This is topic Crazy arm pit sweating....Art, Babs?? in forum Medical Questions at LymeNet Flash.


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Posted by NMN (Member # 11007) on :
 
I have found that my sweat glands under my arm pits run like taps when I take Artemisia.

Does anyone have this?? and do you link it to Babesia in any way??

Its really odd. Nowhere else sweats in the day time just arm pits.
 
Posted by TO LIFE (Member # 12371) on :
 
Hi,

I am having the same problem. Are your sweats in the day as well?
 
Posted by NMN (Member # 11007) on :
 
Yep.. day time only too. Its related to taking art for babs for me.
 
Posted by sutherngrl (Member # 16270) on :
 
It can also be related to Lyme; because lyme messes "everything" in your body up.

Also now that I am exploring autoimmune issues rather than LD, I am finding that the treatment for that is helping with the arm pit sweats.

This has been a symptom of mine ever since I became ill with LD and or autoimmune disorder. It always happens during the day and it comes out of nowhere and its like a faucet was turned on. I think it can be caused from various illnesses.
 
Posted by TO LIFE (Member # 12371) on :
 
Hi,

I am taking humaworm which has Art. in it.

I test neg- for babs but I could be dealing with it, or Parvo virus and some kind of parasite. Viruses and parasites can go together from what I have been reading.

I have been sweating so much I am driping wet at times.

Do you feel better after you sweat? Just curious because I do.
 
Posted by sutherngrl (Member # 16270) on :
 
tosho, I took 3 weeks of steroids for a kick start, then dropped those and am now on plaquenil, which is actually an anti-malarial drug used to treat autoimmune disorders.

I have only been on autoimmune treatment for 5 weeks, but this is the best I have felt in 3 years. One full year of Lyme treatment with absolutely no improvment, well except for the 2 months I was on Malarone, also an anti-malarial drug.

We have not completely ruled out LD, but my LLMD is really leaning toward an autoimmune disorder. I am too now, since I feel about 50% better in a matter of 5 weeks.
 
Posted by CD57 (Member # 11749) on :
 
Sutherngirl wouldn't your improvement on anti-malarials indicate some sort of parasitical infection?
 
Posted by cantgiveupyet (Member # 8165) on :
 
I have this too....wow!! I thought I was the only one. Im not on antimalarials but get this on and off.
 
Posted by btmb03 (Member # 18394) on :
 
I get the underarm sweating thing too. I thought I was the only one!! Hard to know if it is Lyme, or another co-infection (including virus). But one thing for sure, my "inner trembling" is going down a bit with treatment.
 
Posted by sutherngrl (Member # 16270) on :
 
CD57, yes possibly or it could go back to an autoimmune issue which also improves on anti-malarials.

One theory is that the Lyme is gone but not the babesia.

The other theory is a possible autoimmune disorder. This seems most likely at this point, considering my genetics and how this illness was triggered.

I just want to get well, whatever it takes!
 
Posted by TO LIFE (Member # 12371) on :
 
Hi Sutherngrl,

I am wondering if you have had Babs, treatment?

Hugs
 
Posted by heiwalove (Member # 6467) on :
 
i have this too! very frustrating. don't know what causes it, but i assume it's wonky hormones and/or babs.
 
Posted by daniel (Member # 22201) on :
 
I have that too, treated babs for 8 mos, now started bartonella treatment with doxy and levaquin, Plus arte and am sweating again
 
Posted by mbdq (Member # 26277) on :
 
I get crazy armpit sweating when I am on abx. No abx, no armpit sweating, even when I am having flares of other symptoms.

For me, it seemed related to abx treatment.
 
Posted by unsure445 (Member # 15962) on :
 
I think this has been a babesia symptom for me. Usually I am sweating (armpits) and cold at the same time.

Hope it let's up soon!
 


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