Welcome to the Ragdolls UK Charity Blog – Page 2 – Helping girls with Turner's Syndrome achieve their full potential.

A word from our friends!

Volunteering with Ragdolls UK is a wonderful opportunity. Not only do you help those who need support but also share the knowledge and experiences with others about this wonderful, ongoing work.

Emily Toland (Glasgow)

The great work that Ragdolls UK do has provided hope for thousands across the UK who have Turner’s Syndrome as well as their families.

Jenna Waithe (Clydebank)

A little support makes a huge difference!

Have you heard of Turner's Syndrome? It occurs in 1 in about 2500 girls and women across the world and yet there are still many who haven't heard of it.…

Turner’s Syndrome 101 by Patricia Woods

12 Jul 201812 Jul 2018

What is a genetic disorder? Well each of us are made of a unique combination of DNA molecules which in turn determines lots of things about us like hair colour,…

Ragdolls UK Projects

Who’s On The Line? By Marion Kirkwood

24 Apr 201824 Apr 2018

We are a small charity and as such we only have so many people on hand to help. What Ragdolls UK does have to offer are a hard working team…

What is Turner’s Syndrome (A Handy Video Guide)

21 Mar 201821 Mar 2018

For every girl and woman with Turner's Syndrome we support there are several more across the world who have never heard of the condition. Despite occurring in about 1 in…

A World of Information

6 Mar 20186 Mar 2018

We are gifted with being able to find out a whole host of information at our finger tips and yet despite the speed of this information high way there are…

Ragdolls UK Projects…

Happy New Year from Ragdolls UK

3 Jan 20183 Jan 2018

The new year is an exciting time for us because it gives us the opportunity to look ahead and start working towards any fundraising events we may have throughout the…

Turner’s Syndrome and Us; by Racheal Chapman

t was a cool September day and we we’d decided to go for lunch. Normality was what was needed, a lunch date with my husband was perhaps the perfect opportunity…

Too Many Chromosomes Spoil the Broth; by Faye Price

12 Oct 201712 Oct 2017

This can certainly be the case for a minority of unborn babies. Whilst many of our womb bound children are tucked away fully formed, developing that much – loved ability…

Wilson’s Disease: When Copper is the Culprit; by Tetyana Pravytska

9 Oct 20179 Oct 2017

Copper is a naturally occurring element and can be found in various diets. Chocolate, liver, nuts and shellfish contain it in abundance. A great amount of copper in certain foods…

Haemophilia: Improving Lifestyle with Exercise; by Tetyana Pravytska

6 Oct 20176 Oct 2017

In 1904, ten years later after her splendid wedding ceremony, Princess Alix of Hesse, Queen Victoria’s granddaughter, gave birth to her much wanted son. Her happiness faded away very soon…

Autism Spectrum Disorder and Dance Therapy; by Katerina Vasakou

5 Oct 20175 Oct 2017

Body movement therapy approaches support the view that the non-verbal interaction components and body mechanisms of people with autism should be taken strongly into consideration when working in therapeutic and…

Spotlight on Duchenne Muscular Dystrophy; by Tetyana Pravytska

Duchenne muscular dystrophy(DMD) is a rare and inhereted genetic condition . It affects as many as one in 3500 boys. In 1986, researchers discovered the faulty gene on the X-chromosome…

Pet Therapy; by Tetyana Pravytska

Although the great assistance of animals is known for centuries, animal- assisted interventions have not received enough attention from researchers. Even as the number of studies grow, showing therapeutic potential…

Spotlight on Genetic Disorders

Spotlight on Cystic Fibrosis; by Alisha Malik

27 Sep 201727 Sep 2017

Genetic disorders can be caused when a mutation (a random and spontaneous change in the structure of a gene) occurs in a single gene. However, most of these mutations can…

Spotlight on Osteoperosis Imperfecta; by Gemma Bryant

26 Sep 201726 Sep 2017

I was inspired to write this article as a result of realising that if it were not for a couple of friends who happen to have osteogenesis imperfecta (OI), I…

Let’s tell the World!

14 Sep 201726 Sep 2017

When Ragdolls UK was founded we made it our mission to bring awareness of Turner's Syndrome to as many people as we could. It is a condition that occurs in…

Ragdolls UK Projects…

TS Girls Unite; By Tracey Connelly

28 Aug 201726 Sep 2017

I was having a chat recently with Kriss Fearnon of De Montfort University who is conducting research with TS girls and their reproductive decisions. This is one of the most…

Getting the Info you Need: By Anne Lilt

1 Aug 201726 Sep 2017

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…

Ragdolls UK Projects…

Small but Mighty; by Tracey Connelly

24 Jul 201726 Sep 2017

When businesses are built from the ground up it can be a difficult and trying journey. When it is a charity the odds you are up against can be near…

Ragdolls UK Projects

Helping Turner’s Syndrome girls achieve their full potential

27 Jun 201726 Sep 2017

Carrying a genetic disorder can be a scary experience. It can leave the sufferer feeling isolated and lonely. We at Ragdolls UK know this only too well and strive to…