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When we learned that our sweetheart has Turner Syndrome,we had a lot of questions.We hadn't known anything about TS before.The answers we took from doctors have never satisfied us.Also we haven't got the opportunity to speak to the doctors whenever we wish.The hospital which Özlem is being controlled at is 90 km. away to us.The best way was the internet.We have learned much through it.But the real reason for choosing the net was that we wanted to hear or meet the people in our situation.Doctors give medical facts but we need to know the feeling of the people who suffer from TS.Then we decided to set our own site in order to help anyone interested.
As far as I know this is the only site prepared by TS people in Turkey.If we can help anyone,we will be happy.We will also be glad to hear from everyone. Please do send your comments,experiences etc.Everything will be welcomed.

We are not so sorry for having a TS child.She is the most precious thing in our life.In fact, it has added a  new meaning to our life.It's a 1/2500 case and having a TS child cannot be explained just as a coincidence.There must be a deeper meaning in this.We have been trying to do everything for enjoying life.We are sure we'll succeed with the power of LOVE.

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