Author Archives: Aniridia Network

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About Aniridia Network

A charity support group for people with the genetic visual impairment aniridia and their families in the UK and Ireland. Our vision is that people with/associated with aniridia are hopeful, confident, supported and well informed regarding aniridia. Founded in 2000. First registered as a charity in 2011 and fully in 2018.

London meet-up review: A big success

A fantastic 14 people with aniridia, plus relatives came to the meet-up in London in early November. There was great chat about all aspects of life and new friendships created. The evening started at 6pm at Belans bar on High … Continue reading

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Manchester for annual meeting 2012

Manchester, Saturday 19 May 2012 – put it on your calendar right now. That’s where and when the next big Aniridia Network UK meeting will be. It is your chance to hear from and ask questions in person to: people who … Continue reading

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Charity strategy update

Plans for the next two years were the result of the trustee’s latest strategy day. We decided the charity’s priorities for 2011-12 were: increasing the number of volunteers boosting funds raised from donors strengthening how we administer the organisation. Katie, … Continue reading

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Give as you Live – a simple way to raise money for Aniridia Network UK

Would you like to raise money for Aniridia Network UK? Do you shop online? Then why not join Give as you Live? It’s an online shopping portal run by Everyclick.com featuring many well known high street stores such as: Marks … Continue reading

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Harry wins teen “Caring For Others” award

A boy with aniridia has won an award for his caring nature. Harry, 16, from the Exeter area won the “Caring For Others” category in the Teen Awards run by the Exeter Express & Echo newspaper. The awards “show that teenagers … Continue reading

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Fact check on Daily Mail piece about teenager with WAGR/11p deletion syndrome

A recent Daily Mail article aroused our interest. The piece features Gemma who has WAGR, also known as 11p deletion syndrome after its genetic cause. It includes aniridia among its possible symptoms. We were glad to see a national newspaper … Continue reading

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At school with aniridia

My name is Abbie-Rose and I am 14 years old which means I’m in year 9 at school. I live in Norwich and I have aniridia, nystagmus and a cataracts. I also have an auditory processing disorder (APD). My brother, … Continue reading

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Give as you Live – a simple way to raise money for Aniridia Network UK

Would you like to raise money for Aniridia Network UK? Do you shop online? Then why not join Give as you Live? It’s an online shopping portal run by Everyclick.com featuring many well known high street stores such as: Marks … Continue reading

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Protected: On your bike

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New approach to keratoplasty may be better for patients with iris implants

A study has found that Descemet’s stripping endothelial keratoplasty (DSEK) can be better than penetrating keratoplasty in eyes with an artificial iris. In eyes with partial or complete aniridia it helps restore clarity of corneas and may mean quicker improvement … Continue reading

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