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!

Off to the Convenor of Medical Panels with my invisible pain

You know that feeling before something great is going to happen, like just arriving at the airport and knowing you're off on a great holiday? It's a great feeling isn't it? Makes your insides really happy, the body and mind get a lift, and troubles seem to slide away, everything feels like it's going to be alright. Well, I couldn't feel more the opposite right now. I have an appointment with the Convenor of Medical Panels on Tuesday and I'm feeling more like I'm facing a funeral.

Soula Mantavanos…Inside her home and her passion to help others!

Tell us about your history and how you ended up in the position of being an amazing woman advocating for chronic pain? “I was working in our graphic design studio, Origin of Image (ooi.com.au) in March 2007. I was always health conscious so aside from my yoga ritual 4 mornings a week and walking everywhere, I would often sit on a fitball. It was great until the antiburst fitball burst and I fell to the concrete floor. It really was the split second that changed my life. I was 37. I think what tipped me into advocacy was the 4.5 years it took to find a diagnosis and the near miss I had with living out the rest of my life in horrific pain levels if I’d not investigated further. My chronic pelvic pain is more specifically known as Pudendal Neuralgia (PN) or Pudendal Nerve Entrapment (PNE). This is more simply put as Carpal Tunnel in the pelvis. Where Carpal Tunnel affects the hand signals and hand movements, Pudendal Neuralgia affects our biggest pelvic nerve which controls toilet and sexual signals and functions. The pudendal nerve runs under pelvic ligaments and muscles and is attached to nerve roots in the lumbosacral spine so it can be disabling. It feels like that core part of my body has a toothache or as if I have my finger stuck in a powerpoint. BUT, I’m happy to say I’m in a much better place now and that’s why I want to share my story. I believe if I was diagnosed within 6 months of my injury, I would not have this issue now and that makes me want to reach everyone with undiagnosed pain that may be suffering from PN. I’ve also been drawn to advocacy for injured workers since I’ve now had first hand experience with the WorkCover system and its limitations for understanding, assessing and treating chronic pain. In fact my chronic pain issue was not assessable for compensation. Its score was rated at 0% impairment. I’ve also submitted many complaints and questions to WorkSafe and associated organisations, I’m making a heap of noise on social media and gathering a great group of people in the hope of making a change. A network exists now, encouraging other injured workers to speak up, forming communities for support where there were none previously. Injured workers can now vent, speak up, be heard. Social media has provided a voice and is our legs (even when we physically can’t move). So in the process of advocating for PN/PNE the biggest tasks are to change the judgment and misunderstanding of ‘pain’, and misconceptions of the term ‘injured worker’.”

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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