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INTRODUCING OUR NEW “Partners in Wellness” PROGRAM, Calgary

Monday, April 19, 2010

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As the Executive Director for the ME/FM Society of Alberta and on behalf of our board we are proud to introduce our new “Partners in Wellness” program. As someone who suffers from ME/CFS and as most of our board members either suffers with ME or FM the question always comes up, “How do I get back a certain amount of quality of living in order to be able to do some of the things that I once loved?” While studies are underway way or new discoveries are being made, we’re all left with the big question “What do I do in the meantime?” Everyone’s illness takes on different forms, levels of pain and fatigue varying sometimes day to day. The level of frustration for patients can be insurmountable with the lack of knowledge or compassion from the medical community. This leaves patients feeling overwhelmed and “not credible” in the eyes of friends and family. Finally, once you have visited every specialist that the medical community has to offer and are offered little or no answers, we are left on our own. This is where we all must take an active role in managing our health. We must continue to seek medical advice but must also try to find ourselves doctors that are compassionate. Most of us at some point turn to alternative practitioners. By trying to understand the root causes such as dietary intolerances, allergies and hormonal imbalances to name a few, we can slowly start taking charge of our level of wellness.

CANADIAN BLOOD SERVICES FIRST TO TAKE STAND ON ME/CFS & BLOOD DONATIONS

Monday, April 12, 2010

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Canada has become the first country in the world to ban people with chronic-fatigue syndrome from donating blood. The precautionary move is a result of Health Canada’s concern over a virus known as XMRV, which has only potentially been linked to chronic fatigue. XMRV closely resembles the AIDS virus, prompting fears it can be similarly [...]

Discovery of Significant link between XMRV and ME/CFS.

Thursday, October 15, 2009

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Whittemore Peterson Institute Scientists Discover Significant link between XMRV and ME/CFS RENO, NV - A recently identified retrovirus called XMRV has been linked to a debilitating neuroimmune disease that affects more than one million people in the United States. Scientists from the Whittemore Peterson Institute (WPI), located at the University of Nevada, Reno, and their collaborators from the National Cancer Institute and the Cleveland Clinic, have discovered a retroviral link to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).

Recent Podcasts
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Personal account and information about ME/CFS, including Clinical Definitions, Viruses involved, symptoms, some treatments and functioning levels.

Video by the American Centre for Disease Control and Prevention about the condition Chronic Fatigue Syndrome/Myalgic Encephalopathy, titled “Missing My Life”.