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  • What is TS?
  • Treatment
  • Living with TS
  • Join or donate

The following description of Turner Syndrome (TS) and explanation of some of the issues involved in living with the condition are not definitive and a doctor or endocrine specialist should always be consulted whenever a diagnosis of Turner syndrome has been given.

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There are a number of treatments available to those with TS, and each girl/woman should be treated according to her individual needs. TS is a ‘cradle to grave’ condition and as such should be treated throughout life in a variety of ways.

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It should be emphasised that each girl/woman with TS is an individual and what is relevant to one is not necessarily relevant to another.

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Membership of the Society is GBP 30 (UK) per annum (overseas GBP35) and provides many benefits. We are also happy to receive donations which enable the TSSS to continue to offer support to those with TS and their families.

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Diary dates

Sat Nov 28 @12:00AM
Durham & Newcastle meet-up
Sun Nov 29 @ 2:00PM - 05:00PM
Central England Xmas party
Sat Dec 12 @12:30PM -
London Christmas meet
Thu Nov 17 @ 8:00AM - 12:00AM
TS International Conference, Mexico
Fri Nov 18 @ 8:00AM - 12:00AM
TS International Conference, Mexico

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