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FRIENDS

The organizations listed below are members of DSAGNO’s ever widening circle of friends across the country. One of the most critical things parents of a child with Down syndrome can do for themselves is make connections with other parents of children with Down syndrome. This enables us to trade information “through the grapevine” so to speak. Some of the most important things we can learn will come through the experiences of others rather than a book.

In our effort to bring more information to parents and families, DSAGNO reaches out to other organizations in the same way parents reach out to each other. This enables us to bring more parents together, seek out nationally-renowned speakers, and bring more information to our membership.

We’ve listed below a just few of the new “friends” DSAGNO has made and we’ll continue to add friends to the list as our circle of friends grows, so check back frequently.


"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."
CLICK HERE


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.
CLICK HERE

 


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.

CLICK HERE


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.
CLICK HERE


To assist and support, through fellowship and action, the fathers and families of people with Down syndrome.
CLICK 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

 


Expertly helping families with special needs.
Provider Group develops comprehensive plans that can help protect your eligibility for Social Security, Medicaid and other government programs, while supplementing your benefits with income from other assets.
CLICK HERE


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.
CLICK HERE


A family organization representing
Manatee and Sarasota counties in Florida.
CLICK HERE


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


Lousisana Citizens For Action Now
Advocating for individualized community supports for Louisiana citizens who experience developmental disabilities
CLICK HERE


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.
CLICK HERE


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.
CLICK HERE


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

 


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.
CLICK HERE


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.”
CLICK 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.
CLICK HERE


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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