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"Special Reads for
Special Needs publishes books and materials to motivate and accelerate
learning for children and adults with Down Syndrome. Focus includes
transforming nonreaders into eager readers, decoding money management
for teens and adults, and using specific classical music CDs to enhance
learning and brain function."
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To be a driving force
in the Acadiana community in generating acceptance and belonging of
individuals with Down syndrome. It is our strong desire to encourage a
society in which people with Down syndrome can involve themselves in
community activities and be
assisted in their development of the skills
necessary to do so.
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The Down Syndrome Association
of
Greater Richmond
The Down Syndrome Association of Greater Richmond includes parents,
family members, friends and professionals working together to improve
the quality of life of persons with Down syndrome.
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Sharing Down Syndrome
Arizona Inc. is a non-profit parent organization whose goal is to
enhance the quality of life of people with Down syndrome. SDSA is a
501-(c)(3) non-profit organization run by parents in Arizona, and an
Affiliate member of the National Down Syndrome Society and the National
Down Syndrome Congress. Please contact us, we'd love to hear from you!
CLICK
HERE

The Down Syndrome
Association of Central Florida is the leading voice for individuals with
Down syndrome and their families. We offer hope, encouragement and
acceptance through advocacy, education and awareness so that each may
realize their potential as members of our community.
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HERE

CLICK HERE

"Our Children Left
Behind is a parent volunteer-run Web site devoted to issues surrounding
the reauthorization of the Individuals with Disabilities Education Act
(IDEA)."
CLICK HERE
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The Down Syndrome
Research Online Advocacy Group (DSResearch, Inc.) is a non- profit
scientific and educational effort aimed at increasing public
understanding and support for clinical and biomedical research into Down
syndrome.
The DSResearch Online Advocacy Group is a nonprofit
corporation and an affiliate member of the National Down Syndrome
Society.
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A family organization representing
Manatee and Sarasota counties in Florida.
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The Alaska Chapter of
the National Down Syndrome Congress is a non-profit organization of
parents, relatives, professionals and friends of individuals with Down
syndrome. Its membership includes families and professionals from around
the state of Alaska.
CLICK HERE

Louisiana
Citizens For Action Now
Advocating for individualized community supports
for Louisiana citizens who experience developmental disabilities
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TURTLE BOOKS fill the missing gap in children's
literature. Now you have easy-to-read books that honestly talk about
what it's like to be a child with a disability. Warm, colorful
illustrations and simple, beautiful stories offer insights in dealing
with children who have physical and mental disabilities.
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An
Individualized Approach for
Maximizing Your Child's Potential
by equiping families with specific knowledge, expertise, and
methodologies which will assist their children as they prepare for their
fullest, God given potential and destiny.
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Marvin V. Cavallino, D.D.S
Our philosophy is to insure the finest quality
dental care for infants, children, teenagers, and children with special
needs, in the most loving and caring atmosphere as possible.
CLICK HERE
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CREATORS AND
PUBLISHERS OF INTERACTIVE EDUCATIONAL PRODUCTS
For
Preschool, Kindergarten, Special Education, Early Elementary, Speech
Therapists, Educational Therapists, Inclusion Specialists, English as a
Second Language, Resource Specialists, Occupational Therapists, Parents.
CLICK HERE

The Down Syndrome Association
of
Memphis & the
Mid-South
The Down syndrome Association of Memphis began in
1973 as Down's Parents of Memphis. A small group of parents met while
attending the first Early Intervention Program in Memphis at the Child
Development Center. They began meeting to learn more about Down syndrome
and to work to improve public awareness, while providing the most
current care for their children. This group of parents went on to begin
the Special Kids Early Intervention.
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The mission of Bart
Stevens Special Needs Planning is to help families and professionals
plan for the future care, supervision, security, and quality of life for
a loved one with special needs
CLICK HERE

The Down Syndrome
Association of Central Oklahoma (DSACO) was established in January 2000,
and is a certified non-profit organization.
“To raise awareness about Down syndrome in our
community and to provide resources for support and education to families
of children with Down syndrome.”
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HERE

The Canadian Down
Syndrome Society (CDSS) is Canada’s national voice for individuals with
Down syndrome.
Our mission is to enhance the quality of life for
all individuals who have Down Syndrome through advocacy, education, and
providing information.
CLICK HERE

Revolution Earth's first feature-length documentary
film, Shorty, was Executive Produced by Danny Aiello, fully sponsored
and endorsed by the National Down Syndrome Society and premiered in New
York City in October of 2003 to both critical and audience acclaim.
Additionally, fund-raising premieres of the film in numerous US cities
have raised over $50,000 for charities such as the Special Olympics and
numerous scholarship funds.
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The mission of Best Buddies Louisiana is to enhance
the lives of people with intellectual disabilities by providing
opportunities for one-to-one friendships and integrated employment.
CLICK HERE
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