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» LymeNet Flash » Questions and Discussion » Medical Questions » Does anyone get tachycardia & adrenaline rushes?

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Author Topic: Does anyone get tachycardia & adrenaline rushes?
tidegal
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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]

Posts: 44 | From GA | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
tidegal
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Im sorry guys, I meant to say "heart FLOPS" .
Posts: 44 | From GA | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
karatelady
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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

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docjen
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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.
Posts: 393 | From Washington, DC | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
   

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