6 posts • Page 1 of 1
six months into peyronie’sI first started developing symtoms last fall, bent but not broken. My GP doctor sent me to a urology clinic where a person who is not a doctor has given me 4 weekly sonar treatments. With another 4 treatments scheduled for next month. The technician takes a wand from a sonar machine directing sound waves at the affected area on my penis, somewhat like a woman getting a sonagram, petroleum jelly and all. Painless. Before the treatment my sex life was OK with out Viagra now Viagra is necessary an...Read the full article
Re: six months into peyronie’sI have had PD for over 3 years now and I have not heard of anyone getting this treatment. Just like anything with this disease it can come and go. I have used a couple different methods of treatment.
First of all go to a Peyronies specialist. My Dr. Dr. Levine in Chicago gave me a series of 10 varapamil injections along with using the FASTSIZE Extender stretching device. I had a 45 degree curvature and now I am down to about 15 degrees and my erections do not hurt anymore. Dr. Levine did a case study at Rush University. He is legit. http://www.medicalnewstoday.com/articles/71517.php I also did the 2 times a day Vitamin E and took Lj-100 Tankat ali. Expensive but it help with my erections. Best of luck on the treatment. Stay positive. PDGUY
Re: six months into peyronie’sThanks for your comments and advice. How often do you use the vacuum device and for how long? How are you getting along? bb
Re: six months into peyronie’sI use a vacuum device twice a week for about 10-15 minutes at a time but I use the Fastsize Penile Extender for 3-4 hours a day 5 days a week. I just wear it underneath my cloths with pleated pants and you cannot tell I have it on. Get a good vacuum device. They are covered by insurance. Dont get a cheap pump because it may hinder your results.
Cheer, PD GUY
Re: six months into peyronie’sHey, Thanks a lot. I appreciate hearing of your progress and the equipment that you are using. I've been somewhat confused about what to do and depressed about my chances of recovery. I don't know about he Fastsize Penile Extender. You are using it about 15-20 hours a week. Does that seem to be more effective than the pump? I don't know if I have a good pump or not. The cost to my insurance was about $500.00 which seems pretty ridiculous. I can't hardly believe this any of this mess. I just have to keep a good attitude, things hopefully will work out. Again, thanks a lot. bb
Re: six months into peyronie’sI use the pump a couple times a week but the Fastsize Extender I use 3-4 hours a day. I think a combinations of things is good. I ma just glad now I can get erections without pain and it is getting straighter.
Look into talking with Doctors and therapist that know about this specific issue because other Doctors do not know what we go through. just google peyronies and Dr. Levine, who is in Chicago. There is also associations just for peyronies and thats how I found Dr. Levine. As far as your mental aspect. Eat healthier, get exercise and blood flow in your body. Keep your chin up and your penis is just one part of you. Have a great day!
6 posts • Page 1 of 1
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