New member

[islandbumwa]

Greetings fellow peyronies suffers.  I was diagnosed with this disease in early October of this year. I noticed something was happening in early August.  The urologist I saw in Spokane, WA, obviously didn't know much about Peyronies as he told me to take 400 IU's of Vitaim E and we  would revisit it in 6 months.  After reading many of your posts, I realize I need to be proactive now. I'm looking for a doc in the Seattle area who knows what their talking about. Can anyone recommend a good urologist in the great Northwest. Also, I am having skin issues after about 7 weeks on the Vitamin E. Lots of itching. Has anyone else had this side effect?  
Thanks,
Islandbumwa

[james1947]

Islandbumwa

Excellent decision not to wait, excellent decision to see a good Peyronies specialist.
Try to find one close to you at:
https://www.peyroniesforum.net/index.php/topic,4063.0.html
Chicago - Dr. Laurence Levine will be excellent choice if you can get there, it may be far from you but worth.

Welcome to the forum
James