In steroids injection, one is to gently pull the plunger of the syringe before injection to confirm that it is possible to insert the needle into the vein. If in the process of gently pulling, found that the needle inhaled red blood, it means that the needle hit the vein, and direct injection will be risky, and needs to replace the needle and the injection site. If no red blood seen during the process of gently pulling, you can continue to complete the injection. For this injection action, different people show different views, let us have a look.
Different views
Some people do not notice this injection technique at all, and indicate that they have been injecting steroids for many years, and have never hit the vein, and do not intend to add the injection action of pulling the plunger of the syringe.
There are people who not previously aware of this injection, were skeptical after being told about it, and indicated that they did not know if they needed to improve their injection techniques.
Some people who know this injection method think it is an outdated method, as long as you make sure to clear the air in the syringe before injection, basically nothing will happen. At the same time, they believe that the probability of hitting the vein and injecting steroids+oil into the vein is very low, even if it accidentally inject, there is no danger except that it will be a little more painful and cause some bruises.
There are also people who are very cautious and think that need to pull the syringe plunger before injection to avoid risk.
Others who have had experiences after injecting into vein feel that the action of pulling the plunger is necessary.
Possible symptoms after inject Steroids into a vein
According to the user himself, if inject steroids into a vein, difficulties in breathing, dizziness and severe cough can occur, and these symptoms can last for ten minutes or even 45 minutes. During this time, people will feel very uncomfortable and cough is very harmful. like you were going to cough your brains out.
Steroids injection: is it necessary to pull the plunger to confirm that it has hit the vein
This is very necessary. Although the chance of hitting the vein is very low, pulling the plunger before the injection will not cause you any ill effects, but it will eliminate the possibility of steroids getting into the vein. Just gently pull the plunger before injection, if inserted into a vein, during the process of pulling, red blood will appear, you will be very easy to observe this phenomenon. Dealing with this problem is also very simple, you only need to change a needle, change the position to complete the injection. This will help you avoid a bad experience.

Compared with directly supplementing HGH to increase HGH levels in the body, people are more inclined to use some compounds to stimulate the natural release of GH, thereby increasing HGH levels. Hexarelin Acetate, Tesamorelin, and Sermorelin acetate are three peptides that are often discussed in the context of growth hormone stimulation. While they share the common goal of promoting HGH release, they differ markedly in their mechanisms of action, clinical applications, and effectiveness.
Hexarelin Acetate: growth hormone releasing peptide
Hexarelin Acetate, a member of the growth hormone-releasing peptide (GHRP) family, is a synthetic peptide used to stimulate growth hormone secretion. It does this by binding to the growth hormone secretagotor receptor (GHS-R1a), which is located on the surface of pituitary cells. Activation of this receptor leads to increased release of growth hormone. Hexarelin is popular for its potential to promote muscle growth, reduce body fat, and improve endurance, making it a top choice for athletes and bodybuilders.
Tesamorelin: Targets abdominal fat
Tesamorelin, unlike Hexarelin, is primarily used for different purposes. It belongs to the GH-releasing hormone (GHRH) category. Hexarelin activates the GHS-R1a receptor and Tesamorelin acts on the GHRH receptor. Tesamorelin is an FDA-approved drug for reducing excess abdominal fat in HIV-infected patients with lipodystrophy. It does not directly stimulate the release of growth hormone, but rather stimulates the body to produce more of its own growth hormone, specifically targeting abdominal fat, which is a common problem in these patients.
Sermorelin acetate: a precursor for the production of growth hormone
Like Tesamorelin, Sermorelin acetate belongs to the GHRH group of peptides. Unlike Hexarelin, which binds directly to the GHS-R1a receptor, Sermorelin acts as a growth hormone secretor, essentially signaling the pituitary gland to produce and release more growth hormone. Sermorelin acetate is commonly used in anti-aging and health clinics to combat the effects of age-related declines in growth hormone. It can help improve muscle mass, reduce body fat, and enhance overall vitality by supporting the body’s natural growth hormone production.
Key difference in clinical application
While these peptides all have the overall goal of stimulating growth hormone, their clinical applications are very different. Hesarellin is favored for its muscle-strengthening properties and performance benefits for athletes. Tesamorelin is used for the specific purpose of reducing abdominal fat in patients with HIV-associated lipodystrophy. Sermorelin , on the other hand, is more commonly used for anti-aging and health purposes, focusing on general GH enhancement for a more youthful and energetic feeling.

Common injection sites for testosterone include Delts, thigh and gluteus. What might be the cause of pain or swelling when inject testosterone in delts?
Normal reaction
Pain or swelling at the injection site is a common occurrence for novice testosterone injections. Most of the time, the reaction after injection is mild, lasting only 1-2 days. Cold compresses can help relieve pain, redness, and swelling.
The normal injection pain response will greatly relieve as you gradually adjust to the corresponding testosterone ester. It is also related to placebo effect and injection technique and proficiency.
Allergy or inflammation
Testosterone injection dissolved in oil, and the user is allergic to the oil used or the corresponding testosterone, and will also experience injection pain or swelling. In this case, you can change the testosterone oil or replace with another testosterone ester (e.g., from test E to test P).
Needle length
The default recommend needle length is not suitable for everyone, and if the needle is too long (such as a 1.5 inch needle), it can cause unnecessary pain if it inserted too deeply during the injection process. Commonly used needles are 1 inch or 1/2 inch.
Underweight
In underweight people, there is little fat or muscle tissue, so a normal needle injected at the delts site can go deep and cause unnecessary pain. For underweight people, when choosing the injection location, they should avoid delts and choose gluteus or thigh.
Musculess
When you have not gained enough muscle, the muscle in the delts position does not show up well, and you choose to inject in the delts position. The needle can mislocate the muscle and inject into other areas, such as fascia, nerves, or blood vessels, causing local irritation, inflammation, or damage that can manifest as pain, swelling, redness, and even infection at the injection site.
For people with too little muscle mass, injection in the delts position is more difficult, and we can choose the gluteus or thigh position, which is relatively easy to inject. Wait until the muscles have grown to a certain extent before choosing the delts position.
Overinjection
When too much oil is injected in one place at a time, there is also a corresponding injection discomfort, including pain and swelling. The dosage of each injection should not exceed 0.5ml.
Testosterone injection is mainly divided into SubQ and IM <>, of which SubQ injection location is shallow, can use a smaller size of the needle, so it is less prone to injection pain and injection into other pain-prone tissues. For beginners, SubQ injections are more convenient.

When you think about using some supplements to help you build muscle, the most common are these three: sarms, peptides and steroids. Of the three, steroids work better, peptides are safer but more expensive, and sarms are a newer supplement with fewer side effects. For those who are new to bodybuilding and want to start a safe cycle with fewer side effects, the sarms MK677 is the first choice for many.
Why choose sarms MK677 as the first sarms cycle?
For beginners who have just learned about bodybuilding, they can’t properly deal with testosterone inhibition and other side effects brought by the steroids cycle. The side effects of sarms, including the inhibition effect, are smaller. Therefore, compared with steroids,sarms is more suitable for beginners.
Fear of injections is one reason people choose sarms instead of peptides. Peptides are expensive and inconvenient to store and transport.
MK677 acts as an sarms, but it acts like a growth hormone agonist, producing the actual growth hormone. Therefore, MK677 plays the role of peptides HGH to a certain extent. HGH is a popular peptide for bodybuilders, but it is expensive, often out of stock and difficult to find. Therefore, MK677 is an alternative to HGH.
MK677 is a ghrelin (GHS) receptor agonist, and its use increases hunger. During the process of building muscle, eating enough calories and protein can help to better participate in the exercise and provide the material foundation for muscle growth. Therefore, using mk677 can help increase muscle mass faster.
Although we classify MK677 as an sarms, it is not a selective androgen receptor agonist, does not bind to androgen receptors, and therefore, does not inhibit its own testosterone secretion at all.
MK677 plays a similar role to HGH, increasing appetite and helping to rapidly gain muscle while not suppressing testosterone at all. Taking the MK677 orally is simple and quick, with few side effects to deal with, making it ideal for novice users.
MK677 cycle and dosage
The MK677 dose is 10-25mg/day. The daily dose is controlled under 25mg, and there are almost no side effects. After the dose exceeds 25mg, fluid retention and headache may occur. In the course of using the MK677, timely supplemental levels help alleviate these side effects.
MK677 does not inhibit its own testosterone secretion, and its cycle length can be appropriately extended. Under normal circumstances, the cycle length of sarms is 6-8 weeks, and the common cycle length of MK677 is 12-16 weeks.
MK677 has the effect of improving sleep quality, and if you choose to use MK677 at night, it will help you sleep. If you are aiming for rapid muscle gain, take MK677 in the morning, as it will increase hunger and allow you to eat more, providing a material basis for muscle growth. Of course, it is also possible to split the daily MK677 dose to provide a more stable HGH level.
After you get used to the MK677 , you can consider stacking it with the sarms, the real sarms + MK677 provides faster muscle gain. But before you fully understand each sarms, it is best not to stack directly, because the side effects of each sarms are not the same, blind stacking, will make you do not know which sarms is working, and do not know how to deal with the corresponding side effects.

Semaglutide is a GLP-1 single receptor agonist, Tirzpatide is a GLP-1 and GIP double receptor agonist, and Retatrutide is a GLP-1, GIP and GCG triple receptor agonist. From their mode of action, we would think that there is a progressive relationship between them. If there is a progressive relationship between modes of action, does that mean there is also a progressive relationship between their effectiveness? So, if we are using the triple receptor agonist Retatrutide , is it necessary to stack Semaglutide or Tirzpatide?
In the use of weight loss peptides, many people are stacking these three peptides, and it has been shown that the effect is better after stacking. If Retatrutide is already the best of the three of them, is it necessary to stack it with weight loss peptides that are not as good as it?
Recently, the idea that Retatrutide doesn’t need stacking has gained a lot of support, and the reasons are summarized below.
Do not understand the mode of action of Retatrutide
Retatrutide not simply synthesize to stimulate GLP-1, GIP and GCG receptors, respectively. Reta design to lose weight in a way that is exactly eight times as effective as naturally occurring GIP (Tirzpatide is twice as effective as naturally occurring GIP), while having less effect on GLP-1 receptors than Tirzpatide. Both Semaglutide and Tirzpatide work by getting you to eat less and weigh less. It’s different with Reta, where you can eat normally and then lose weight normally and get better results than with Sema and Tirz. Retatrutide is a non-equilibrium triple receptor agonist by design. Other companies designed balanced triple receptor agonists to lose weight, but eventually stopped the trials. The action of balanced triple receptor agonists is similar to the pattern of stack, so the failure of these drugs illustrates that the effect of simple stack is not obvious.
The idea of controlling calorie intake
People experienced significant appetite suppression when using Semaglutide and Tirzpatide. Controlling calorie intake is the basic operation of weight loss. When you use Retatrutide and you can eat again, you worry about eating too much to lose weight, and you want to control your appetite with Sema or Tirz. Reta actually loses weight by converting fat into glucose, the part of fat that provides the body with energy and can fight hunger, but only if you reach the optimal dose of Reta. The optimal dose of Reta is 9mg, which needs to titrat gradually from 2mg to 9mg over a period of 4 months. Some people expect to see the weight loss effects of Reta soon and therefore do not give Retatrutide enough time to reach the optimal dose.
In pursuit of rapid weight loss
For the above reasons, the best weight loss from Retatrutide comes after 4 months, and people want to stack up when they haven’t seen significant results after 3 months of using Reta. During these months, you may eat more than you do on Sema and Tirz and worry that excessive calorie intake will lead to weight gain, and stack Sema or Tirz can solve this problem. Therefore, make many people will stack.
This part of the theory supports the idea that Retatrutide doesn’t need a stack. What do you think? Do you stack Retatrutide with Semaglutide or Tirzpetide?

Experienced sarms users are no longer satisfied with the sarms solo cycle, but explore the sarms stack which can increase muscle to a greater extent. Here’s a sarms stack Rad140 +MK677 +YK11 +Enclo for your information.
Rad140
In this stack, RAD140 is a true Sarm, targeting muscle mass by binding to androgen receptors in skeletal muscle. RAD140 also encourages the body to burn fat, thereby gaining lean muscle.
MK677
MK677 is a ghrelin (GHS) receptor agonist and a growth hormone secretagogue, similar to a growth hormone agonist, that activates the hypothalamic pituitary gland to produce actual growth hormone, which improves metabolic activity, builds muscle mass, controls hunger levels, and lowers cholesterol levels, among other things.
in addition to having an anabolic effect, in this stack, MK677 helps provide appetite during the cycle, enabling the user to consume enough nutrients to provide a material base for muscle growth.
YK11
Yk11 is a selective androgen receptor modulator (sarms), but it is also a myostatin inhibitor. As a myostatin inhibitor, YK11 unlocks myostatin and promotes greater muscle growth. For people with genetic traits that have a low potential to gain muscle mass, yk11 help to break down genetic barriers and promote muscle growth.
In this stack, the YK11’s special mode of action helps users gain muscle mass quickly, even though the sarms RAD140 has put on enough muscle.
Enclo
Enclo stands for Enclomifene citrate, a non-steroidal SERM(Selective estrogen receptor modulator). By antagonizing the estrogen receptor in the pituitary gland, it reduces the negative feedback effect of estrogen on HPGA(hypothalamic-pituitary-gonad axis), thereby increasing the release of LH(luteinizing hormone) and FSH(Follicle-stimulating hormone) and promoting the production of testosterone.
Rad140+MK677+YK11+Enclo
In this stack, RAD140 has a small inhibitory effect, but yk11 has the structure of steroids, which has a large inhibitory effect on endogenous testosterone secretion. Use enclo in cycle helps to maintain testosterone levels during the cycle and avoid low testosterone.
In the sarms stack, the principle of using only one real sarm is generally followed. in this stack, it looks like two sarms are used, the RAD140 And the YK11. In fact, yk11 is not exactly the same mode of action as SArms for structural reasons. So RAD140+YK11 is also a common stack.
Rad140+MK677+YK11+Enclo is for bulking, not cutting. Because Cutting needs to control caloric intake, the increase in appetite provided by MK677 makes it difficult to control calories, and Yk11 also helps to rapidly expand muscles. Use this stack build muscle, need to deal with testosterone suppression issues, blood pressure issues, and add liver protection as appropriate.

Androgenic alopecia is a topic of increasing concern. Does the use of exogenous testosterone to boost overall testosterone levels cause androgenic alopecia hair loss?
I did a little poll on that question. Of the 351 male testosterone users, 43 experienced hair loss after using testosterone, and 351 reported no hair loss after using testosterone for more than a year, and some even had thicker hair after using extrinsic testosterone. The proportion of participants with and without hair loss is shown in the figure below.
Relationship between exogenous testosterone and hair loss
The reason why it is believed that exogenous testosterone causes hair loss is because the higher the level of testosterone, the more DHT will be converted, and thus the androgenetic alopecia. This is indeed the theoretical cause of baldness.
People who use exogenous testosterone instead of other steroids usually do so for the purpose of testosterone replacement therapy (TRT). Therefore, the dose of testosterone used is relatively low, about 200-300mg/wee, and the maximum will not exceed 500mg/week. This dose is used to make up for testosterone levels that decline with age or that are low due to hypogonadism. The purpose of using testosterone in these people is to raise the overall testosterone level to the normal level, or at the position of the normal testosterone level. If testosterone did not affect his hair when he was young and his testosterone level was the highest in his life, chances are that it will not affect his hair after increasing his testosterone level.
People with a family history of hair loss are more likely to lose hair. Therefore, if your hair is more sensitive to DHT, you belong to the population prone to hair loss. Before you use testosterone, your testosterone level may not be enough to convert enough DHT to cause hair loss, and when you use exogenous testosterone to convert more DHT, it may cause hair loss.
Why do I not lose hair after using exogenous testosterone?
First of all, genetics plays a big part, and if your genetics are good, you’ll always be able to keep your hair easily.
Estrogen levels have a lot to do with hair health. Elevated levels of testosterone, in turn, lead to elevated levels of estrogen. Proper estrogen contributes to the health of hair and makes hair grow better. But too much estrogen can cause more side effects in men. Testosterone users will use aromatase inhibitors (AI) to lower estrogen levels. If estrogen is reduced to too low a level, it can make hair quality worse and may lead to hair loss.
In addition, stress and emotional problems can also cause hair loss. After the male testosterone level increases, it will enhance self-confidence and improve physical health to a certain extent. Therefore, if you are not prone to hair loss, hair quality can be improved.
For the vast majority of people who use exogenous testosterone, it is done thoughtfully. They no longer want to experience the side effects of low testosterone levels, compared to which hair is less important. They are willing to give up some others for something more important.
It can also be seen from the vote that the proportion of people who lose their hair because of testosterone is about 12%, and most people are well adjusted to testosterone.
You don’t have to give up your hair. Androgenic alopecia is due to DHT. Reducing the production of DHT while using testosterone can prevent hair loss. Of course, if you are prone to hair loss, hair loss should be prevented in time. Finasteride and Minoxidil are widely used to prevent hair loss.

When Bodybuilders used testosterone esters to build muscle, they found that long ester Test Cypionate had more sexual side effects than short ester Test propionate , and these side effects mainly showed inhibition of HPTA(natural testosterone levels) and low libido.
The use of exogenous tests can suppress natural testosterone production, but exogenous tests can replace some of the effects of testosterone. Therefore, most of the time, if use an exogenous Test, rather than other forms of androgen, such as Nandrolone and Drostanolone, you will not feel significant symptoms of low testosterone. Extensive user data has shown that people who use test long ester are more likely to experience side effects in terms of sexual function. The possible reasons are as follows:
Shorter esters are closer to natural testosterone
The half-life of naturally secreted testosterone is very short, and the half-life of testosterone after the addition of ester can reach as long as 15 days. Test Propionate half-life is about 4 days, test cypionate half-life is about 12 days.
Bodybuilders use long esters to pursue long-term stable testosterone levels because stable testosterone levels help users better engage in bodybuilding, which benefits muscle mass and strength growth. However, maintaining high testosterone levels in the body will continue to inhibit HPTA and affect HPTA’s response to the hormone.
Most hormones in the body are produced intermittently, including testosterone. Natural testosterone levels in the body are different from time to time, with distinct peaks and troughs. Over-stable testosterone levels are contrary to the naturally secreted testosterone levels and are not conducive to maintaining the function of HPTA.
Advantages of long esters
One reason people don’t like the short ester is that it requires frequent injections and is more cumbersome. In fact, unless it’s TRT, bodybuilders actually never wait a week to Test Cypionate with a second injection. They will choose M/W/F, EOD, or even ED for better results. In fact, short esters, in addition to benefiting HPTA, also help control side effects, including estrogen side effects. So frequent injections aren’t a problem for bodybuilders.
People prefer long esters because of the stable testosterone levels they provide. When using test short ester at a low testosterone level, users who have been at a high testosterone level suddenly drop in testosterone levels, just like people who have been excited for a long time suddenly quiet down, will be a little tired and lost. But why not take a good rest at this time and give your body a time to recover. It is impossible to stay in a high phase without rest, and HPTA is the same.
conclusion
Having said all this, I’m not telling you to switch to test short ester. Long esters (such as Test Cypionate) do provide stable testosterone levels, and long-term stable testosterone levels help build muscle quickly, so if on test long esters, there is no low libido, no high estrogen, etc., you are well adapted and it is suitable for you. If you are experiencing these side effects, consider a short ester, such as Test propionate.

Semaglutide , a peptide drug approved by the FDA to treat type 2 diabetes and obesity, achieves weight loss by acting on GLP-1 receptors to control appetite. In short, Semaglutide allows you to reduce your food intake without feeling hungry, thus promoting weight loss. If you do not feel appetite suppression after using Semaglutide, you are still gaining weight, what is the reason?
First, Semaglutide doesn’t work for everyone. If you have been using Semaglutide for a long time and the dosage has been increased to the highest level and still has no effect, then there is no need to continue using Semaglutide. If you’ve just started using Semaglutide and haven’t seen results yet, that’s our topic for today.
Many people start Semaglutide treatment after hearing about the weight loss results of Semaglutide from various sources. Once you don’t see results in time, you start to wonder if Semaglutide is useful.
Related to the dose of Semaglutide
The therapeutic dose of Semaglutide is 1.7-2.4mg per week. To reduce side effects and allow the body to adjust to the drug, it is usually titrated from a low dose to a therapeutic dose. In the process of titration, it takes several months to experience, so during this time, the effect of the drug is not obvious.
Some people start with 0.5mg, continue for four weeks, then increase to 0.75mg, and then to 1mg. Others start at 0.25mg, increase to 0.5mg after a month, and then need to increase to 0.75mg after four weeks on 0.5mg, and then 1mg. However, when he was still at 0.5mg and did not see appetite suppression and weight loss, he became suspicious of the effects of Semaglutide.
In fact, when the user is still at 0.5mg, this dose has not reached the therapeutic dose, so the suppression of appetite may not be significant. If you still maintain your previous eating habits and caloric intake, you will gain weight in the past, but now even on Semaglutide, the caloric surplus will still cause weight gain.
Therefore, on Semaglutide, it is necessary to remain patient and wait for the actual dose to reach the therapeutic dose.
Individual related
The actual effect of Semalutide varies from individual to individual, which is also the reason why some people cannot achieve weight loss by using Semaglutide. Some people feel the effects and start to lose weight when they start using Semaglutide, while others need to reach a therapeutic dose to lose weight. Our bodies are complex, and many drugs take time to show their effects.
If you have increased your dose to a therapeutic dose and are still not losing weight, it is time to consider whether Semaglutide will work for you.
Develop good eating habits in semaglutide for weight loss
Many people who are severely obese are unable to control their desire to eat. Semaglutide makes it easier for users to fill up and lose the desire to overeat, thereby starving them to their target weight. This also shows that the basic weight loss is to reduce the intake of calories.
The common thinking of Semaglutide users is: because I can’t control my desire to eat more, use semaglutide to help control the appetite, and if the appetite is not best controlled on Semaglutide, then Semaglutide is not working well.
While using Semaglutide, we can rely on it to some extent to control our food intake, but it is still important to develop healthy eating habits. If you stop using Semaglutide after you have successfully lost your goal weight, it is still possible to regain the weight if you still eat excessive calories and do not exercise. Good eating habits can help you keep the weight off without gaining it back after you’ve lost it.
Therefore, in the process of losing weight, you should be patient and pay attention to the cultivation of habits.

YK11?is a compound with the characteristics of both sarms and steroids, Some people think it is better to stack use, others think it is better to use alone. What is the situation?
Effect of YK11
YK11 is a myostatin inhibitor that breaks down genetic restrictions on the body and allows people who cannot grow muscle to achieve muscle growth. So, it’s effective for people with genetic traits that have low potential to gain muscle mass. Because some people are naturally high in myostatin, it can be difficult to gain muscle mass. YK11 acts as an inhibitor of myostatin, and even if bodybuilder does not have the right genetic structure, it can grow muscle and improve muscle performance with the help of YK11.
At the same time, it is an androgen receptor modulator that binds to AR in skeletal muscle through the same mode of action as sarms to achieve the purpose of muscle growth.
Therefore, the muscle-building effect of sarms YK11 is not weaker than that of testosterone, and at the same time, as sarms, it has less inhibitory effect on the body than AAS. If yk11 is used alone, there is great muscle mass gain.
YK11 stack
Because yk11 has the structure of steroids, its suppression is much higher than some other sarms. In order to avoid the possible effects of a decrease in naturally secreted testosterone levels due to suppression during yk11 use, some bodybuilders prefer to add testosterone to the yk11 cycle. This is equivalent to using the YK11 stack.
One reason bodybuilders choose sarms is that they have less suppression of natural testosterone levels and thus fewer side effects. If the use of yk11 also requires stack testosterone, it further suppresses natural testosterone levels. If you forgo yk11 in favor of rad140 or lgd4033 cycle, you can also gain a significant amount of muscle mass with less inhibition. Therefore, many people will choose the safer sarms cycle instead of the yk11 cycle.
And yk11’s muscle-beneficial effects have attracted more bodybuilders to use it, even when stacked with testosterone. Because YK11’s mode of action is not exactly the same as sarms, it is also a partial agonist of the androgen receptor and can be stacked with other sarms for better effects. Both yk11 cycle and yk11 stack cycle ultimately require PCT to restore testosterone levels, so using yk11 stack cycle is more cost-effective.
Although yk11 has a large suppression effect, it still has fewer side effects than steroids. It is androgenic, but does not cause problems like prostate problems and androgenic alopecia like testosterone does.

Forums are full of people discussing the side effects of testosterone <astersteroids.com/steroids-pow… injections, why are so many people still using testosterone, and are they worth it?
Why do so many people discuss the side effects of testosterone injections on forums? This is because so many people are getting testosterone injections. Except for those who are well tolerated, have no side effects, or have all side effects resolved by the doctor, the base of people who come to the forum because the problem is not resolved is still that large. The fact that more and more people are talking about it indicates that the range of testosterone users is expanding.
We can see that in the process of using testosterone, many people talk about having to check their blood pressure regularly, quit smoking, control drinking, adhere to injections (may be lifelong injections, but also need to spend more money), and even need to take some additional drugs, such as liver protection, anti-estrogen and so on. That sounds like a complicated thing to do. Are the benefits of using testosterone worth all the things we do?
Except for the few who quit because of problems they couldn’t solve, most of them are sticking with it. So, the results are clear: worth it, especially for those with low testosterone levels.
When you are too tired to function every afternoon; When you want to participate in some outdoor activities, but are discouraged halfway up the mountain; When you lose muscle mass with age and your belly gets bigger… These little problems can knock your confidence and affect the quality of your life. However, problems such as fatigue, decreased self-confidence, decreased libido, muscle loss, and osteoporosis can all be solved by testosterone.
Will there are side effects of using testosterone?
Of course there will be. But every side effect has a solution, you just need to check regularly and follow your doctor’s advice.
Afraid of injections? Oral testosterone has even been developed to solve the injection problem. Worried about pain from intramuscular injections? Subcutaneous injections have also been found to be a good solution.
Long-term testosterone injections cost money? Compared to the libido, muscle mass, less effort, better fitness results, more extroversion, more confidence, more energy, spontaneous erections on demand, etc., increased testosterone levels are worth the cost (money). At the same time, isn’t making money for a better life?
Of course, before deciding to use testosterone, you should do a blood test, fully listen to the doctor’s advice, and do not start blindly, lest you will end more blindly.

For bodybuilders, we’ve talked a lot about how to boost your testosterone levels, such as exercising, Enclomiphene, or extrinsic testosterone. In talking about these topics, we are assuming that you are building muscle for the purpose of bodybuilder, today we are talking about normal conditions to increase testosterone levels.
Testosterone levels are important for bodybuilders, and equally important for every man. Testosterone makes men men. When we say someone has higher testosterone than others, it’s like saying they’re more masculine than others. How to increase testosterone levels is crucial for every man.
Maintain a healthy lifestyle
A healthy lifestyle helps boost testosterone levels. This includes eating a healthy diet, maintaining a balanced diet with protein and minerals and healthy fats, and eating less processed foods. In addition to eating a healthy diet, avoid smoking and excessive alcohol consumption, which would lower testosterone levels and also carry a number of health risks.
Maintain a healthy weight
Obese men have low testosterone levels that have been proven by studies, while overly thin men seem to have low testosterone levels. Therefore, maintaining a healthy weight will make you look like you have higher testosterone levels, which is actually the case. Regular exercise helps maintain healthy weight gain and increases testosterone levels. Getting enough sleep and managing your own stress can also help boost your testosterone levels and lead to a healthier body.
Avoid exposure to chemicals
With the development of agriculture and industry, the number of people with infertility and infertility is increasing, which is link to some chemicals present in pesticides and personal care products, which can interfere with hormone balance and affect male testosterone levels and fertility.
Consider natural supplements
Proper supplementation of vitamin D and zinc both help with testosterone production, but medical advice should be followed and may have the opposite effect if taken in excess.
Consider TRT
If your testosterone level is already very low and is beginning to affect your normal life, and natural ways have not been able to increase testosterone levels, you can consider TRT(testosterone replacement therapy).TRT is the use of external testosterone? <astersteroids.com/testosterone… replace the role of your own testosterone, so as to treat the problem of insufficient endogenous testosterone levels.

In the use of bodybuilding supplements, the most direct impact on the body is the inhibition of their own testosterone level, is there a growth of muscle mass without affecting their own testosterone levels of supplements?
AAS
AAS is an exogenous androgen. The use of exogenous androgen in the bodybuilding cycle will definitely affect the secretion of testosterone. During this process, the level of testosterone in the body may still in homeostasis, but this balance is not controll by HPTA(hypothalamic-pituitary-testicular axis), but the secretion of endogenous testosterone gradually decreases, and AAS supplements this part of testosterone and balances the levels of testosterone in the body at a higher level.
Sarms
SARMs are not androgens, and the use of sarms in the bodybuilding cycle theoretically does not affect endogenous testosterone levels. However, this is not the case. sarms work by binding to androgen receptors, and by taking up a portion of the androgen receptors, the body produces an extra portion of testosterone. The brain detects that there is more testosterone secreted and reduces testosterone production. Therefore, if you use sarms, you will still reduce some of your own testosterone levels.
How can I maintain a stable testosterone level while using AAS and sarms
Since both AAS and SARMS use reduce endogenous testosterone levels, is it possible to maintain normal testosterone levels in the process? It is possible to use these supplements to stack testosterone to replenish the testosterone that less produced. But in doing so, it still suppress the testosterone level.
So bodybuilders began experimenting with the use of gonadotropins in the cycle, which unblocks the inhibition of HPTA by high testosterone levels so that testosterone is release continuously . Enclomiphene is commonly to maintain the level of endogenous testosterone.
Are there supplements that don’t affect testosterone level at all?
In addition to natural additives and strengthening exercises, only a few that are classified as sarms are other receptor agonists (which do not act on androgen receptors) that do not affect testosterone levels. gw501516 <astersteroids.com/safe-shippin… for example, helps build muscle by regulating metabolism to boost energy levels and endurance. However, these supplements are not as effective as sarms and AAS in building muscle.

Testosterone and AAS injections are intramuscular injection (IM) and subcutaneous injection (SubQ), which of these two injection methods is better?
IM vs SubQ basic info.
§ IM refers to the injection of AAS into the muscle and SubQ refers to the injection of AAS into the subcutaneous tissue.
§ IM injection is shallow and SubQ injection is deeper. As a result, IM injections requires longer needles.
§ IM inject at a 90-degree Angle, while SubQ inject at a 45-90 degree Angle.
§ The injection site of IM is mainly Thigh(Quads), Delts, Hip and Gluteus. SubQ inject in areas with fatty tissue, such as the abdomen and upper buttocks.
Advantages and disadvantages of IM
Because there are larger and more blood vessels in the muscle than in the subcutaneous tissue, AAS absorb faster when injected into the muscle. Therefore, AAS injection by IM can take effect quickly, and the maximum efficacy peak appears earlier and the peak value is higher. Because of the rapid absorption rate using IM injections, the peak of serum testosterone levels after IM injection of AAS is more predictable. Therefore, after IM injection, it is easier for individuals to determine the time when their own serum testosterone level will peak, and thus easier to control the peak testosterone level.
The disadvantages of IM are also obvious, that is, because the injection is deeper, it is more likely to cause pain, and because there are more blood vessels in the muscle, inexperienced users may stick the needle into the blood vessel.
Due to the depth of IM injection, the subcutaneous tissue and fat are thicker for overweight or obese users, and SubQ may actually do when doing IM, which they may not know.
Advantages and disadvantages of SubQ
Some injection sites suitable for IM are not convenient for personal injection, SubQ injection into the subcutaneous tissue, which is easier to operate. SubQ inject in a shallow location and with a smaller needle size, which is less likely to cause injection pain or problems with blood vessels.
In terms of drug absorption, SubQ is injected under the skin and into the fat, and absorption is slower, so the time to reach the peak concentration of the drug is slower. However,SubQ provides more stable testosterone levels than IM.
For bodybuilders, the goal of injecting AAS is not just to stabilize testosterone levels, but for more muscle mass and strength. The user would think that injecting AAS into the muscle would preferentially bind to the androgen receptors in the muscle, thus achieving the purpose of muscle building.
During the use of AAS, the main source of estrogen is the aromatization of testosterone. In general, there are more aromatases in fat, so user thinks that if AAS is injected into fat, more of it will be aromatized into estrogen.
Natural testosterone production fluctuates, with different testosterone levels at different times of the day. The main difference in the effects of IM and SubQ is that one provides a higher testosterone peak and one provides a more stable testosterone level. You can choose the injection method according to your own purpose.

Weight-loss drugs have a plateau, after which further weight loss is slowed or stopped. What should I do when semaglutide weight loss plateau appears ?
Semaglutide plateau
Semaglutide weight loss As with other weight loss methods, the body will eventually stabilize at an appropriate weight, which may or may not be the user’s goal weight. If you want to continue to lose weight after reaching the weight loss plateau of the drug, or to avoid weight regain, you need to take the drug for life.
Semaglutide is an FDA-approved weight loss drug. It mimics a naturally occurring hormone that provides the brain with a sense of fullness, slows digestion, and allows food already consumed to leave the body more slowly, successfully helping many obese people lose significant amounts of weight. However, after the weight reaches a certain point, the rate of weight loss slows down until it stops.
Semaglutide plateaus after about 60 weeks of continuous use. At this point, the user has usually lost a significant amount of weight and is gradually approaching a healthy weight, and the body is more inclined to retain calories to protect itself.
At the beginning of weight loss, when you reduce your energy intake, your body will meet its energy needs from other sources such as glycogen (including breaking down fat), which will lead to weight loss. Over time, as the weight lost gradually increases, the body compensates by slowing down the metabolism. When your metabolism is equal to the amount of energy you take in from food, you’ve hit a plateau. This is the genetic protection of the body, which also leads to the cessation of weight loss.
How to solve the semaglutide plateau
If you need to cross the plateau and start losing weight again, you need to change the body’s energy balance again. This can be done by changing your diet or increasing physical activity.
Another way to change the plateau is to increase the dose of the drug. The dose of Semaglutide is 1mg to 2.4mg per week, with gradual increases from the lowest dose to the highest dose. However, after reach the maximum dose, we can’t increase the dose, otherwise it will bring more side effects. So increasing the dose of the drug is limite.
The slimming peptide Tirzpatide <> and Retatrutide <astersteroids.com/triple-recep… developed successively also indirectly solved the problem of plateau of Semaglutide <astersteroids.com/type-2-diabe… Semaglutide is a single receptor agonist of GLP-1, Tirzepatide is a double receptor agonist of GIP and GLP-1. Retatrutide is a triple receptor agonist for GIP, GLP-1 and GCG. Thus, there is equivalent to a progressive relationship between the three drugs, and after reaching a plateau with single-receptor agonists, dual-receptor agonists would work.
However, in the actual process of weight loss, if not only rely on weight loss drugs, but can cooperate with physical activities, it will be more healthy weight loss. After reaching the plateau, actively participate in physical activities, even if the weight is no longer loss, but the body composition is changing. Your body will be more symmetrical, your posture will become better, and your health will be greatly improve.

SRAMS, as selective androgen receptor modulators, are less androgenic and, therefore, bring fewer androgenic side effects to bodybuilders’ bodies, whereas the effects of sarms on the liver are universal. Before starting a sarm cycle <>, you should prepare liver support in advance to avoid damage to the liver. Common liver support is NAC, Milk thistle And TUDCA, let’s take a look.
NAC(N-Acetyl Cysteine)
NAC, or (N-Acetyl Cysteine), convert to the antioxidant glutathione in the liver and is an FDA-approved prescription drug.
Intravenous NAC can reduce kidney and liver damage caused by acetaminophen overdose.
Due to its antioxidant and anti-inflammatory properties, NAC helps detoxify and detoxify, preventing and reducing the effects of medications or heavy metals that may affect kidney and liver health, among others.
NAC can also improve liver function in patients with nonalcoholic fatty liver disease.
Long-term or high dose use of SARMS such as rad140, lgd-4033, etc. will affect the health of the liver. In the sarms cycle, a lot of liver support can protect the liver and prevent liver damage.
NAC is orally, and when use NAC to protect the liver, the usual dose is 600-1200mg per day.
Milk thistle
Milk thistle is a plant that has the effect of clearing heat and dampness and soothing liver and gallbladder, and has been used in clinical studies to treat liver diseases and cancer.
As a plant extract, Milk thistle is also safe for long-term consumption. When people have to take drugs to treat diseases, in order to prevent damage to the liver from the drugs, Milk thistle is a plant-based dietary supplement to protect liver health.
When bodybuilders use Milk thistle as liver support, the oral dose is 140-420mg per day.
TUDCA (Tauroursodeoxycholic acid)
TUDCA, full name tauroursodeoxycholic acid, is a naturally occurring hydrophilic bile acid that counteracts the toxicity of conventional bile acids and also protects and repairs the liver.
Bile acids are the most functional component of bile, aiding digestion and absorption, breaking down food and cholesterol, and eliminating harmful pathogens from food that enter the digestive system. When the liver and gallbladder overburdene, bile production becomes difficult, then need TUDCA. TUDCA also use for liver damage and cholestasis occurs.
For bodybuilders, when the sarms used affect liver health, TUDCA can alleviate and treat these effects. TUDCA is available in oral doses ranging from 250 to 1500mg.
Sum up
The liver has the ability to repair itself, and in general, using sarms at low doses does not have a significant effect on the liver. However, sarms users say that using it can help reduce problems that may occur when running a sarms cycle, compared to not using liver support.
From the above description, we know that NAC and Milk thistle have the effect of early prevention in the sarms cycle. TUDCA, on the other hand, is usually not use in the low-dose sarms cycle. TUDCA should only be used in cases where it is very powerful and has a significant effect on the liver.

For bodybuilders, a high or low level of testosterone is closely related to gaining and maintaining muscle mass and strength, and we generally think that the higher the level of testosterone, the easier it is to build muscle, so what is the maximum level of testosterone our body can effectively use?
Testosterone levels in relation to muscle mass and strength
The older you get, the more difficult it is to build muscle and maintain the muscle mass you’ve gained, mainly because testosterone levels in adult men decline with age. Similarly, men’s strength levels and bone health tend to decline as they age.
It is clear that low levels of testosterone are not conducive to building and maintaining muscle mass and strength, and are not conducive to the health of bones.
500mg/week testosterone dose could raise testosterone to what level?
Normal testosterone levels range from about 10-30 nmol/L, and under special circumstances, some people’s normal testosterone levels will exceed 30 nmol/L. So, with greater testosterone levels, can our bodies use them effectively?
The study showed that on day 14 after the first 500 mg (15.02±0.76 nmol/L) Test T, the participants’ testosterone levels increased by 360%, that is, about 54.07nmol/L (1557ng/dL), which is well above the maximum value of the testosterone range.
500mg/week is the dosage for novice bodybuiders and 1000mg/week for experienced bodybuilders. There is no experimental data on 1000mg/week doses, but if inject 1000mg of testosterone weekly, The maximum testosterone level in the blood is much higher than 1500ng/dL.
Is it necessary to use higher testosterone doses?
Bodybuilders use exogenous testosterone to build muscle by putting their bodies through tough workouts, they work very hard to make these testosterone would be use in building muscle mass and increase strength, Not to make yourself angry, aggressive, or more self-centered. However, they are still not immune to the side effects of high doses of testosterone, so the corresponding side effects need to be addressed in cycle and PCT.
So, if you do not have a reasonable plan, blindly increase their serum testosterone levels, perhaps the final result will not be as you want.

For many people, 300ng/dL is a very low testosterone level. If the testosterone level is this value, there may be certain symptoms of low testosterone. However, normal testosterone levels range from 264 to 916ng/dL, indicating that 300ng/dL is a normal value. Why is there such a wide range of testosterone levels?
This is because men’s testosterone <> levels are constantly changing throughout their lives, and this change generally follows the same rule, that is, “with the growth of age, and year by year.” The age of 20 is about the highest level of testosterone in a man’s life, and after that, testosterone levels will decline every year.
Does anyone’s testosterone level rise from year to year?
It is true that there are people whose testosterone level rise with age without the use of exogenous testosterone and other drugs that promote testosterone production. Here is a case study of a 40-year-old man with a blood test result of total T=1082 and Free T=10. According to him, he did not use exogenous testosterone, nor did he use other drugs that would promote testosterone production.
The hypothalamic-pituitary-testicular axis (HPTA) controls the secretion of testosterone. When the body’s testosterone levels are low, HPTA activates positive feedback to start promoting testosterone secretion. When the body’s testosterone level reaches the maximum threshold, HPTA initiates a negative feedback that begins to inhibit the secretion of testosterone, so that the testosterone level is in dynamic equilibrium.
The normal testosterone level is between 264 and 916ng/dL, the maximum 916 is about the testosterone level of a man when he is 20 years old, and the minimum 264 is the testosterone level of an elderly man. What happens if a man reaches the age of 40 and finds that his testosterone level exceeds 1,000 ng/dL? Of course, at first you might be happy, like you’re 20 again. Then, you might worry, is there something wrong?
What’s the problem?
When the testosterone level exceeds the maximum of this age, the first thing to consider is whether there is a problem with HPTA, at this time, the pituitary gland is usually checked, whether the pituitary tumor affects the function of HPTA.
If the test is completed and no physical problems are found, it is also possible to have a testosterone level of 1000ng/dL at the age of 40, and it is said that some young men in the Colombian army test for testosterone levels as high as 1500 ng/dL, which may be related to genetics.
Are there other factors that cause testosterone levels to rise? It is said that this man measured his testosterone level above 1000 after he lost weight. Do you know how much weight he lost? Two hundred pounds. And he’s still on a diet.
Some experiments have shown that fasting increases testosterone levels. At the same time, he has lost a lot a weight and is a new him now. People who are overweight have lower testosterone levels than people of normal size. If a person is severely overweight at a young age, then his testosterone levels are low, and when he loses weight and keeps building muscle, more muscle requires more testosterone levels to maintain, then his testosterone levels will be much higher than if he is obese. At the same time, if he is still on a diet, testosterone levels do rise naturally.
Of course, if there is a sudden natural increase in testosterone levels, it is necessary to seek medical attention in time to rule out the factors of disease.

Normal testosterone levels are between 264 and 916ng/dL, while some men with high testosterone level around 1000ng/dL still have low testosterone symptoms, including severe fatigue, slow recovery from exercise, libido problems, mild ED, depression, anxiety, and even reduced erections in the morning. Today we talk about possible causes.
Production and form of testosterone
The hypothalamic-pituitary-testicular axis (HPTA) controls the release of testosterone. After testis release the testosterone , this part of testosterone does not enter the blood circulation directly, but part of it bind to SHBG (sex hormone binding globulin), part of it bind to albumin, and only a small part (about 2%) unbind and can bind freely to androgen receptors. To make a difference. Therefore, this part of the unbound state of testosterone is Free T. The higher the level of Free T, the more benefits of high testosterone levels.
In addition to Free T, a portion of testosterone binds to albumin. Albumin is a carrier protein that has a low binding force with testosterone and can easily separate from the bind testosterone. This testosterone, which binds to albumin, arrive various parts of the body in the blood circulation. And then when testosterone separate from albumin, it also acts as testosterone.
The part of testosterone that binds to SHBG is difficult to separate from SHBG because it has a high affinity with SHBG. Therefore, this part of testosterone is equivalent to being wasted, unable to produce corresponding effects.
Conclusion
So, Free T is the most potent testosterone, followed by albumin bound testosterone, and finally SHBG bound testosterone. When we take a blood test, the total testosterone measured includes the part of the testosterone that is bound to SHBG, so when the total testosterone level is high, it does not mean that the body has a high level of available testosterone.
When you have a high testosterone level and, at the same time, a high SHBG level, then you are still likely to have low testosterone symptoms.
Boron helps reduce SHBG levels. There is also Proviron <>, a weak anabolic steroid that preferentially binds to SHBG, increasing the level of free testosterone and improving the utilization of testosterone and other AAS.

GHRH (growth hormone releasing hormone) based on the development of growth hormone secretadotropin, because it is a synthetic form of GHRH or a cut from the amino acid sequence of GHRH, and has a similar role to GHRH in promoting HGH secretion. Hexarelin Acetate , on the other hand, has a different structure than GHRH, but is rather similar to GHRP-6, mimicking the effects of Ghrelin by acting as a Ghrelin receptor agonist. So, what is the relationship between Hexarelin Acetate and Ghrelin, and how do they increase HGH levels?
Hexarelin Acetate: a synthetic peptide
Hexarelin Acetate is a synthetic peptide derived from the growth hormone releasing peptide (GHRP) family. It was originally developed to stimulate the release of growth hormone and promote growth in laboratory animals. The main mechanism of action of Hexarelin involves binding to the auxin receptor, the growth hormone secretagotor (GHS-R1a). By activating this receptor, Hexarelin effectively stimulates the pituitary gland to release more growth hormone into the blood.
Ghrelin: The natural hunger hormone
Ghrelin is a natural peptide hormone that plays an important role in regulating hunger and appetite. It is produced mainly in the stomach and is released when the stomach is empty, signaling the brain to eat. Ghrelin also binds to the GHS-R1a receptor, much like Hexarelin, but its main function is to stimulate the release of growth hormone during fasting or calorie restriction.
Hexarelin Acetate and Ghrelin: growth hormone stimulation
Both Hexarelin Acetate and ghrelin have the unique ability to stimulate the release of growth hormone in the body. This common mechanism of action makes them valuable tools in the fields of research, medicine and exercise science. Increased levels of growth hormone can have a range of benefits, including promoting muscle growth, reducing fat, improving energy, and potentially anti-aging effects.
Key differences between Hexarelin Acetate and Ghrelin: natural and synthetic
The most significant difference between Hexarelin and Ghrelin is their origin. Ghrelin is a naturally occurring hormone, while Hexarelin is a peptide synthesized in the lab. The main role of Ghrelin is to regulate hunger and appetite, while Hexarelin is specifically designed to stimulate GH release. Although the two compounds activate the same GHS-R1a receptor, their effects differ due to the synthetic nature of Hexarelin.

The main advantage of Sarms compared with AAS is that androgen side effects are less. PCT is required for every AAS cycle (except TRT). Does the sarms cycle need PCT?
It depends on the type of SARMs
A major problem that PCT addresses is the suppression of endogenous testosterone, so One criterion for determining whether a PCT is required for One sarms cycle is whether the sarms inhibit endogenous testosterone secretion.
Endogenous testosterone secretion is suppressed because the compounds used replace the role of testosterone in the body, fooling the body into thinking that sufficient levels of testosterone have been secreted, thereby reducing endogenous testosterone levels to maintain the total testosterone level in the body within the normal range. Therefore, whether an sarms needs PCT depends on whether it will replace the role of endogenous testosterone.
sarms are selective androgen receptor modulators, which act by binding with androgen receptors in skeletal muscle. Therefore, sarms will replace the role of endogenous testosterone (androgen), so that more self-secreted testosterone can be left, thus achieving the result of testosterone inhibition. Therefore, the sarms cycle requires PCT.
However, there is also a subset of receptor agonists, which are classified as sarms but do not actually work by binding to androgen receptors. mk677, for example, is a ghrelin receptor agonist and a growth hormone secretagogue that mimics the growth hormone (GH) stimulating effects of the endogenous hormone ghrelin. For example, GW501516 is a PPARδ receptor agonist that provides energy to the body by regulating lipid and protein metabolism, thereby greatly increasing endurance levels.
This type of sarms does not require PCT. Therefore, before using sarms, it is necessary to understand what kind of receptor modulator it belongs to in order to have the corresponding use.
Depending on the dose of SARMs used
When the sarms you use are true sarms (i.e., selective androgen receptor modulators), in principle, they inhibit endogenous testosterone secretion, so they need PCTS. But the advantage of sarms is that it is more secure. When you use it at low doses, it doesn't cause excessive side effects, including testosterone suppression. For example, lgd4033, studies have shown that when the daily dose is not more than 5mg, basically zero side effects, and the dose is 5-10mg, side effects are also very small. When the dose exceeds 10mg, the corresponding PCT should be selected according to the actual situation.
To sum up, do I need PCT after SARMs cycle? It depends on which sarm you're using, with what doses, and the cycle length, if there is any side effects.

If we do have a certain disease, and the doctor prescribes the corresponding drug and tells us that this drug will have multiple side effects such as this and that, we will still take that drug. And when there is a healthy person, going to try a drug, we’re going to pay more attention to the side effects of the drug, and in the meantime, we’re going to think over and over again, do I want to use it?
People had the same idea before they tried steroids or sarms, not sure if they were going to start using them. At this point, many people will tentatively think, I try to do one cycle, and then stop. I will do the PCT correctly, get the body indicators back to normal, and then the muscle mass retained during this cycle (maybe 10 pounds, more or less) will be enough to achieve my goal.
Is this feasible? Of course you can. The use of steroids or sarms is a bodybuilding cycle, then follow by a PCT, and we can start the second cycle after the body indicators return to normal. If you finish the first cycle, it’s perfectly possible to stop and not go to the next cycle.
However, can you really stop after one steroids /sarms cycle?
Unless your experience in the first cycle is so bad that you jump out of the cycle without lasting even one cycle, you won’t hesitate to stop.
Suppose you get 10 pounds of muscle mass after the first steroids cycle, and you feel a lot of energy, a lot of power gains, a lot of confidence in the cycle, or you get the best performance ever on sports. After the cycle, you run the PCT cycle correctly, and all the side effects are eliminated and your testosterone <astersteroids.com/steroids-pow… levels are restored.
Then, you stop and don’t do the next cycle. It’s doable. You may be able to hold yourself together for a few months during this period and not start a second cycle. But when everything settles down, you’ll be in the same state as you were before you started the first cycle. You can’t help but think, if you don’t use steroids, you’re not going to be able to get any further than you are now, and what’s more interesting to you is that the last cycle was so good, you want to run another cycle.
Whether it’s improving your appearance or increasing your confidence, it makes you a better version of yourself. This kind of improvement is addictive, and it’s hard to suppress your thoughts. A lot of people with a trial mindset will go through one cycle and then go through the second cycle and then the third cycle, and that’s probably why steroids are so widely used.
So, it’s possible to just run one steroids/sarms cycle. The premise is that you need to find the right supplements for your use, develop the right cycle, deal with possible side effects, and have a correct pct. Otherwise, you may not last a cycle.

In the process of using AAS or sarms, you can choose to use different AAS or choose one from a number of sarms, but you can hardly avoid SERM clomiphene or enclomiphene. men with low testosterone levels also use Clomid or enclo to boost their testosterone levels. In the course of the use of various drugs, there may be some side effects, but most of the side effects are reversible. Because clomiphene has a possible (rare) irreversible ocular side effect, those who know it will choose it carefully. If you were told that enclomiphene has the same benefits as clomiphene, but without the ocular side effects, would you choose enclomiphen over Clomiphene ? So when it comes to the ocular sides, what does clomiphene vs enclomiphene actually look like?
Clomiphene Ocular sides
Studies have shown that it is possible to have ocular sides when use clomid, such as blurry vision. Although this side effect is very rare, once it develops it is permanent.
Enclomiphene Ocular sides
A large proportion of the population claims that enclo has no ocular sides. If you still have ocular sides after using an enclo, you’re not getting enclo, you’re getting clomid. It is possible that someone might sell clomid as enclo. But the assumption is that enclomiphene does not introduce ocular sides, otherwise, whether you use clomid or enclo, ocular sides are likely to appear.
There’s not a lot of data on Enclo, and there’s no evidence that it causes eye problems. However, users reported that they had eye problems when using clomiphene, and enclomiphene continued to have eye problems after they changed to Enclomiphene following the advice. If it uses real enclomiphene, enclomiphene will also cause ocular sides.
Why Clomiphene vs Enclomiphene cause Ocular sides
There are many theories as to why clomiphene and Enclomidphene may cause eye problems, and since there is no official explanation, here is only an explanation.
Some explain this phenomenon from the way clomid and enclo function. They inhibit the negative feedback of HPTA by blocking the action of estrogen in the brain, thereby maintaining the release of testosterone. So they also blocks estrogen receptors in the eye, causing ocular sides.
Some explain this phenomenon in terms of the biological characteristics of clomid and enclo. Most SERMs, including clomid and enclo, are inhibitors of the enzyme DCHR24, whose role is to convert desmosterol into cholesterol. The first drug used to lower cholesterol was Triparanol, which worked by inhibiting DCHR24, but with serious adverse effects, including irreversible vision loss. Similarly, clomid/enclo inhibits the action of the DCHR24 enzyme, preventing desmosterol convert into cholesterol, which accumulates in the eye and causes ocular sides.
Clomiphene vs Enclomiphene. clomid is composed of enclomiphene and Zuclomiphene. As an inhibitor of DCHR245, enclo has about 10 times the potency of zuclo. At the same time, the structure of enclo is more similar to Triparanol. Therefore, enclo may have fewer side effects than clomid, but enclo is no less effective than clomid on the Ocular sides.
Clomiphene vs Enclomiphene Ocular sides review
Based on the above information, both Clomiphene and Enclomiphene may cause Ocular sides, but the probability of irreversible ocular side effects is very low. And the appearance of this side effect is also related to the individual, some people are easy to appear, and some people basically do not appear. Some have shown continuous use of clomid for 15 years without ocular sides. Some people have mild eye discomfort, such as floaters, light sensitivity, etc., and will recover on their own after stopping the drug.
Many side effects are related to the time of use and the dose of use. In the process of using clomid and enclo, controlling the dose can reduce the probability of side effects. If you do need to use clomid or enclo, don’t be afraid to use it; the probability of Ocular sides appearing is very low. PDE5 inhibitors like Sildenafil or tadalafil also have known eye side effects, but they are widely used.

Some sarms, such as gw501516 and sr9009, we believe do not inhibit endogenous testosterone secretion and therefore do not need to use SERM clomiphene or enclomiphene. Other sarms, such as mk2866 and rad 140, mimic the mode of action of testosterone and inhibit endogenous testosterone production, requiring the use of SERM. Regarding when to use SERM, is it at the beginning of the cycle, in the middle of the cycle, near the end of the cycle junction, or after the cycle (PCT)? Different people have different opinions, and we have summarized these opinions.
We have talked a lot about the use of SERM after cycle (PCT), and if SERM is used during the period, sarms users prefer to use enclomiphene rather than clomiphene. In fact, in pct, they also use enclo. Today, we will not talk about the difference between enclo and clomid, but about which phase in the cycle they use serm.
Use SERM enclomiphene on the first day
A large percentage of bodybuilders prefer to use a SERM enclo on the first day of the cycle. They believe that sarms (mentioned here are inhibitory Sarms such as rad140, not non-inhibitory Sarms such as gw501516) mimic the action of testosterone, and it will start to exert inhibitory effects from the moment it enters the body, so you need to use serm enclo to maintain your endogenous testosterone secretion levels.
In terms of inhibition, the idea is correct. Doing so keeps endogenous testosterone levels uninhibited and at normal levels.
Start using serm enclomiphene in the second week of the cycle
Bodybuilders, who hold this view, believe that with stronger sarms like RAD140, which have a very high inhibitory effect, there is a possibility of more severe testosterone inhibition or shutdown in the fourth week of the cycle, so it is necessary to start enclo earlier, preferably no later than the second week of the cycle.
Many people agree with this view, because for safety reasons, no one wants to have their testosterone levels severely suppressed or shut down. There is a dosing issue involved, rad140 is given in doses of 10-30mg ED. Low doses of rad140 can be effective, and rad140 is used at low doses without severe testosterone suppression.
The serm enclo starts on the fourth week of the cycle
Some sarms start in the fourth week, with noticeable changes in muscle mass to strength levels, which is when hormone levels in the body are thought to be highest, after which total testosterone levels begin to decline (inhibition begins to show). At this time, SERM enclo is used to block the negative feedback effect of estrogen on HPTA, ensure the continuous release of testosterone, maintain testicular function, and maintain the testosterone level after the cycle.
Use a SERM enclo after the end of the cycle (PCT)
Post-cycle therapy (PCT) is the official procedure for the sarms or AAS cycle. Compared with AAS, SARMs is safer and has fewer side effects, and basically does not have serious inhibitory effects when used in prescribed doses and prescribed cycles. Even in AAS cycles where inhibition is more severe, users tend to focus on getting gains in the cycle while addressing inhibition in the PCT. Because of the continued use of exogenous aas or sarms, the inhibitory effect will remain. This is equivalent to solving the problem while still suppressing it. Therefore, the inhibition effect brought by sarms can be solved in time after the cycle (pct), and it should be done.
Enclo maintains the release of testosterone by blocking the effect of estrogen on HPTA, except in the treatment of hypogonadism, in people with normal gonadism, it is usually used at a low dose, EOD or E3D frequency, equivalent to intermittent use to stimulate HPTA without the need for long-term high dose use.
The use of enclo during the cycle blocks the brain's response to estrogen, and even if excess estrogen is produced in the body, it will not be reflected through the body and will affect the accuracy of judging estrogen levels (reflected in bloodwork).
Why do many people use enclo at the beginning of a cycle, or during a cycle? This may be dose-related. They may have experienced side effects from high doses of the drug, so they prevent them in advance. Each sarms has its guiding dosage, the right dose to keep itself safe, rather than focusing on prevention.

Estrogen in men is produced by the action of aromatase on testosterone, and this part of estrogen plays a key role in male health. When male bodybuilders take AAS, testosterone levels rise rapidly in the body, and estrogen levels rise accordingly. High estrogen levels can have a range of effects on male bodybuilders, including bone health, moodiness, gyno, and more. How to solve the problems caused by high estrogen levels that may occur during AAS use?
Use AI(Aromatase inhibitors)
Where does estrogen come from in men? Because aromatase converts testosterone into estrogen. We couldn't try to lower testosterone levels, so we targeted aromatase. Both AI letrozol and arimidex bind to estrogens converted by aromatase, so that this part of the estrogen cannot bind to the corresponding estrogen receptors, thus reducing the effect of estrogen. The effect of AI ememestan/Aromasin is more direct, it directly kills aromatase, so that testosterone can not be converted into estrogen.
How these three AI are selected is related to the estrogen levels of the bodybuilders, but also to the corresponding estrogen symptoms. Used only to prevent high estrogen levels or early estrogen symptoms, Arimidex is usually used at 0.5mg per week or every 3.5 days. aromasin needs attention because it kills aromatase, the body needs time to produce new aromatase, in the process, there may be low estrogen symptoms. Letrozole reduces estrogen levels by 98%, so it is not often used in the AAS cycle, but in PCT or for the treatment of gyno.
Use AAS that do not convert to estrogen
AAS can be divided into two main categories, testosterone and DHT. Testosterone is converted to estrogen, whereas DHT is not. So using DHT-type AAS can avoid the side effects of estrogen. Testosterone AAS include testosterone, trenbolone, nandrolone, boldenone, dianabol. DHT AAS include Masteron, primobolan, anavar, winstrol, anadrol, proviron, superdrol. Some bodybuilders are better tolerant to estrogen, and some bodybuilders are more sensitive to estrogen and are prone to high estrogen symptoms. Therefore, it is possible to choose whether to use testosterone aas or DHT AAS based on this category. This is not to say that DHT-like AAS are better, DHT does not have estrogenic side effects, but there are androgenic side effects that belong to it.
Within these AAS, there are also special presence that give bodybuilders more options. Testosterone use aromatizes the production of estrogen, so estrogen side effects need to be dealt with. However, if masteron is combined with testosterone, there is no need to worry about estrogen side effects. Because masteron itself does not aromatize into estrogen, it also has anti-estrogen effects, and when it is used with testosterone, it enhances the effects of testosterone and avoids high estrogen side effects.

In the use of AAS, how to deal with estrogen is a compulsory course. When it comes to estrogen side effects, the first symptom that usually comes to mind is gyno. In fact, gyno is a late symptom of elevated estrogen levels. Before gyno appears, there are many symptoms that remind you that estrogen levels have been elevated and you need to start dealing with estrogen side effects.
When these symptoms occur, it is time to start dealing with estrogen side effects.
Sensitive nips
Gyno symptoms do not appear suddenly. Some people worry too much about gyno symptoms and start dealing with estrogen early, a condition that has the potential to drop estrogen levels too low, and low estrogen levels can have corresponding symptoms and affect their health. When you use AAS in the process, there are sensitive nips, nips itching or hardening, indicating that estrogen levels is too high, at this time to deal with estrogen, will not develop to gyno.
Sleeping trouble
Sleep trouble is a common symptom of high estrogen and includes frequent waking during the night, insomnia, hot flashes, cold sweats and other symptoms. These symptoms are a warning to keep an eye on your estrogen levels.
Soft or No morning wood
High levels of estrogen can affect your sex drive, and low levels of estrogen can also give you low libido, even if you have high testosterone levels. So when you suddenly don't feel so good, it may be because you've messed up your hormone levels.
Acne
Too many androgens can cause acne, as can high levels of estrogen. Estrogen acne is the cystic kind that is huge and can't pop usually.
Face bloating and Body bloat
Bloating face is also called Moon face, you may have a round, swollen face, which is the effect of high estrogen. High estrogen levels are reflected in the body, which can make the whole person look very bloated. When you use AI(aromatase inhibitors - anti-estrogen), you will find that you are thinner because the water weight is gone.
Emotional
If you are Easy getting weepy during pharmaceutical commercials or rom-coms, that's not a good thing. For an AAS user, this means your estrogen levels are too high, and it makes you are easily emotional.
Anxiety is a form of emotional anxiety, a hormone that controls a person's mood and behavior. When you experience an emotion that is not normal for you, you need to consider what external factors are causing the result. One manifestation of high estrogen levels is anxiety.
If you are becoming paranoid for no reason while using AAS, it may not be a mental problem, but an emotional one.
Brain fog
Brain fog often manifests itself in mental exhaustion and an inability to concentrate. brain fog can be caused by a variety of factors, but both low and high estrogen levels can lead to confusion and some brain fog symptoms.
When bodybuilders start to experience one or more of these symptoms while using AAS, you need to be concerned about your estrogen levels and start dealing with it before it leads to more serious consequences. Options to deal with high estrogen levels are AI(aromatase inhibitors), including letrozol, arimidex and exemestan. Which of these three is the best? -Here

The three most commonly used AI are letrozol, arimidex and exemestan, which AI should I choose when I want to block the effects of estrogen.
Which one lowers more estrogen
If the purpose is to block the effect of estrogen, then which AI can reduce the level of estrogen to a greater extent, then it is better, right?
Let's look at how these three AI reduce estrogen levels. Studies have shown that Letrozol can reduce estrogen levels by 98 percent. arimidex can reduce estrogen levels by 50-60%, a percentage that accumulates if used consistently. Exemestan can reduce estrogen levels by 58±21%.
From the above data, letrozol is the more effective one. So letrozol was the first choice of the three AI, right? The answer is not so. Let's keep looking down.
Different object
Although all are used to reduce estrogen levels, the three AI's target objects are different. The target of letrozol and arimidex is the estrogens transformed by aromatase, while the target of exemestan is aromatase and all estrogens attached to aromatase.
Aromatase converts testosterone into estrogen, and excess estrogen accumulation produces corresponding estrogen side effects. Letrozol and arimidex do not act on the aromatase and bind to the estrogen converted by the aromatase, so that this part of the estrogen cannot work. Exemestan differs from them in that it directly interacts with aromatase, killing the aromatase as well as the estrogens attached to the aromatase.
Their different ways of acting make them a clear difference after use: at the end of the cycle, AI stops using, and the estrogen accumulated during this period is suddenly released, estrogen levels surge, and high estrogen symptoms are more likely to occur. Unlike using exemestan, which kills the aromatase, even after stopping using exemestan at the end of the cycle, it takes some time for the body to recover the original aromatase levels, so your estrogen levels will always be low.
From this perspective, it is clearly better for exemestan to lower estrogen levels. So, should you choose exemestan? Let's keep looking down.
Role of estrogen
Is lower estrogen the better? Not really. Estrogen levels have an impact on libido, mood, skin quality, hair, nails, bone health and more. Low estrogen levels can lead to stiff joints, loss of sex drive, drowsiness and more. So it's not about lowering estrogen levels as low as possible.
So, of the three AI's, the one most commonly used to reduce estrogen levels during the cycle is arimidex, especially for novices. For the experienced, of course, there are other options, such as exemestan. Although it kills aromatase, it lowers estrogen levels by 58±21% and also increases total and free testosterone levels, making it a good option for bodybuilders to gain muscle mass if they can control the dose and frequency of exemestan use. Since letrozol reduces estrogen levels by 98% and is really very effective, it is not usually used for cycle, but to reverse gyno symptoms that have already occurred.

Most AAS are used injectable, and there are many sites available for injection, which are the specific ones, which is our topic today.
The usual injection sites
The commonly used AAS injection sites are Thigh(quads),Delts,hip and gluteus. These location targets are larger, large muscles are usually found in these areas, and if people choose these locations to inject, it will be easier to find a place. At the same time, because these areas usually have more muscle and less adipose tissue, when AAS is injected, it is easier to inject into the muscle than into the fat. There are more aromatase in fat than in muscle, so injecting in these locations will correspondingly reduce the probability of contact with the aromatase. And, bodybuilders use AAS with the goal of increasing muscle mass, injecting it into the corresponding muscles to help build muscle mass more targeted.
Thigh(Quads)
This is the one in the thigh, located between the lateral and rectus femoris muscles, making up the so-called muscular quadriceps (quads). This is the easiest place to inject when self-injecting and is therefore the most commonly used injection location.
Delts
The injection site is on the upper arm, under the shoulder. To find this injection site, you need to find the bone at the top of your arm where it meets your shoulder and inject it about 2 inches below that point. Note that the injection is in the center of the muscle where the thickest muscle is. This injection position is more difficult than the previous site, and you may need help.
Hip
Also known as the ventrogluteal muscle, it is located near the buttocks. It is a large muscle, relatively easy to find, and it is far away from vulnerable nerves, such as the sciatic nerve. More suitable for injection. However, because it is on the back of the person, it is not easy for individuals to find the location when injecting.
Gluteus
Also known as the dorsogluteal muscle, it is a large muscle located in the buttocks and is one of the largest muscles in the body. Therefore, although it is located on the back of the body, it is very easy to find and very popular with injectors. But with intramuscular injections, this position is risky. Because there are major blood vessels and nerves, including the sciatic nerve.
The best place to inject
Of these four injection sites, which is the most common used?
From the perspective of safety and convenience, the best injection location should be thigh(quads). In fact, people choose all these four injection sites. Gluteus may seem like a dangerous place to inject, but in fact, gluteus has a very large number of people who choose to inject AAS. Especially in the AAS injection process, which requires frequent changes of injection locations, Gluteus is really a big target.
No matter which location you choose to inject, at the beginning, you will experience a certain degree of muscle pain, this is a normal phenomenon, usually disappear within a few days, choose the right size of the needle, do not worry too much. However, always be careful to avoid nerves and blood vessels.

Handling estrogen is an essential lesson in the use of AAS. Gyno is the result of the accumulation of excess estrogen. What should I do if I have gyno symptoms? In the treatment of gyno, there are three processes, namely gyno prevention, gyno flare-up and gyno reversal. These three cases are described in detail below.
Gyno prophylaxis
Gyno formation is due to the accumulation of estrogen, so preventing estrogen levels in advance and preventing them from rising above normal levels can prevent gyno formation.
During the use of AAS, the source of estrogen in the body is mostly androgens. The key factor that converts androgens into estrogen is aromatase. Aromatase works by aromatizing testosterone molecules and converting them into estrogen. Therefore, the key to preventing gyno is estrogen and aromatase.
By controlling the conversion of testosterone to estrogen by aromatase, you can block the production of estrogen, thereby avoiding the occurrence of estrogen beyond normal levels and producing gyno symptoms. This is how Exemestan(Aromasin) works. Aromasin directly destroys the aromatase and kills the estrogen attached to the aromatase, avoiding the production of estrogen at the root.
Another way to prevent the effect of estrogen is to occupy the estrogen receptors in the body, so that the estrogen produced by the body cannot bind to the estrogen receptors, thus blocking the effect of estrogen. This is how Arimidex and Letrozol work.
Gyno flare-up
If AAS used in the cycle will produce a large amount of estrogen, and it is not well prevented in advance, resulting in long-term estrogen control, and the initial symptoms of gyno such as nipple swelling, pain or itching begin to appear, it is the gyno flare-up stage. This indicates that you are not using enough anti-estrogen (AI) dose and need to increase the dose of AI. SERM is also added as a treatment.
Serms (selective estrogen receptor modulators) also bind to estrogen receptors to block the effect of estrogen and avoid the occurrence of gyno. They are mostly used in PCTS. Common SERMs are Tamoxifen(Nolvadex), Reloxifene and Clomiphene.
Because AI Arimidex affects the use of Arimidex when used with SERM Nolvadex, Reloxifene can replace Nolvadex when AI is used with SERM.
Gyno Reversal
The Gyno reversal stage means that gyno symptoms have developed, and at this stage, surgery is usually required. If your gyno development comes from the use of AAS, SERM can also be used therapeutically in most cases. When SERM is used to treat gyno reversal, Tamoxifen is not usually suitable, tamoxifen is usually used for PCT, not gyno flare-up or gyno reversal. SERM reloxifene is often used to treat gyno reversal, along with the addition of Cabergoline.

No matter what age you are, once you talk about weight loss, there is always a lot of resonance, especially among women. Here are some weight loss tips for your information if you are interested in it.
Make a weight loss plan
After making up your mind to lose weight, just relying on the consciousness to keep telling yourself to eat less, to eat healthy things, or to exercise more, and in actual life, can not pay action, or occasionally act once, is basically not practical significance. In the long run, it will also bring psychological suggestions to yourself: Clearly already paying attention, why did you not lose weight? Create anxiety for yourself. Only reasonable planning and strict implementation can produce practical significance.
Make your own weight loss plan, such as how many calories you eat each day and how much exercise you do. Buy a weight scale and a scale in grams to measure the food intake. Make a small chart of the number of calories you eat each time, and you will know how many calories you can eat for the rest of the day to reach your goal. If you end up eating fewer calories than you planned, that’s a good thing. For exercise, you don’t need to do much exercise if your goal is just to lose weight and not gain muscle. Proper exercise can keep you healthy during weight loss, walking is the easiest exercise, in fact, if you stick to walking 30-45 minutes a day, also help to lose weight.
Choose the right foods
Eat more foods rich in protein and fiber, fruits, vegetables, protein and fat are all good foods, eating these can be a good aid to weight loss. Try to eat staples like chicken and roasted vegetables, salmon + broccoli, lentil soup, etc. When the main food has fed your stomach, you will not be so easily attracted to snacks. Snacks are more about texture, and more often than not, they can be delicious and cause you to consume too many calories without realizing it.
No liquid calories. It can make you drink too many calories without even realizing it.
Sauces are needless calories. sauces like ketchup.
You can replace butter or oil in cakes and cookies with can pumpkin
Don’t be anxiety
In fact, believe it or not, being in a good mood also contributes to weight loss. When you’re stressed out, your body is more likely to store fat. Also, stressful situations can make you crave high-fat foods. Some strategies to reduce stress include getting enough sleep, exercising moderately, being in nature, and doing things you enjoy.
Sleep is also a tips to weight loss. Maintaining normal sleep duration and sleep quality will reduce the body’s production of hunger hormones. Ghrelin can make you hungry for simple carbohydrates and junk food, or keep you awake at night. So, getting more sleep can also help you lose weight.

The appeal of Anabolic steroids to bodybuilders is hard to resist. It brings tremendous muscle mass and strength gains, accelerates the process of bodybuilding, and breaks through the limitations of the body, which is difficult to achieve by relying on exercise alone. If I want to start an anabolic steroid cycle, how do I do it safely and effectively?
Have a blood test before start
Before starting the anabolic steroid cycle, having a blood test will help you understand your physical condition, including testosterone levels, estrogen levels, liver health, etc. It is helpful to choose the appropriate type and cycle of anabolic steroid, and also provides a reference standard for the recovery of endogenous testosterone level after the cycle.
Prepare your gears
There are many Anabolic steroids, but not all of them are suitable for beginners, and it is important to choose the right Anabolic steroid that suits you. Most male bodybuilders start with testosterone (Test, Test C, Test P, Test E, etc.). Because testosterone is a natural hormone in the body, it can be used for both bulking and cutting. Female bodybuilders basically start with Anavar because it has less androgenic action and is less masculine compared to other AAS.
We can see that experienced bodybuilders often use more than one AAS in their cycle, and they stack different aas based on different goals. For people who are new to steroids, they should start with an anabolic steroid.
Develop a training plan accordingly
The effects of Anabolic steorid in bodybuilding are difficult to achieve with exercise alone, but if you rely on anabolic steorid alone, without a targeted training plan and implementation, you will still be difficult to gain significant muscle mass or strength. Steroids along with hard work to get there.
Diet is important
Clean eating is an important lesson in bodybuilding. Calorie intake is also important for bodybuilders, not just for dieters. Too many calories will turn into fat instead of muscle, and too few calories will not be enough to support the energy needed to participate in exercise. At the same time, muscle synthesis requires a large amount of protein/amino acids. Consuming high-quality protein, vitamins, minerals, and maintaining a clean diet are equally important for bodybuilding.
Handle possible side effects
During the use of anabolic steroid, some side effects related to androgens may occur, including acne, hair loss, low libido, high libido,gyno(estrogen side effects), edema, liver toxicity and other effects. Knowing the possible side effects of each anabolic steroid in advance will help prevent them in advance and effectively avoid side effects.
PCT
PCT(post-cycle therapy) is an important part of anabolic steroid cycle. No matter which anabolic steroid is used, it belongs to exogenous androgens, and long-term use can inhibit the production of endogenous testosterone. The role of PCT is to help restore the secretion of endogenous testosterone, freeing bodybuilders from dependence on exogenous androgens and restoring the function of their own gonadal axis. If the corresponding estrogen side effects have not been dealt with properly in anabolic steroid, the PCT is an opportunity to remedy them.

Rather than directly using exogenous testosterone replacement therapy (TRT), some men diagnosed with low testosterone levels prefer to try Enclomiphene to help promote the production of endogenous testosterone, thereby increasing their testosterone levels. Compared to TRT, enclomiphene <astersteroids.com/enclomifene-… brings low libido side effects, so some men have to give up using it.
How does Enclomiphene increase endogenous testosterone levels
Enclomiphene is a selective estrogen receptor modulator, acting in the same way as Clomiphene. By antagonizing the effect of estrogen in the pituitary gland, Enclomiphene makes HPTA (hypothalamic-pituitary-testicular axis) continue to act positively and stimulate the production of testosterone by testis, thereby increasing the level of autocrine testosterone.
Enclomiphene cause low libido
A 40-year-old man who normally felt fine had no obvious symptoms of low testosterone. Influenced by his friend, he also went to test his own testosterone levels, which showed that his Total T was 380 ng/dl and his Free T is 7.3 ng/dl. Tests showed he had low testosterone and he was given 12.5mg of Enclomiphene a day. A month later, his total T had risen to 798ng/dl and his Free T had also increased to 16.4 ng/dl.
Enclomiphene doubled his testosterone levels, however, in addition to the benefits of high testosterone levels, his libido was greatly suppressed.
Another 50-year-old male user takes Enclo at a dose of 25mg three times a week to treat low testosterone levels. Enclo does help raise testosterone levels, but sex drive is rarely experienced while Enclo is being used, and can return when the drug is discontinued.
Another man who used 9.37mg of Enclo a day to treat low testosterone levels also experienced low libido (but still can get hard).
Why does Enclomiphene inhibit libido compared to Clomid?
Clomid is equivalent to 38% Zuclomifene (estrogen receptor agonist) and 62% enclomifene (estrogen receptor antagonist). Therefore, Enclomiphene is used to reduce the side effects of estrogen. There are many factors that affect libido, and estrogen levels happen to be one of them.
Enclomiphene dosage
The usual Enclomiphene dose is 12.5mg or 25mg per day. However, the recommended dose for most people who have used Enclo is 6.25mg ED. enclomiphene, at a low dose, maintains the function of estrogen without affecting libido. If the libido problem does not improve, the dose may be changed to EOD, or E3D.

For dieters, calorie control is the easiest and most direct way. However, after you gradually reduce your calorie intake, the feeling of hunger caused by an empty stomach can be unbearable. At this time, you will want to eat something to relieve that uncomfortable feeling, is there zero calorie food to eat ?
What is zero calorie food?
Zero calories is just a concept, there is no such thing as zero calorie food. If the calorie content of a food is low enough, the user believes that the calories they consume in the process of eating the food, chewing and digestion, etc. will offset the calories of the food itself, or consume more calories than the calories of the food itself. Therefore, it is called zero calorie food or negative calorie food. We don't know exactly how many calories we burn in our chewing and digestion processes, so it's actually impossible to determine whether the calories in the food we eat will be offset or not. In general, foods with fewer than 5 calories are defined as zero-calorie foods.
Are there recommended zero calorie foods?
Based on the above definition, people have found some foods with lower calories to be used as leisure time snacks or fat reduction meals to help control weight or lose weight.
Apple
Apples are a must-have fruit for dieters. Its high water content and dietary fiber help to produce a feeling of fullness. Dietary fiber can also help slow down digestion and keep you feeling full for longer.
broccoli
Broccoli is low in calories and carbohydrates, while rich in essential vitamins, minerals and dietary fiber, and is recognized as one of the zero calorie foods. Boiling is the best recipe for cooking, if you add oil or other high-calorie ingredients, it is no longer a low-calorie food.
celery
Celery is low in calories and carbohydrates, and its high water and fiber content helps you feel full. Celery juice is also a common way to eat celery.
cucumber
The calorie of cucumber is very low, the taste is very good, and the way to eat is various, which is loved by people who lose weight.
Black coffee
A cup of about 237g black coffee contains about 2.4 calories, it does not contain milk, cream or sugar and other added ingredients, ideal for weight loss people.
popcorn
Plain or just salted popcorn is also a low-calorie food that tastes good and provides a good sense of fullness. It can be used as a small snack to ease hunger.
Zero-calorie foods help dieters create a calorie deficit to control their weight. At the same time, it increases the sense of fullness, which can alleviate the negative emotional impact of hunger caused by the dieters in the process of controlling diet, and help users lose weight better. Even in the process of losing weight with peptides, you need to control your diet, and these zero-calorie foods can help you control your calorie intake.
In the process of using zero-calorie food, we should pay attention to the balance of nutrition and supplement the body's necessary proteins, fats, vitamins and minerals, so as to avoid malnutrition and affect health.

As one of the latest weight loss peptides, Retatrutide's triple receptor activation has attracted the attention of many Semaglutide users and Tirzpatide users. At the same time, like Semaglutide, it acts on GLP-1 receptors, and like Tirzpatide, it acts on GLP-1 receptors and GIP receptors. As a result, users tend to experience fewer side effects when they switch to Retatrutide, which leads to more people starting to use Retatutide to lose weight. However, many people find that Retatrutide does not seem to work after switching to it, what is the reason for this and what should be done?
Real Retatrutide
First of all, you need to make sure that what you buy is real Retatrutide. As a new product, Retatrutide has a large audience. Some suppliers may not be in stock and sell other weight loss peptides as Retatrutide for money. This is not just a hypothetical question, several people who have bought Reta from us have reported having been cheated before. Astersteroids sells real Retatrutide with 100% guaranteed quality.
There are also people who buy Reta, it is the real Reta, but after using it, you can not see the obvious effect. It was later found that the purity of the product was not enough, it contained Reta, and also contained other things. Astersteroids sells Retatrutide with a guarantee of quality and purity.
Dose accumulation
Secondly, the use of Reta has a cumulative process in the body and does not work as soon as it enters the body. Some users didn't feel the effects until two weeks later, and others didn't feel the effects until three weeks later. A GLP-1 dose accumulation formula has also been developed to calculate the accumulation of drugs in the body, and interested users can try it.
The effectiveness of Retatrutide is also related to its half-life. The half-life of Reta is about 6 days, and we usually choose to inject it once a week. In order to achieve better results, user will divide the weekly dose into two injections. This method increases the frequency of use, but in principle it will obtain a more stable Reta concentration to achieve a better useful effect.
Individual constitution
Finally, the actual use effect is related to the individual physique. Semaglutide and Tirzpatide have helped many people lose weight successfully, however, some people report no results after using them, which is individual. In fact, no one has reported that Retatrutide has no effect on them at all.
To sum up, if you find that your weight loss peptide Retatrutide has no effect after use, you first need to rule out whether you have got real Reta, after making sure that you are using real Reta, you need to be patient and wait for it to work, basically Reta can help everyone lose weight.

When testosterone or testosterone esters are used, the frequency of injection is usually related to their half-life. If the corresponding ester has a shorter half-life, the injection frequency will be higher. If it corresponds to a long ester, the corresponding injection frequency is lower. Some people pursue daily injections in the belief that they can achieve more stable testosterone levels. Is it necessary?
Relationship between half-life and injection frequency
The half-life is the time it takes for the concentration of testosterone or testosterone ester to drop to half of the initial dose after it enters the body. A half-life is usually when the concentration of drugs in the body is at its highest. Therefore, in order to maintain the maximum concentration of testosterone in the body, the next injection of quasi-testosterone is usually started at the time of the first half-life to maintain the stability of testosterone levels in the body.
It is important for bodybuilders to strictly adhere to the half-life injection. Stable testosterone levels help bodybuilders stay active and have enough energy to engage in exercise. For TRT, because the body's testosterone levels fluctuate greatly, from 300 to 1000ng/dL is a large range, therefore, once a week or once every two weeks injection can maintain basic testosterone levels.
Does the frequency of injection affect the effectiveness of use?
For TRT, many people say that if they get an injection every two weeks, they may feel more tired during the last part of the second week. When changed to weekly injections, it can be a good relief from fatigue. People with TRT need continuous injections over a long period of time, so they are not inclined to increase the frequency of injections because that would bring more work.
For bodybuilders, they rarely choose to give a second dose a few days after the half-life has passed, so if they follow the half-life to determine the frequency of injection, there is little impact on the effectiveness of use. For a while, testosterone users pursued higher injection frequency, believing that it would lead to better results. If their weekly dose is 600mg, they can inject 600mg once a week, or they can be divided into two weekly injections of 300mg, or they can be divided into three weekly injections of 200mg, and some people pursue daily injections, thinking that they can get more stable testosterone levels. Is it necessary?
A frequency of injections based on the half-life gives you a relatively stable testosterone level. Some people think that daily injections can better simulate the level of natural testosterone, which is actually more equivalent to a psychological comfort. We're already using exogenous testosterone, which is testosterone with esters, which is inherently different from endogenous testosterone. Excessive frequency has no additional benefit other than to find yourself more things to do.
Of course, things are not absolute, some people who are sensitive to testosterone respond that if they inject once a week, testosterone levels fluctuate more and estrogen levels spike, never bringing serious estrogen side effects, if they divide the weekly dose into once a day, there will be no estrogen side effects, and there is no need to take AI.
However, this is a rare phenomenon, Bodybuilders who use testosterone. The most common frequency of use is three times a week (Monday, Wednesday, Friday) and two times a week. They say the once-a-day injection makes no difference other than the need to use more pins and prick yourself more times.

Testosterone is the basis of all anabolic steroids. When bodybuilders start the steroids cycle, testosterone is usually the first thing they consider, which can help build muscle quickly and reduce fat, improving boybuilders' exercise ability. When bodyuilders use testosterone to build muslce, what are the other effects? Let's take a look at what testosterone users have to say.
Relieve social anxiety and increase self-confidence
“My anxiety has reduced a ton in social situations. I’m able to relax and completely unaware of how people perceive me anymore. My partner was like...when did you turn into such a chill cool guy?”
“Same here I went from extremely mentally unstable and even suicidal to MUCH happier, more confident, higher energy within just a couple months.”
Hair loss may occur, but body hair may increase
“I thought ‘I’m hairy as is. It can’t get much worse’. It got worse.”
“I had to trim my thigh hair with clippers.”
Hot flash
“Menopause lol. Hot flashes aren’t fun but it’s temporary”
“My endocrinologist told me this was a symptom actually haha, but it isn’t permanent. She told me that it usually comes back when you go off of Testosterone though. ”
Increase libido
“Libido, went from getting off 1-2 times a week to 1-2 times a day.”
Muffled voice
“With the singing, it took me 6-7 months to really start singing again because my voice was changing too rapidly to sing without sounding horrible. As it’s settled I’ve found I don’t have the same tone and stuff as I did before, but almost like a completely new voice. Just give it some more time.”
Sweat easily
“No more hot showers, less resistance to hot weather and sweating all over my body when i’m exerting myself was a surprise to me.”
Muscles get stiff if you don't exercise
“It will make you bulk up muscles even if you don’t work out, but you need to stretch like you are going to exercise every day otherwise you can get stiff and uncomfortable.”
“Stretching is super important. I had been wondering for a while why I was always so stiff and then I read a post here about someone experiencing stiffness on Testosterone, it all made sense.”
Increased appetite
“You will want to eat the entire house lol.”
“The fridge tempts me in ways I never experienced before. And I have no idea whether to listen to the urge to eat everything or resist it.”
Knowing the possible effects of testosterone in advance can help you prepare for entering the cycle in advance, and don't panic if you encounter these conditions in the cycle, many symptoms will ease over time, if a certain symptom has affected your daily life, please seek medical help in time.

Women make up a large proportion of Retatrutide's users. There has been a lot of concern about whether Retatrutide causes headaches or migraines in women. Today I have put together a summary of this problem, and I hope it will be helpful to you.
Common female headache
Common causes of headache include excessive drinking, lack of sleep, excessive stress, and underlying diseases. For women, the most common cause of headache is related to hormone levels. Estrogen and progesterone play a key role in menstruation and pregnancy, but when their levels fluctuate, they can cause headaches in some people. During menstruation, women experience changes in hormone levels, and as a result, many women experience headaches during menstruation (early, middle, late). Headache symptoms improve when hormone levels stabilize.
So, do these women get headaches/migraines from using Retatrutide?
Does Retatrutide cause headaches/migraines in women?
As to whether Retatrutide causes headaches/migraines, we can first listen to what users has to say.
“I have chronic migraines. It hasn’t triggered migraines for me, thank goodness but I am getting dehydration headaches way faster than normal. ”
“I have chronic migraines from a TBI I suffered as a child. Retatrutide does not trigger them at all. I have not suffered an abnormal migraine since starting Retatrutide several weeks ago.”
“I rarely have migraines, unlike my friend that gets one wigh the start of her cycle literally every month. However, I woke with a migraine today and my cycle just started, so it could be a coincidence, but I’m on week 3 of Retatrutide.”
As can be seen from their experiences, Retatrutide does not cause headaches/migraines in women. In the process of using Retatrutide, headache problems occurred, mostly related to electrolytes.
Headaches from electrolytes
When using Retatrutide, because dehydration is faster than usual, if you do not pay attention to water and electrolytes, you will experience headaches. Make sure to drink enough water every day and replenish your electrolytes, and your headaches will be relieved.
Therefore, women using Retatrutide to lose weight will not induce migraines, and the headache symptoms it causes are basically caused by dehydration. Keep your fluids and electrolytes balanced so you don't get headaches.

Retatrutide is the latest weight-loss drug, and many people may have been using other weight-loss peptides, such as Semaglutide and Tirzepatide, before discovering it. What dose should I start with if I switch from other weight loss peptides to Retatrutide, and will the starting dose still be the minimum?
Dose range of Retatrutide
The Phase II clinical trail dose range for Retatrutide is 1mg, 4mg, 8mg, and 12mg. The doses of Phase III clinical trail are 2mg, 4mg, 6mg,9mg, and 12mg. Therefore, the standard dose of Retatrutide should start at 2mg per week and the maximum dose should not exceed 12mg per week.
When people first use peptides to lose weight, the principle of peptide use is to start with an initial dose of 2mg and then gradually increase the dose depending on drug tolerance and actual use effect. Retatrutide 2mg is a safe dose and was well tolerated when used in the experiment, so choosing a 2mg weekly dose is a very safe dose. Then increase to your target dose, such as 6mg,8mg, etc., up to 12mg per week.
In the phase II clinical trail, there is another data with reference significance, that is, the target dose. When the target dose is 4mg, the starting dose can be 2mg and 4mg respectively, and when the starting dose is 4mg per week, the weight loss effect is better after 36m weeks. When the target dose was 8mg per week, the starter dose was 2mg and 4mg, respectively, showing similar weight loss after 36 weeks. This data suggests that the most stable starting dose should be 2mg per week, or 4mg if your target dose is larger.
If you are already using Tirzepatide, what is the starting dose when switching to Retatrutide?
In the clinical trail, there is no relevant data. What you can see so far is some user experience data.
A user who switched from Tirzepatide 10mg to Retatrutide 5mg reported no side effects other than a little irritating effect and good weight loss.
Another user switched from Tirzepatide 15mg to Retatrutide 4mg with no side effects but no significant weight loss and will be followed up with a weekly dose of 8mg Retatrutide.
There are also users who switched from Tirzepatide 7mg to Retatrutide 4mg and lost weight very quickly, but experienced some head-passing side effects. (Headache side effects may be related to electrolyte imbalance, which should be replaced during the use of weight loss peptides such as Retatrutide.)
We can see that after using Tirzepatide and then Retatrutide, people tend to start with 4mg. Therefore, as a reference, a starting dose of Tirzepatide starting at 4mg and then increasing as needed would be a good choice. Of course, it is still more stable and safer to start with 2mg per week and gradually increase the dose.

One of my friends used Test E to increase his testosterone level to build muscle mass. After a cycle, he have had a blood test and found both his ALT and AST levels are raised. He is quite worry about it and concerned if the exogenous testosterone is responsible for this phenomenon. In response to his problem, we consulted a number of professional users, and they told us several possible reasons.
First, his ALT and AST levels were respectively 137 U/L and 64U/L, ref <50, on the high side, but not very high. It may be because he is just starting to use exogenous testosterone, and his body is still adjusting. Test E will cause a temporary increase in liver enzyme levels, but it will not have a major impact on the human body, and will gradually return to normal as the body ADAPTS to Test E. This is obviously what happens when people use drugs. Most drugs are metabolized by the liver after entering the body, temporarily affecting the value of some liver enzymes, and the symptoms will disappear over time or when the drug is stopped.
Another professional wondered if he was infected with the virus. Because he had been in a situation where normally his AST and ALT levels were 22-35, it was found after a blood test that the AST rose to 147 and ALT is 143. He was later diagnosed with streptococcus.
At this point, someone asked, "Did you exercise intensely before taking the blood test?" "Does exercise affect test results?" "Yes," he said. Strenuous physical activity can cause muscle damage, and broken muscle fibers cause enzymes such as ALT, AST, etc. to be released into the blood stream, resulting in elevated liver enzyme levels in blood test results. Therefore, exercise should be avoided in the 2-3 days before the test. my friend confirmed that he had run long distances and lifted weights before taking the blood test. If it is caused by this reason, then after a full rest, you will find that all the values will return to normal.
In addition to the above, they also tell us that using other things like AI(aromatase inhibitors), creatine, etc. can cause a temporary increase in liver enzymes. It's not necessarily caused by testosterone. In fact, some AAS do have hepatotoxicity, but the effect of testosterone on the liver is not obvious. However, this is not to say that testosterone does not affect liver enzyme values at all. One user who started using testosterone at a dose of 300mg per week saw his ALT and AST levels rise from 30 to 60. After that, he divided the weekly dose into two doses, and his ALT, AST levels remained around 40.
Therefore, the elevation of ALT and AST is actually affected by many factors, what we have to do is to do a good blood test, communicate with the doctor and seek professional advice in a timely manner, do not put yourself into a panic.

I started clomid in late April. At that time I had lost 55 lbs in 15 weeks(3.7 lbs per week). Since then, I have lost 10lb in 5+ weeks(2 lbs per week). When this statement appears in front of your eyes, do you wonder: Clomiphene can lose weight?
What does Clomiphene do?
Clomiphene citrate is a non-steroidal selective estrogen receptor modulator that was approved by the FDA in 1967 to treat fertility problems. By blocking the effects of estrogen on the hypothalamus, Clomiphene promotes the production and release of luteinizing hormone (LH) and folliclestatin (FSH).
In its scope, Clomifene does not have a weight loss effect, so why do users lose so much weight after using clomifene?
Continuing to look down and see that the reason why users use Clomid is to increase their testosterone levels.
I do not know my current T levels. The doc put me on 3 months of Clomid, 25mg/day and I get tested again in mid-July. At that time, I will also get my E tested and go on an E-blocker, if needed. When I'm not on Clomid or something similar, my T levels are very low: 180-220s. I've been on Clomid, and another I can't remember the name of, before and it gets my levels up to normal-ish (400-650). I'm hoping to get my levels to 800+ with help, weight-loss and lifting heavy weights.
Clomiphene raises testosterone levels
It's not hard to see how Clomiphene has the ability to raise testosterone levels. How does it do it? In men, the negative feedback regulation of the hypothalamic-pituitary-testicular axis (HPTA) is influenced by estrogen, and by blocking the hypothalamic action of estrogen, the HPTA axis will continue to respond positively, resulting in more testosterone production.
The weight loss caused by using Clomiphene is actually the result of increased testosterone levels.
Adults tend to get fatter as they get older; Adult men's testosterone levels gradually decline as they age. It seems that weight gain in adult men is associated with low testosterone levels. While low testosterone does not directly lead to obesity, people with low testosterone do tend to be more likely to gain weight. Using Clomiphene to boost testosterone levels, combined with exercise, makes it easier to lose fat and gain muscle, and the technical word is that testosterone changes the composition of the body.
So, Clomiphene has no weight loss effect, but people with low testosterone levels who use Clomiphene have fat loss and muscle gain effect.