We are updating the TBRS Community website in major ways!
We are currently working on a new website that will have two sections - one for families and one for researchers!
There will also be a calendar of events, and more updated information on TBRS!
I am hoping to have this completed by the end of the year!
We are increasing accessibility for disabled individuals to fill out the Patient Priority Survey
It now has a new color scheme, is easier to read, and is available in spanish
We are also planning to conduct one on one interviews with diagnosed individuals that are interested in filling out the Patient Priority Survey to help them!
NORD registry 2.0 is in development
As I mentioned before, we are including all germline DNMT3A variants
We still have a long road ahead of us, adding in standardized surveys and changing this up, but still a work in progress
Again, I will make a post when it is complete!
Genomics video
Some of you participated in a genomics video for Dr. Kate Tatton Browns team to describe your experience with genetic testing and diagnosis of TBRS
This is almost completed and was super impactful! Such a beautiful video!
Kate Tatton-Brown still needs to give us feedback, but we will share this video when we are able to
Webinar with Virginie McNamar about Ciitizen
Monday Nov 27, 1-2pm EST
Join to learn more about this tool and what it can offer to TBRS Families.
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2026 TBRS Community Summit!
The 2026 TBRS Community Summit will bring our community back together in San Antonio, TX, USA.