Our little girl was diagnosed with Turner Syndrome at our 20 week scan. This is chromosome abnormality affecting 1/2500 females in the UK. 

Whilst frantically trying to find out about the condition we came across the Turner Syndrome Support Society. Since the very moment we made contact with them, their help, care and support has never wavered and has been invaluable. 

This is is our way of "Just Giving" something back to help the society and all those magnificent people that have helped us since that daunting day in March 2011!!

As 2014 is the 15th anniversary of the TSSS Annual Conference they are asking its members to help raise funds and awareness centered around the number 15. They are calling this "club 15".

The money which we hope to raise will enable the TSSS to:

>Continue to offer support to those with TS and thier families

>Help to create greater awareness of Turner Syndrome amongst health professionals and the general public

>Enable them to provide information on all aspects of living daily with Turner Syndrome

Thank you so much off taking the time to visit our page! 

Please donate as every little helps!

Emma & Andrew x