We couldn't do this without help

Synapticure partners with best-in-class clinics, and advocacy groups to advance brain health. Together, we are dedicated to improving patient outcomes through cutting-edge research and innovative solutions.

Dementia

Hilarity for Charity

Luna

Bayada

Senior Helpers

Parkinson's Disease

American Parkinson Disease Association

PMD Alliance

The Michael J. Fox Foundation for Parkinson's Research

PD Avengers

Amyotrophic Lateral Sclerosis (ALS)

Hope Loves Company

Hark

Lisa's Legacy for ALS

Live Like Lou Foundation

Augie's Quest

Voices for ALS

ALS Therapy Development Institute

Les Turner ALS Foundation

I am ALS

Massachusetts General Hospital Neurology

Amyotrophic Lateral Sclerosis

ALS Therapy Development Institute

A non-profit organization dedicated to finding effective treatments and a cure for Amyotrophic Lateral Sclerosis (ALS). It is the world's largest ALS-dedicated research organization and uses innovative approaches to accelerate the discovery of treatments and a cure for the disease.

Augie's Quest

A charity organization that raises funds and awareness for Amyotrophic Lateral Sclerosis (ALS) research. It was founded in honor of Augie Nieto, a fitness industry pioneer who was diagnosed with ALS, and aims to accelerate the discovery of treatments and a cure for the disease through funding cutting-edge research.

Hark

An active ALS charity organization that was founded by Donna Dourney York in memory of her father, Charles W. Dourney, a lifelong athlete, coach, and father of seven, who courageously battled ALS until his death in November 2009, and who was affectionately known as “Hark” by his wife Ann.

Hope Loves Company

A non-profit organization that provides support and resources for children and families affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The organization offers a range of programs and services designed to help families navigate the challenges of ALS, and works to raise awareness and funds for research towards finding a cure for the disease.

I am ALS

Provides financial assistance, emotional support, and advocacy services to individuals living with ALS and their families. The foundation also works to raise awareness and fund research for treatments and a cure for ALS. The I Am ALS Foundation is committed to helping those affected by ALS to live their best life and to ultimately find a cure.

Les Turner ALS Foundation

A non-profit organization dedicated to providing support, education and advocacy for people affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The foundation funds cutting-edge research to find a cure for ALS, while also offering services such as patient care and support groups, equipment loans and home modifications to help people with ALS and their families cope with the disease.

Lisa's Legacy for ALS

A community dedicated to raising awareness and support for people affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The group provides a platform for members to share information, resources, and support with one another, and works to raise funds for ALS research and advocacy initiatives.

Live Like Lou Foundation

A non-profit organization that raises funds for research and provides support for people affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The foundation funds innovative research to find treatments and a cure for ALS, and provides support to families and individuals impacted by the disease through community building initiatives, resources, and advocacy.

Massachusetts General Hospital Neurology

A world-renowned center dedicated to providing comprehensive and compassionate care to patients with neurological disorders. The department is composed of leading experts in the field of neurology, and offers a full range of services including diagnosis, treatment, rehabilitation, and research. The team works collaboratively to meet the individual needs of each patient, provide advanced diagnostics and treatments, and deliver cutting-edge research. The department is committed to providing the highest quality of care and advancing the field of neurology.

Voices for ALS

A non-profit organization that aims to provide support for people affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The organization provides resources and advocacy to help people with ALS and their families navigate the challenges of the disease, and works to raise awareness and funds to support research towards finding a cure.