Hello,
I am have been lurking on this forum for several months now. I am already familiar with the survival guide and general information. Just posting this as a way to finally engage with the community a bit.
Age?30 years old
What did your medical doctor conclude?I have yet to consult a specialist. I initially visited a general practitioner last year to discuss
erectile dysfunction. He concluded my
erectile dysfunction was connected to depression and prescribed Wellbutrin. I continued to do research and became worried I was presenting some symptoms of Peyronie’s and found the resources of this forum and Neo-V. However, I concluded that my case was overall very mild and that the best course was to take measures at home. Even so, I am looking into seeing a specialist. Thankfully, one of the recommended Peyronie’s doctors (Dr. Anthony J. Bella) lives in my town, so I should be in good hands if I can see him. However my symptoms are confusing and the measures still in place due to Covid-19 makes accessing healthcare difficult.
How long have you had symptoms?I have suffered from some form of
erectile dysfunction for a few years. I believe a combination of smoking, antidepressants, poor masturbation habits, and a sedentary lifestyle were to blame. I have quit smoking, moved onto Wellbutrin, and started doing lots of exercise to combat this. The possible Peyronie’s symptoms emerged only in the last several months (Oct-Nov 2019 approx).
What are your symptoms?My symptoms are confusing and I am unsure how to properly classify them. I have diminished erectile quality. I do not get any spontaneous erections in the day but I do get some night time erections. During the day, I can only get erect by physical stimulation to essentially force it but, once erect, there is little loss in quality. The problem is getting there. I have experienced very mild shortening and some slight deformity that is most pronounced in a semi-erect state but are almost not noticeable when fully erect. There is no deformity when
flaccid but at times my
flaccid penis feels tougher and denser. However, this is inconsistent and might indicate more of a pelvic floor issue than any calcified
plaque. From what I have read on this forum,
plaque is noticeably hard and consistent and I do not have that. For a few months, there was some mild discolouration and two varicose veins appeared on the upper part of the shaft but the discolouration has subsided in recent months. During this period there was some mild pain but it was not severe and would frequently subside. I see slight evidence of a atrophic scar forming a slight indent underneath the head of the penis and some feeling of roughness at other parts which I believe indicate scarring specifically of the tunica. I believe the visible deformity is the result of this scarring making the tunica less elastic than it previously was. I used to be able to almost feel it in a way. In the process of getting an erection, it would feel like the blood was pushing against something. I suspect the scaring is the result of a combination of smoking,
erectile dysfunction leading to a loss of elasticity, and from masturbation.
Although I did not realize it at the time, I believe I have had an unhealthy approach to masturbation for many years. I always enjoyed the act more than the climax and would frequently “edge” to delay ejaculation. This led to a pattern of prolonged sessions of masturbation and sex that I believe has resulted in a toughening of the tunica. Much of the deformity matches up with where my hand would make contact and so this seems like the likely cause.
What treatments have you tried and what were the results?I found this forum several months ago and immediately began all of the over the counter treatments recommended in the survival guide. Recently, I have added the daily Cialis. Therefore, I am taking the following:
Acetyl L-Carnitine
L-Arginine and L-Citruline
CoQ 10
Vitamin E
Vitamin D
A “Men’s Health” multivitamin
Omega 3 supplements
Pycnogeol
Daily Cialis 5mg
Heated rice bag before I sleep
I do not have a prescription for
pentox but I have been drinking coffee and tea after reading a post from Neo-V that said there were many similarities between caffeine and
pentox. My hope is that caffeine combined with regular use of ibuprofen to reduce
inflammation and act as a blood thinner should have a similar total effect.
I am considering purchasing a
VED but, to be perfectly honest, that treatment is a little frightening for me. I am looking into using a water based one because I have read that that has less chance of damage compared to air based pumps but I am unsure.
I am unsure about the results. Because I do not present any curve and the deformity is most present when semi erect, I feel like my case is very mild and all my treatments are more preventative. Deformity does not seem to be worsening but I cannot say what aspect of the treatment works or where I would be without it. I do feel like there is some improvement. I no longer feel like the blood is pushing against a constricted tunica in the process of getting erect and the discolouration that used to be present has disappeared almost entirely.
Also, I have been trying to control my masturbation but this has been difficult to find a balance. On the one hand, I believe my masturbation habits are a large factor in my mild deformity. On the other, I recognize that inducing erections is an important aspect of healing and preventing
fibrosis. So I am trying to find a balance but I find this difficult because after inducing an erection via masturbation I find it difficult to exercise the will power to not masturbate the way I used to. I am doing my best to overcome this. In November, I tried full no fap but I have been more complacent and compulsive recently. I am considering doing a full no fap month again but I want to keep the healthy benefits of erections. Perhaps I will finally buy a
VED to find a way to eliminate masturbation while still inducing regular erections. We will see.
Do you have insurance or means to get medical treatment?Nationalised healthcare covers most aspects.
Where are you in dealing with the psychological aspects of Peyronies Disease?Very mixed. Some days are better than others. I do find myself obsessing and being fearful for my sexual future. At times, I have found it difficult to work and my confidence to perform sexually and pursue a partner is greatly hampered. Still, perhaps it is the Wellbutrin or whatever, but I am not as completely broken as I have seen in some other cases. Thankfully, my case seems very mild and that helps me be hopeful of an eventual improvement and recovery. I recognize that this is a disease that takes time. As has been said on this forum, this is a marathon, not a sprint. All I can do is educate myself and take the proper preventative and restorative steps and see how things will progress in the months and years to come.
Are you in a relationship?No, I am single. I have been told I am attractive but I have always been an awkward person. The previous few years of mild
erectile dysfunction hurt my confidence to put myself out there and the recent mild deformity has amplified that feeling. Thankfully, I do have a loving and supportive family of siblings and parents who help me.
Thank you for reading. Any feedback is appreciated. I am not sure if what I have is true Peyronie’s. I do not understand where simple scarring ends and where full Peyronie’s begins. I suspect at the very least I have what Neo-V referred to as a pre-Peyronie’s but I am trying to be smart and proactive. Also, I would like to thank the moderators of this forum. This collection of information has been very helpful during a very worrying time.