There are more than 300,000 new Lyme Disease infections annually, and the CDC and medical community is just now acknowledging this astonishing number, MUCH higher than their previous rates of "30,000 annual cases."
If you are one of the annual 300,000 diagnosed with Lyme Disease stand up and represent. The Lyme community is launching a photo campaign to get more media attention for Lyme Disease. They are asking for your photos.
It's simple and powerful, be a part of it here:
http://lyme300000.wordpress.com/
My fibromyalgia journey - complementary and alternative medicine, an integrative approach, for treating fibro and chronic fatigue, what has helped me - information, resources and research I've found that I want to share to help others regain their wellness!
Showing posts with label chronic lyme disease. Show all posts
Showing posts with label chronic lyme disease. Show all posts
Tuesday, December 3, 2013
Sunday, December 1, 2013
Lyme Disease and the CDC
And we wonder why we can't make any progress with Lyme Disease??
This is sad and sickening. And yet another reason I skew towards the all-natural alternatives and way from the medical community. Are the ever really our for our best interests, or just our to line their own pockets with more money??
Lyme Disease Community Blows the Whistle on Corruption Within the CDC http://www.prohealth.com/library/showArticle.cfm?libid=18502&B1=EG112713
This is sad and sickening. And yet another reason I skew towards the all-natural alternatives and way from the medical community. Are the ever really our for our best interests, or just our to line their own pockets with more money??
Lyme Disease Community Blows the Whistle on Corruption Within the CDC http://www.prohealth.com/library/showArticle.cfm?libid=18502&B1=EG112713
Friday, November 29, 2013
Lyme Disease and Fibromyalgia?
I've always held the theory that my fibromyalgia and chronic fatigue has been hereditary and lying dormant, and was kicked into full gear when I was bit by tick and faced Lyme Disease attack (stressor) on my body in 2009. Looking back now, I don't think I had the traditional "bullseye" rash but just a big pink blot. Thus I delayed treatment, even diagnosis for the Lyme Disease. It took 4 months to get a diagnosis of Lyme Disease, then fibro and chronic fatigue.
Long story short, I still keep one eye out on Lyme Disease research, studies and community involvement.
When I was diagnosed in South Florida with Lyme Disease it was very hard to find treatment, get any straight answers. I was told Lyme Disease is not common in Florida, in fact many doctors didn't even believe I had it.
I recently came across some articles on a brave young woman, also a Lyme Disease sufferer, who is working to promote better research and education on Lyme Disease, especially in Florida:
Long story short, I still keep one eye out on Lyme Disease research, studies and community involvement.
When I was diagnosed in South Florida with Lyme Disease it was very hard to find treatment, get any straight answers. I was told Lyme Disease is not common in Florida, in fact many doctors didn't even believe I had it.
I recently came across some articles on a brave young woman, also a Lyme Disease sufferer, who is working to promote better research and education on Lyme Disease, especially in Florida:
An upcoming symposium on Lyme Disease at The University of Florida:
Has anyone else had experience with Lyme and Fibro / Chronic Fatigue?
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