Weekly Updates! - April 4, 2025

Weekly Updates! - April 4, 2025

Weekly Updates! - April 4, 2025

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:
      • 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!
      • To support, visit the TBRS Exercise Challenge website.
        • All of the funds raised go to improving the Patient Registry and making data more easily accessible for research!
        • If you have any questions or need help, please contact me at kit@tbrsyndrome.org.
  • Upcoming: TBRS Friends and Family Support Group - April 26, 2025
    • This event will take place Sunday, April 26, 2025 at 2:00 PM Eastern Time via Zoom
    • 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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