Posted 8/1/2014 7:27 PM (GMT 0)
Good Afternoon,
I posted recently for the first time regarding my situation and am thankful for the many thoughtful responses that I received. In brief, I have been experiencing many things that are symptomatic of Lyme Disease over the past couple months. Saw my PCP, blood test negative. I think I've run my course with the PCP, so have scheduled with an LLMD but have to wait roughly two months for the appointment (every LLMD within 3 hours of me is scheduling out quite a ways).
Absent a firm diagnosis, I'm looking for suggestions of things that I can do naturally (or otherwise) that have a chance at improving my symptoms until I see the LLMD. Symptoms are muscle twitching (all over) and aches, heavy/weak arms and legs, increasing joint pain, foggy brain, sensitivity to light and sound, and a bit of tingling in the extremities. Also what feels like a tightening of the esophagus and facial muscles that ebbs and flows. I do have doxyciline and am considering 100mg 2X per day for a month. I've done a couple Epsom salt baths, and I have Magnesium Glycinate pills that I started taking 4x per day. What else might work and is there anything I'm doing that I should cease?
Thanks in advance!