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Migraine Resources & Support | American Migraine Foundation
The American Migraine Foundation provides education, support and resources for the millions of men, women and children living with migraine.
Migraine Health Information & Community
Find out about migraine including symptoms, diagnosis, treatment, patient stories, support, and more from a migraine community perspective.
Author: Amanda Workman
Home - The Migraine Trust
The Migraine Trust is dedicated to helping people affected by migraine. We are the only UK migraine charity providing information and support, campaigning for awarenessand change, and funding and promoting research.
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Top migraine wellness community for patients. Discover trusted insights on what causes migraines and your migraine symptoms. Get help and hope for living with all types of headaches and migraine aura.
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Home - Urology Care Foundation
Welcome to UrologyHealth.org, your trusted resource for reliable urologic patient education. The Urology Care Foundation is educating patients and funding answers.
Home | The Heart Foundation
The Heart Foundation saves lives and improves health through funding world-class cardiovascular research, guidelines for health professionals, informing the public and assisting people with cardiovascular disease
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A Breath of Hope Lung Foundation fights lung cancer through funding research, raising awareness, and providing patient support.
Home - Autism Society
The Autism Society, the nation’s leading grassroots autism organization, exists to improve the lives of all affected by autism. We do this by increasing public awareness about the day-to-day issues faced by people on the spectrum, advocating for appropriate services for individuals across the lifespan, and providing the latest information regarding treatment, education, research and advocacy.
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Nick Everton Trust Home Page
The Nick Everton Trust, The Nick Everton Trust for Genetic cancers & Familial Adenomatous Polyposis (FAP) The Trust has been established to increase public awareness of genetic cancers in young people and particularly Familial Adenomatous Polyposis (FAP), provide better and more accessible information on the disease, promote wider and more comprehensive screening within "at risk" families and, by improved genetic testing, identify more of those at risk from FAP, establish a nationwide counselling network for sufferers and their families, set up a national network of specialist FAP clinics, assist research into genetic forms of cancer, principally FAP
Home - Phelan-McDermid Syndrome Foundation
Improving lives affected by Phelan-McDermid Syndrome Join Donate Newly Diagnosed International DataHub Upcoming Events Resource Library It is the mission of the Phelan-McDermid Syndrome Foundation to improve the quality of life of those affected by Phelan-McDermid syndrome worldwide by providing family support, accelerating research, and raising awareness. Latest News & Blog Post We are Phamily […]
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