AnneSommers said...
I know it’s a very old thread but I’ve finally found someone who has experienced similar symptoms - Lyme induced dysarthria (speech problems). I see st0rch hasn’t posted in a very long time; does anyone know whether he/she still visits this forum or how to contact them.
Has anyone else gone through similar symptoms? Is recovery possible? How is st0rch today, in remission or still battling the disease? Any help would be really appreciated.
I had slurred speech from Lyme and/or Bartonella, it was one of the reasons I was misdiagnosed with Multiple Sclerosis. Mine usually only came out in the heat or if I was exhausted or really stressed.
It is gone now, and my heat intolerance is gone as well.
I have had Lyme and Bartonella my entire life, I suspect I was bit by ticks more than once, and I have 15 lesions on my brain (although maybe they're gone now, I don't know, I haven't had a follow-up brain MRI).
I am not fully in remission yet, but I am getting there, after over a year of Buhner herbs, LDN, diet changes, lower stress, and no antibiotics (had c diff, won't take them now). I was pretty shocked this summer when my heat intolerance was completely gone, after 7 miserable years of dealing with it.