When you receive news of a new health condition, it can cause anxiety and worry. Our Patient Services Team understand and are here for you to help you through your patient journey. If you have SVT or have received an ablation to treat SVT, then your experience can help provide reassurance, comfort and support to those, who may be finding themselves at the beginning of a similar journey. If you can help, please contact our team on info@heartrhythmalliance.org
Would you like to share your SVT pati... - Heart Rhythm Diso...
Would you like to share your SVT patient story to help others?
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Having SVT can be frightening and disruptive, but it is not life threatening. I had SVT basically my whole life, and it would rev up in times of stress, dehydration, or prior to my period. During menopause it was awful requiring trips to the ER to convert my rhythm, so my doctor prescribed a beta blocker which helped considerably. Then my husband became terminally ill and after he died my SVT episodes were daily and lasted hours, so I followed my doctor's advice and had an ablation in 2014 which ended the abrupt tachycardia episodes. Since then I have had the odd bump or flutter, but no more SVT. It has been a blessing.
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