Spastic Paraplegia Foundation, Inc.

Hereditary Spastic Paraplegia #hsp & Primary Lateral Sclerosis #pls together we are #HSPandPLS The Spastic Paraplegia Foundation is committed to promoting research to find cures for Hereditary Spastic Paraplegia and Primary Lateral Sclerosis, to educating people and their families affected by these conditions to help them live full and productive lives and to creating opportunities for mutual support and sharing.

• Birth Defects, Genetic Diseases Research

• 38.

SMS Research Foundation

The mission of the Smith-Magenis Syndrome Research Foundation is to advance scientific research leading to innovative treatment options for people living with SMS.

• Fund Raising and/or Fund Distribution

• 39.

Ellie White Foundation for Rare Genetic Disorders Inc

We will not give up until a cure for Wolfram syndrome is found for Ellie and the children suffering from this disorder.

• Birth Defects, Genetic Diseases Research

• 40.

Fam177a1 Research Fund

Founder and President, FAM177A1 Research Fund The mission of the FAM177A1 Research Fund is to improve the lives of those affected by FAM177A1 Associated Disorder through research and development of transformative therapies.

• Education N.E.C.

• 41.

Aarav S Time To Shine

Our goal at Aarav’s Time to Shine is to bring awareness and raise funds to assist the Cystinosis Rese AARAVS TIME TO SHINE Home About News Donate Past Events ATTS Grand Gala 2023 More WHO WE ARE Your support is important to our work at Aarav39s Time to Shine.

• Professional Societies & Associations

• 42.

Sturge-Weber Foundation

Embracing our uniqueness. We may be rare, but we're also one in a million.

• Specifically Named Diseases

• 43.

SETBP1 Society

President of SETBP1 Society and Parent Advocate for SETBP1-HD SETPB1 Society's mission is to provide support to individuals with SETBP1 haploinsufficiency disorde Our Mission is to provide support to individuals with SETBP1 disorder and their families, to promote discussion and fund research, and to bring awareness and education to the public.

• Birth Defects, Genetic Diseases Research

• 44.

Rare Olive Org Inc

Our mission is to push forward the scientific understanding and treatment options for a rare neurodevelopmental disorder.

BEYOND THE DIAGNOSIS

Beyond the Diagnosis unites art and science to bridge the knowledge gap in healthcare, promote inclusivity, and raise awareness for children living with life-altering diseases.