Last week, we held our first Medical Outreach Meeting meeting of 2025! In this meeting, Dr. Stephanie Meredith presented on how to apply for CMEs and CEUs for presentations or webinars. Dr. Meredith shared a number of helpful tips and Read more…
Mitchell Levitz, a Self-Advocate with Down syndrome and Co-Author of Count Us In, shares a recorded presentation for medical students, physicians and other health professionals about how to discuss disabilities and to offer clinical care to people with disabilities and Read more…
Happy New Year from all of us at Lettercase! We are looking forward to another year of developing and translating resources, carrying out new and exciting research, and providing training to providers and advocacy leaders. We are also excited to Read more…
This week, we held our last Medical Outreach Meeting meeting of 2024! In this meeting, participants shared their incredible progress and successes in 2024, and Dr. Stephanie Meredith led a discussion on meeting topics for 2025. Participants who shared their Read more…
This month’s Medical Outreach Meeting presenter is Nicole Terry! Nicole is an experienced marketing professional with over a decade of diverse experience working in Corporate America. Nicole is also a parent of a child with Down syndrome, which led her Read more…
In this Medical Outreach Meeting, Brian Skotko, MD, MPP, answers questions and provides insight into Down syndrome care. Brian Skotko’s experience includes: DSC2U (Down Syndrome Clinic to You) is a resource for caregivers and medical providers of individuals with Down Read more…
For more than a decade, Lettercase has been a trusted resource for expectant and new parents, as well as healthcare providers, delivering accurate, accessible, and evidence-based materials about genetic conditions. Now, as part of GSF, our mission is strengthened with the support of Read more…
One of our genetic counseling student colleagues at Wayne State University, Maryam Ijaz, and her program director, Angela Trepanier, performed an analysis of the data we collected from patients about their genetic counseling experiences, as a subset of the data Read more…
Storytelling session at the Genetic Support Foundation event in 2018 discussing the top 5 things Stephanie Meredith wishes doctors or genetic counselors would have told her when her son, Andy, was diagnosed with Down syndrome back in the year 2000.
Learn how you can build relationships with medical providers, engage in medical outreach, and meet more new and expectant parents by collaborating with Early Intervention specialists and programs. Featuring Roxane Romanick, LCSW whose experience includes: Experience includes direct parent support, Read more…