Dufresne
almost there...
- Messages
- 1,039
- Location
- Laurentians, Quebec
@juniemarie
@@juniemarie , I also relate the night sweats to babs, and Bart gives me heavy head day sweats, also I don't sweat at all normally. Babs gives me a light dry cough, but it seems that I get more chest pain and also spasms of the respiratory track with what I identify as been bart flares.
And sorry, I had forgotten, the come and go heel and sole pain especially when I get up, which comes with bart flares too.
@Dufresne , thanks for the quote. Bart treatment before Babs. That's a pity, my LLMD treated Babesia first. He insisted in saying that babesia treatment was the first line to go with, according to what he learnt from Dr Horowitz. Babesia should be treated first otherwise we couldn't reach nor borrelia nor other coinfection (he said).
In the end it's all anecdotal. Whatever infection is doing the most damage is the one you go after first.
A lot of people talk about the night sweats and other pesky inconveniences, but what about the core ME/CFS symptoms? I always found it discouraging that so few people treating Lyme and co ever improved these. Yet that's what I'm experiencing. I generally don't suffer night sweats and air hunger with my babesia. Instead it oxidizes the f*#k out of my system, and this leads to brain fog, cognitive dysfunction, and I think it's complicit in my PEM. Also I'm quite sure it's a toxin the bug produces that causes a sort of CIRS reaction that absolutely messes up my terrain.