Peyronie’s Treatment Help – Right Now
Every day I talk to men who need Peyronie’s treatment help. As a result, they take control of their Peyronie’s disease treatment. They no longer feel like helpless victims. They are in control and less stressed because of the work they do to eliminate their Peyronie’s disease scar.
Consequently, PDI receives reports from 8-10 men with moderate to marked Peyronie’s treatment help and improvement for every one failure. That is nice success!
What we propose at PDI is not earth shattering or extreme. It all starts with a simple question: If half of men naturally cure or self-heal their own Peyronie’s disease, why not me? That is all we attempt to do. PDI tries to help men heal better. This is not such a strange idea. You are looking for Peyronie’s treatment help, to do a better job of healing.
Peyronie’s treatment concept in a nutshell
The PDI approach is simple: Do everything you can – all at the same time – to help your body heal your Peyronie’s disease. As someone once said, “PDI treatment is like ganging up on Peyronie’s disease. I supply myself with all the things I need to do a better job of curing my Peyronie’s disease.”
If you did not heal your PD in the first 12-18 months like so many men do, perhaps you just need a little Peyronie’s treatment help. You will only know if it can work, if you try.
Help Peyronie’s treatment naturally
All PDI Peyronie’s disease treatment ideas and strategies come from this Alternative Medicine website and the “Peyronie’s Disease Handbook.” If your Peyronie’s curved penis creates sexual distress, read Dr. Herazy’s second book, “Peyronie’s Disease and Sex.”
Read success stories. Click on Peyronie’s disease treatment testimonials.
Why Buy from PDI? It’s all about getting the best Peyronie’s disease treatment possible:
Three simple steps for Peyronie’s treatment help:
Learn about natural Peyronie’s treatment. The doctor who diagnosed your Peyronie’s disease told you next to nothing about it. Now you are on the internet looking for help to avoid penis surgery. Get clear and practical Peyronie’s treatment help from a doctor who had PD and cured it. Learn what he used and how he used it. Peyronie’s treatment help starts with education.
Start the most aggressive therapy plan you can use for 3-4 months. Larger treatment plans give better results than smaller plans. Read about the “Large (Best) Plan” for personal treatment. The “Medium (Better) Plan” is perhaps the most popular of the three plans. The “Small (Good) Plan” is a good starting point. Modify any plan by subtracting or adding, to suit your personal Peyronie’s disease treatment philosophy.
Stop being discouraged. Sign up for the Peyronie’s Disease Treatment Forum blog and get motivated, inspired and educated. Remember, everyday men around the world are actually getting natural Peyronie’s treatment help.
The PDI website offers helpful information about Peyronie’s disease treatment. Most of these ideas will be new to you. It actually gives real answers you are looking for. If you are looking for a different PD treatment option, this is it.
Lastly, please email questions about any Peyronie’s treatment help you need. info@NaturalHealthEducationLLC.com . You will receive a prompt response. I will be happy to assist you in any way I can. TRH
41 thoughts on “Peyronie’s Treatment Help Starts Here”
I have been clicking all over this site looking for what "Peyronies disease natural treatment" IS and can't find it. Perhaps you can enlighten me?
It is necessary to do more than click over this site. You have to read the explanations and understand the philosophy of Peyronie’s disease treatment.
I assume you are looking for one page that lays out the whole thing in one easy to follow series of steps – one page that gives you the Silver Bullet that will get rid of your Peyronie’s disease. Well … there is none. Each man has to work out his own Peyronie’s treatment plan based on how his scar tissue responds in terms of size, shape, density and surface qualities of the scar.
Medical health care is based on the idea that there is one drug out there that will take care of what ails you. It is so strong and universal that all people who use it for a particular problem respond to it and get well. If you look at the declining health of this country and all modern societies you will see that this idea is difficult – if not impossible – to put into action.
Alternative health care is based on the idea that the body has a great ability to heal itself and all efforts are designed to assist the healing response for Peyronie’s disease. Since there should be no argument that each person is different in countless ways, each person needs different things to get well. On the PDI site we lay all of the possible options out in front of you to use to your best advantage. It is a difficult thing to do for some, but we have had so many successes that I know when it is done with diligence and aggressiveness the body is capable of healing or eliminating the Peyronie’s disease scar in a reasonable percent of cases.
Perhaps your difficulty comes from looking for something complex and huge, when the answer is really rather simple. I hope this helps; if not let me know, OK?
Happy New Year to you, John
Is any of this a one time fix for Peyronie’s disease; or is it the start to a life time of prescriptions?
How will this treatment perform with other types of penis enhancement?
Are there any other publications regarding your'e claims (beside your'e 2 books); as I've become a sceptic over the years since I've become afflicted with this curse.
All plans sound fine; but do they work for all cases of Peyronie’s disease?
Great question. I have been doing this work since 2002 and in that time no one has written back saying their PD has returned or worsened after starting the PDI method of Peyronie’s disease treatment. Since the PDI concept has been used less than 10 years at this time, our results have not been extended out far enough in time to really see how permanent these changes are. So far, so good, but only time will tell.
We do not do penis enhancement; that is for the people who sell magic pills and those mechanical $350 stretchers with the wild claims. Our method is based on the idea that if 50% of men who develop Peyronie’s disease get well on their own, then it is obvious that a “self cure” happens in PD with great frequency. That is a good thing. What we advocate is the use of a wide and diverse series of Alt Med therapies that when used in combination will increase your capability to heal the PD scar like in the lucky 50% of men whose body heals itself. We promote ways that are intended to help you heal and repair the PD scar. I like to day that we do not treat Peyronie’s disease, we work with the man who has Peyronie’s disease so he can help himself.
At this time no publication or drug company is interested in what PDI does. There is not enough profit in vitamins, minerals and enzymes to stir their interest. They always look for multi-billion dollar opportunities, and this is not one of them.
Nothing medical procedure or drug works in all cases. Nothing. Aspirin does not work in all cases. Why would you expect or demand that the PDI concept must help all cases of Peyronie’s disease for it to have value or credibility? Look at it this way: Novocain is a highly successful and popular medication, but it does not work in all cases. Your dentist does not know if and when and how much must be used to get the desired results, so your dentist will ask you, “Are you numb here?” Sometimes the Novocain does not work for someone, and another numbing drug must be used. Yet Novocain is considered a successful and valuable drug. And so, there are people who do not heal and repair their PD scar with the PDI method, and there are many who do. The only way to learn if and how well you respond is to do the work and see what kind of results your body can achieve. You might be surprised what you can do for your Peyronie’s disease. TRH
My question is… why is my penis getting shorter?? I understand the reason for the curvature is my Peyronie’s disease, however my penis appears to be getting shorter even when it is not erect. Can you answer this??
I had an injury about a month ago and am reading through your Peyronie’s disease website. I am getting pain during intercourse and am wondering if I should abstain from sex for a few months. Can intercourse make scarring worse at this point and decrease the healing process? If this is Peyronie’s disease I want to do the right thing and not make it worse.
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my penis started to curve from peyronie’s disease about 8 years ago.was not too worried until my penis started not being as hard and big.the next thing I know I have a hard time getting hard and my penis is small when I do get hard.it bends very sharp to the right at the base,as this in it's self does not cause trouble having sex.it is the not being hard enough to have sex or being embarassed because of the size.I have been all through the manhood thing being embrassed not feeling like a man any more with my peyronie’s disease.I used to be very happy with my size and hardness and felt like a real man.I am 60 and still think I have a lot left in my penis,it is just the bend in my penis that makes me feel less of a man.
Your Peyronie’s disease story is a lot like other men, sorry to say.
Even though you do not ask for help or pose a question for me, I would suggest that you get busy looking into Alternative Medicine treatment ideas for your Peyronie’s disease. Even though it sounds like you have been dealing with Peyronie’s disease for eight years there is still ample reason to believe your body could be capable of some resolution of the internal scarring that is probably the cause of your current situation. I suggest you get yourself to a competent urologist for a confirmatory diagnosis and if it is Peyronie’s disease that you are dealing with you can begin to do some basic therapy to start some level of recovery. I also suggest that you get my book, “Peyronie’s Disease and Sex” so that you can start to work out some of your issues about your sexual identity. TRH
Hi, I have been diagnosed with Peyronie’s Disease, however my case is the rarer form and instead or curvature I have narrowing and shrinkage. I have looked far and wide and have found a few reference to L-Carnetine but I have been unable to collect any hard facts. I do like your sight and would like to pursue some of the avenues reccommended here. Can you reccommend a specific treatment relative to my so called rare instance of Peyronie’s disease? Any information is greatly appreciated.
I am a 63 yr old man with some questions about Peyronie’s disease. Until about a year ago, I had no sexual problems at all. Erections were fine and my wife and I had a good sex life. Then I started to get pain with erections and didn't know what the heck was going on. Now I have a 90 degree upward bend in my erection and penetration is almost impossible, since my penis is weak where the bend is. I am still able to climax with masturbation. And oral sex with my wife gives her satisfaction, but she craves the feeling of me inside her. I am embarrassed that I can't seem to do that, even though I get really hard when I give her oral sex. I have been using Super CP Serum and vitamin E and DMSO for several months. The pain seems to be diminishing, but the scar seems to be larger. I am embarrassed to let my wife see my bent erection. The first time she saw what I was dealing with she made me feel wierd. I know that I can still satisfy her with oral sex, but I am hoping that eventually I will be able to have normal intercouse again. I need encouragement at this point.
Sorry to learn of your problem. What you describe is typical of many men with Peyronie’s disease.
Concerning your self-directed treatment, I think it is too limited. Using the same few therapies for three months is not what we recommend and not what you will read on the PDI website or my blog entries. On top of that you are only using the external therapies for your Peyronie’s disease and no internal therapies – no wonder you are getting only limited results. It seems to me you are not following what I have suggested in the printed instructions that are included with each order you receive from Peyronie’s Disease Institute. If you wish to get better using Alternative Medicine for your Peyronie’s disease then you should follow the recommendations you have been given. Since you are not following the PDI concept of treatment you cannot expect to get the kind of Peyronie’s disease results you read about.
Men are getting help with the Peyronie’s disease methods I propose. If you want to get started in right direction please read again the information you were sent and follow those instructions.
Please let me know if you have any specific questions about Peyronie’s disease treatment. TRH
You only have to read the information that is available on the Peyronie’s Disease Institute website. There is not much more that I can add to what you see to tell you more or explain better about Peyronie’s disease than what is on our huge website.
When you have a specific question about Alternative Medicine treatment, please send it to me and I will try to assist you. TRH
You are not correct to think that your distortion is all that rare or unusual. Penile distortion of one kind or another is the hallmark of Peyronie’s disease. I communicate often with men who have a bottle neck or an hourglass deformity. Shrinkage is extremely common, in both length and girth.
You do not want to use L-carnitine, you want to use acetyl-L-carnitine for your Peyronie’s disease. The PDI store sells a high quality acetyl-L-carnitine that we have used with great success for almost ten years, and the PDI website has a large discussion explaining what you need to know about acetyl-L-carnitine and Peyronie’s disease. TRH
I am a 50 year old man with Peyronie’s disease and due to the fact that i live in Iran and considering the situation in USA as developed country you can imagien our condition in this regard so here by i would like to ask you to help me to get rid of this bad conditions please
hello, i am 25 and i have had this Peyronie’s disease scar since a year now. There is no bending yet but i can feel one scar in the middle of the pinus which slows down the flow of blood from the middle of the pinus up to the head.. this makes my top part of the pinus take time before hardening and growing up fully… only thing i would want is to make this scar smaller or softer so that blood flow will go better.. can you help me ?
i am willing to come to your institute if necessary. I live in london uk.
please let me know
Dr. H . – a urologist diagnosed Peyronie’s disease..but I cannot detect the plague that he advised he located on the dorsal side ofteh the penis…how do I id these plaques so I can monitor the progress I will have under your medium plan to which I will be subsribing. Further as to those 50% of men who are lucky to recover from Peyronie’s disease without attentions how long on aveage would you say that healing takes place. Thanks
How does the Peyronie’s disease treatment effect internal scarring, or those as previously mentioned where the scars are internal and do not as much cause bending as much as lack of rigidity? Do any of the external products help with internal plaque buildup or is that a different treatment? Is there one treatment that covers both Peyronie’s disease and Dupuytrens?
And when you order is there a listing of how much to take of the various ingredients or is that left up to the individual? I see some people take more E or more C, but how do they know where to start? And is it explained how to use the external ingredients and if there are combinations?
Hello Dr , we’ll I have this problem. I have peyronie’s disease. Hour glass top and bottom are good strong erections . But the area where the plaque is a strangle hold on me. I know its a lack of an enzyme . But i also read blood pressure medication is a contributing factor. I been staying up nights , lost my lady. Lost my job . This pyronies has taken a a bite out of me. No medical insurance . But is also have other underlying health issues. Thyroid, low t. HBP. Diabetes. I pray everyone with this can get real help. I certainly need a push in the right direction. Support for Peyronie’s disease is Not existing. I just stumbled on this site. Thanks
All scaring of Peyronie’s disease is internal. PDI treatment uses internal therapies (vitamins, minerals, enzymes) that are taken by mouth to work internally, and it uses external therapies (DMSO, manual stretching, ultrasound, etc.) that are done directly over the area of the Peyronie’s disease scar and are intended to influence the internal scar chemically as well as physically.
Depending on the location of the Peyronie’s disease scar it can affect in two basic ways: A Peyronie’s scar can alter erection quality (making the penis flaccid or less erect) in all or just part of the penis by preventing the closure of veins that should normally create hydrostatic pressure, as well as cause the penis to deform (bend, dent, hourglass, etc.) if and when it does become erect.
When a man has both Peyronie’s disease and Dupuytren’s contracture the different therapies affect those same dense fibrous tissues equally; many men who have both problems but start out wanting to treat one problem in particular will report that both problems are responding. This occurs because there is no way to control of limit where the internal therapies travel and work inside the body. When a man has both problems we suggest he apply the external therapies directly to the hand (DC) and the penis (PD) for maximum direct treatment to assure the best possible results.
When you place your order from PDI or DCI you will receive a large amount of information that tells you exactly how to use whatever it is that you are ordering. No one complains they do not know how to use their Peyronie’s disease treatment plan after reading the information we provide. TRH
Sorry to learn of your current problems with Peyronie’s disease. I urge you to review the information on the PDI site and learn how you can use this information to support your immune system for a natural healing response. There is a tremendous amount of help and information available if you seek it out.
Yes, Peyronie’s disease can disrupt a person’s life to the core. A lot of damage done is determined by how the individual responds to it. I am not saying it is a walk in the park, I am saying to limit the amount of your life and personal identity that you give to this problem. It is your penis that is involved when you have Peyronie’s disease, a part of you, not all of you. Keep things in perspective. You are more than your penis.
It would be good for you to look around the PDI website to learn more about how you can gain control of your Peyronie’s disease situation and perhaps help your body heal this terrible problem. TRH
Hi Dr. some ppl have peyronie’s disease but if you palpate, you can feel the scar how can their own will improve
Not all Peyronie’s disease scars can be located; maybe half are easily found. Of the other half of PD scars maybe 10 percent will never be located. And, yes, some men with Peyronie’s disease will get better on their own. This self-healing is the idea behind what we try to do at PDI: Help the body self-heal Peyronie’s disease by supplying extra vitamins, mineral and enzymes that it uses to get rid of the scar tissue. It is really a simple idea, don’t you think? TRH
If you contact directly I will send you a long and detailed explanation how to go about locating your Peyronie’s disease plaque or scar material.
On average a typical spontaneous natural healing (the kind in which the Peyronie’s disease goes away on its own without any direction intervention), can take from 6-18 months or so.
There is help all over the PDI website explaining and advising men how to help your body heal its Peyronie’s disease. It is necessary that you read and understand that this is a process using Alt Med to help the body heal as normally and naturally as possible. There is no need to come to the US since everything that is needed is available on the website, and it is necessary that you conduct the plan at home everyday making decisions for your self-treatment. You will be in charge of this work, while keeping in close contact with your local family doctor who can monitor and supervise what you are doing for your Peyronie’s disease treatment. We send to all customers all the information and suggestions how to do this work with Peyronie’s disease, so that your doctor can review and approve the process for you before you get started. TRH
Yes, Peyronie’s disease is just part of the problems that you are dealing with. I hear from many men in the Middle East who have Peyronie’s disease but are unable to do much about it due to the complex social and political problems of that part of the world. The best I can tell you is this is that if you have a friend who is in the US who can send products directly to you it is possible to get your Peyronie’s disease therapy in that way. TRH
Whether you have Peyronie’s disease developing right now will not be known for at least 6-12 months from now; you might have just slightly strained some of the soft tissue of the shaft during your injury and it will heal fine perhaps. Time will tell. In the meanwhile it would be foolish to take any chances or abuse yourself in such a way that you might provoke additional injury resulting in Peyronie’s disease because of secondary trauma that occurs after the first trauma. You must assure that you do not engage in any sexual activity that will result in more trauma.
I am not saying to avoid sexual intercourse. I am saying to avoid injury during sexual intercourse. Avoid techniques that put you at risk of injury; this usually occurs when the woman is on top while in the missionary position and she pulls back so far that the man pops out of the vagina while she then thrusts down on his erection (this is probably how you got injured last month, right?). Go slow, go easy, use light and gently thrusts, use short thrusts that do not risk you exiting the vagina. No teenage-like sex until you are feeling back to normal, and even then you always want to avoid penis injury because Peyronie’s disease is always a potential after this kind of trauma. You might want to read the book I wrote, Peyronie’s Disease and Sex” http://peyronies-disease-help.com/pdi-product/peyronies-disease-sex/ that goes into hundreds of sex strategies and techniques for those who have Peyronie’s disease or want to avoid getting it. TRH
If you have Peyronie’s disease you have a lot of fibrous tissue being laid down internally in the penis. This causes a bent penis to develop, and it can cause the penis to not only shorten but to become smaller in diameter or girth. The fibrous tissue does not stretch out as the normal penis tissue does, resulting in loss of size of the penis.
If you have Peyronie’s disease and your penis is smaller, you are still a worthy and lovable human being; you are still Bruce, just with a smaller penis. You have to keep in mind that you are not a penis and your total self-worth is not determined by the size of it. Your penis is attached to you; you are not attached to your penis. Your penis is the most important and valuable and lovable part of you — only if you make it that way in your mind. A good woman can love a man with a small penis. Do all that you can to heal your Peyronie’s disease using Alt Med ideas found on this website.
To get your thinking straightened out so you are not approaching this problem like a teenager, get my book, Peyronie’s Disease and Sex” http://peyronies-disease-help.com/pdi-product/peyronies-disease-sex/ It will put things in perspective for you, and give you hundreds of solid ideas how to use what you have. TRH
I’m a 50 yr old man with self diagnosed peyronie’s disease. About a year ago my girlfriend and I were having sex “doggie style” and I was aggressively thrusting in and out and I popped out and it hurt immediately. But afterwards, no pain or side effects. But now I have scar tissue approximately one inch down from the head and all the way around causing the bottle neck affect. From the base of my penis and 4″ up my erection is normal. But from the Peyronie’s disease scar tissue and up it stays flaccid and painful. Its not extreme pain, but very uncomfortable and painful. I’ve lost girth and length. I’ve read that a penis pump may help. Not only is the physical part taking a toll, I’m a little sad and depressed by my situation. I’m anxious to try your peyronie’s disease treatment but I know I may never be the “same” again. Thanks for any help and response
Your doggie style injury is a classic way to injure the penis that can eventually result in Peyronie’s disease. Another variation is the missionary posture with the woman on top during which she pulls back too far and loses the penis from the vagina, and thrusts back down with full force onto the erection thus bending it (painfully) against her pubic bone or inguinal area. I mention this so readers are aware and forewarned that both these common sex postures can lead to Peyronie’s disease if they are performed carelessly or with such teenage abandon that injury results. Should they be abandoned and forgotten? No. They should be used slowly, carefully, , skillfully and with much practice, deliberately and with relish, while being mindful to NEVER pull back so far as to lose insertion once in the vagina. Guys: if you keep your head and be reasonable during sex, you are safe. Let her go crazy, you stay sane and make sure you remain in that slippery sleeve of hers where you are safe. A good way to stay safe is to put one arm firmly but gently around her waist to limit her movement and yours; do not squeeze her, just keep both of you two together if thrusting gets too wide. Your hold with your arm keeps the thrusts short so she cannot lose you. OK? These ideas and a lot more are in my book, Peyronie’s Disease and Sex.” http://peyronies-disease-help.com/pdi-product/peyronies-disease-sex/
Peyronie’s disease does not have to so greatly curtail sexual activity as it often does; men stop sex unnecessarily because they do not know what they need to know to make it happen even with a bent penis.
I do not like penis pumps (or vacuum erection devices or VEDs) because they can cause more penis injury when used to excess. Given the way that men react when they see their abnormally large erection when it is in a VED, they easily injure themselves because it seems than men cannot control themselves when it comes to their penis. Ask the average woman. For this reason I think the VED is not a good approach to use because it can easily be abused and lead to more injury that leads to more Peyronie’s disease. In fact, read the PD forums. You will encounter many men whose Peyronie’s disease started when they were using a VED in an effort to enlarge the penis. There are better and safer strategies to naturally help your Peyronie’s disease heal, next paragraph.
Back to your concern about treating your Peyronie’s disease. All I can tell you after doing this work with thousands of men since 2002 is that we help more men than we do not help. And of the men we help the progress ranges from slight to complete; progress and recovery seems to depend on how aggressively and faithfully a man will work on his Alt Med plan that he puts himself on. It is vitally important that you locate and monitor the size, shape, density and surface features of your PD scar tissue that is causing your bottleneck and reduced size; you will use this information to guide your treatment. All this is explained in great detail in almost 20 pages of notes that are included with the treatment plan you order. I encourage you to learn as much about Peyronie’s disease as you can from the huge PDI website. Please let me know if you have additional questions. Since this is December 24th, Merry Christmas. TRH Peyronie’s disease
Many men with Peyronie’s disease have difficulty locating their Peyronie’s disease scar tissue, that is true. What is also true is that many of them do find it once they know what they are looking for. Many people,, even doctors, have trouble locating the fibrous tissue. I have sent you some special instructions that explain in great detail how to locate your Peyronie’s disease scar.
If anyone else reading this communication wants to get special detailed instructions how to find their PD scar, just send an email directly to me with the note “How do I find my Peyronie’s disease scar?” I will send you notes to help you. TRH
Doctor Herazy. l have linked your answers to peoples concern for Peyronie’s disease. l have been battling with a similar situation for years now. l have a curved penis which has affected my sex life. l cant penetrate a woman because of this curve. l always stop at the surface of the woman organ. This has always made them not to enjoy sex neither do l. Is there any way l can get help / treatment so that my penis goes to the normal size. Please help am hurting feel disturbed
You say you do not have Peyronie’s disease, yet you mention you have a bent penis and it is not your normal size. These are two findings of having Peyronie’s disease. I suggest you ask your medical doctor to diagnose your situation.
Regarding your problem with penetration related to your bent penis and smaller size, my book, “Peyronie’s Disease and Sex” could be very helpful to you. This is a 180 page book filled with helpful sex advice and insights if you have sexual difficulty related to Peyronie’s disease. It has helped thousands of couples to improve their ability to engage in sex again. It also discusses the feelings of embarrassment, insecurity, confusion and loneliness that bothers men who are going through Peyronie’s disease.
Lastly, it is possible to help the body reduce Peyronie’s disease. Please look around this website for information about using Alt Med to help your body remove the Peyronie’s disease fibrous tissue that could be causing your bent penis and reduced size. Good luck. TRH
Hi Dr Herazy. My Peyronie’s disease started approx 3 years ago. I woke up one night with a painfull erection. I saw a urologist who said i had scar tissue and would report back to me. Her report was the scarring will go away after 3 months or so and to see her again if i started to bend. At that stage i had no major bend. Not knowing I had Peyronie’s disease and not being advised to not have intercourse my wife and I continued to do so. It hurt! Also resulted in a peyronies bend! I started taking Neprinol in July 16 and vitamin e with that in November 16. I bought 3 bottles of PMD from you in October 16 and have almost finished the second one. I have no more pain but not a lot of bend reduction. Reading the current newsletter it would seem i should start to utilise your big/large plan plus manual stretching? Your thoughts please?
Having Peyronie’s disease does not necessarily mean you should not engage in sexual intercourse. The only proviso about Peyronie’s disease and intercourse is that you should be careful to not be aggressive or careless lest you injure yourself during insertion or thrusting. As long as intercourse is slow, gentle and careful, continue as you normally would. Your pain during intercourse suggests that what you were doing, and how you were doing it, was stressful to the already injured area of PD scar. Someone should have explained all this better to you while they were telling you about Peyronie’s disease.
Your current Peyronie’s disease treatment regimen is piecemeal and only partial, and it is a common way for people who only read around the edges of this website to get started with partial information and partial treatment; they are often disappointed with small and partial results. In order to expect better Peyronie’s disease scar reduction it is important to use a diverse complement of the internal and external therapies that you see discussed on this website. Now that you have started a partial and imbalanced treatment I suggest that you go back to the PDI website to determine what level of treatment you should follow; a good place to start is http://peyronies-disease-help.com/new-customer-how-to-select-treatment-plan/. From there simply decide which plan to use, and order for yourself those elements of that plan you do not have. You will be given all notes and suggestions for correct use of whatever you order.
You have experienced some improvement with your pain using a partial approach so it seems reasonable that better care should result in further reduction of your Peyronie’s disease scar and straightening of the bent shaft.
Let me know if you have any more questions about your Peyronie’s disease treatment. TRH
What do you think of the P-Shot for Peyronie’s disease?
My urologist did not mention it as an option. He only wants to give me the shots of Xiaflex, or whatever it is. Or pills, or surgery. I was going to consider the P-Shot. Any thoughts??
The Priapus Shot (P-shot) has been around for only a few years and was not initially intended as a Peyronie’s disease treatment.
The P-shot website opens with the statement, a “Description of how the penis can be rejuvenated and enlarged using platelet derived growth factors (or Platelet Rich Plasma).” This indicates the P-shot is really about how the penis looks, about vanity. This same secondary usage is also seen with the penis extenders or mechanical stretchers that were designed to fulfill every man’s fantasy of a larger penis, not anything related to PD. Every man wants this P-shot thing to work because he would get a larger penis in the process – a win/win. What a simple and easy idea to sell to people. Please look up the other PDI posts for more information where I have commented on this subject. Overall, I have strong doubt that time will prove the P-shot to have much if any positive affect on Peyronie’s disease.
We know that the body heals Peyronie’s disease in a good percent of cases. PDI was started in 2002 after I was able to use Alt Med nutrients to encourage my own healing of PD. I get 8-10 reports of moderate to marked success of reduced Peyronie’s disease fibrous tissue (and related improved penis curvature, return of lost size, improved erection quality) for every one report of failure. Not bad. People daily tell me that we present here makes more sense to them than anything they have found on the internet. Please look around our site for information that will help you decide how you want to treat your Peyronie’s disease. Please let me know your questions. TRH
do you have step by step instructions on how to use you peyronies treatments
Yes, whatever you order comes with instructions how to correctly use each product. Peyronie’s disease is not an easy problem to treat correctly, so we knew we had to give our customers good information to use. Our instructions earn praise from the folks who order from PDI, and we very seldom get questions from anyone after they go over the notes. TRH
HELLO dR. hERAZY, i READ THROUGH YOUR pEYRONIE’S TREATMENT ADVICE BUT NOTICED YOU DID NOT MENTION ANYTHING ABOUT USING THE uLTRASONIC DEVICE YOU SUGGEST FOR dpi CONDITION OF THE HAND. oR dID i MISS THAT. i HAVE READ NUMEROUS ARTICLES ABOUT USING uLTRASONIC TOOTH BRUSHES AND SAW YOU DEVICE WHICH DOES LOOK MORE EFFECTIVE FOR TREATING MY PEYONIE’S.
Greetings Charlie and a Happy New Year to you and yours,
More ideas for a shortcut to Dupuytren’s contracture treatment. Someone somewhere must have recently started to spread the idea of using a vibrating toothbrush (that is called “ultrasonic” even though it only vibrates a few times per second). For this reason, people are assuming that it is the same thing as ultrasound therapy. However, a true ultrasound machine vibrates at the rate of a minimum of a MILLION times a SECOND, not 10, 25 or 100 times a second, but at least a million times a second. There is no comparison. The therapeutic difference is significant. I have not yet read how the relatively slow vibration of a toothbrush is supposed to help Dupuytren’s contracture. However, even before seeing the information, I am very skeptical.
Yes, the Dupuytren’s Contracture Institute definitely recommends 3MHz treatment as part of a larger natural protocol to increase and support the ability of the body to reduce and even eliminate the DC palm nodule and finger cord. Some people try to use only ultrasound therapy for their Dupuytren’s contracture, and it helps a little. They eventually learn that it is a whole lot smarter and faster to treat their DC as DCI recommends with a larger and more inclusive treatment plan. DC is a tough problem. There are no shortcuts or easy answers.
When Dupuytren’s contracture treatment is done the way DCI suggests, we get 8-10 people reporting moderate to marked improvement (up to and including complete reversal and elimination of DC) for each person who reports failure. When just ultrasound is used, we get reports of some softening and a little regression, but then improvement typically stalls. The recovery process must be supported fully, with a host of vitamins, minerals and enzymes, for good results to occur.
The specific ultrasound machine that is recommended and sold by DCI operates at 3,000,000 cycles per second (three million vibrations a second), which is typically written as 3MHz. The higher 3MHz (3 million cycle) vibration penetrates less deeply that the relatively slower 1MHz (1 million cycle) vibration. Since the DC nodule and cord are at and just below the surface, the 3MHz unit works much better for DC and PD, than the more common 1MHz US machines that are routinely used to treat sprains and strains of various body parts.
There are many places ultrasound therapy is explained on the DCI website; just search around a bit. TRH