• Medical Specialty Research

• 73.

Cure 2 Children Foundation

Fondazione a carattere internazionale, per la cura delle malattie ematologiche ed oncologiche, la ricerca scientifica ed il trasferimento di know-how It is our vision that every child, whether suffering from leukemia, cancer, thalassemia, or sickle cell disease, has the chance for an affordable and reliable cure, locally.

• Fund Raising and/or Fund Distribution

• 74.

Harmony 4 Hope

Leading Nonprofit Mobilizing Community & Raising Funds 4 Rare Disease through the Universal Power of Music & Storytelling.

• Birth Defects, Genetic Diseases Research

• 75.

Ataxia Telangiectasia Children's Project, Inc.

The A-TCP organizes & supports innovative research to optimize disease management strategies, develop new treatments and find a cure for ataxia-telangiectasia.

• Fund Raising and/or Fund Distribution

• 76.

Curears A NJ Nonprofit Corporation

Our mission is to spread awareness, connect and provide support to affected families and fund research for the ultra-rare mtARS genes.

• Alliance/Advocacy Organizations

• 77.

Trpm3 Foundation

Patient advocacy and support for those affected by #TRPM3 #ionchannel related disorders.

Be Still Foundation Inc

To empower and uplift those with tremors, along with their families.

• Birth Defects, Genetic Diseases Research

• 79.

Channeling Hope Foundation

Channeling Hope Foundation A community of researchers and families driven to advance care and develop treatments for those affected by NALCNrelated disorders.

• Nonmonetary Support N.E.C.*

• 80.

Global Neuro Ycare Inc

The mission of Global Neuro YCare is to educate through the creation and translation of materials and programs for children, youth and families; advocate with national and international organizations to guide the creation of regional, cultural and country specific programming; and support research addressing the needs and experiences of young carers.

THE TYLER'S TRIBE FOUNDATION

The Tylers Tribe Foundation Lets WipeOutALS Together About The Tylers Tribe Foundation The Tylers Tribe Foundation was founded by Meghan Decker after her brother Tyler was diagnosed with ALS at just 26 years old.