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:

http://hhp.ufl.edu/index.php/2013/07/biting-back/

An upcoming symposium on Lyme Disease at The University of Florida:

http://www.epi.ufl.edu/?q=tick-borne-disease-symposium

Has anyone else had experience with Lyme and Fibro / Chronic Fatigue?