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Our mission as the central voice in Michigan is to help prevent Lyme Disease and other Tick-Borne Disorders while providing support and education to Lyme Disease patients, caregivers, Health Care Professionals and the general public.

ALS Arizona is dedicated to improving the quality-of-life for persons with ALS. We provide movement to those who have lost the ability to walk; communication to those who have lost the ability to speak; support to those who have lost the ability to cope; and a voice and role in the fight against Lou Gehrig's Disease in Arizona.

To support the needs and well being of affected individuals and families, to promote awareness and education, to advance research for more treatments and ultimately a cure for Spasmodic Torticollis.

Our mission is to provide continuing education to those who prepare braille and to provide braille materials to persons who are visually impaired.

COMMUNICATION SERVICES AND COMMUNITY OUTREACH FOR THE DEAF, BLIND CITIZENS OF MINNESOTA. DEVELOPMENT OF LEADERSHIP SKILLS THROUGH IMPROVED SOCIAL INTERACTION.

TO IMPROVE THE QUALITY OF LIFE FOR THE SICKLE CELL PATIENTS LIVING WITHIN THE GREATER BOSTON AND SURROUNDING COMMUNITIES.

Our Mission is to provide a social support environment for professionals and families of individuals affected by Sotos syndrome so they can meet, exchange ideas and help one another cope with the condition. Sotos syndrome is a genetic condition causing physical overgrowth during the first years of life. Children with Sotos syndrome are often taller, heavier, and have larger heads than their peers. Because of the distinctive head shape and size, Sotos syndrome is sometimes called cerebral gigantism. Ironically, this rapid physical development is often accompanied by delayed motor, cognitive and social development. Muscle tone is low, and speech is markedly impaired.