Anyone still struggling after AVM removal?
My AVM was 10+ years ago. It developed on my brain stem at the base of my skull by the cerebellum. I am not experiencing the symptoms that led my doctors to discover it but have been living with the aftermath of my surgery from removing it. The podcast from Radiolab, Song of the Cerebellum, nails my experiences. It's worth a listen (can't post URLs)
Interested in more discussions like this? Go to the Stroke & Cerebrovascular Diseases Support Group.
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