Once in a while it's good to do some creative spring cleaning, and that is what has happened to our website.
The stored content looks a bit different from what we have had in the past. The content has been updated, and redesigned
using some pretty zippy tools, templates and resources offered by Siteground.com.
I have used some other free resources to add a bit more variety and to keep the costs of running the website down. As a
non-profit group, no donations or money is ever are asked for. Membership is free and open to all peoples in all countries,
who are either born with TBS, or their family and friends have been.
It is also open to health professionals, in particular geneticists researching the syndrome. No personal information
regarding your current residential address details are requested or displayed on our website to protect your privacy.
If you would like to join our group, please click on the Feedback Link below to request membership. You can also use the
Feedback Link to request information about this group, the condition and symptoms of this rare syndrome.
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