Re: Diagnosed with fibromyalgia and Meniere's Disease

Forgot to add that I am now 90% better, after having lyme 8 years. It would have eventually progressed to MS I believe, as I was having the jerking symptoms, and twitching, especially my facial muscles and extremities. Go pursue lyme disease heavily, until you find a LLMD that will run a western blot through Igenex. Don't pursue MS until you rule out lyme for sure, as lyme is a very tricky SOB and is what causes MS in my eyes. It's a re-engineered bioweapon, which broke out from Plum Island, NY. Why do you think it evades testing and diagnosis by many mainstream professionals?! $$$$, they diagnose you with lyme right away they treat you for 4 weeks and you are good.

If they stall you and say they cant find your problem, then the lyme sets in and by the time they make a diagnosis whether it be lyme or MS or whatever they say you "have", you are fighting an uphill battle while they get to make $$$ by prescribing expensive MS or ALS drugs, & even if you find a good LLMD, they get to prescribe you long-term Antibiotics which then rake in tons of $$$ for the big pharma industry. They want you sick for a while before they treat you, or they want to misdiagnose the lyme as something else. Believe it or not, it's true. I hope you find some actual help, and stay away from the mainstream medical professionals.