Hey regtam25. I stopped using the snake
hanger because with the constant pge1 soreness that my dick goes through, I can’t tolerate the pain from old school compression style hangers right now whole doing chemical Penis Enlargement. Vacuum based hangers allow for just suction force to grip my glans and shaft for comfortable
hanging while on this protocol.
Hey Falcon88. With VEGF administration of it was to be handled with care from what I’m learning. VEGF is actually more dangerous to use if you have any cancer cells then any other growth factor peptide because VEGF creates new blood vessels and blood pathways in tissues that are starving of oxygenated blood.
I’ve learned for VEGF to work on whatever tissue it’s administered on, that tissue has to be receiving a poor blood supply thus sending the stress single for the body’s natural VEGF to come into play to help upgrade the starving tissue’s vascular system.
If the tissue is already receiving blood from having good vascular pathways then I’m thinking VEGF will not chance anything. There has to be a lack of oxygen to the tissues to send out the distress signal for VEGF to work.
I have a theory that if one were to do a few semi erect clamping sets to completely cut off blood circulation in 10 to 15 minute sets, then administer VEGF, the effects would be enhanced.
Still researching VEGF. We need to find out what dosage this growth compound needs to be administered in and what frequency to do so.
For your other question it’s IGF-DES. Not MGF-DES. To learn about MGF and IGF-DES do a google search to get general knowledge but here’s some info from me.
MGF is a form of igf but with MGF meaning mechano growth factor this peptide is naturally released in muscles that have been just trained and damaged. Mgf causes immediate stem cell activation and cell proliferation in skeletal muscle and smooth muscle. With the penis being composed of smooth muscle Mgf is able to attach to receptor sites in the penis to cause stem cell division. Where talking thousands to millions of new stem cells being created with each injection. With all of these new stem cells they don't have a purpose yet. MGF only works on recently damaged tissues which is why bodybuilders use it immediately post workout. This is the reason why I inject it into my penis immediately after I’m done with my morning Penis Enlargement workout.
Now with IGF-DES OR IGF-RL3, these peptides cause hyperplasia to a smaller degree but mainly they cause cell differentiation. This means that the igf turns the new stem cells into a permanent cell type. So with skeletal muscle the new stem cells created by mgf get turned into muscle cells after igf therapy. The same thing happens in the penis. After new stem cells are created in the penis after mgf therapy they don't have a purpose or cell type yet. Hours later the igf-des therapy differentiates the new cells turning them into smooth muscle cells.
So basically MGF proliferates and IGF differentiates.
Hey bigdaddy777. It’s funny you say that hopefully a protocol will be pain free, because I’m actually about to take the pain to a whole new level unfortunately. I'll explain on this in a moment after I address Ramrod360's question.
Hey Ramrod360. With the ratio, I don’t have one yet bro. I have mixed vitamin E, powdered acetyl-carnitine and arginine just yet. I’m still researching to see if these supplements will be able to dissolve in DMSO and if there molecular structure is small enough to be carried through the skin with DMSO as the carrier.
Ok guys. So far it’s been 6 days since I’ve been using DHT cream. So far I’ve noticed that my flaccid penis feels more dense and heavy but that’s about it so far. No libido increase or erect size increase so far. It’s still too early to look for results but that’s my status report with DHT so far. I’ve been applying 4 drops of DHT gel on the shaft and rubbing it in, letting it sit on my penis for 10 to 15 minutes. I then apply dmso/paba on it to drag any remaining dht into the penis. I do this twice a day. Once in the morning and once in the evening during my chemical erection workout.
Now after having a Skype convo with Ronielle I realized that by finding ways of using the least amount of pge1 for a 2 to 3 hour erection is the wrong way to go about this. The thing is pge1 unlinks collagen bonds in the tunica which weakens it and makes it extremely susceptible to enlargement through stretch force.
The more pge1 floating in the penis, the better. I’ve been doing my pge1 erections at night time since my body responds better allowing me to use a small dosage to avoid the pain but, I’m short changing myself with 10 mcgs. As you guys know I’ve been avoiding going beyond 12 mcgs because of the pain associated with the pge1 erection. BIG MISTAKE from what I’ve learned during my Skype confo.
The fact of the matter is. When you get injured. Lets say punched in the face and left with a broken jaw. Your jaw becomes inflamed and your body releases natural pge1 to the injury site to diolate the blood vessels so fresh blood can get to the injury site and start the repair process. The massive pain at the injury site is partially because of the pge1 being released in the area for blood vessel expansion.
Now when injected into the penis, pge1 is a massive vasodilator, forcing an erection for a certain length of time depending on how large the dosage. PGE1 excites the nerve endings of the penis, especially right below the glans and through out the shaft causing pain for most men. So basically you can look at PGE1 as liquid PAIN.
I’ve been trying to avoid this liquid pain but I’ve learned that I need to be trying to move up in mcgs with PGE1 slowly so massive amounts of pge1 is circulating through the penis during the erection delinking collagen bonds at a massive rate.
Coughroniellecough has told me that I need to slowly climb my way up to 100mcgs and beyond of pge1 for this much pge1 will delink a shit ton of collagen bonds making the tunica like puddy. Being erect for 3 to 4 hours does cause biomechanical creep and angiogenesis in the penis since the organ is being put under an internal pressurized boner for 3 to 4 hours with the cause of the internal pressure being nutrient filled oxygenated blood. However, it’s the massive amounts of PGE1 delinking the tunica that makes the tunica weak enough to give in to the internal pressure of the erection for permanent enlargement. Coughroniellecough had reached past 300 mcgs of PGE1 during his 4 year journey and had to add other vasodilators to get a decent length erect response.
So basically I’m going to bite the bullet here and man up with pge1. In the evening it takes about 20 mcgs of pge1 for a 1 ½ to 2 hour erection at about 60 to 75% erect most of the time but at night time it takes 10 mcgs for a 2 to 3 hour erection. I will be returning to doing my chemical erections in the evening. Starting tomorrow I will inject 25 mcgs of pge1 which is the highest amount I’ve ever injected, hoping for a good 3 hour or more erection. The pain is going to be excruciating but to hell with the pain. I just have to be strong minded and strong willed to deal with it. No more playing around. If 25 mcgs doesn’t give me at least 2 hours of solid wood with another hour of being 60 to 70% erect then I’ll move up to 28 to 30 mcgs the next time.
We want the penis swimming in pge1 for maximum tissue elasticity and collagen delinking of the tunica. Not to mention PGE1 actually increases DHT receptors in the penis so the increase in pge1 should make my penis more sensitive to the DHT gel treatments I’m implementing.
I will also be taking more evening primrose oil caps and borage oil caps since these two supplements increase the body’s natural PGE1.
My new found interest in not running away from the pain of pge1 has also come from rereading Dr Adam’s chemical pe patent. Some good info in this patent fellas. Some of the test subjects were not just doing 3 to 6 hour chemical erections. Most of these test subjects where also receiving testosterone injections directly into the penis not to mention the pregnancy hormone called relaxant which increases elasticity of male and female genitals.
Here’s a link to the original chemical Penis Enlargement patent by Dr Adams. Definitely a good read fellas. In the link though it seems that Dr Adams is against pumping but I'm all for pumping. Pumping serves an important place in my Penis Enlargement protocal.
http://www.faqs.org/patents/app/20100112027
Here’s a direct quote in the patent on one of the test subjects called EXAMPLE 1.
EXAMPLE 1
“[0080]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.
[0081]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 8 1/2 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 2 1/2 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.”
The patent has 10 more test subjects in it showing there protocol and there results so read the whole article in the link I posted above. Good stuff.
