Lettercase

We are a Genetic Support Foundation program that offers reliable, up-to-date information about genetic conditions.

06/12/2026

A recent viral video posted by a popular YouTuber has brought renewed attention to a topic that we care deeply about: the quality of information available to pregnant patients at the moment of a prenatal diagnosis.

Our latest blog article addresses common misconceptions about Down syndrome and explores why the quality of information provided at the time of diagnosis matters so much.

Read now by visiting blog.geneticsupportfoundation.org!

05/28/2026

For this month's Medical Outreach meeting, we discussed how to host a "Lunch and Learn" presentation! Together, we created a template presentation based on what matters most to both the Down syndrome community and the medical providers who serve them.

Ready to bring a Lunch and Learn to your area? Visit lettercase.org/lunch-and-learn to watch a recording of this month's meeting and download the template presentation!

05/20/2026

Join us for the 2026 DNA Dash on Saturday, June 13th! Whether you walk, run, roll, or complete a personal goal, every step supports our important services. 💙

🔎 What does your DNA Dash ticket fund?

Your registration helps us send free, balanced resources to families learning about a new diagnosis, including conditions such as:
📚 Down syndrome
📚 Klinefelter syndrome
📚 Turner syndrome
📚 Jacobsen syndrome
📚 Spina Bifida

🔎 Why do we need your help?

Too many new and expectant parents are not provided up-to-date, balanced resources when learning about a genetic condition in their baby. But these resources can help families find support and services and improve long-term outcomes for families.

By joining DNA Dash, you can help us send trusted resources to parents and healthcare providers nationwide to support families when it matters most.

💙 Learn more, register, and share by visiting GeneticSupportFoundation.org/dna-dash-2026!

05/08/2026

This Mother's Day, help us ensure that every new and expectant mom receives the support and information they need following a diagnosis of Down syndrome!

💌 A donation of just $21 helps us send a free printed book on Down syndrome to a new or expectant mom through Priority Mail.

💌 Larger gifts help us maintain, update, translate, and create new resources. Larger gifts also help us share resources with healthcare providers nationwide so families receive thoughtful, accurate information from the very beginning.

Please consider making a gift today and sharing our campaign with your loved ones: https://donorbox.org/mothers-day-campaign-2026 ❤️

05/05/2026

DNA Dash is BACK!

Join us on Saturday, June 13th for our second annual DNA Dash virtual 5K fundraising event! This event is your chance to walk, run, roll, or accomplish a goal to help raise funds for Genetic Support Foundation.

💬 How does it work?
This event is virtual, so complete your 5K anytime, anywhere on June 13th. You can also choose a different activity or goal to complete, like a crafting, coloring, or reading race! If you'd like to complete the event with a group, teams can register together at a discount.

💬 What will I get?
Once you register, you will receive a package in the mail with a DNA Dash wristband and sticker. If you raise $50, you will also receive a GSF tote bag with extra goodies!

💬 What will my ticket fund?
All money raised from this event will directly fund GSF's important work, from direct patient care to disability advocacy.

Register, donate, and learn more by visiting GeneticSupportFoundation.org/DNA-Dash-2026!

04/30/2026

For this month's Medical Outreach Meeting, Dr. Stephanie Meredith presented on supporting children with Down syndrome who also have another genetic condition.

We discussed:

❤️ Connecting with a genetics provider
❤️ Connecting with other condition-specific organizations
❤️ Finding resources
❤️ Supporting families after loss
❤️ And supporting children with Down syndrome and autism spectrum disorder

Watch a recording and read a summary of this meeting by visiting lettercase.org/news!

04/21/2026

Each year, about 70,000 parents, advocacy leaders, and healthcare providers turn to our Lettercase and Down Syndrome Pregnancy websites for trusted information and support following a new diagnosis. All of our resources are available online at no cost, and we provide nearly 3,000 free printed books annually to families and providers who need them.

Our goal is simple: to ensure that every new and expectant mom receives the information and support they need following a diagnosis of Down syndrome.

This Mother's Day, you can help make that possible. Your donation allows us to ship free printed resources to families through Priority Mail, and to hand them directly to healthcare providers at medical conferences.

❤️ Give today to provide a lifeline for moms when it matters most: https://donorbox.org/mothers-day-campaign-2026

❤️ Set up an easy peer-to-peer fundraising page to help us raise funds for Mother's Day: email [email protected]

04/17/2026

Why become a Genetic Support Foundation recurring donor? Bernice Hall shares her story!

"My grandson with Down syndrome was born in 2000 and is now my part-time roommate. He says my house is his place too, and he helps me take out the trash and blow the leaves in my yard. He is such a blessing to me! I know how much it meant for my daughter to get support after he was born 26 years ago, so I donate $21 per month to Genetic Support Foundation to cover the cost of sending a book packet to a family of a new baby with Down syndrome. By the end of the year, I will have supported 12 families! As Andy's "Mama" and Stephanie's mom, I'm so happy to support this meaningful work."

Join Bernice in sending resources to families with Down syndrome by visiting GeneticSupportFoundation.org/donate and choosing to support us with a monthly donation. ❤️

04/09/2026

Dr. Jason Eberl and Dr. Stephanie Meredith teamed up as guest editors for the latest issue of Narrative Inquiry in Bioethics: Narrative Symposium on Parenting Children with Down Syndrome.

This special collection highlights stories from a diverse group of parents raising children with Down syndrome. As the editors note, "These stories convey that parents of children with Down syndrome are not a monolith. They are funny; they are insightful; they are frustrated; they are vulnerable and raw; they come from a range of backgrounds; they represent an array of prenatal diagnosis, postnatal diagnosis, and adoption experiences; and most importantly, they authentically love their children who also reflect a constellation of identities."

Thank you to NIB Managing Editor, Heidi Walsh, for keeping us on track and to Rosemarie Garland-Thomson for bringing us together and for her ongoing leadership as a trailblazer in disability rights!

These narratives can be accessed for free at the following link: https://muse.jhu.edu/pub/1/issue/56243

04/03/2026

Spent yesterday morning talking to genetic counseling students at the University of South Carolina about the history of disability rights, how to sensitively share a diagnosis, and where they can find resources for support. So grateful for their program and their historic leadership in the 2008 Down syndrome Consensus Group, and we're so grateful to share that legacy with the new generation of students!

Address

PO Box 2649
Olympia, WA
98507

Website

http://www.lettercase.org/

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