Links

The following links are to external sites of interest.

My Links

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http://www.youtube.com/user/Emz1402?feature=mhee
My YouTube Video Channel with a few personal videos I made about TS.
 

Other Pages Of Interest

 
 
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http://www.coeliac.org.uk/
Coeliac UK is the leading charity working for people with coeliac disease and dermatitis herpetiformis (DH)
   
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http://www.southend-on-seacarnival.org.uk/
Southend-on-Sea Carnival Association is a voluntary organisation which was formed in 1926. Each year the association organises and runs Southend Carnival which helps local charities and provides countless amenities to various local organisations.
   
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http://www.visitsouthend.co.uk/
With seven glorious miles of seafront, the longest pleasure pier in the world and a host of exciting events and festivals all year, it's no wonder Southend-on-Sea leaves visitors smiling time after time.
 
 

Turners Syndrome Pages

 
 
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http://www.childgrowthfoundation.org/
The Foundation is the UK's leading charity relating to children's growth.
   
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http://kidshealth.org/teen/diseases_conditions/genetic/turner.html
Turner syndrome (TS) is a medical disorder that affects about 1 in every 2,500 girls.
   
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http://www.tss.org.uk/
The Society provides accurate and up to date information on Turner Syndrome and the many aspects of living with the condition on a daily basis. We hope you find our website useful and friendly.
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http://www.turnersyndrome.org/
Create awareness, promote research and provide support for all persons touched by Turner syndrome.
 
 

Turners Girls Links

 
 
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http://www.youtube.com/user/CherryBlossomGirl85
A TS Girls YouTube channel with videos of her experiences and topics for discussion about TS.
   
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http://www.facebook.com/?ref=logo#!/pages/CherryBlossomGirl85/150155775052105
A TS girls Facebook group for everyone to discuss any topics surrounding TS and share their experiences.
   
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http://www.freewebs.com/colleenjoyce/
I am a full blown Turner's girl, all of the cells in my body are missing a chromosome. I thought that this website would be a good idea for TS girls to learn a little more about each other.
   
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http://turnerssyndrome.tripod.com/tsyndrome/id10.html
I'm Jessica I set this website up because I have a condition called Turners Syndrome and wish to share my experiences.
   
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http://www.facebook.com/?ref=logo#!/groups/90864331453?ap=1
A TS girls mums Facbeook group to help raise doctors awareness of TS trying to arrange fundraising events and allows discussions about various issues.
   
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http://www.thirtysomethingblog.com/turnersyndrome.html
When I was in 3rdgrade my parents took me to my pediatrician telling him they were concerned with my size.  He sent me to the hospital for 3 days of genetic testing. The result was a diagnosis of Turner Syndrome.
   
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http://www.angelfire.com/tn/Anita/
I have Turner's Syndrome, and I set up this web page to inform other people of this chromosomal disorder.