Re: Hi my first post

[pjwpdsj]

This is my first post also, I was diagnosed with peyronies disease about 6 months ago.  It has not gotten any better and my urologist has said we are at the point of the injections or do nothing.  Trying to weigh the risk vs. benefit to see what I should do.  He said there is a remote possibility of a penis fracture to total ED.  I am 66 years old and still active sexually with my wife of 43 years.  Anyone been through the injections with positive or negative results?
Thanks

[kuaka]

Here is my standard "welcome to the place no man wants to be" post...

Start here.

https://www.peyroniesforum.net/index.php/topic,3180.msg44057.html

A humorous and informative talk on penis anatomy.  This will help you understand what is happening, by understanding how it is supposed to work.

http://www.ted.com/talks/diane_kelly_what_we_didn_t_know_about_penis_anatomy

Dr's members here have experience with.

https://www.peyroniesforum.net/index.php/board,37.0.html
https://www.peyroniesforum.net/index.php/topic,4063.0.html

Dr's who have published papers in this area of expertise.

http://expertscape.com/ex/penile+induration

Another external source of expertise.

http://www.peyroniesassociation.org/

Nutritionally, consider that you might be Magnesium Deficient.  Peyronie's (PDS) is a fibrosis condition, and most such conditions seem to be associated with Magnesium Deficiency.  Modern farming techniques strip Magnesium out of our food supply.  Magnesium Chloride is a good place to start.  Magnesium Citrate is a bit more bioavailable.

This condition has many varieties, and what works for one may not work for you.  Don't despair if you don't have success right away.  Patience is key.

Traction and VED (Vacuum Erection Device) are both tools in this battle.  Old Man is the resident VED expert.  In either traction or VED, caution is important.  Introduction of "new" injury will only make things worse.

Good Luck,

kuaka