Hope for Hemiplegic Migraine Sufferers — rare migraine variants
Community. Support. Healing. Hope. And always, much love!
Community. Support. Healing. Hope. And always, much love!
My name is Jennifer S., and my mission is educating people about a little-known disease called hemiplegic migraine (HM). and other rare migraine variants
I've suffered from chronic migraine for years, and was diagnosed with hemiplegic migraine six years ago. I also suffer from fibromyalgia and chronic fatigue. My mission is educating those fortunate enough to not suffer invisible illnesses or rare migraine variants, as well as letting those in the chronic illness community know they are not alone.
Because HM is a rare migraine variant, even many neurologists fail to understand the disease. My goal is to provide first hand insight into what living with this disorder or other rare migraine variants is like.
There's much to see here. So, take your time, look around, and learn all there is to know about living with chronic illnesses like HM. Please note: the messages here are for informational purposes only. Please consult with a doctor when making health-related decisions.
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