Last night I received this comment from David and was so excited that I was trying to write this post in my broken sleep:
“…an interesting research finding published recently titled ‘Unveiled: First gene link to common migraine.’ In short, this genetic variant allows a messenger chemical called glutamate to accumulate between brain cells, and this unleashes the migraine.” (more…)
A simple question with a not-so-simple answer. This post is dedicated to Diana Lee and her Somebody Heal Me blog. It appears in the August 2010 Headache and Migraine Disease Blog Carnival where this question is the theme.
I am 56, and I have migraine disease. My first migraine attack came out of the blue when I was 16. What follows is my history and how over the 40 years I have ‘coped’ (or NOT) with migraine disease.
My attacks were sporadic in the early years and I took tons of aspirin and tried to figure out what was wrong with me – why I was violently ill in bed with head pain and vomiting for two to three days at a time. Doctors I discussed it with told me they were tension headaches and I needed to relax. Hmmm… (more…)
This is National Massage Therapy Awareness Week (Oct. 25-31,2009), and I know a fantastic therapeutic massage therapist in Sarasota, Florida, if you’re looking for one. Massage is great for migraine and I wish I could afford regular massage therapy! I guess my husband could learn it… 
Our ‘Express Migraine to Congress!’ campaign is launched at the wonderful suggestion of Vicki Gewe!
Vicki sent a book to Tom Harkin (D-IA), Chairman of the Senate HELP Committee, and I sent a copy to each of my senators, Barbara Boxer and Dianne Feinstein. Seven books are on their way to Congress now!
AND for every book sold in this effort, we will donate $1 to the Alliance for Headache Disorders Advocacy. You can make a dual impact with your purchase.
Anyone can purchase a book for Congress to promote awareness and migraine research here: http://www.wordmetropress.com/congress.html. Simply make a note in the PayPal purchase form which Senator or Representative you would like to receive your book. (more…)
Shared by Teri Robert (thank you) – and completed by me:
Anyone who has Migraine disease or another headache disorder knows what it’s like to live with an invisible illness. People can’t see our illness. There are no outward signs. Invisible illnesses are easy for “healthy” people to ignore. This adds to the burden of disease and makes lives even more difficult.
Each year, National Invisible Chronic Illness Awareness Week is observed to educate the public and raise awareness about invisible illnesses. One of the blogging activities this year is a “meme,” 30 Things About My Invisible Illness You May Not Know. So, here’s my meme… (more…)
Would the migraine world be much different if migraine hadn’t been so invisible for so many years? If it hadn’t been considered a woman’s ‘headache,’ particularly because often it was wrapped around hormones and the menstrual cycle? If more men had migraine disease or more men had spoken up about it over the years? If women had been more vocal and assertive – or aggressive – about their real symptoms? If Virginia Woolf, Joan Didion and others had been men?
Yes, it would.
I was raised as a good little Midwestern girl, to be seen and not heard, to have a superwoman’s work ethic, an obligation to help others and to be responsible and accountable for my actions. Not that any of these things are bad, just that for 15 years or so, this is why I listened to doctors who said my horrible ‘headache’ attacks were just a part of menstruation, that I needed to relax and ‘stroke my chin’ so I wouldn’t develop ulcers to go with that ‘headache.’
All those years of hearing in some way or another that migraine was my doing – you need more exercise, more sleep, better food, more relaxation, change your personality – blah, blah, blah… while I stoically suffered through too many two-to-three-day sick episodes per month with pain, nausea, diarrhea, and life between two sheets in a dark room with my friends, the ice packs and vomit buckets. (more…)
While I’ve never written about migraine in my family before, even in a journal entry, it’s a mystery that I and my family members have tried to solve once or twice.
As one of five girls – yes, I have four sisters and no brothers (my poor father!) – and one of the three of us who have migraine disease, naturally I’ve wondered (and lamented) over the years, “Why me/us – what’s the reason or connection?”
Imah Widai
I’m Mad as Hell and What I’m Doing About It…
Yes, we still need painful and frightening migraine art
…and everything else possible to help the migraine awareness effort!
Well, National Headache Awareness Week (June 7-13) is reaching its end, but our efforts to promote awareness and understanding while advocating for more research and better treatments must go on!
Dedicated migraine professionals, advocates and overcomers are leading the charge online with excellent, informative migraine and headache sites, providing support and sharing knowledge and experiences. Some can be found on this blog under Resources and more will be added here soon. (more…)
I’ve wondered for quite a while about this recipe of minerals and serotonin and migraine. Every time I try to add magnesium to my supplement regimen, which does include calcium, I seem to experience more or worse migraine attacks.
But that contradicts everything I read about many migraineurs having low levels of magnesium and how magnesium helps. So I have been left to wonder if this is coincidental for me and to try adding magnesium periodically to see what happens — and to suspect that perhaps I am just an anomaly in this regard!
Please read this brief article by Mamta Singh I was glad to find about the role of calcium in the mix with magnesium, potassium and serotonin. Maybe eventually I will find just the right amount of each ingredient for me!
*Obviously, I am a student and not an expert in this area, so please check with you doctor about supplements you consider taking.
The week of April 20 and so much you can do!
MIGRAINE, anytime, urgent: Contact your senators and urge them to sponsor S 660, the National Pain Care Policy Act of 2009, to improve “research, education, training, access, outreach and care” for all painful conditions, including migraine. It’s fast and easy to send an e-mail to your senators through the Alliance for Headache Disorders Advocacy. (more…)
I wanted to publish a book of written and visual art, creative expressions of people who live with migraine, to help promote awareness and understanding of it. The book is done. Now I want to talk about it, feature some of the work, writers and artists, and provide a place for anyone with an interest in the book, migraine, other chronic pain issues, art, poetry, essays, photography, publishing, health and advocacy issues, and maybe even a sprinkling of current events and politics, to connect. Welcome to this migraine and life journey!
