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Chronic Migraine Awareness

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  • Receiving Migraine Infusions During a Pandemic

    Receiving Migraine Infusions During a Pandemic

    Written By Victoria White Presented by Chronic Migraine Awareness Inc. It is beyond surreal entering a hospital in an almost empty center city Philadelphia right now. I cannot help but feel anxious about the possibility of accidentally spreading COVID-19 to another patient or to a healthcare professional if I’m an unwitting carrier and also some…

    May 28, 2020
    Advocacy and Migraine, Covid-19, Get Real About Migraine, Medication & Treatments, Migraine In Real Life, Patient Perspective
    #chronicmigraine, #chronicmigraineawareness, #CMA, #migraine
  • Part Two – Covid-19 VS Chronic Pain 24/7

    Part Two – Covid-19 VS Chronic Pain 24/7

    Written by Rachel Huley Presented by Chronic Migraine Awareness The difficulty of finding a doctor for an invisible illness is hard enough every day of the year when hospitals aren’t flooded with contagion and warranted mass hysteria. During a world-wide health pandemic, finding a new, trustworthy doctor would be a miracle.  I called the neurologist’s…

    May 18, 2020
    Covid-19, Get Real About Migraine, Medication & Treatments, Mental Health and Migraines, Migraine In Real Life, Patient Perspective, stigma
    #chronicmigraine, #chronicmigraineawareness, #CMA
  • Part One – Covid-19 VS Chronic Pain 24/7

    Part One – Covid-19 VS Chronic Pain 24/7

    Written by Rachel Huley Presented by Chronic Migraine Awareness It was the first week of working from home that my latest migraine attack began. Mid-March covered the South in pollen and misinterpreted the Atlanta population’s allergies for Coronavirus symptoms. Regardless of the presidential promise and close proximity of the CDC, the tests weren’t available yet…

    May 9, 2020
    Advocacy and Migraine, Covid-19, Get Real About Migraine, Mental Health and Migraines, Migraine In Real Life, Patient Perspective
  • #LetsGetAfterIt

    #LetsGetAfterIt

    Written By: Catherine Charrett-Dykes Founder and President of Chronic Migraine Awareness, Inc. Dear Chris, For the past month or so now, the nation has watched you live and report on your experience with this new disease, this new pandemic – Coronavirus.  Your reporting connected with me in a way that gives me hope that we…

    April 28, 2020
    Advocacy and Migraine, Covid-19, Get Real About Migraine, Migraine Community, Migraine In Real Life, Patient Perspective, stigma
  • My Thoughts on Receiving Botox During Covid-19

    My Thoughts on Receiving Botox During Covid-19

    Written By: Peggy Artman, for Chronic Migraine Awareness, Inc. I have been getting Botox injections to help with my chronic migraine attacks every quarter for more than five years. My migraine disease is stubborn and has not responded to very many medications. I wondered in the past if it was still worth the effort to…

    April 25, 2020
    Covid-19, Medication & Treatments, Migraine Community, Patient Perspective
  • My Impasse

    My Impasse

    Chronic Migraine Awareness, Inc. is pleased to present The Struggle of Understanding My Migraine Disease Written By: Alexes Elizabeth It was too hot, maybe? Did I just faint on the schoolyard playground? After many hours of traveling out-of-state, it was at a park that I wondered, how much time has passed since this unexplainable occurrence?…

    April 19, 2020
    Get Real About Migraine, Migraine Community, Migraine In Real Life, Patient Perspective
  • Get Real About Migraine: Peggy’s Story

    Get Real About Migraine: Peggy’s Story

    Chronic Migraine Awareness, Inc. is pleased to present Part Six in our continuing series. Written by Peggy Artman My journey with migraine began when I started having what I believed to be sinus headaches. I went through a phase where I caught a lot of upper respiratory viruses, which turned into sinus infections. I had…

    April 4, 2020
    Advocacy and Migraine, Get Real About Migraine, Migraine Community, Migraine In Real Life, stigma
  • Self-Care During the Covid-19 Crisis

    Self-Care During the Covid-19 Crisis

    Written by Peggy Artman for Chronic Migraine Awareness, Inc. In my state, we are not officially quarantined, but we might as well be since we are required to follow the federal and state protocols. I don’t know about you, but I’m tired of all the worries about paper products and hand and surface sanitizers. We…

    March 29, 2020
    Get Real About Migraine, Mental Health and Migraines, Migraine Community, Migraine In Real Life, Patient Perspective
  • I’m already prepped, how about you?

    I’m already prepped, how about you?

    Written by Kristen Estep for Chronic Migraine Awareness, Inc. I would like to start by saying that I hope you are not quarantined, but if you are there are some lessons you can learn from the invisible illness community.  We are experts on self quarantine, this is our lives.  I’ll let you in on some…

    March 21, 2020
    Advocacy and Migraine, Get Real About Migraine, Mental Health and Migraines, Migraine Community, Migraine In Real Life
  • The Global Pandemic

    The Global Pandemic

    Written by Catherine Charrett-Dykes, President and CEO of Chronic Migraine Awareness, Inc. pan·dem·ic /panˈdemik/ – (of a disease) Prevalent over a whole country or the world. You might expect this to be about the coronavirus, however it’s about the other global pandemic – migraine disease. Migraine has existed for over 6000 years and impacts one…

    March 19, 2020
    Get Real About Migraine, Migraine Community, Migraine In Real Life
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