Hello! I’m Soula, welcome to pudendalnerve.com.au2026-05-24T13:34:31+10:00

Hello, welcome to my website!

I hope you’re not living with ongoing pain, but if you are, this website was created to prevent people who are experiencing chronic pain from misdiagnosis.

Created in 2011 – 4 years into this terrible lived experience, I realised I could help many people by building a website. The aim is to empower you so you can manage your health issue and to also avoid ongoing chronic pain –yes, it’s possible!

I want you to know that what you might be feeling right now won’t last forever, and that you will be able to change your situation, even if you’re stuck in negative thoughts and feelings, and all your efforts aren’t working. Change can be slow and will take longer the longer you have been living with pain.

I couldn’t hold my mobile phone or a glass of water without triggering my nervous system. Yet, here I am… working part-time, with very low pain levels and symptoms and a returned quality of life – I even founded My Health Story, a health tech platform to help people with chronic illness.

You’ve got this!

San Diego Pain Summit

Pain Management Conference The 9th Annual International multidisciplinary conference helping clinicians translate pain research into patient centered care. Rajam Roose is the CEO/Founder and sole organizer of the San Diego Pain Summit, LLC. She was a massage therapist for 16 years and ran a digital marketing consulting business (special skills: social marketing, SEO, & SEM) for [...]

The Business of Advocacy

Over some years and after a third time being banned in some way or form from an official pain organisation's social media, I now feel encouraged to make a point - advocacy is not a business. I began this website to advocate for people living with chronic pain and share helpful resources to avoid the impact of misdiagnosis on their lives. I aimed and achieved gratitude on a global scale, which has fed me. I also started this website to connect people living with chronic pain to professionals who understood them very well and could possibly treat them. I've asked none of these amazing professionals to pay me to be included on this website – we're all working for the same cause, right?  This was never intended to be a business. What I'm seeking is more respect and understanding for the voluntary position of the advocate. So let's pull the bandaid off and frankly define it: Advocacy is costly and time-consuming. It earns us no income; it causes pain and uses a significant portion of the little and precious uptime we get and, advocates are also much greater than their cause. I repeat; advocacy is no business. 

Rebrand Announcement: My Health Story

I was so close to throwing the PainTrain My Health Summary idea out the window when COVID-19 hit.  There was no way I could be positive about pushing on with my little train startup while a pandemic was approaching. But as it turned out COVID-19 catapulted telehealth behaviour and with that came increased interest in health tech and a newborn... the digital patient!  My creative communication experience always encouraged me down this complex path – I found healthcare primitive! The way people manage their health and the way appointments are managed has not changed for eons. If you live with an ongoing medical condition, we know now that it takes teamwork to manage it and you have to be responsible for your own health information (or it all gets documented incorrectly!). Clearly, I believe that we need to step up and manage our health and all things relating to it. We especially need to do this because we all have such lengthy stories to tell! So on that note, here's my big news from my humble little train which is now planning to go way beyond its destination... if you help me, there's a lifetime subscription in it for you!

Can’t read without pain levels soaring?

Then, here are my top recovery suggestions.

Stop repeating yourself at appointments and forgetting your important information – subscribe to My Health Story. I founded it so you can store and share your story and support yourself.

Get it in your App Store or at myhealthstory.com.au/shop

Yes, this amazing human with all her pelvic health and trauma experience is available to you via What’sApp. Get on there and search for Anne-Florence Plante.

Download the Pelvic Sense Program (use HELLOPS for a discount at sign-up), as this is something in your hands that you can do right now to start easing that screaming pelvis.

I know it’s hard to activate yourself when you’re feeling terrible and you can’t move but just move for a minute.. just watch something, just listen to this program and do whatever part of it you can to get that ball rolling.

Evelyn Hecht, a powerhouse physiotherapist who founded Pelvic Sense, is there for you if you need her.

Another on hand powerful resource is MoreGoodDays and that’s because you have oncall help if you need it as well as all the education resources you need to understand and treat chronic pain.

Find a GP who understands chronic pain (who will ask about your sleep, diet, and exercise) and knows the latest pain research. Here’s a test question for your GP – have they heard of Professor Lorimer Moseley and his research? If the answer is no, move on!
This might not be your issue, but it was mine and it still is today. I take my cushion everywhere even on a good day as prevention is a huge part of your health management.

A good day can easily bring on a bad day if you go past your limits. So stay your best by doing everything need to.

Here’s my cushion

Wow, this was an eye-opener. It explained everything to me about my body and how the trauma of misdiagnosis caused my harm – not my actual accident.

Read how I investigated my DNA and how it change my diet.

RUN to a pain specialist. Here’s some info about my life-saving specialist, whom I’m sure you won’t need if you prioritise your recovery.

Who am I?

My name is Soula and I live in Australia. I literally fell into the land of pelvic chronic pain – specifically Pudendal Neuralgia (PN), on March 1, 2007 when a fitball I was sitting on burst and I fell to a concrete floor.

At the time, I was working at ooi, a design company that I own with my husband Theo in our beautiful Collingwood warehouse. I was also an exhibiting artist until pain put an end to that for a few years.

Since my accident in 2007, I’ve learned a lot about chronic pain – especially that you can prevent it from becoming chronic and that you will manage it (I know you’re thinking I’m nuts, but you really can).

I want people to learn from my experience because I believe the ongoing issue I now live with was totally avoidable. I was undiagnosed for 4.5 years and that was THE most tragic part of my accident.

Me in pictures

Love my advocacy?

Well you can thank me! It will also help me keep my advocacy going. Donate from $10 via PayPal by hitting the button!

Thank you so much xx

Get ready to recover

Do you believe in yourself? Do you find yourself thinking, ‘hey, I know more about my experience than my health carers do? That’s because it’s true.

Sure, chronic illness is confusing and complicated and it fatigues you so you can’t think but know that underneath all that is the information you need to get better.

Are you prepared to learn a great deal about yourself and make changes to your life?

This is the road back to YOU. And some of you will return to a 100% version of you and others will return to a new version of YOU. But know that you will get there.

Despite what you’re feeling right now and despite thoughts like, ‘my pain is different’, ‘this is more serious’, ‘no one can help me’, I encourage you to take a huge breath and get ready to drive because you are leading the way forward. Yes, you!

Galleria Vittorio Emanuele IIMilan

Me in pictures

My treatment

Since my diagnosis 4.5 years after my fall, I’ve been able to find treatment that is slowly chipping at the glacier. Remember, you won’t need this – I had no resources like this to guide me which is why I fell into the big hole.

For me, recovery included/includes;

I was living with unbearable pelvic chronic pain that made me feel like I had my finger stuck in a powerpoint. I was sleeping my life away and, when not sleeping, in so much pain it was impossible to achieve much at all.

I was existing, not living. But I’m living now. That’s me below, in Venice (getting my cushion out of my bag).

Soula's cushion & handbag action Venice

Love my advocacy?

Well you can thank me! It will also help me keep my advocacy going. Donate from $10 via PayPal by hitting the button or this link!

Thank you so much xx

My journey

Not only did I find a way to move forward, but I traded the unfortunate experience with advocacy so I could further support people living with chronic illness and Victorian injured workers.

It’s been an overwhelming emotional journey since 2007. As well as the endless hunt for treatment, I have:

Let’s clarify whether you need to read on:

  • Do you have chronic pelvic pain?
  • Have you had this pain since injury, pregnancy, giving birth, or other trauma to your pelvic area? Perhaps you are an elite athlete or cyclist?
  • Does it feel like a toothache?
  • Does it itch and gnaw?
  • Do you feel like you’re on fire?
  • Do you feel spasms, fluttering and glitchy?
  • Are your toilet and sexual signals and functions irregular?
  • Is there no obvious issue with your x-rays and MRIs?
  • Do you find distraction can often work incredibly, but afterwards, the pain becomes excruciating?
  • Is the pain often worse after activity rather than during?
  • Do you feel no one quite understands you, your explanations, and your pain descriptions?
  • Have you been told you have a Psychological Condition and been left to feel like you’re crazy?
  • Do you associate your pain with ringing in your ears and feel you can’t pinpoint where it is?
  • Would you say it’s sometimes painful to speak and that sounds and speaking hurts?
  • Have you had endless appointments with no relief?
  • Do vibrations, a fright, or bumps send a surge through your spine?
  • Do your legs feel weak?
  • Do you find sitting unbearable?
  • Have you fallen on your coccyx or had an accident, and after years it still feels like it happened yesterday?
  • Are you part of an Australian Workers’ Compensation system and feel you are being treated poorly and that the whole system is like a circus?
  • Do you feel the Australian Workers’ Compensation system can’t help with return to work because the VWA Agent treats you poorly?
  • Do you feel the system is outdated and primitive and has no understanding of chronic pain or your situation?

Then I sadly welcome you (NOT) to my website but please know, there is a way to change things. That road is unique to each of us. Strap in, prepare to really get to know yourself and be prepare to slow down in order to speed back up again.

Acknowledgment

I have to acknowledge my diagnosing physio, Anne-Florence Plante who lent me her research and encouraged me to put this website together. Also, a huge thanks to the contributors who wrote letters of support and allowed me to share their valuable information.

Another reason why I made the site is that I felt Victorian injured workers needed some advocacy also. My experience with the Victorian Workcover Authority (VWA) and their health insurer buddies has been the most significant trauma of my experience. WorkSafe is a system constructed to avoid liability for work injuries – it has sadly nothing to do with helping people get better and back to work.

A reminder that this website is a documentation of my experience and my treatment (appropriate and not!). No information provided on this site is a form of recommendation in any way. Each of us has a unique experience with chronic illness, and each has to find our way through it.

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