Cornelia de Lange Syndrome Foundation, Inc.

Cornelia de Lange Syndrome, promoting research & providing support to individuals with CdLS & their families 860.

• Specifically Named Diseases

• 245.

The Corneal Dystrophy Foundation

http://www. cornealdystrophyfoundation.

• Medical Specialty Research

• 246.

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

• 247.

Rare Village Foundation

TO FIGHT FOR CURES FOR RARE DISEASES AND EMPOWER INDIVIDUALS WITH RARE DISEASES TO LIVE THEIR BEST LIVES THROUGH LOCAL COMMUNITY EDUCATION, INSPIRING ADVOCACY, AND TIMELY CONNECTION TO CRITICAL RESEARCH THAT LEADS TO CURES We Empower Families to Create Cures for Rare Disease.

SCLERODERMA FOUNDATION OF CALIFORNIA

https://t. co/zM9Em1IIrP We EMPOWER the scleroderma community to live BETTER lives through programs dedicated to SUPPORT, EDUCATION, and RESEARCH We EMPOWER the scleroderma community to live BETTER lives through programs dedicated to SUPPORT, EDUCATION, and RESEARCH Signed in as fillergodaddy.

• Single Organization Support

• 249.

For A Cure NW

For A Cure NW's sole purpose is to raise funds in support of patients and research involved with The High Risk Leukemia Program at Seattle Children's Hospital.

• Fund Raising and/or Fund Distribution

• 250.

DHPS FOUNDATION

Leading the way in DHPS Deficiency Disorder research and education in order to find treatment, and a cure #curedhps #raredisease Our genetics make us unique our struggles and triumphs unite us.

• Single Organization Support

• 251.

THE MED13L FOUNDATION INC

Supporting MED13L families through awareness, research, and community.

• Birth Defects, Genetic Diseases Research

• 252.

ADLD CENTER

The ADLD Center is focused on raising awareness about Autosomal Dominant Leukodystrophy ADLD and developing a network of clinicians researchers patients and their caregiversadvocates in order to raise funds as we move forward towards finding a cure.