livingwithbrugada

My name is Lynn Tincher Calvert. In September of 2010, I was diagnosed with Brugada Syndrome, a rare and fatal genetic heart disease. This diagnosis came after twenty years of hospital visits, heart medications, and years of worry. I’ve started this blog as a way to shed a light on this horrible disease. As more and more are diagnosed, I hope to provide an avenue for information, shared stories, and a place to come for support. If you or anyone you know is affected by this disease or any unknown heart problem, please share this information so that we all have a place we can call home…

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