Sjögren’s Foundation

Creating a community where patients, healthcare professionals & researchers come together to conquer the complexities of Sjögren's.

• Fund Raising and/or Fund Distribution

• 65.

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.

• Specifically Named Diseases

• 66.

K-T Support Group

Information, education and support for combined vascular malformation patients and families coping with Klippel-Trenaunay syndrome K-T Support Group, a non-profit group supporting Klippel-Trenaunay syndrome, CLVM, Parkes-Weber syndrome.

Cri Du Chat Research Foundation Inc

CDCRF is a 501c3 Non-Profit supporting the development of a treatment for Cri du Chat / 5p- Syndrome.

• Fund Raising and/or Fund Distribution

• 68.

Eleanor Kaplan Foundation Inc

To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.

• Specifically Named Diseases Research

• 69.

Plasminogen Deficiency Foundation

A 501(c)(3) public charity dedicated to improving the lives of patients with plasminogen deficiency (PLGD).

• Research Institutes and/or Public Policy Analysis

• 70.

American Institute for Dyscalculia Research

It is estimated that as many as 4 million children in the U.

• Residential, Custodial Care (Group Home)

• 71.

Place of Purpose Community

The Place of Purpose Community POP Giving physically disabled adults community to live and grow Building relationships with other disabled adults and finding their purpose in life Take our survey Help us help you.

• Professional Societies & Associations

• 72.

American Autonomic Society

Diverse disciplines that share interest in the autonomic nervous system and the pathology, treatment, and prevention of disorders.