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AAP Health Supervision for Children – In Your Language

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Help us ensure a healthier, brighter future for our children
Follow these important, free guidelines

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Health Supervision for Children
and Adolescents with Down Syndrome -
In Your Language
American Academy of Pediatrics
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Health Supervision for Children
and Adolescents with Down Syndrome -
In Your Language
American Academy of Pediatrics

Healthy Children with Down Syndrome Campaign

 

A Commitment to Free Resources For All​

The Global Down Syndrome Foundation (GLOBAL) is proud to announce our collaboration with the American Academy of Pediatrics (AAP). The collaboration ensures that the AAP Health Supervision Guidelines for Children and Adolescents with Down Syndrome (the AAP Pediatric Guideline) is available in multiple languages at no cost to families and professionals around the world. GLOBAL has a network of world-class clinicians and scientists who help to create many important resources including our AAP Pediatric Guideline and our Prenatal & Newborn Down Syndrome Information pamphlet.​

The Impact of YOUR Support​

Your generous support allows us to provide thousands of free downloads and print mailers to local Down syndrome organizations, universities, medical centers, research institutes, families and professionals. People with Down syndrome have a dramatically different disease profile than those without Down syndrome. They are at high risk for certain diseases ​(for example, autoimmune disease and Alzheimer’s) but highly protected from others (for example, solid tumor cancers). Following evidence-based guidelines is crucial to healthy outcomes and can significantly impact cognition.

Access the AAP Health Supervision Guidelines for Children and Adolescents with Down Syndrome

For Families: Available in English, Español, Italiano, Shqip, and Kiswahili

For Professionals: Available in English, Español, Italiano, Shqip, and Kiswahili

Healthy Children with Down Syndrome
By the numbers

100% of the proceeds from GLOBAL’s Healthy Children with Down Syndrome Campaign go to AAP Pediatric Guideline translations and to our Prenatal & Newborn Down Syndrome Information pamphlet.

Envelope icon31,200
Downloads & Print Distribution

Seminar icon200
Webinars & Conferences

Earth icon105
Countries Covered

People icon5
Languages Translated

Trusted GLOBAL Partners & Supporters
Supporters at the $10,000 level or higher receive special recognition

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Logo Chadron's Hope Foundation
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Charles Monfort

The Napoleone Family

The Stephens Family

Testimonials
Amy Navejas
It is so important to have GLOBAL’s evidence-based Prenatal and Newborn Down Syndrome Information pamphlet, a resource medical professionals trust. We were fortunate to be able to distribute 500 copies at no cost to our local providers last year.

Amy Navejas, J.D.​

Executive Director​
North Carolina Down Syndrome Alliance​

Karen Kelminson
At the Sie Center at Colorado Children’s Hospital we provide the Prenatal and Newborn Down Syndrome Information pamphlet to pregnant people who have received a prenatal diagnosis for Down syndrome. It is a vital resource!
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Kelminson-Karen

Karen Kelminson, M.D.​

Medical Director​
Sie Center for Down Syndrome​
Children’s Hospital Colorado​

Carissa Carroll
We provide thousands of new parents with a beautiful welcome basket each year. We are proud to include the Prenatal and Newborn Down Syndrome Information pamphlet and to refer parents to the AAP Pediatric Guideline in multiple languages thanks to GLOBAL.
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Carissa Carroll

Carissa Carroll

Jack’s Basket

Recent News & Resources​
Help Us Spread the Word

DeOndra Dixon advocacy

📣 CALL TO ACTION: Contact Your Senators TODAY!

Please help GLOBAL ensure we have funding to elongate life and to improve health outcomes for our loved ones with Down syndrome!​

Take five minutes to urge your two Senators to Co-Sponsor and Pass the DeOndra Dixon INCLUDE Project Act (S. 3981). Just plug in your address, press “Send Email,” and your Senators and a pre-drafted letter will auto-populate. ​

Named after Jamie Foxx’s little sister, DeOndra, who tragically passed away in 2020, this legislation will secure increased federal funding for Down syndrome research and medical care for our children and adults for years to come.