This is topic Does anyone get tachycardia & adrenaline rushes? in forum Medical Questions at LymeNet Flash.


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Posted by tidegal (Member # 8262) on :
 
I get tachycardia and adrenaline rushes along with alot of other symptoms. It seems this always happens at night. I also get "hear flops". I have dysautonomia as well and was wondering if this gets better with the lyme treatment.

Thx all [Smile]
 
Posted by tidegal (Member # 8262) on :
 
Im sorry guys, I meant to say "heart FLOPS" .
 
Posted by karatelady (Member # 7854) on :
 
If you do a search on here, you will see a lot of people have this problem.

I use to get that a lot at night. Even went to the cardiologist, they put me on a holter monitor (laughed at me because I was too young to have heart troubles-this was years ago), they even did echogram and never found anything.

Now I know it was the lyme.

The abx seem to do that to me now.

Sandy
 
Posted by docjen (Member # 7510) on :
 
I've had problems like that for years. I would get a huge jolt of adrenaline and then paroxysmal palpitations, which unfortunately caused a couple of fainting episodes. I had all the tests (also told I was "too young" to have these problems). Nevertheless they found mitral valve prolapse, and tachycardia, so I have been on beta blockers for years. LLMD thinks that it's all due to lyme infection, and once I clear some 'chetes I can ditch the beta blockers. If it is bothersome, you might want to talk with your doc about beta blockers or another rhythm drug.
 


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