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Author Topic: Peyronies Survival Guide - Information for New Members  (Read 33783 times)

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Hawk

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    • Peyronie's Disease
Peyronies Survival Guide - Information for New Members
« on: February 19, 2013, 09:39:43 AM »

Welcome to the PDS Forum.  We sell nothing and we run this off of our own work and money.  We do this to provide a place where you can find support and education from other men and women who have fought back against this condition.  We know you have a thousand questions ranging from what can I do to fight this, to how can I face life.  We know because we have all been there. Our ages range from 17 to 85 years old.  Some of us have experienced our first symptoms several decades ago.  Many of us have survived, improved, even prospered.  This is our best attempt to give you one short article to read to help answer some of your questions.  These answers do not come directly from doctors but they come from fellow patients and spouses that have traveled this road.

What is going on? - If you have Peyronies, you have a condition that caused your body to replace normal elastic tissue in your penis with non-elastic scar tissue called plaque.  It has no association with plaque in your arteries or elsewhere in your body.  You have Peyronies when your body forms scar tissue in the penis in places where it is not needed to heal a wound.  It replaces normal elastic tissue, often far from any injury and it can cause deformity much like putting a piece of Scotch tape on a balloon and then blowing it up.

What Caused this? No one can give a definitive answer to that question.  There are clear indications that there are genetic predispositions that are the underlying problem and that the actual event known as Peyronies Disease is then triggered by an obvious injury or by a micro-trauma you may not have even noticed.  If either the underlying condition is not present, or the triggering event does not happen then Peyronies Disease may never develop.  The greater the underlying conditions, the less of a trigger it presumably takes to start the Peyronies Disease process.  There are many factors that increase our risk for Peyronies but for now, lets discuss some practical tactics to deal with it.

What do I do to cure this? While there is no cure, there are several things that can help stabilize the process and even reverse the symptoms of Peyronies Disease.  It usually makes sense to try these in a certain order.  In ranking this order we consider:
   The likelihood the treatment will work
   The risk of the treatment (either to general health or to the Peyronies Disease)
   The cost
   How invasive is the treatment – Most patients and doctors proceed from less invasive to more invasive (oral meds, shots, surgery)

Unfortunately no single treatment works for all, and every case seems to progress or respond to treatment in its own way.  Very rarely (less than 5% of cases) reverse on their own.  A slightly higher percentage improve somewhat over time without treatment.  Most remain the same or progress (symptoms worsen) without treatment.

Best initial treatments / things you can do immediately - The list of first-line treatments recommended by the PDS are a combination of those recommended by leading urologists combined with over-the-counter treatments that have resulted in the best reports of success from our thousands of members.  Some of these have clinical studies supporting their benefit in treating Peyronies. These are first-line treatments because they are less invasive and have the least risk of negative side effects.  They are supplements (food based nutrients) or lifestyle changes with few if any risk of negative side-effects.  In fact they are likely to benefit your general overall health.
CO Q10 - 200 - 400 mg daily divided into 2 or 3 doses. (If over 40 yrs old, consider substituting the more expensive Ubiquinol)
Acetyl L-Carnitine 1.5 - 3 grams per day divided into 2 or 3 dose
L-arginine 1.5 - 3 grams per day divided into 2 or 3 doses
Try to minimize stress by getting plenty of good sound sleep and moderate exercise.
DO NOT USE TOBACCO PRODUCTS
Consider researching and going on an anti-inflammation diet
Erections with oxygen laden blood supply are good but any rough sex or intercourse with an inadequate erection is risky.

Pain - Pain varies greatly from case to case.  Pain can be non-existant, constant during erection only, or only when the penis is flaccid.  Some of these first-line treatments help resolve pain.  You can also take Ibuprofen or Celebrex to help with pain and inflammation if needed.  Pain usually runs its course during the initial acute phase and resolves within 6 to 18 months even without treatment.

It is critical to establish a baseline - There are few times where a subjective impression is less reliable then when a stressed man is looking at his penis for signs of improvement or further damage.  That is why it is critical to get objective baseline measurements.  For now just trust me on the best way to do this.  First Get a BPSFL measurement (just mouse over the abbreviation).  If you get natural erections then measure your erect girth at 2 points on the shaft that are easy to duplicate the next time.  I recommend right behind the head and at the base.  As an alternative you can go for the largest and smallest diameter spot if you choose.  Now try to measure your angle of bend with a protractor (you can print one online) or by photo or tracing.  Write these measurements down! These measurements are critical and will tell you if Peyronies is advancing or if you are recovering ground.  Otherwise it is just a guess if a treatment is slowly working.

OK, what is my first official step? Step number one is to get a sound diagnosis.  Preferably from a urologist that specializes in Peyronies Disease.  Most urologists see Peyronies Disease as a frustrating condition that makes up a tiny part of their practice, a practice that treats male and female urinary tract conditions.  A sexual Dysfunction doctor with an interest in Peyronies Disease is often a better choice.  Depending on your area and your insurance this may mean the first step is getting a referral from your family doctor.  Sometimes you can contact a specialist without a referral, depending on the requirements of your particular insurance coverage.

How do I find a good doctor?  While well known doctors with a specialty in Peyronies Disease are relatively few, most men in the U.S. will live within a couple hundred miles of a doctor that is known by the patients on this forum.  There are likely many more doctors that we do not know.  Sometimes patients have good luck finding a doctor on their own either by asking questions in advance or simply by the luck of the draw but the odds are against that since national surveys show that most urologist have many totally false notions about Peyronies.  Doctors recommended by this forum would usually do the following:
        Give you a hands on examination to check for plaque (scar tissue)
        Order or perform a duplex Doppler ultrasound to check plaque and blood flow.
        Prescribe Pentox and an ED drug along with over-the-counter, L-Arginine.  The            combination of these 3 items is referred to as a PAV cocktail
        They would be open minded and supportive of using therapy such as a VED or traction.
        They would consider surgery a last resort after a year or more of other treatments failed, and mutually satisfying intercourse was difficult.
        They would also consider injections to be a last resort.

Preparing for my doctors visit To some degree, this will depend on whether your doctor is one from our list or whether you decided to take a long-shot on a random urologist. To cover all bases I will assume you are unsure of your doctors expertise with Peyronies.

1. Do not be shy.  Doctors deal with such issues as a routine part of their day.

2. Take a photograph of your erect penis from an angle that shows any deformity accurately.  This may reduce the extent of the examination required or simply be an added piece of information

3. If you have a spouse or partner take them along to take notes or remind you of questions. Begin writing down questions a few days in advance.

4. Read and take information on Pentox studies from the following FOUR (4) links Pentoxifylline Attenuates Transforming Growth Factor- β1-Stimulated Elastogenesis in Human Tunica Albuginea-Derived Fibroblasts Part 2: Interference in a TGF- β1/Smad-Dependent Mechanism and Downregulation of AAT1
   
Smith et al. 2011, Pentox treatment and penile calcifications in men - Peyronies Society Forums   
CLICK ON THE ATTACHMENT FOUND AT THIS LINK. 

Click the attachments below.  Both are good resource to take to your doctor when asking for pentox.
  CLICK ON TWO ATTACHMENTS FOUND AT THIS LINK.

5. Ask your doctor for a complete blood panel including Vitamin D, total testosterone, free testosterone, estrogen, and PSA testing.  The information in these tests will be necessary to make decisions about your treatment plan.

Beyond Diagnosis - Hopefully you had a positive experience with your doctor.  If you got a diagnosis of Peyronies Disease then you should also have gotten a prescription for Pentox (400 mg 3X a day with food) which is probably the single best first-line treatment for Peyronies Disease.  Pentox does not cure Peyronies Disease.  In many men it does help with everything from reducing pain to partial correction of deformity, or at least stopping progression.  You should next consider getting a VED or a traction device.  This means it is necessary for you to read those boards on the PDS forum to make the best decision for you.  Traction takes more of commitment from you but there are many factors to consider such as "can you get a natural erection", what is your daily life style, is cost a factor.....    Many members have both traction and VED units.

Remember, this is a marathon not a sprint.  If you are fortunate enough that the recommended first-line treatments help you, the process will be very gradual.  Do not expect to see significant improvement in a few weeks. Also there are other supplements and routines like gentle heat that may help.  There are also more invasive treatments if these first-line treatments fail.  However, the treatments in this article are the stating point.  They are the ones that will give you the best result for the money and the time spent.

Psychological Aspects - The PDS has an entire board discussing just the psychological aspects of Peyronies.  It is clearly at least half of the challenge and maybe the part that you have the most control over.  Men with similar physical symptoms have dated, gotten married, had children, and lead close intimate relationships with their spouse.  Others have lost wives, jobs, dropped out of school, and become social shut-ins.  Attitude and perspective is everything.  If you have not already learned this it is time to learn that your penis does not define you.  It has little to do with the intimacy you can offer to a mate.  Many marriages have become stronger because instead of counting on a "perfect penis" to carry a relationship, men learned to include new levels of intimacy that their spouse had been craving.

The most common complaint of women is that their partner withdrew, shut them out, would no longer hug, hold hands, or kiss.  They refused to discuss their issue of Peyronies but instead got angry and confrontational.  What Peyronies does to the penis very seldom ends a good relationship.  What some men allow it to do to them psychologically has often ended relationships.  Sadly this is the one area over which they had total control.  If need be, seek good professional counseling.  If you grow and rise above the psychological impact, you have already won half of this battle.

Best Wishes!
Hawk, Founder/Administrator

PS: Please do NOT ask me private questions about Peyronies Disease.  Post on the open forum.  We have several thousand members.  Most know things I do not know.  The point of the forum is to post where several minds can consider, suggest, and learn.  I just cannot reply to thousands of members privately.
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