Introduction!

[nevertheless]

Hello all!

Glad to be here. Will update signature soon.

Age? 31

What did your medical doctor conclude? Have only talked to my GP/PCP but he did manual exam and said he felt plaque. Seems like I may have combo of congenital curvature as well as peyronies. He told me I should follow up with urologist soon.

How long have you had symptoms?
Downward curve around maybe 30-40* as long as I can remember. Remember hurting myself masturbating as a teen but have never brought it up. First inch or so of penis is a bit more slim than the rest of the shaft it seems. Might be optical illusion because of curve though.

What are your symptoms?
Mostly just downward curve. No pain during sex but very sore after. Doctor explained because of downward curve I am rubbing wife's pelvic bone probably which would certainly cause soreness. Feel like I have lost some length over last few years. Also have low T and on weekly shots, which has helped erection strength but worsened soreness and maybe curve more prominent when harder.  

What treatments have you tried and what were the results?
Currently starting RestoreX. On day 3! Going well so far. Obviously no results yet except my wife has even noticed I look much larger flaccid basically all the time since starting. Usually a grower but looking much more like a shower.

Debating asking doctor about Cialis so open to any ideas about that!

Do you have insurance or means to get medical treatment?
Yup. Currently hit medical deductible for the year. Just submitted RestoreX for reimbursement with letter from my doctor so we will see.

where are you in dealing with the psychological aspects of Peyronies Disease?
I'm mostly fine. A little self conscious but nothing awful. Wife doesn't mind except sex can be uncomfortable for both of us at times.

Are you in a relationship?

Married for almost 10 years!

[PeyroniKirai]

nevertheless,

Welcome to the Forum and thanks for the full detail intro.

Please put a few summary lines in your profile as well.

The Forum is here to support you, so always feel free to ask any questions you may have and also to post your experiences if you think they could help other Peyronies Disease sufferers.

Best regards,
PK