Volunteer Spotlight on Kelly Amspacher
How did you get involved with Miles for Migraine?
I became involved with Miles for Migraine 3 years ago and wish I would’ve become active much sooner. My Headache Specialist told me about Miles for Migraine for many years but with intractable chronic daily migraine and a daughter playing field hockey year round throughout her school years, and then college, I felt that I wouldn’t be able to devote/commit 100% of my energy – the only way I know.
When I finally went to my first Patient Education Day, I was hooked! My next experience was at a run/walk event where being part of a migraine community was electrifying. From there, I attended local Meet-up sessions to broaden my horizon and migraine support. I’m honored and thrilled to be a Migraine Community Group Facilitator.
How did it help you with your migraine journey?
Being involved with Miles for Migraine has been, and continues to be, an awesome life experience. I have made new friends and my “tribe” has grown immensely! The relationships that I have developed are an integral part of my life; bringing me hope, support, joy and caring that only other people with migraine can offer. I don’t feel alone in my journey.
Miles for Migraine has given me a sense of belonging, a sense of purpose and self-esteem. I’ve been able to put my passion for education and advocacy into action…”making the invisible…visible”.
I’m a FANATICAL University of Notre Dame football fan as well as a Villanova University men’s basketball fan!!
Jill Dehlin’s advocacy story is written and told by Jill Dehlin and edited by Miles for Migraine team. Miles for Migraine’s Advocacy Stories highlights the many different ways that health advocacy shows up as individuals advocate for themselves and others. This project is not limited to migraine and other headache disorders, nor is it limited to…
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