Heat intolerance with Lyme's

Does anybody have heat intolerance?  Winters seem better for me.  I am dragging with the sumemr heat.  I have neuro symptoms and never had the joint pain.  Thanks for your help.  I am also getting tested for Addison's.

Thanks all! Well, Congress just gave funding of $4 million for Lyme's research. It's a start. In five years I think this will become a major epidemic and insurance companies will be forced to comply. I am sorry that we are having these symptoms but glad there are others like me.

Well, the representative from Loudoun County (number 2 in new Lyme cases...yes, that's where I got mine) is really pushing this awareness. So it's finally getting out there. And thank God for Under Our Skin. It's just a matter of all of us starting to make people aware. Whenever I get into small talk..Like, "How are you?" I immediately say "Crappy. I have Lymes." And I give people a short lesson on it. Awareness is key.
I actually love the cold. I feel much better. I am wondering last fall after the summer I actually went into remission until December when my symptoms reappeared...if this is b/c a lot of the toxins were released in the summer? Hummmmm....

Toxins will also damage your autonomic nervous system which then makes you unable to tolerate extreme temps, hot or cold. I have what they call autonomic deregulation but I do better in the heat than the cold.  D

Hi, I am new too, I have many symptoms for a year now, probably had lyme about 10 yrs with other not so extreme symptoms as i have now. Has anyone heard of the Wellness pro Rife machine? Then also the Douglas Coil?

I cannot tolerate heat or sunlight due to a combination of lupus and Lyme disease. If I'm in the sun more than a few minutes I break out in a rash and my lupus symptoms flare up. Sometimes even I end up in the ER with chest pains! Just like the other posters, the heat makes me even more exhausted than usual.

We're trying to move to the coast where it's cooler and frequently cloudy, which may help!

How will the 4 million be used do u know? did u read this? thanks lisa

I have a really hard time with tolerating heat, too. Heat from the Summer sun, and the heat from even a lukewarm bath sucks the energy out of me completely.

It's not uncommon for me to continue sweating after drying myself several times once I'm out of the bath. I have to sit down, drink water, and rest for awhile before getting ready. I can't seem to tolerate the cold, either.

And the heat from my laptop often zaps my energy and makes my head sweat, too. Maybe my laptop is doubling as a rife machine.

Heat, cold, bright lights (even the TV at night), too much noise...all aggravating to my system.

Indeed, it really sucks to have Lyme disease.

I do better when I'm warm...the cold does me in. I already feel numb and desensitized - so when I get cold I feel worse.

Both heat and cold intolerance for me, too...
miserable...
I also get a rash in the sun...tanning during the summer used to be one of my favorite things. Now it just makes me sick.

Sitting at work with no A/C for second day and just can't take it. Yesterday left my physically ill. I was doing so well for so long but seems the heat is sucking the life out of me. Of course, the recent stress hasn't helped but this disease is just so baffling, that the heat, something I used to love, can just drag you down so bad. :(

 

I'm sensitive to heat and cold.

I'm aware that people use Rife machines to treat Lyme and other illnesses, but I don't know a lot about it.  I've never used one myself.  In her books, Hulda Clark discusses using them for parasites and cancer, I believe. 

From what I understand, a few decades ago, doctors were diagnosing Lyme left and right, and since it's so difficult to fully treat, insurance companies didn't want to pay for treatment, in turn prompting doctors to diagnose it less.  That leaves us where we are today. 

Secondly, some of the doctors on the front lines have been trying to get the CDC to listen to their research, experience, and information for years, but the CDC continues to ignore them most of the time.  Ritchie Shoemaker discusses his battle with the CDC in his book, Desperation Medicine.

Also, the army has the most accurate tick dispersal information, because they don't want their people getting Lyme during boot camp.  For some reason, the army and the CDC do not communicate with each other.

Best wishes for good health!

Yes, definitely yes.