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Pain Train featured in the AMA Victoria’s VICDOC magazine

By | 2018-02-16T10:12:28+00:00 February 16th, 2018|Help, Pain Train, Print, Professional, Read|

Pain management has come to me in various forms. It’s a pretty special feeling that my 11 years of experience with chronic pain may be useful for learning and inspiring change in the way pain [...]

Melbourne Leader story, Soula bares soul over pain

By | 2017-12-11T15:09:55+00:00 December 5th, 2014|Advocacy, Print|

The following story was published in support of the current National campaign: Nerve Pain is Different. Please help us raise awareness for those with debilitating invisible pain. If you think you have nerve pain, talk to your doctor and visit [...]

ANZCA Bulletin: Simple Accident Leads to Life of Pain

By | 2017-12-11T15:03:47+00:00 October 7th, 2014|Advocacy, Print|

It took nearly five years of chasing answers, of tests and interventions, frustration, grief, and constant, unbearable pain to reach a diagnosis. The fall caused nerve damage in the pelvic area, very real but invisible on MRIs, examinations, X-rays and CT scans. “It is still a primitive time in pain. Being told for four and a half years ‘this is chronic pain ... go home and live with it, there’s nothing that can be done’ is brutal not to mention primitive.”

The book: Art & Chronic Pain – A Self Portrait

By | 2017-12-11T09:42:17+00:00 October 30th, 2013|Print, Read|

Yes, I've found another medium to express my pain and you can own your own copy of it! I didn't see the point of creating a long description of my living with pain, sharing my tips, turning journal entries into a pain story. I am, first and foremost, before the pain life, an artist... so my book had to contain many pictures and few words, just 32 pages in fact, but I believe it's a complete story. It doesn't hold the solution for PN but it'll allow you to explain it to someone else, leave it on the coffee table, and it will be light enough to carry around. Above all I created it to express my experience so far and so that it is a bit of a companion to another PN family member. The idea was for the reader to feel empathy in a world where no one seems to understand, and to ease the pain as you look through it.

My_Space, My facade, living with Pudendal Neuralgia

By | 2017-12-11T13:46:29+00:00 May 9th, 2013|Blog, Creativity, Print|

We don't usually love media, but a little attention after some lengthy hibernation from work was bound to be very valuable for our (Theo's and my) 12 or so year old business, Origin of Image. The lovely Sunday Style (Herald Sun) offered an interview in their 'My_Space' feature... hmmm, quite funny for us as there's nothing 'my' about 'our' life. We share work, living, we even share Pudendal Neuralgia (PN). However this media attention and the snap of me in Sunday's weekend paper had me staring at my portrait (thank you Marija Ivkovic) with curiousity at that captured second of my able life. I looked incredibly independent, active, like I was working full-time and like the issue I confessed to was clearly easy to live with. We are all judged on our facade... and although it was stated in the article that I have PN, I often wonder: can it (or any other invisible issue) ever be understood by my friends, family or community at a glance? The answer is obviously 'no'. I myself battle to understand this conflicting issue with its high sensitivity, on/off maddening, screaming and confusing signals and failing functions, and that's no surprise because even I can't see it! Theo puts it well, "I can't understand Pudendal Neuralgia but I believe Soula".