About the blog

As part of my new year resolution, I have decided to get a grip on my health. I’m on a mission to finding out as much as I can about Large Vestibular Aqueduct Syndrome, LVAS for short. I have dealt with vertigo, attacks, inner ear pressure, and tinnitus my entire life and I want to see if there is something I can do, if anything, to make my life a little more stable. It can’t hurt to try, however, I already know there is no cure for it. Only 1 in 10,000 people have LVAS so there is little knowledge about the syndrome. I did not know what it was until I was diagnosed with it in 2008. This occurred after I was previously diagnosed with Meniere’s disease. I still do not know whether I have both or if I just have LVAS. Basically I’m starting this blog to let people know about LVAS, share my story, and to get feedback, information, or advice. Hope you enjoy 🙂

That’s me on the right with my boyfriend

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