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SHADES FOR MIGRAINE PARTNER DIRECTORY
The Shades for Migraine partners consist of over 45 organizations and bloggers, all offering unique resources to the migraine community.
The Association of Migraine Disorders (AMD) is devoted to expanding the understanding of migraine disease and its true scope through education, research and awareness. Because migraine is a full body disease with a broad spectrum of symptoms, AMD is focused on including many medical specialties in the management of this disease. The centerpiece of this effort is a comprehensive online course to accelerate the training of more medical professionals. For patients, AMD shares the opinions of experts in its series of short podcasts. AMD believes that migraine has yet to capture the support of the general public, and therefore it runs Shades for Migraine, a collaborative public awareness campaign.
The Associação Brasileira de Cefaleia em Salvas e Enxaqueca (Brazilian Association for Cluster Headache and Migraine) is a cluster headache and migraine advocacy association aimed at improving patients quality of life by raising awareness, promoting disease education, and fighting for disability rights.
Achy Smile, LLC is a blog and migraine awareness shop run by Erica Nicole Carrasco (Dallas, Texas). Erica lives with Hemiplegic Migraine, several headache types, Fibromyalgia, and other comorbid conditions.
The Alliance for Headache Disorders Advocacy is comprised of nonprofit organizations who are vitally concerned about the health of patients with headache disorders including migraine disease, cluster headaches, chronic daily headache, new daily persistent headache, tension-type headaches.
Alicia Wolf is a cookbook author and recipe developer who lives with vestibular migraine. The Dizzy Cook is dedicated to spreading awareness about vestibular migraine from a patient's perspective, new treatments in layman's terms, and recipes that follow a migraine elimination diet but without feeling so restricted.
Alleanza Cefalalgici is an Italian patient association dedicated to facilitating the dissemination of headache-related information and supporting patient management.
The American Migraine Foundation (AMF) is a non-profit organization dedicated to the advancement of research and awareness surrounding migraine
Argentine Migraine and Headache Association's (AMyCA) mission is to improve the quality of life of people who suffer from migraines and headaches through education, support, and advocacy. They are committed to supporting patients, training healthcare professionals, and raising awareness in society about the impact of these conditions.
The Associazione Cefalea Ticino is a nonprofit association in Switzerland that promotes communication, discussion, and mutual support among people with headache or migraine.
Carenity’s motto has been “patient comes first”. Their site allows you to share your experience, find comfort and useful information provided by other patients, and hopefully, improve your everyday life. Their goal is to better correspond to the needs of patients and their families.
Chronic Migraine Awareness, Inc. (CMA, Inc.) is the voice of the chronic migraine community. We offer support, information and education to empower individuals to advocate for their health.
Club de la Migrana is a Spanish-speaking digital community and non-profit foundation representing migraine and chronic migraine patients in Chile. It educates and informs about the disabling effects of migraine.
Clusterbusters supports research for better treatments and a cure while advocating to improve the lives of those struggling with cluster headaches.
Austria's first cluster headache Association specifically dedicated to supporting people with cluster headaches and their families
CHAMP provides support to people with headache, migraine and cluster diseases who are often stigmatized and under-served by together organizations and leaders to enhance communication, coordination and collaboration.
The European Migraine & Headache Alliance is a non-profit, patient umbrella group which was launched in 2006. Since then, the Alliance has grown to represent 30 patient groups from across the continent.
The Estonian Migraine and Headache Patients Association is to help migraine and headache patients better understand their condition and encourage them to take more responsibility for their illness.
The Global Patient Advocacy Coalition for Headache (GPACH) is a non-profit organization registered in Belgium. It is formed by patients and headache specialists collaborating together as volunteers to advance patient-centered advocacy for people with headache disorders across the globe.
The Greek Society of Migraine and Headache Patients is a nonprofit organization established in 2017 and a member of both the Pain Alliance Europe and the European Migraine & Headache Alliance.
HMPF is a non-profit advocacy organization comprised of diverse stakeholders with a mission of advancing public policies and practices that promote accelerated innovation and improved treatments for persons living with headache disorders and migraine disease.
The Headache Society is a non-profit association of headache patients and medical professionals, aiming to increase the level of medical education in the field of headache and facial pain, and facilitate access to modern treatments forheadache and facial pain patients
Headache Norway is a nationwide independent association that will organize and work to ensure that everyone suffering from migraine or other headache disorders has a meaningful and well-functioning life
Migraine & Headache Australia has supported Australians living with migraine and headache for over 20 years through advocacy, support and funding research.
Migraine Again is run by people with migraine, for people with migraine and frequent headaches. Everyone on our editorial team lives and works with migraine attacks. We’re here to support and empower you with evidence-based information and tips that will help you work, play, eat, and thrive – until there’s a cure.
Ireland’s only charity dedicated to migraine and headache disorders, which provides information, support and reassurance to those who suffer and their families.
Migraine at School is a national movement to guide families through the complicated journey of migraine.
Migraine Australia is a support and advocacy organisation, run by people living with migraine, working to improve the lives and wellbeing of all Australians living with migraine.
Migraine Canada improves the lives of Canadians with migraine and other headache disorders through awareness, support, education, advocacy, and research.
Migraine Meanderings is an online community for people who live with migraine and other headache disorders, their family and friends.
Advancing migraine education, awareness, and advocacy across Africa. We strive to bridge the knowledge gap among healthcare providers, workplaces, and communities by promoting evidence-based information and improving access to quality care.
Migraine Strong is a health and wellness website featuring information about migraine disease in a way that encourages our readers to find hope in a situation that often feels hopeless.
The Migraine World Summit is the largest patient event in the world for those with chronic headache and migraine disease. Its mission is to reduce the global burden of migraine through world-class education. It is available free and online.
Migraine.com is a Health Union community. Health Union reaches millions of people through condition-specific online health communities and a Social Health Network of patient leaders across virtually all health conditions.
Helping people with migraine live freely. The first patient organization supporting people with migraine and their loved ones in the Czech Republic
The offical website of the Migraine Sufferers Association in Lithuania
Miles for Migraine is a nonprofit organization with the mission of improving the lives of people with migraine and other headache disorders, and their families, by raising public awareness about this disease, and helping to find a cure.
My Migraine Life is an advocacy, awareness and community building blog. Sarah shares stories of how she lives life through migraine with children, travel, teaching and daily life.
The National Headache Foundation is the oldest and largest foundation for patients with headache. The foundation is the premier educational and informational resource for those with headache, healthcare providers, and the public.
Parenting With Migraine is a motherhood and wellness blog that offers support, resources, and hope to parents who live with migraine.
Raising awareness among the general public, employers, policymakers, and the medical community about the impact of migraine and headaches on patients' daily lives, and increasing understanding of those who suffer from these conditions.
Rock for Migraine mission is to spread awareness of migraine disease as a true neurological condition that both women and men live with. We strive to provide migraine support and enhance understanding of this serious condition. We also strive to be a voice for those who cannot speak for themselves and to assist in advancing anything we can, in any way possible, regarding this condition.
A non-governmental organization dedicated to supporting people suffering from brain disorders, supporting them and their families through information, education, support programs, awareness campaigns, advocacy, and the creation of an informed and supportive community.
Danielle Byron Henry Migraine Foundation was founded by Dan Henry, M.D., his wife, Diane, and their daughter, Elizabeth Henry Weyher, in honor of their daughter and sister, Danielle, who battled with migraine disease for almost 10 years until her death in 1999 at age 17.
The German Headache Foundation has been informing the public about headache disorders as an online platform for over 20 years.
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.
The Migraine Trust is dedicated to helping people affected by migraine. They are the only UK migraine charity providing information and support, campaigning for awareness and change, and funding and promoting research.
Michelle Tracy is a patient advocate, writer, and keynote speaker who speaks about her life migraine. The Migraine Warrior educates, advocates, and fundraises for migraine and other headache disorders.
Judy has lived with migraine since she was 7 years old. Her blog aims to support and foster understanding among patients and their loved ones living with chronic illnesses around the world.
The U.S. Pain Foundation is the leading advocacy organization for people with pain. Their mission is to empower, educate, connect, and advocate for individuals living with chronic illness that causes pain, as well as their caregivers and clinicians.
VeDA supports and empowers vestibular patients on their journey back to balance through education, advocacy, and by connecting them with vestibular healthcare specialists.
Interested in becoming a Shades For Migraine Partner? Email us at sara@migrainedisorders.org
