TheStick;407272 said:Just pray you don't ruin your dick with all that stuff.
I dont think that.With these alkaloids i may have problems with heart,but in normal doses there is no problem.But i will see how my body response to the mix of all that staff.In the end of first month i will go to my doctor to make a cardiogram.Quote Originally Posted by TheStick View Post
Just pray you don't ruin your dick with all that stuff.
alati6;407454 said:I dont think that.With these alkaloids i may have problems with heart,but in normal doses there is no problem.But i will see how my body response to the mix of all that staff.In the end of first month i will go to my doctor to make a cardiogram.
My idea is replacing injections into cc with transdermal gel (DMSO+papaverine).I find that DMSO dissolve Papaverine.DMSO softents collagen,but I never readed that inhibits cell generation(please tell me your source).All meds are from pharmacy,not from UG lab.Testosterone injections are intramuscular.PABA replacing POTABA(oral form) .Arginine is aminoacid(oral form).So nothnig injecting into my penis.Will be work that staff with effect-i will find out.And again sorry for poor english.A method for causing a permanent increase in the length and girth of a male subject's penis, said method comprising the step of (a) administering to said male an effective amount of a vasodilator selected from the group consisting of papaverine, chlorpromazine, atropine, phentolamine, and prostaglandin E1, or a mixture thereof, and relaxin, which potentiates the effect of the vasodilator and compositions thereof comprising a pharmaceutically-acceptable diluent or carrier, to induce a cumulative prolonged engorgement of the subject's penis; and (b) repeating step (a) as necessary to cause said increase during said treatment
alati6;407577 said:First at all this is experiment and my advise for your safety ison't do like me!the gereneral idea is from here www.freepatentsonline.com/7671091.html.
My idea is replacing injections into cc with transdermal gel (DMSO+papaverine).I find that DMSO dissolve Papaverine.DMSO softents collagen,but I never readed that inhibits cell generation(please tell me your source).All meds are from pharmacy,not from UG lab.Testosterone injections are intramuscular.PABA replacing POTABA(oral form) .Arginine is aminoacid(oral form).So nothnig injecting into my penis.Will be work that staff with effect-i will find out.And again sorry for poor english.
tester8888;407607 said:http://www.scientistsolutions.com/t8064-dmso+in+cell+based+assays.html
http://www.sigmaaldrich.com/life-science/stem-cell-biology/stem-cell-protocols.html
From your previous postings, I got the impression, that your plan was to inject all of this stuff into your body:
-"Next week I plan to start chemical Penis Enlargement.I will use PapaverineHCL powder dissolved in DMSO,Viagra,PABA,L-Arginine,Yohimbine HCL and Testosterone E inj"-
There are things in that list that are NOT meant to be injected. Additionally, you need to understand about synergy and kinetics of drugs. The easiest way to explain it is this, 2 + 2 = 7 Injected DMSO is a dangerous game, it allows anything to end up anywhere in your body. Yes, DMSO softens collagen, so why would you inject it, and take the risk of it going straight to your heart, and softening the papillary muscle tendons of your heart valves and causing you to now need heart valve transplants?!
I read your source in it's entirety, a couple of times actually.
Your source, is simply someone that has a THEORY on chemical Penis Enlargement, and is wanting to get it patented--which is not the same as FDA approval.
After the patent, then he would go to FDA and request a review to start clinical trials, and then if they approved his request, he would go out and find his lab rats and start the experimenting.
Basically, you are voluntarily going to be using yourself as them guys lab rat. Why risk loosing your penis or your general health just because someone out there in cyberland has some theory about Penis Enlargement? I promise you, that in my 17 years of working in emergency medicine I HAVE seen guys fuck up their penis really bad. It really DOES happen.
I do not worry about you as much as I did, as I now see, or think I see, that you are not going to be injecting ALL of these things, some you will take orally.
What is your plan for aromatization and PCT from the Test E? Have you made a plan for that?
I guess I can't understand why someone would risk damaging their body with chems when there are other alternatives.
I am not an asshole, I am legitimately concerned for you or others that would attempt what it is I thought you were going to do.
I didn't found anything about inhibiting cell generation.Please give a Quote.
Do you read this?I read your source in it's entirety, a couple of times actually.
Your source, is simply someone that has a THEORY on chemical Penis Enlargement, and is wanting to get it patented--which is not the same as FDA approval.
After the patent, then he would go to FDA and request a review to start clinical trials, and then if they approved his request, he would go out and find his lab rats and start the experimenting.
and 4 other examples.EXAMPLE 1
A male patient, age 41, was treated with intracavernosal injections of a vasodilator, prostaglandin E1, on a regular basis (approximately four to five times per week) over an 18 month treatment period. A sufficient quantity was administered to maintain a prolonged engorgement of an erectile response between 40-75% over a period of several hours, generally 3 to 6 hours. The quantity of medication was adjusted from time to time in accordance with the patient's response, which was monitored at least weekly.
The size of the patient's fully erect penis increased from 5.8 inches to 8.6 inches in length (about an 48% increase) and 3.7 inches to 5.8 inches in girth (about an 56% increase) over the 18-month treatment period. Following the discontinuation of this treatment, the erect penis length remained stable for two years at over 8½ inches. Treatment was re-institued combining intracavernosal injections 3-4 times per week of a mixture of testosterone (0.5 mg) and vasodilators with low dose oral Potaba (500-1000 mg) 3-4 times per day. After a short treatment period of 2½ months, the patient's erect penis was over 9 inches in length, which means he has gained an additional 0.4-0.5 inches in length (about an 6% increase). The total increase in length was therefore about 3.2 inches (about an 55% increase) in length.
EXAMPLE 2
A male patient, age 30, was treated with intracavernosal injections of the vasodilator on a regular basis (approximately four to five times per week) over a 6-month treatment period. A sufficient quantity was administered to maintain a prolonged engorgement over a period of about 3 to 6 hours. The quantity of medication was adjusted in accordance with the patient's response. The potentiator potaba (aminobenzoate) (1000 mg/4 times per day) was administered orally to the patient for the last 60 days of treatment.
The patient's erect penis increased from 5.6 inches to 7.7 inches (about an 38% increase) in length and 3.2 inches to 5.3 inches (about an 65% increase) in girth over the 6-month treatment period.
EXAMPLE 3
A male patient, age 52, was treated with separate intracavernosal injections of vasodilators, Papavarine, phentolamine and prostaglandin E1, on a regular basis, selected from treatments of 0 to 4 times per week, over a 7 month treatment period along with daily subcutaneous injections of a prostaglandin F analogue. A sufficient quantity of vasodilator was administered to maintain a prolonged engorgement of an erectile response greater than 70% for 3.5-5 hours duration. The quantity of medication was adjusted from time to time in accordance with the patient's response, which was monitored initially weekly then monthly once the patient had mastered the IC technique and the responses were consistently of the same duration.
The size of the patient's fully erect penis increased from 5.0 inches to 6.3 inches in length, i.e. about a 26% increase, over the 7-month treatment period. Following the discontinuation of this treatment, the erect penis length remained stable.
EXAMPLE 4
A male patient, age 34, was treated with intracavernosal injections of a triple mix of the vasodilators Atropine, Chlorpromazine and Papavarine on a regular basis (approximately two to five times per week) over a 4-month treatment period. A sufficient-quantity was administered to maintain a prolonged engorgement of 60-90% over a period of about 3 to 4.5 hours. The quantity of medication was adjusted in accordance with the patient's response. The potentiator, Potaba™—potassium aminobenzoate (1000 mg/3-4 times per day) was administered orally starting 1 month before starting the IC injections of the vasodilators Atropine, Chlorpromazine and Papavarine.
After 5 months of treatment the patient's erect penis increased from 6.0 inches to 7.1 inches (about an 18% increase) in length.
EXAMPLE 5
A male patient, age 44, was treated with intracavernosal injections of a quadruple mix of the vasodilators prostaglandin E1, Atropine, Chlorpromazine and Papavarine on a regular basis (approximately two to four times per week) over a 4-month treatment period. A sufficient quantity was administered to maintain a prolonged engorgement over a period of about 3 to 5 hours. The quantity of medication was adjusted in accordance with the patient's response. The potentiator dihydrotestosterone 5% ointment was administered orally starting two weeks before starting the IC injections of the vasodilators Atropine, Chlorpromazine and Papavarine and prostaglandin.
After 4 months of treatment the patient's erect penis increased from 5.2 inches to 6.5 inches (about a 25% increase) in length.
EXAMPLE 6
A male patient, age 44, was treated with intracavernosal injections of the vasodilator phentolamine on a regular basis (approximately two to four times per week) over a 4-month treatment period. Phentolamine was frequently combined with indirect vasodilating effects of oral Viagra to produce and maintain a prolonged engorgement of 60-90% over a period of about 3 to 5 hours. The quantity of medication was adjusted in accordance with the patient's response. The potentiator dihydrotestosterone gel was administered orally starting two weeks before starting the IC injections of the vasodilators Atropine, Chlorpromazine and Papavarine and prostaglandin.
After 4 months of treatment the patient's erect penis increased from 5.2 inches to 6.5 inches (about a 25% increase) in length.
The chance this hapen to me by using 1 ml dmso ED is like to hit me an airplane while I'm writting this reply.Look here http://www.youtube.com/user/DMSODV#p/a/u/1/SjDb_p5uXXo He drink DMSO like it's a water.Yes, DMSO softens collagen, so why would you inject it, and take the risk of it going straight to your heart, and softening the papillary muscle tendons of your heart valves and causing you to now need heart valve transplants?!