The American Headache and Migraine Association is a nonprofit organization for patients who live with Migraine and other Headache disorders, as well as their families and friends. AHMA's mission is "to help those affected by Migraine and other Headache Disorders find and use our voices to empower patients, family members, friends, and care partners. Through education, support, advocacy, and research we will bring hope and banish the feelings of hopelessness that too often accompany these disorders. We will work to dispel myths and misconceptions, thereby working to eliminate the stigma we face all too often and replace it with compassion and understanding."
Check out the AHMA web site, www.AHMAIsHope.org.
Life hasn't slowed down as some people thought it might after I hit 60. I'm busier and busier between my "regular" job and volunteer activities. My personal site and blog have fallen behind, but I keep hoping to find time to update them more often.
You can find most of my "work" on:
My personal blog is:
Cyndi Jordan and I have been working on this new site:
Another new site I've been working on is Migraine Clues. This site is meant to bring together information, images, links to educational articles and more — to make it easier for Migraineurs to find information.
Last, but certainly not least, please check out the American Headache and Migraine Association. This relatively new nonprofit organization is a patient-focused and patient-driven organization for patients with Migraine, Cluster Headaches, NDPH, and other Headache disorders as well as their families and friend. I'm one of the founders of AHMA and the current chair.
last updated July 31, 2015
All content © Teri Robert, 2004 - Present, unless otherwise noted. Site last updated July 31 2015.