Topic: Can we ever be sure Peyronies Disease ever truly stabilizes - (Completed) (Read 10988 times)

Hawk · « **on:** February 24, 2006, 10:08:35 AM »

This poll question deals with when is stabilization really stabilization? Does true stabilization ever occur or does Peyronies Disease just cycle through active and dormant cycles.

Temporarty posts with comments or questions about this poll can be posted here, However, posts and general discussion about the progression or course of Peyronies Disease shoud be posted on the main Peyronies forum under "Progression of Peyronies Disease".

phatkatwun · « **Reply #1 on:** February 25, 2006, 12:42:09 PM »

I have had Peyronies Disease for about 5 years and the condition has changed about every 6 to 12 months. No treatment except vitamin E.

emersonchief · « **Reply #2 on:** March 22, 2006, 08:14:49 PM »

I have had Peyronies Disease for 3 years and for the last 1 1/2 years it has stabilized with the exception of the small plaque moving.

Mick · « **Reply #3 on:** March 23, 2006, 01:45:53 PM »

No, have been stable for more than 5 yrs.

j · « **Reply #4 on:** March 23, 2006, 05:02:18 PM »

Stable for a couple of years now, after several months of rapid progression.

jess99504 · « **Reply #5 on:** March 23, 2006, 05:06:18 PM »

I've been stable for almost 10 years

Larry H · « **Reply #6 on:** March 23, 2006, 06:05:02 PM »

I've had Peyronies Disease for over 6 years and it's never been stable and continues to change.

Hawk · « **Reply #7 on:** March 23, 2006, 07:03:49 PM »

Just vote. It will only let you vote once. There is no need to post unless you need to explain why you can't find a suitable choice to vote for.

Barry · « **Reply #8 on:** March 24, 2006, 12:49:36 AM »

I have had Peyronies Disease for 11 LONG years. I have had two periods in time that I was stable for about 18 months,otherwise I have had numerous events of loss of girth and degree of angulation both lateral and dorsal. Furthermore I have had three incidents of loss of length, first in the beginning,second about seven years into the disease and lastly have noticed a small but evident loss taking place currently that started about 5-6 weeks ago. To date, I have lost over three inches.

Barry

bob · « **Reply #9 on:** March 27, 2006, 03:09:28 PM »

I lost one-half to perhaps an inch, but that was back at the beginning. The most annoying development was the indentation which seems to have become more pronounced.

TopperCR · « **Reply #10 on:** March 28, 2006, 08:12:08 AM »

I have had Peyronies Disease for 3.5 years & am stable.

Hawk · « **Reply #11 on:** March 28, 2006, 09:08:20 AM »

I appreciate you participation and patience as we try to fine-tune this process.

These polls are of utmost importance in beginning to glean some real information on issues surrounding Peyronies Disease. Please help in fine tuning these polls so Peyronies Disease suffers have access to some real information.

I notice there are many posts in the area reserved for those that "cannot answer the question as it is currently worded". EVEN THEN, YOU SHOULD VOTE: "I cannot answer the question as it is currently worded. (Please post why)"

The point of the poll is to vote in the poll. When you post in this area it indicates you cannot answer the question as it is currently worded. This is confusing since many of the posts indicate the person could have voted for another choice. It is further confusing since only 5 members voted "I cannot answer the question as it is currently worded. (Please post why)" yet many more than 5 posted.

If you voted in the poll for any choice other than I cannot answer the question as it is currently worded. (Please post why)" , please delete your post from this section.

Thanks

Old Man · « **Reply #12 on:** March 28, 2006, 11:06:43 AM »

I have had Peyronies Disease for over 50 years now and currently stabilized. It has come and gone several times during this long period of time.

Old Man

Hawk · « **Reply #13 on:** March 28, 2006, 11:40:01 AM »

I would like to know if everyone that posted below actually voted in this poll, and if so, which choice they voted for.

Larry H · « **Reply #14 on:** March 28, 2006, 02:01:07 PM »

Yes, the last choice.

Larry

emersonchief · « **Reply #15 on:** March 28, 2006, 02:13:57 PM »

Yes I voted on the last choice also!

emersonchief

Barry · « **Reply #16 on:** March 28, 2006, 02:40:43 PM »

Yes, last choice.

BF

number1 · « **Reply #17 on:** March 28, 2006, 10:19:28 PM »

I've had Peyronies Disease for 3+ years. no change after the first year.

dcaptain · « **Reply #18 on:** March 29, 2006, 12:17:00 PM »

I have just reached the one-year mark with Peyronies Disease, so I can't say whether or not it will recurr. TO DATE it has not progressed or gotten worse, but I cannot speak furhter than the one-year mark.

dcaptain

zigwyth · « **Reply #19 on:** March 29, 2006, 12:26:22 PM »

Have only had it 3 months

SteveW · « **Reply #20 on:** March 30, 2006, 10:40:08 PM »

I couldn't vote with the current wording. I am not quite 1 year.

concerned · « **Reply #21 on:** March 31, 2006, 02:26:07 PM »

Have only had it two months

phil · « **Reply #22 on:** April 07, 2006, 10:18:08 PM »

I think I am stable but it has been less than a year since I seemed to stabilize.

Tim468 · « **Reply #23 on:** April 18, 2006, 10:30:31 AM »

I developed it over 30 years ago. It has been so slowly progressive that change is imperceptible - but it has continued to worsen. The changes come in mini-bursts of activity, followed by periods of no change. For whatever reason, I can *feel* the changing going on. It is not so much painful as it is a tightening up of the penis (similar to what it feels like when you are in cold water), with a slight aching feeling. When I get that feeling, I increase my self-therapy ("use it or lose it", and vitamin E, NSAIDs and warm baths to relax things). This seemed to work for me until this year when it got busier, and I am now doing carnitine and iontophoresis.

Tim

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