Yes, I do exist - as a real person, not some trick of the imagination :)
I live in Australia and was born with TBS. I created and run this International Support Group via the internet and have met some pretty amazing and fantastic people along the way, who have come on board to offer their support and friendship in making this group such a positive and successful group. I don't receive any profits from the Support Group and sincerely hope members or other interested people who wish to make profits do so by making a commitment within their local community to raise awareness for their children living with the symptoms of TBS.
I also recommend that they, in doing so also support research in TBS and pass on their knowledge to assist the growing evidence now known of TBS.
I am grateful to Professor Juergen Kohlhase who operates independently of this website project, but kindly endorses this Support Group without receipt of any funding or benefits. The success and recognition of the TBS Support Group has been assisted by his involvement with moderating information and content regarding TBS within the website.
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