Ocean
Frequent Contributor (1K+ posts)
Member # 3496
posted
This is the only thing I've been told so far about my heart. My mom says she has it too. Kids have it, but usually outgrow it. My mom also was dx with MVP. I am seeing a new PCP next week and am hoping she will do some heart tests due to the missed beats, had some tachycardia this am, but probably due to the start of meds for me yesterday.
CD57
Frequent Contributor (1K+ posts)
Member # 11749
posted
Hi--I have sinus tachycardia show up on two EKGs and when I asked about a link to this and MVP I was told no.
Posts: 3528 | From US | Registered: Apr 2007
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posted
I have sinus arrthymia and mvp among other things such as Right bundle branch block, PVC's and sinus tachycardia. I am on a beta blocker that helps some w/the tachycardia but not hte PVCs.
Posts: 146 | From Midwest | Registered: Feb 2005
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-------------------- i am not a Dr. any info is only for education, suggestion or to think/research. please do not mis-intuprest as diagnostic or prescriptive, only trying to help. **
dx in 08:lyme, rmsf, bart, babs, and m.pneumonia. Posts: 422 | From TX | Registered: Oct 2008
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sutherngrl
Frequent Contributor (1K+ posts)
Member # 16270
posted
I have MVP, PACs, and lately my heart races but only for about 20 seconds.
I had an echo at the beginning of my illness, that has been almost 3 years ago. I wonder how often an echo should be done?
I was trying to hold off until I am well to see what is left of my heart at that time. Hopefully most of this stuff is minor and some will clear up when the Lyme goes away.
Posts: 4035 | From Mississippi | Registered: Jul 2008
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