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.
The American Parkinson Disease Association (APDA) is a nationwide grassroots network dedicated to fighting Parkinson’s disease (PD) and works tirelessly to help the approximately one million with PD in the United States live life to the fullest in the face of this chronic, neurological disorder. Founded in 1961, APDA has raised and invested more than $252 million to provide outstanding patient services and educational programs, elevate public awareness about the disease, and support research designed to unlock the mysteries of PD and ultimately put an end to this disease. To learn more about the support APDA provides nationally through a network of Chapters and Information & Referral (I&R) Centers, as well as their national Research Program and Centers for Advanced Research, please visit www.apdaparkinson.org.
A non-profit organization that aims to raise awareness and provide support for people affected by Parkinson's disease. The organization strives to improve the quality of life for people with Parkinson's and their families by providing resources, education, and advocacy, and by funding research towards finding a cure for the disease.
The PMD Alliance is a non-profit organization dedicated to improving the lives of individuals and families affected by Parkinson's disease and other movement disorders. Through education, support programs, and community engagement, the PMD Alliance provides valuable resources, empowerment, and a sense of belonging to those living with these conditions. Their comprehensive approach aims to enhance awareness, knowledge, and quality of life for individuals impacted by Parkinson's disease and related disorders.
The Michael J. Fox Foundation for Parkinson's Research (MJFF) is a leading nonprofit organization committed to accelerating the development of improved therapies and finding a cure for Parkinson's disease. Since its inception in 2000, the foundation has raised over $1 billion for research funding, driving innovation and fostering global collaboration in the field.
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.
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.
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.
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.
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.
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.
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.
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.
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.
An advocacy group that works to raise awareness about Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease, and to encourage greater funding for research and treatments. The group is made up of individuals and families affected by ALS, who advocate for increased government funding, improved access to care, and increased public awareness of the disease.
A non-profit organization that raises funds for research and provides support for people affected by Amyotrophic Lateral Sclerosis (ALS). The organization funds innovative research to find treatments and a cure for ALS, and provides support to families and individuals impacted by the disease through advocacy, resources, and community building initiatives.
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.
