“Do You Want to Have a Better Quality of Life
with Pudendal Neuralgia?”

  Hi, my name is Vanessa and I have survived Pudendal Neuralgia.

  During the weekend of Thanksgiving 2007 I suffered a serious fall in my bathroom
  that led to a severe case of chronic pelvic pain.

  My life became a living hell. I could barely walk, I couldn’t sit, and I couldn’t  
  drive anywhere. I would often need one of my parents to carry me to the toilet
  because walking hurt too much. And to add insult to injury I started suffering from 
  frequent bouts of urinary incontinence and extreme constipation.

I was completely bed bound, unable to get out of bed for more than a few minutes a day. I could only lie on the right side of my body as the pudendal pain was mostly on the left. I ate most of my meals lying in bed. And I was only able to wash occasionally when I could bare to have my Mum hold me up in the shower. And this lasted for nine months! (Want to see proof of my illness?)

And all the while I had to deal with horrific levels of unending pelvic floor pain. You know the pain that I’m talking about: that unmistakable feeling of acid burning, stabbing, aching, twisting, knife-like pain. 

I felt as though I had no dignity left. And even worse than that, I felt helpless.

None of my doctors knew what was going on. I went through endless hospital tests until a specialist in Paris finally diagnosed me with Pudendal Neuralgia. But even after we received the diagnosis none of my doctors really knew what to do. The treatment options seemed limited, and the doctors mostly wanted to avoid dealing with my case. I felt like I had no control over my situation.

I found some information on the internet, but most of the time it was just a repeat of the same basic information, or it was complicated medical reports aimed at surgeons. I found the search for information confusing, frustrating, and overwhelming. Furthermore, I was feeling so sick so much of the time that the last thing I wanted to do was to troll through the internet looking for answers.

I knew that most Pudendal Neuropathy sufferers never fully recover, but I persevered in my research none the less. And it paid off, because I eventually found a treatment that resulted in my complete recovery.

In the process of doing this research I discovered a huge amount of information about the condition. After I recovered I realized how important it was to pass on all this information. I didn't want any other Pudendal Neuralgia sufferer to have to go through what I had. And so I decided to complete my research.

In the process of doing all this research I was shocked to discover just how much I was ignorant of during my illness. I regretted how much more effectively I could have handled my treatment if I'd only known what I was now discovering.

In my experience a big issue is that much of the information available on the internet regarding pudendal nerve damage is highly subjective. It can be a great help to hear about other sufferers experience of pudendal pain, but each case is so different that this isn't the most practical of information. And when the majority of information available on pelvic nerve pain that one is reading is completely subjective one can easily feel overwhelmed and depressed.

Furthermore, it's just not very practical to have to drudge through large amounts of personal stories just to try to obtain factual information. Sufferers need a comprehensive overview of Pudendal Neuropathy and Pudendal Nerve Entrapment summarized in just one place.

It seemed to me there was a need for subjective, researched information. This information needed to  cover every facet of life with pudendal nerve damage, from the physical, to the emotional, and financial. It needed to start by clearly explaining the basics such as how a nerve works, where the pudendal nerve is located, and the reasons behind the symptoms. It needed to expand on what the options are for working and living with the condition. It needed to provide clear information about the psychology of dealing with chronic pelvic pain and the ramifications for friends and family. And all this information needed to be summarized in just one place.

It seemed to me that the best solution would be a comprehensive guidebook. It needed to be of such a quality that it would equip sufferers to deal with every aspect of their Pudendal Neuropathy. After all, why should someone have to spend years in trial and error when they could be fast tracked through the process and immediately provided with a high level of information about their pelvic floor pain?

And so I created a solution - a comprehensive, factual, objective guide book.

• The details of the cure that allowed me to recover from Pudendal Neuralgia
• What conditions can develop as a result of pudendal nerve damage
• Every major diagnostic test available
• Every major pudendal treatment available
• The various kinds of pudendal nerve entrapment surgery available
• The many gadgets that are available to PN sufferers, and where to buy them
  

       “I wish someone had placed this book in my hands
                                                   when I was first diagnosed"

This book - "Living with Pudendal Neuralgia" - is the result of my personal experience of Pudendal Neuralgia, plus several months of extensive research. All of this valuable information is available for your use. Simply place an order via the PayPal link and a copy will be delivered straight to your door.

                           When you think of the thousands of dollars you spend on medication,
                      hospital visits and doctors appointments, doesn’t spending just $36.99
                               to learn about all your options seem like a good investment?

$36.99 is less than what the average Pudendal Neuralgia sufferer spends
in just one month on medication!

I know what it feels like when money is tight because your pelvic floor pain doesn't allow you to work, and you're under financial pressure due to the cost of medical tests, medication, and countless doctors appointments. I've been there - I was unemployed for two years as a consequence of pudendal pain. During most of that time I received no unemployment benefits, had substantial medical bills, and I was basically was completely reliant on my family for survival. I know how careful one has to be with money when chronic pelvic pain is causing financial pressure.

On this basis I can tell you with complete integrity that this is an investment that is worth making. The cost of this book is small in comparison to the medical bills and medication bills you are likely paying. And the value of what you are gaining - an in depth knowledge of your condition - is substantial.

Understanding your pudendal pain is one of the most powerful things you could do to equip yourself for what is ahead. It's absolutely crucial.

The information contained in this book will allow you to be empowered in your fight against pelvic nerve pain. It will potentially provide you with knowledge of other treatment and lifetstyle options. And potentially it might save you from living in an unnecessarily difficult situation.

Buy my book to learn:

• How to deal with friends and family who don’t understand your illness
• How to recognize the signs that your loved ones are dealing with caregiver burnout
• How you can still have a scintillating sex life, despite your injury
• How to use a whole range of effective pain coping mechanisms

Sure, you could just do the research yourself. You could do months of tedious work to get somewhere near what I've managed to put together. You could battle through your exhaustion and pelvic floor pain to try to replicate this book.

Or you could simply invest a few dollars, leverage all the work I've done, and possibly start dealing with your condition in a more efficient manner. Empower yourself today by clicking the "Buy Now" button below and equipping yourself in your battle with Pudendal Neuropathy!

Buy my book to access:

• A complete list of Pudendal Neuralgia symptoms
  
• An extensive list of all the support groups available to you
• A full explanation of the most commonly prescribed medications
• A detailed glossary of all the most frequently used medical terms
  
  If you are struggling to understand what Pudendal Entrapment is, you want to know what a pudendal  block is, you keep hearing terms such as "Alcock Canal", "Pudendal Canal", "Vulvodynia" and "Levator Ani" and you want to know what they mean, then this is the book for you!
  

"This book is absolutely invaluable to anyone
suffering from Pudendal Neuralgia"

Ask yourself: 

• Why should you stay ignorant about Pudendal Neuralgia?
• Why should you rely on doctors who have never even heard of PN?
  
• Why risk not knowing about something that might improve your condition?
• Why spend months researching the illness when you could simply order this book and instantly have all the answers?
• Who better to teach you than someone who has personally experienced pudendal damage and has  fully recovered from it?

As they say, if you want to know what the road ahead looks like,
ask someone who is on their way back!

In my experience there is nothing worse when you’re sick than feeling completely out of control. By buying this book you will regain some control over your situation. You will learn how to effectively adapt your life to your condition. You'll gain access to powerful information as to how to handle your finances, your emotions, and your lifestyle. You will learn what worked for me when I had Pudendal Neuralgia. And you will learn the many things I wish I had known at the time.

Today I am able to fully enjoy life. I am able to walk, run, and sit for as long as I want. I’ve been on long distance flights on my own, and carried heavy bags along the way. I’ve climbed mountains, and swam in my local lake. I’ve taken up dance lessons again, and occasionally enjoy doing pilates. I’ve done more than I would ever have thought was possible when I was lying in bed, overwhelmed with pelvic nerve pain. It is possible that you could recover to this extent. And if you don't there are many treatments and gadgets reviewed in this book that could significantly improve your quality of life.

                         "This book is the best investment
           a Pudendal Neuralgia sufferer could possibly make"


Having Pudendal Neuralgia need not feel like the end of your life. By learning about the many options on offer you can discover ways to regain some of your independence, reduce your pain, and enjoy life more.

My book will not cure you. But it will give you a chance of finding a cure, and of having the best possible quality of life in the meanwhile.

                               
                                    This is the first ever full length book on Pudendal Neuralgia.

                                It is also currently the only full length book on Pudendal Neuralgia.


This book features:

• 133 pages
• Thirteen chapters dedicated to every aspect of life with Pudendal Neuralgia
• Extensive illustrations and photographs
• Contact details for the associations, gadgets, and treatments discussed in the book
• Comb binding, for easy reading for the bed-bound
  
  
  Do the right thing and empower yourself over Pudendal Neuralgia. Why wait?! Order your copy today for just $36.99 + shipping via PayPal and get it delivered straight to your door!
  
  

 
LEGAL DISCLAIMER: The author is not a doctor, or qualified medical practitioner. All information, opinions, and data shared in "Living with Pudendal Neuralgia" is subject to the assessment of the reader, and the advice of their doctors. By purchasing this product the buyer is accepting sole liability for their use of the information contained.

Has my book helped you? Do you have questions for me? Any thoughts? Email me and let me know!