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What is TS?

The following description of Turner Syndrome (TS) and explanation of some of the issues involved in living with the condition are not definitive.

 

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

Please support this study and help us understand Lymphodema and how it impacts on those with TS and how we can help better in the future.

Your experience will help others.

This study is a joint study with the US, UK and Canada.

More info

Diary dates

Sat Sep 20 @ 1:00PM - 04:00PM
Gtr Merseyside & Manchester meet-up
Fri Oct 10 @12:00AM
TSSS annual conference
Sat Oct 11 @12:00AM
TSSS annual conference
Sun Oct 12 @12:00AM
TSSS annual conference
Sat Nov 01 @11:00AM - 04:00PM
Newcastle open day
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Fundraising ideas

Click the wheel

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15,000 ft tandem skydive

in aid of the TSSS

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Visit our online shop

For TSSS publications, goodies and more.

Shop now!
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Join POW Health!

and raise £1 for the TSSS at the same time.

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