Calming My Storm is a New Jersey nonprofit organization that works to help people with concussions and migraines thrive. Our mission is to support people with concussions and migraines through expert interviews and advice, educational resources, and personal narratives. We hope to help migraine and concussion sufferers find ways to continue to achieve their goals and reach for their dreams
Parenting With Migraine is a motherhood and wellness blog that offers support, resources, and hope to parents who live with migraine.
The Dizzy Cook is dedicated to spreading awareness about vestibular migraine from a patient’s perspective, new migraine treatments in layman’s terms (with a focus on more natural treatments that can be used while trying to conceive/pregnancy), and fun recipes that follow a migraine elimination diet but without feeling so restricted.
Migraine Strong is committed to empowering individuals through education and hope while helping them gain control of chronic migraine. Their Facebook community is dedicated to managing chronic migraine through lifestyle, best medical practices and pure tenacity. They celebrate their members’ little victories and encourage them to thrive with this chronic illness.
VeDA supports and empowers vestibular patients on their journey back to balance. We do this through education, advocacy, and by connecting them with vestibular healthcare specialists. Many of the patients we support suffer from vestibular migraine. “VeDA supports vestibular migraine patients in their journey toward recovery. We believe that by connecting with others we can learn coping strategies and a
The U.S. Pain Foundation is the leading advocacy organization for people with pain. Our mission is to empower, educate, connect, and advocate for individuals living with chronic illness that causes pain, as well as their caregivers and clinicians.Through our multiple programs and services, we work to enhance the quality of life for people with pain, improve patient outcomes, address access
The Migraine Warrior Blog and its companion Facebook page were created by Patient Advocate Michelle Tracy after being diagnosed with chronic migraine disease at age 19. While trying to find meaning in her pain, Michelle realized that her thoughts and experiences had the potential to help others even as she lay in a dark room, unable to lift her head.
Jaime Sanders is a blogger and patient advocate who lives in Virginia with her husband and three children. She has had a life-long journey with migraine disease and lived most of her adult life with depression. From a toddler with abdominal migraine to a wife and mother with chronic migraine, Jaime has learned to turn her pain into empowerment over
The Migraine Chronicles is where author, editor, and Migraine.com writer Sarah Hackley gets candid about life with intractable chronic migraine. From parenting and relationships to individual responses to new medications and unusual treatments, Sarah takes a frank look at it all. Regular round-ups of other great sites and bloggers included!
Established in memory of our daughter and sister, Danielle, our mission is to raise awareness and provide support and access to treatment for those living with migraine disease, especially young adults and children. On June 21, we are proud to join the Shades for Migraine Coalition at our “Shine Her Light” celebration in Salt Lake City.