Tag: #migraine
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RetreatMigraine 2023; Sharon’s Experience
Chronic Migraine Awareness, Inc. would like to thank Sharon for sharing her experience with us. I attended RetreatMigraine 2023 which was held in Minneapolis, Minnesota. It was absolutely amazing! The inspiration I receive there helps me learn how to take care of myself, so that then I can help others with this invisible neurological…
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Copay Accumulator Legislation
Written by Kristi Estep for Chronic Migraine Awareness, Inc. Last week I and two other advocates were invited to attend an Advocacy Day with The Global Healthy Living Foundation at the Ohio Statehouse. We were all highlighting our specific chronic diseases and what the copay accumulator legislation means to our specific communities. We were accompanied…
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Lucy’s Story; Longing to be Pain Free
Chronic Migraine Awareness, Inc. would like to thank Lucy for sharing her story. *TRIGGER WARNING* This blog post contains material of a highly sensitive nature including ‘thoughts of suicide’ that may be triggering for some individuals. Hello, my name is Lucy, I have lived with Chronic Migraine daily for the past 39 years. Every morning…
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Gelcys’s Family Migraine Story
Chronic Migraine Awareness Inc. would like to thank Gelcys for sharing her story with us My name is Gelcys, I am a wife to a Military Veteran and a mother to a soon to be 14 year old son. We all battle with varying levels of migraine disease. I have the worst of it, I…
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Advocacy Beats Stigma
“Stigma is a process by which the reaction of others spoils normal identity.” Quote ~ Erving Goffman In the last few years, I haven’t encountered much stigma, and to be fair, I don’t work outside the home. Due to the high levels of head pain and other migraine symptoms, I don’t even leave my house…
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Getting to know CMA’s Co-Director of Admins; Elizabeth’s Story
Elizabeth Arant has been a migraine patient for over 30 years and a chronic migraine patient for over 20 years. While having chronic migraine she received her Undergraduate and Graduate degrees in Nursing. Although she is not practicing Nursing at this time, she volunteers her time with various headache and migraine groups to increase awareness…
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Getting to know CMA’s COO & VP; Nancy’s Story
Nancy Harris Bonk, the Chief Operating Officer and Vice President of Chronic Migraine Awareness, Inc, is a patient leader and educator who has been helping those living with migraine disease since 2003. She developed episodic migraine disease during puberty. Then, in December 1996, Nancy slipped and fell on a patch of black ice in her…
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Getting to know CMA Directors; Gina’s Story
I have had migraine for as long as I can remember. Migraine has been a part of my life for nearly all of it, which is well over 40 years! I became chronic daily 19 years ago and my currently diagnosis is chronic intractable migraine with aura. I have been spreading migraine awareness as well…
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Black Men Have Migraine Too
Written by Jaime Sanders and originally published on TheMigraineDiva.com Generously shared with Chronic Migraine Awareness I was extremely amazed and humbled by how many people reached out to me after the Good Morning America segment aired that featured my story. To say it was overwhelming would be a gross understatement. The vast majority of comments,…
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Roni’s Reflection from RetreatMigraine
Redondo Beach, California Written by Ronetta Stokes for Chronic Migraine Awareness Inc. Hmm… hmm-hmm-hmm-hmm Hmm-hmm-hmm-hmm Hmm-hmm-hmm-hmm-hmm Sometimes in our lives We all have pain We all have sorrow While attending RetreatMigraine in person these words resonated with me. We all have pain, we all have sorrow. The weekend brought together a community of people living…
Chronic Migraine Awareness 