posted
Hi I m wondering, do you think heat has any effetc on babs as it has on lyme?
Posts: 723 | From Montreal | Registered: Oct 2010
| IP: Logged |
ktkdommer
Frequent Contributor (1K+ posts)
Member # 29020
posted
The heat makes me sick. I feel like heck, heart starts beating fast, get dizzy and nauseated. Even mild temps like 75 with humidity makes me start to melt. My symptoms flare up and I get fatigued. My doctor said he would write a letter for AC at my work place because of babesia, so I infer he means babs acts up with heat.
-------------------- Things are never dull. After 3 fighting Lyme, 2 are in remission. Youngest is still sick, age 22. He has new diagnosed Chiari Malformation and Ehlers Danlos Syndrome. Posts: 1366 | From Perrysburg, Ohio | Registered: Nov 2010
| IP: Logged |
posted
That would make sense. I too get sick in the heat---feeling fatigued, nauseated, faint, and heart palps.
I had the room a bit too hot and steamy during my shower last night and almost bit the dust.
Posts: 303 | From Pennsylvania | Registered: Jul 2010
| IP: Logged |
posted
So is treating babs with FIR sauna not a good idea?
My body temp has been around 97.0. when i was running fevers regularly i didn't want to get in the sauna. now i want to get back in there and sweat some stuff out.
posted
I feel like I am sufficating when it's hot and humid outside. I would think that with Babs and Bart. you would be a bit hypoxic anyway due to the red blood cells being effected. You have to work harder to get oxygen into your body and the heat makes it worse.
Just MHO:0
Posts: 131 | From Maryland/USA | Registered: May 2011
| IP: Logged |
posted
Well, guys, I have Lyme, Bart and Babesia. I can't tolerate the cold. I live in Florida and feel much better since moving here from the cold Northeast.
Posts: 671 | From Fort Myers, Florida | Registered: Jun 2009
| IP: Logged |
payne
Frequent Contributor (1K+ posts)
Member # 26248
posted
If i dont have a fan on 24/7... ready set sweat..any humindity. and melt down.. not a fever..97.3 and not a masses sweat either. after a shower wow, it takes an hour sitting quietly to cool off enough to dress... ugh. CLD more then 10 yrs.
-------------------- TULAREMIA/rabbit fever ? Posts: 1931 | From mid-michigan | Registered: Jun 2010
| IP: Logged |
posted
Fyrecracker, get back in the sauna. I use my FIR sauna at least 4 times a week. Seems like it works better when I feel worse.
Clinically on Babs and Bart for me, also. But, I have more Babs symptoms than anything. The Bart is very apparent on my skin. Although, that is really changing with treatment.
Give me the heat, anyday.
Posts: 671 | From Fort Myers, Florida | Registered: Jun 2009
| IP: Logged |
mojo
Frequent Contributor (1K+ posts)
Member # 9309
posted
I have a very low tolerance for heat. I hate humidity - I feel like I can't breathe. I don't like hot at all. I can even be uncomfortable being warm. I'd rather be a little chilly.
I DO use my sauna (not much in summer, though). It works miracles for me and I highly recommend it. I go full blast for 45 minutes several times per week.
I purposely bought the kind where the head sticks out - I can't breath hot air.
I've been using my sauna for several years now and it's the best thing I bought (as well as my rife machine!)
Posts: 1761 | From USA | Registered: May 2006
| IP: Logged |
BoxerMom
Frequent Contributor (1K+ posts)
Member # 25251
posted
I also have the three Bs and I love my FIR sauna. I feel like a million bucks after a sauna.
But I tolerate the heat just fine. I run cold, and would love to move farther south!
mojo
Frequent Contributor (1K+ posts)
Member # 9309
posted
My husband treats his colds in a similar manner. He drinks a lot of hot water and/or tea and bundles up at night (sweats, hat and layers of covers) and sweats it out!
quote:Originally posted by chiquita incognita: I've been reading in one of my alternative medicine manuals that heat therapy is helpful to the immune system, so long as it doesn't go overboard....and it helps us to sweat out bugs, toxins et al.
As adjunct support to cold/flu therapy when I was a kid, we used to drink hot sage tea and put strong sage tea into the bath. Sage makes you sweat if you use enough of it. Then we would bundle up in our pj's under lots of covers and sweat. Drink more tea to keep hydrated and replace lost fluids, cool/wet washcloth over forehead to prevent excess overheating. Shower off again afterward to release sweated-out toxins on the skin.
I wonder if this could be good adjunct support in lyme? For those of us who can tolerate the heat,that is....I hate these babs heat waves but sure as hell wanna knock these bugs out. I don't know or even claim that this is the whole piece of the pie but do again wonder if it could be helpful as adjunct support. Gonna start trying it myself, thank you guys!
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
Printer-friendly view of this topic