Getting the Info you Need: By Anne Lilt

We are so pleased to see our website up and running with some new changes. We hope you can take the time to check it out.

The site features some basic information on Turner’s Syndrome, our volunteer vacancies as well as some information on our organisation.

We have information packs with more in depth details on Turner’s Syndrome. These are on an on demand basis to keep down the printing costs but if you are a Turner’s girl, a family member or if you would like learn more about a condition that occurs in 1 in every 2000 girls worldwide then please contact ragdolls.uk@gmail.com and we will be happy to send out any information you may need.

INFORMATION PACKS AVAILABLE

What is Turner’s Syndrome?

If you are newly diagnosed or would like to learn the basics this may be for you.

Turner’s Syndrome and the teen years

Is your TS girl reaching her teens? Are you a teen TS girl and would like to learn more about how puberty will affect you?

Turner’s Syndrome and Health

We run over all of the information you need to know to be a healthy, happy TS girl!

HELP US CONTINUE ON OUR MISSION

You can also make secure one off donations on our website! Any amount, large or small, is greatly appreciated. It goes a long way to helping us continue our projects as well as build new ones.

If you would like to make your donation monthly you can select the option as you complete the PayPal transaction.

To donate to Ragdolls UK monthly via Direct Debit contact us.

Your generosity will help a small charity thrive and grow!

YOUR OPINION MATTERS

Finally, our website also contains a link to our online survey. Just a few minutes of your time can help shape the future of Ragdolls UK. This is open to our members, TS girls, families of TS girls, medical professionals as well as the general public. We use your responses to focus our efforts to where you think they are needed most.

Click HERE to visit our website.

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