I am convinced I have Lyme + Bart. But never had the bottom of the foot pain always mentioned. If I was infected 3 to 6 yrs ago, would these symptoms sound right to you? Progressively weakening muscles that began suddenly 4 months ago. Weak and painful neck..tender shinbones, extreme headach every day, nausea and bad heartburn fluxuating. No appetite, but not loosing weight, muscle atrophy ,like all weight has moved to stomache! No way I can leave the house, when I forced myself to the bank in this darn snow (cental MA) since then all symptoms have been much worse. can't even make myself a cup of tea. Just getting scared maybe this isn't from Lyme and I really do have ALS, MS OR worse. Thanks - I am not meaning to complain or whine, just seriously wondering if I'll be traveling to LLNP soon to find out it is not the lyme! I hear so much about people here that are very sick with lyme, but still functioning...could I be mistaken? diagnosed over and over again positive for lyme at doctors, then western blot at mayo clinic negative. Hence, the reason for my asking you guys to confirm symptoms. (sorry, I may be being redundant) Thanks for your patience!
Beagle
Posted by Hambone (Member # 29535) on :
quote:Originally posted by Beagle: I am convinced I have Lyme + Bart. But never had the bottom of the foot pain always mentioned.
My Bart foot pain didn't surface until I was 3 months into antibiotic treatment for Lyme.
Posted by Lymetoo (Member # 743) on :
diagnosed over and over again positive for lyme at doctors, then western blot at mayo clinic negative
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Mayo does NOT want to find Lyme because they WILL NOT treat it. Go with the many positive tests you already have!
Also consider yeast/candida in addition to the Lyme and possible coinfections.
Posted by Lymetoo (Member # 743) on :