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The Irish Football Association is expecting to run a small number of Basic Referee’s Courses in 2014. They will be held in different locations around Northern Ireland with details appearing on this page over the next few months.
The next introductory course will be on Monday 21st July 2014 at Shamrock Park, Portadown. A beginners course will run at the same venue from Monday 4th August 2014.
Release Date: 28/02/2011
LIBBIE Spiers is the precious, two-year old daughter of IFA Grassroots Development Officer Kyle Spiers and his wife Gillian.
For the first few months of her life Libbie appeared to be a healthy baby, however at the age of six months she endured her first seizure. This was, at first, attributed to common febrile seizures resulting from a high temperature during teething or a cold, however when the seizures became more frequent and prolonged it became apparent that this was something much more serious.
Kyle and Gillian have left no stone unturned to achieve a proper diagnosis of Libbie’s condition – and this has been difficult as appropriate medical expertise in Northern Ireland is very limited.
Eventually, Libbie’s condition was diagnosed as Dravet Syndrome. This is a condition caused by a gene mutation (SCN1A) and is extremely rare – only six children are known to have the condition in Ireland and even in the USA, where there are more cases, knowledge about the Syndrome and its long-term effects is very limited.
What is known is that Dravet’s Syndrome affects almost every aspect of a child’s life, including cognitive development, mobility, speech and language development and behaviour.
The Libbie Trust is being established to raise funds to be held in trust for Libbie’s future, so that anything and everything possible can be made available for her in terms of treatment, knowledge and care.
The Trust will be administered by a Committee and will work closely with the Dravet Syndrome UK, a charity set up in England for support of UK sufferers and their carers. It is hoped that, in addition to providing care and support for Libbie and her parents, it can also help raise awareness of this Syndrome and help other parents find support and information more easily.
There will be collections taking place at Northern Ireland Home Internationals during 2011 - please support The Libbie Trust, and you will also be helping other Dravet Syndrome sufferers and their families.
Should you wish to learn more about the condition, you can email Kyle: email@example.com or telephone 07765 463 946.
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