Searching for hope

[curvedcarnivore]

I haven't been coping mentally with Peyronie's Disease at all lately - and I would love some help.

I think a few things have caused my thinking to hit rock bottom. One is that at the beginning, I had a lot of hope that RestoreX, diet, supplements, and Cialis would be able to straighten out my bend – at least a little. Yet, after 73 days with no improvement, I've now lost that hope, and I'm worried I'm a lost cause.

The second issue was that I made the mistake of going to Reddit and a few other places that were full of absolute despair, which rubbed off on me. I felt just as horrible and hopeless as the men doom posting – yet I couldn't stop scrolling.

Anyway, I'm really hoping you guys may be able to share some more hopeful resources, studies, stories or anything regarding successful healing from this disease.

I desperately need to get some hope back that recovery is possible and it's not "all over" living with this disease, so even if you have a more positive way of looking at this situation, I'd love to hear it.

[Sonic]

73 days may sound as much but it's not. Wait at least 1 year and I know this sounds hard but during this 1 year keep remaining positive and imagine yourself getting great results within that year. Each day going forward. Keep using the restorex, use it correctly and never skip a day. You will get results. Be patient friend.

[RexRG]

I agree with Sonic. It took at least six months to get to this result for me (before on the left). Although additional plaque was involved, the curve and length improved. I used no other method but RestoreX.  

[Hawk]

No one who educates themselves on Peyronies Disease would expect correction in two months.  That was never a practical expectation, and I think that is pretty clear just reading the forum.  This is a marathon, not a sprint. Failure to respond in 2 months does not equal no hope.  In fact, it does not indicate much of anything.

Next, even if non-invasive procedures completely fail, you still have other options up to and including. An implant that will assure a 100% reliable penis with no future Erectile Dysfunction as you age.  You are barely beginning first-line treatment.  It is not time to despair.

The most important first lesson you must learn about Peyronies Disease is that it affects your mind at least as much as it affects your penis.  Your mind is completely your responsibility to treat and improve.  It sounds like not only do you not have a program to treat the mental aspects, but you are abusing your mind with an obvious negative environment. That is the equivalent of squishing your penis under a rolling pin every day.  Instead of treating the mental aspect, you are suffering from self-inflicted injury.

Stay away from the negative and add a little positive. https://www.peyroniesforum.net/index.php/topic,13846.0.html

We are all rooting for you!

[curvedcarnivore]

I appreciate this so much, as I keep getting mentally worse and worse to the point I think "checking out" is my only cure.  

[dioporcolorisolvo]

I haven't been coping mentally with Peyronie's Disease at all lately - and I would love some help.

I think a few things have caused my thinking to hit rock bottom. One is that at the beginning, I had a lot of hope that RestoreX, diet, supplements, and Cialis would be able to straighten out my bend – at least a little. Yet, after 73 days with no improvement, I've now lost that hope, and I'm worried I'm a lost cause.

The second issue was that I made the mistake of going to Reddit and a few other places that were full of absolute despair, which rubbed off on me. I felt just as horrible and hopeless as the men doom posting – yet I couldn't stop scrolling.

Anyway, I'm really hoping you guys may be able to share some more hopeful resources, studies, stories or anything regarding successful healing from this disease.

I desperately need to get some hope back that recovery is possible and it's not "all over" living with this disease, so even if you have a more positive way of looking at this situation, I'd love to hear it.

I have your age, but I've this disease since I was 27 years. You are not so unlucky after all (don't be angry, but you can't imagine what this disease is at 27y old).
The only thing I can tell you is that the acute stage lasts much more than 6-12 months. Don't expect too much improvement for the first 2-3 years.

In my case:
2011-2015: HELL
2016-2022: situation improved
2023- now: relapse of the disease with more pain than the first stage. Mentally I very close to suicide, but I'm not desperate with the same intesity of the first years. I've no illusions any more, life sucks and I'm a man now.

Every case is different, you could improve next month or never, nobody knows.