Astressin-B Research report – Norma – Parcel C
Sarah Campeau 
Parcel C consists in subjects that have been injected with distinct dosages of the compound. The main variable consists in the duration and consistency of the dosages. This means that the sub-groups within this parcel are helping us determine the efficiency of the compound given different dosages, and how the subjects react to an interruption of the injection cycle, the additional inconsistency of the dosages and duration of the treatment.
This Parcel has been divided in 8 sub-groups, all of which have ongoing experiments that require a constant and prolonged evaluation. Below is the fundamental data being collected on Parcel C;
• Does the compound leave any traces after the treatment has been interrupted?
• Do the side-effects cease after the treatment is interrupted?
• Do the results maintain after the interruption of the treatment? If so, how long are they maintained for.
• How do subjects react to extreme dosages of the compound
• How to the test subjects react to dosage fluctuations
One of the most common questions we keep getting is in regards to the efficiency of Astressin-B used in a treatment to treat hair loss in Androgenic Alopecia patients. While I cannot release a great deal of specifics at this moment, rest assured this is being fully contemplated, particularity in this Parcel.
Since most of the data on this particular parcel is still volatile, as it’s an ongoing experiment, we cannot release a lot of information, but we can safely publish the following preliminary data:
• So far the side effects have disappeared after the treatment has stopped on all sub-control groups.
• An unspecified percentage of subjects who had the treatment interrupted started losing hair again.
• An unspecified percentage of subjects who had the treatment interrupted did not start losing hair again
• High dosages of the compound increase significantly the noted side-effects
• High dosages of the compound did not increase the overall efficiency of the compound
I apologize for not being able to specify the subject conditions, but the purpose of these updates is to give our readers an idea of what we are doing and how the experiment is being conducted, not to provide the definite results.
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You stated that high dosages of the compound increase significantly the noted side-effects. Are the only side effects still noted increased saliva production and hypersomnia? Or at higher dosages were other side effects noted? As always, so grateful for all your hard work and this website sincerely gives me the will power to get out of bed everyday!
Thank you!
Hello Kenny, in addition to the previously documented side effects, we have noted other detrimental effects, particularly in the intensive dosage sub-groups.
sarah -
is there any way you can state what these other detrimental effects were?
marcus, most of the side effects I mentioned were gastrointestinal related.
Hi Sarah,
In an earlier post the following question was asked:
“If astressin-b proves to do no harm to any mice at all and it ends up being totally safe will there be a way to administer the drug to the public if people were to sign a disclaimer or something?”
And someone on your end responded:
“there are thousands of commercial drugs out there that are being sold legitimately without FDA approval, so the answer to your question is yes.”
Can you elaborate on how a drug can be sold legitimately without FDA approval and how this may occur with Astressin-b? I feel like the drug should be released soon to help those with Cushings syndrome, is there anyway people dealing with Cushings or Chronic Anxiety can get the drug without waiting years to improve the quality of their lives.
Thank you.
Are any of the mice subjects being given an oral dosage of the peptide and do any of you know whether or not astressin-b can be absorbed through the intestinal tract and into the bloodstream?
Also are any of the subjects being given a topical dose?
One last thing… Was this post the final report you had mentioned in earlier posts?
Also, I feel like there has been a lot of mention about explaining why it will work in humans and be effective for humans with AGA, can we get that explanation?
Thank you.
I think the post has given a response to that question already,
” I cannot release a great deal of specifics at this moment, rest assured this is being fully contemplated, particularity in this Parcel.”
sarah,
i know you cant be certain, but would you assume that the side effects for humans will most likely be the same as they were in the mice?
Hello Sarah, I got back all my results and everything seems to be really good except for my DHEAS are at 20.3 which is just barely in range (on this it shows 23 as the highest in range) and also my cortisol levels are kind of high, but only for morning, evening, and night is kind of high but still in range. C (morning) 13.6, C (noon) 1.8, C (evening) 2.8, C (night) .8. I’m not sure Exactly what this means, but I have been following Astressin-b for 6 months now and it seems that this peptide is going to be right in line for helping me lower my cortisol levels? Thanks for any advice you can give me and for all the hard work you all do as always!
How is androgenic alopecia being fully contemplated in this parcel? Do any of the subjects have AA ?
Hello Sam,
In reality most natural supplements are not patentable, which is why they are feely available to the public without having given through an FDA approval process. FDA assures that a given drug is safe, and has passed through rigorous procedures before it is released into the market.
Having said that, there are thousands of drugs in the market that are not FDA approved, and while it takes time for the authorities to crack down on these cases, they eventually do and the products are taken off the shelve, but not before having had a good run in the market turning a good profit.
astressin-b:All subjects are being administered the compound intravenously, we are not testing the compound topically.
What do you think Sarah? It is possible to work topically?
Can i guess a major side effect? Over-active gal bladder / gal stones?
Thinking further about it. Systemically blocking cortisol in high dosages is a terrible idea and long term it will reek havoc on a number of bodily functions including drop in blood pressure, lower body temperature, weakened immune system, overactive digestion, shitting yourself, etc. Our bodies do need to have a sense of when to repair or maintain themselves.
@Brad M: We want to get cortisol levels back to normal range, not to an abnormally low level. That’s why probably every single person will need to get their cortisol level measured, and the optimal dosage determined right for him/her. A couple of weeks later check the cortisol level again, etc, until it’s back to normal. Like endocrinologists do, when they set the dosage for a hormone, for example thyroxine, in case of hypothyroidism. I guess, most of the people, who has hair loss by high cortisol levels, the real cause is psychical, and not the need of stronger immune reactions or higher blood pressure. I think the facts are the opposite, I will be able get asleep easier, have lower blood pressure, heart rate, etc. Only good things!
@Robert
I agree with you completely. What would be most helpful to have is a cortisol tester similar to a blood sugar insulin tester for diabetes.
@Brad M You still have not posted a link about your mix and results… There have been numerous other posts since you said yours has been awaiting moderation? I would have thought it would have posted by now. Sarah, other moderators, do you think there is legitimacy to this claim that a mix containing a cortisol blocker applied topically to the head could help hair regrow?
@Kenny
It’s under another thread. The mod approved it.
http://www.hairloss-research.com/latest-astressin-b-research-update/
Hello. Is there any news to keep our hopes up? God knows we could do with some.