Do you have LVNC? I have spent the past 6 years living with this diagnosis of LVNC and trying to meet others like me. I have created a safe place that we can all talk and discuss things such as diagnosis, prognosis, fears, aspirations and of course all the fun stuff like doctors, location, treatment, and just regular life. I know we are a rarity in the heart world, which is why we need to come together. If you are interested in more information please feel free to fill out the form below and I (Bonny) will personally reach out to you!
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