TARLOV CYSTS - Canada the misinformed!!!

The rare diagnosis of Tarlov Cyst Disease poses significant challenges in the realm of medical care. Most Canadian Medical Practitioners lack the expertise to accurately diagnose, treat, or manage this condition. As a result, patients often find themselves navigating a healthcare system ill-prepared to address their needs, leaving them feeling lost, scared, and isolated. This lack of medical understanding perpetuates feelings of misinformation and uncertainty among Canadian patients. Through this blog, I aim to share my journey of navigating the Canadian Healthcare system while living with multiple rare disease diagnoses. I have dedicated myself to learning as much as possible about my rare diseases, hoping that my experiences and hard-earned self-education can support and guide others on their own rare disease journey. Together, let's shed light on the challenges those living with rare diseases face and work towards a more compassionate and informed healthcare system.

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Thursday, October 13, 2011

Canadian Pain Management Series of Recent News Articles

CANADIAN PAIN COALITION

For every patient with Chronic Pain, to hear the story of another person feeling similar pains and facing similar barriers is never a good thing. But sometimes it can be a great thing!


I received an email from the Canadian Pain Coalition (CPC) informing members that there is a recent Pain Management Series of news articles written in publications across Canada.


Below are all of the links to the published stories for anyone interested in knowing more about what Canadians are facing, and what's being said and done to improve current pain management options for Canadians.



'The worst part is you can't see pain'; Former administrative assistant can no longer work now that her entire body has been affected






Who will stop the pain? Canada's invisible epidemic of suffering / Treating the invisible affliction; Inside the world of unrelenting, incapacitating and life-altering pain.




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