• Alliance/Advocacy Organizations

• 64.

PCD KS FOUNDATION

Working together to find a cure and improve care for those with ciliary disorders and their families by increasing awareness, research and support.

• Birth Defects, Genetic Diseases

• 65.

Tennessee Prader-Willi Association, Inc.

We provide support and information for people with PWS & their families.

• Specifically Named Diseases

• 66.

ASSOCIATION FOR GLYCOGEN STORAGE DISEASE

Created for support and awareness of the various types of Glycogen Storage Disease.

• Reproductive Health Care Facilities and Allied Services

• 67.

Everlasting Hope

Home About Resources Grant Program Insurance Coverage Events Donate Shop More Everlasting Hope is here to walk with you through infertility How can we help.

• Specifically Named Diseases

• 68.

Watch 4 Wegeners

It could save a life. Home Sarahx27s Story About Our Board Contact Us Run To Raise Testimonials More Watch 4 Wegeners It Could Save a Life Our daughter Sarah River Whitmire was a college student in pharmacy school when she died suddenly at age 20 from complications of undiagnosed Granulomatosis with Polyangiitis GPA also known as Wegener39s Disease a rare autoimmune disease that no one knew she had.

Kidney Disease Research and Assistance Fund

Minister who has worked for 21 yrs with non profits 501C.

• Nerve, Muscle, and Bone Diseases

• 70.

Lynk Up World (LUW)

Lynk Up • World (LUW) is on a mission to bring meaningful connection to children & families impacted by rare diseases through art, support and innovation.

SEATTLE CHILDREN'S HOSPITAL

The I Can And I Will Guild was created as a non-profit in December 2019 to support Seattle Children's Hospital and raise money for Uncompensated Care.

• Health (General and Financing)

• 72.

MAKENAS RAY OF HOPE INC

WE ARE MAKENAS RAY OF HOPE OUR VISION Makenas Ray of Hope Inc.