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If this is your first visit, be sure to
check out the FAQ by clicking the
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before you can post: click the register link above to proceed. To start viewing messages,
select the forum that you want to visit from the selection below.
Your Participation in this message board is strictly voluntary. Information and comments on the message board do not necessarily reflect the feelings, opinions, or positions of the Hypertrophic Cardiomyopathy Association. At no time should participants to this board substitute information within for individual medical advice. The Hypertrophic Cardiomyopathy Association shall not be liable for any information provided herein. As a good practice screen names should not be "full legal names" as we can not full assure your privacy from search engines if your FULL name appears on the messageboard
All participants in this board should conduct themselves in a professional and respectful manner. Failure to do so will result in suspension or termination.
WONDERING HOW MANY OF YOU HAVE HAD CARDIOVERSION DONE AND WHAT YOUR SUCCESS WAS WITH IT? ALSO, DID YOU REMAIN ON COUMADIN AFTER? I RECENTLY HAD ONE FOR SUSTAINED A-FIB.
I HAVE AN ICD
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Everyone is very different with HCM and you can't go by someone else's progress as a guide to your own. For example, in my family, three of us have afib and one has been cardioverted a handful of times but is in sinus (normal rhythm) and tends to stay that way. Two of us are always in afib and one of us has been cardioverted 20 times, the other 4 times.
Most people do better than my family, though, with afib.
Oh yes. Everyone with afib does. Mom, me, brother, aunt, cousin, other aunt.
Yup. Whaddya want to know?
They key to coumadin is to not drink or have the same amount of alcohol each week and keep your weekly vitamin k content even, too.
Be aware that fish oils, vitamin E and some plant oils like primrose and flax will thin your blood too. if you take supplements, always take them and don't skip or double up.
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