Stichting Rubinstein-Taybi

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find a answer to your questions


Thanks to working together worldwide we were able to collect a lot of useful information and experiences about the Rubinbstein-Taybi syndrome. After many researches, articles and stories down our road we have collected all of this on this platform. Using the 'search' function; you can have all this on your fingertips!

Do you need help

Are you new here? Do you find it overwhelming? Start at the beginning and let us, step by step, guide you and introduce you with Rubinstein Tayby Syndrome.


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Information

More about RTS

Knowing what your child has is important! What is this syndrome? Why do you get it? How can you treat it? We have collected all available information to tell you!

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Experience stories

Share your stories and hear those of others

RTS is a long journey; sometimes difficult but often you arrive at a sunny place. Talking about it helps you cope with the journey.

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Meeting others

There are others in the same situation as you. If you connect with us we can help you find them. Maybe you want to meet someone with similar experiences.

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Ask the expert

Ask our experts

We all have questions on the care and wellbeing of our loved ones with RTS. Search the questions others have asked before. No question is too big or too small to ask.

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Our vision

Our movie

Rubinstein-Taybi Syndrome (RTS) is difficult to understandThe best way to find out is by watching our introductory video.

Our community worldwide

Our friends

Your national group

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Network of expertise Rubinstein-Taybi syndrome

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About the website contents

 

All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at: 

Send a email: info@rtsyndroom.nl