Hello. I hope everyone has had a great week. I have a few updates to share:
Launching the TBRS and DNMT3A Registry (2.0)!
We have been working to update our Patient Registry for some time now, and are excited to announce that the TBRS and DNMT3A Patient Registry has officially launched!
Our goal with this new registry is to collect data more efficiently and make it easier for families to complete!
Some of the other changes included in our new registry are using standardized surveys, adding Heyn Sproul Jackson Syndrome to our Registry (HESJAS is a different syndrome also caused by the DNMT3A gene), and translating the Registry into other languages.
Steps to participate in the updated Registry are below:
IF YOU PARTICIPATED IN THE REGISTRY IN THE PAST:
You should have received an email from iamrare-help@rarediseases.org with instructions to continue with the new Registry.
Please email me with any questions! kit@tbrsyndrome.org
THANK YOU to our TBRS Challenge participants!
We have officially launched the 2025 TBRS Exercise Challenge!
Through this challenge, individuals with TBRS commit to a daily exercise of their choice in exchange for pledges and donations to the TBRS Community. This presents an exciting fundraising opportunity while encouraging healthy practices for individuals with TBRS.
Thank you to all of the superstars participating in the Challenge this year! It's amazing to see what you can do!
The TBRS Community offers a monthly Friends and Family Support Group via Zoom. Families from all around the world can participate. We create a safe place to share thoughts, feelings, concerns, and emotions without judgment. The meeting seems to take a different shape every time we gather—sometimes we focus on sharing resources or experiences, but we always seek to make everyone feel comfortable and supported.
Any parents or caregivers of someone diagnosed with TBRS are welcome.
Thanks! Please reach out to me with any questions at kit@tbrsyndrome.org.Kit Church, CARE Manager
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