Olly the Owl's is going around the world to raise awareness of XP.
He is currently in Canada. We are now selling Olly Jnr's - Olly XP's baby brothers and sister for individuals to take on their travels. They cost £8 each and we ask that purchaser take him on their travel and send us a photo for our website. We are posting the pictures here and on Facebook. |
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Funding announced for national centre for rare childhood disease |
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Guy’s and St Thomas’ is to become the national centre for treating children with a rare inherited disease that leaves them vulnerable to sunlight. In collaboration with the University of Sussex and Ninewells Hospital Dundee, the Trust will tackle the recessive genetic disorder Xeroderma Pigmentosa, or XP, which impairs the ability of the body to repair damage to DNA caused by ultraviolet light. It affects about 100 people in the UK and can be a very severe disease, causing skin cancers, eye problems and neurological problems such as hearing loss, learning difficulties or difficulty walking. Dr Bob Sarkany, consultant dermatologist, St John's Institute of Dermatology (Guy's and St Thomas'), led on the application to the National Specialised Services Commissioning Group – a Department of Health committee which commissions highly specialised services – to fund the centre. "Until now, it has been difficult to coordinate all the different specialists," Dr Sarkany said. "But now we can have a clinical set-up where specialists in dermatology, neurology, ophthalmology and other relevant fields can work closely together." The Trust will work with Professor Lehmann's internationally famous diagnostic laboratory service at the University of Sussex, and the photobiology unit at Ninewells Hospital, to formalise a dedicated service for patients suffering from this debilitating disease. Working together, the team will build on their expertise to provide an expert and comprehensive service for patients. The service will be based not only at the Trust in London, but around the country with the XP team working with patients and consultants wherever they are. The centre will also work with the XP Support Group, a charitable Trust founded in 1999 by the parents of a child with the disease. Sandra Webb and her husband Steve first became concerned about their son Alex when he received a sunburn through a car window at just seven weeks old. At seven months he burned in the shade and at 11 months he had his most serious burn on a holiday in Austria; on both occasions he was wearing full sun block. Sandra said: "It is a strikingly difficult way to live for a child, and for the families concerned. Alex's school has been fitted with protective film on all the windows, lights have been checked for their emission of UV light and a welfare assistant has been provided to help apply his sun cream." Alex has to wear a visor whenever he goes out to protect his skin against cancer-inducing damage from daylight. Click here to read more.... |
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The XP Support Group Charity Auction takes place on Saturday 31 October |
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Please make sure you send you contact details with your bid. If you are successful you will be informed on Sunday 1st November. You can then pay by cash, cheque made payable to the XP Support Group or by credit/debit card on-line at https://xpsupportgroup.workwithus.org/Fundraising/Donate.aspx?page=5294 If you would prefer to make a donation to the group. This can also be done through the above link. Thanks. |
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The Patient Information Pack is on-line! |
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With this Newsletter patients and their families will have received a copy of our new Patient Information Pack. Ever since the Charity was set up , it as been a dream to produce an information pack that will help patients and heir families from diagnosis through the different stages of their life. We have been able to achieve this with a grant that we received from Jeans for Genes in 2006.
The pack consists of 12 Information Leaflets as follows:
• What is the XP Support Group?
• What is XP?
• Getting Medical Advice
• Getting help from Social Services
• Out and About
• Protection from the Risks of UV
• Genetics of XP + XP Top Tips
• XP at the different stages of Life
• What is UV?
• Owl Patrol weekend Camp
• XP Fundraising
The Patient Information Pack is on-line
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Owl Patrol Wins Charity Award! |
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We are delighted to announce that the Owl Patrol night time camp was awarded “Charity event of the Year” at the Express Yourself awards by Halo Living. Sandra Webb collected the award at the Feathers Ball in Manchester.
She is seen here collecting the award from Coronation Street star Scott Wright. The evening was especially poignant as the Band played Lean on Me”, the Owl Patrol song as Sandra was leaving.
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