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thegreycat

Just want to extend my appreciation of this forum.

The users, moderators and admins are all a source of comfort, information and sanity for myself and I'm sure to countless other men too who feel we can't discuss this terrible thing with friends or family IRL.

You only have to look at most intro posts to see the level of support offered to people here, no matter who you are or where you're from, you're among friends here.

I am glad this place exists.
35. No injury. Lump Feb 22.
Pain, dent, left & upward bend ~50deg. Bad EQ.
Cialis Dac 22 - ear issues.
Diagnosed Feb 23.
VED Oct 22. PMP Feb 23.
Lump reduced May 23, dent remains, angle a little better. EQ improved.

Supportive partner, depression.

Sonic

And we should also thank people like you, greycat, who do journals/diaries of traction or VED journeys. These are basically like mini versions of clinical studies and are very helpful. It is a shame though that many who get better/healed move on and never drop by anymore. All in all it is a great forum, no other peyronies related forum will ever beat this.
30 years. Sudden rightwards curve detected in June 2020
Narrowing on right side and about a 20° curve to the right.
ED + instability due to narrowing.

FrankPD

Yes, I'm thankful for everyone here being so open and honest.  

It helped/helps so much.
I have a girlfriend
Age 48, No injury
Diagnosis January 2022  
Six plaques
Hourglassing when flaccid and semi-erect
Only have my congenital curve
Massaging with vitamin E cream twice a day 
5mg Tadalafil, Healthy diet
Discomfort/aching sometimes

Pfract

Thank you for the words, Greycat!

Mikel7

It makes the heart glad to read words of sincere thankfulness! Thank You!
Lump 4/2020, age 62 , Dr Levine 6-26-20, Dors Curve 11/2020, Peyronies
Vit E400mg, COQ10, Heat Therapy, Penimaster, Pentox, Cialis, Restorex
SNHL 7/2020 - Stopped all Meds because ototoxicity  Heat/traction/VED are working. CPPS Diagnosis - Stable :)

ohnoohno

Wholeheartedly agree. To those in charge big hats off to you. I can't imagine where I would turn to without this forum. Peyronies Disease can be such a heavy weight on ones mind but coming here makes me feel less alone. I see a light at the end of the tunnel for everyone.
29 y/o diagnosed 13 Jun 22.

went from a slight 30dg bend at glans to whole thing being deformed/loss of length over a year.

trying to find a way out of this all

Stabler

This is a great forum. We all try to help one another. It's not every day that you see a group withstand time like this one has on volunteer alone and those who have been helped over the years has to be in the thousands maybe tens of thousands. I am so very proud to be part of this forum

Stabler
Moderator since 2015- Missouri- I work in the medical field and have strong knowledge of insurance and how to obtain coverage for medication and other treatments. Being a woman I do not have Peyronies but you can ask me anything. I am happy to help.