For families with Rubinstein-Taybi Syndrome.
You are not alone.
Your central hub for community, guidance and lifelong support.
Bi-Annual Conference.
Our bi-annual conference is happening this year at Drayton Manor where you can meet other families, learn about the condition, and have a fun weekend at the theme park.
Connecting families.
The RTS Support Group started off with a small number of families being contacted by Barbara Baron who kept in touch by phone and letter.
Over the years, the number of families involved has significantly increased, links have been made with relevant medical professionals and experts, and the charity communicates regularly with families by email and holds large well attended events.
Barbara’s ethos continues and the charity remains dedicated to bringing RTS families together to help provide support and to share information.
What our families say
Jack’s story
Jack’s story
Jack’s story
Jack’s story
Research and Impact.
RTS funds a student on a research PhD at Aston University, Birmingham. Put some more information about that here as I cannot find anything on the current website and this would be interesting to know about.
Meet our Team
Medical Advisory Board
I realise this is just the governing board photos but Gemini recommended demonstrating medical trust and expertise. So it could be good to show bios, links and credentials here.
Dr Jane Sharpe
Senior Lecturer, Sheffield Teaching Hospital
A note about their credentials
Zohra Lakha D.Phil
Counsellor and Advisor
A note about their credentials
Jo Mullins
PhD Research Student, Aston University
A note about their credentials
Dr Jane Sharpe
Sheffield Teaching Hospital
A note about their credentials