posted
I had a regular follow-up visit with my PCP today and told him that I was now more sure than ever that my Fibromyalgia was actually Lyme Disease...
I informed him that I was waiting to hear from my caseworker at Social Services, before making an appt. with an LLMD that I had been researching.
Caseworker told me at our last visit that she may be able to get at least my first visit paid for, because I told her that this doctor does not take Medicaid and I don't have the money to pay...
But in the meantime, he agreed to put me on an antibiotic just to see what happens...
He was going to use Doxy, but I just recently read that Minocycline actually was found to be more effective in treating Lymies w/Neuro symptoms...
He agreed to 30 days of the Minocycline 100 mg 2x daily..
Anyone else ever heard this and what should I be looking for if it actually starts working??
Thanks Ellen
Posts: 50 | From Port Crane, NY | Registered: Apr 2007
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lou4656
Frequent Contributor (1K+ posts)
Member # 10300
posted
Hi Ellen!
I was on this dosage of mino for 7 months. You may feel dizzy and off balance for the first two weeks. Hang in there -- it gets better. Also, take mino with a big glass of water, and do not lay down for 30 minutes after you take it.
Mino worked for me, but I noticed the most improvement after 3 months. Good luck to you!
-------------------- LouLou Posts: 1276 | From maryland | Registered: Oct 2006
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