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
The “Stiftung Kopfschmerz” (Headache Foundation, Germany) ist a non-profit organization. For more than 20 years, the Headache Foundation has been informing the public about headache diseases as an online platform. It is important to us that new research results are not only accessible to experts, but also to those affected and their relatives. With our information and education offers, we
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.
Our mission is to empower people living with migraine and other headache disorders through training and mentoring. We are developing a patient advocate incubator to train and mentor patients and caregivers with the skills necessary to take an informed, active role in their own health care, encourage, educate, and advocate for others, raise awareness through involvement in local, regional, national,
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
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.
Patient Advocate Foundation (PAF) is the leading direct patient services organization with a mission to eliminate obstacles for patients trying to access quality healthcare. PAF case managers serve as active liaisons between the patient and their insurer, employer and/or creditors to resolve insurance, job retention or debt crisis matters as they relate to their diagnosis of a chronic, life-threatening and
Founded in 1970, the National Headache Foundation is the oldest and largest foundation for patients with headache. Its mission is “To cure headache, and end its pain and suffering.” Its vision is “A World Without Headache.” The foundation is the premier educational and informational resource for those with headache, healthcare providers, and the public. The work of the foundation is
My Chronic Brain is a new magazine designed specifically for people with Chronic Migraine and those they interact with–from caregivers to families, friends, and healthcare providers. We arm readers with information in simple, easy to understand formats to help them live their exceptional lives.We’re accessible online, for free. We know that taking care of your health is expensive. We don’t