The Transverse Myelitis Association

Our Mission is-
-To support and advocate for individuals and their families diagnosed with rare neuro-immunologic disorders of the central nervous system
-To promote awareness and to empower patients, families, clinicians and scientists through education programs and publications
-To advance the scientific understanding of and therapy development for these rare disorders by supporting the training of clinicians-scientists dedicated to these rare diseases and by supporting basic and clinical research.
OUR GOAL IS TO IMPROVE THE QUALITY OF LIFE OF INDIVIDUALS WITH THESE RARE NEURO-IMMUNOLOGIC DISORDERS

Pediatric Brain Foundation

Pediatric Brain Foundation’s Mission is Three-fold:
1. Expedite scientific research to find treatments and cures for ALL of the more than 14 million children, in the U.S. alone, living with some form of neurological disorder

2. Provide families and health care professionals with up-to-date information and resources on the latest discoveries in pediatric neurology

3. Educate the public and public officials on the critical importance of funding pediatric neurological research

Contact a Family

Contact a Family improves the lives of all families with disabled children. With them, we transform their lives, break down barriers and tackle disadvantage through ambitious, collaborative and innovative work. We make a real and lasting impact and are a force for positive change.

Advocacy for Patients with Chronic Illness, Inc.

To provide free information, advice and advocacy services to patients with chronic illnesses, in areas including health and disability insurance, Social Security disability, employment discrimination, school-based accommodations, and resource location.

Any Baby Can, Inc.

Any Baby Can serves families that have a child under the age of 13 with a chronic illnes, developmental delay or health risk, through case management and other support services.