The Guthy-Jackson Charitable Foundation is dedicated to funding research in the quest to understand the pathophysiology and biochemistry of Neuromyelitis Optica (NMO) Spectrum Disorder.
The Sumaira Foundation for NMO is a 501(c)(3) organization dedicated to generating global awareness of NMOSD, fundraising to help find a cure, and creating a community of support for patients + their caregivers.
The Transverse Myelitis Association supports individuals living with rare neuro-immune diagnoses and their families, promotes awareness to empower patients, families, clinicians and scientists, builds a collaborative and dedicated clinical care network and helps advance scientific understanding and research.
The National Kidney Foundation is the leading organization in the U.S. dedicated to the awareness, prevention and treatment of kidney disease for healthcare professionals, patients, their families, and Americans at risk.
The American Kidney Fund is the nation’s leading non-profit working on behalf of the 30 million Americans with kidney disease.
HelpHopeLive is a non-profit organization that supports community-based fundraising for people with unmet medical and related expenses due to cell and organ transplants or catastrophic injuries and illnesses.
The Kidney Transplant/Dialysis Association is a patient-run, non-profit organization dedicated to providing financial aid, information, and emotional support to chronic renal disease patients, donors and supporters.
MGFA is committed to finding a cure for myasthenia gravis and closely related disorders, with a vision to create a world without MG.
The Myasthenia Gravis Association’s mission is to increase public awareness and provide MG-specific educational opportunities.
The Myasthenia Gravis Hope Foundation acts as the voice of patients, to focus on bridging the gap between patient needs and clinical interaction, to create positive clinical partnerships, to bring advocacy and education to the forefront and to engage in the arts to help foster awareness and challenge the stigmas faced by the growing Myasthenia Gravis community today.
Sjögren's Syndrome Foundation, recognized as the national advocate for the disease, provides patients with practical information and coping strategies that minimize the effect of Sjögren's.