Statement launched on behalf of Ed Slater & Gloucester Rugby
Gloucester Rugby is deeply pained to announce that Ed Slater has been identified with Motor Neurone Disease (MND).
Following six months of trying out, Ed’s analysis was once showed closing week and in consequence, with the strengthen of his circle of relatives, pals and Gloucester Rugby, he has made the tough determination to retire from skilled rugby with fast impact.
Everyone at Gloucester Rugby – avid gamers, control and group of workers – are completely dedicated to supporting Ed, his spouse Jo and his 3 youngsters in no matter method required. We know the similar can be true of Gloucester and Leicester lovers, and the broader rugby group.
While Ed, his circle of relatives and the Club take time to resolve subsequent steps, Gloucester Rugby have opened a JustGiving web page. The path of those finances can be decided in the end, whether or not it’s supporting Ed and his circle of relatives at once and/or a decided on MND charity.
To donate, please click on right here.
Neither the Club nor the Slater circle of relatives can be making to any extent further remark at the moment and kindly request that the ones needs be revered.
For additional info on MND please consult with www.mndassociation.org.
My Name’5 Doddie Foundation
Gloucester Rugby is thankful for the strengthen already supplied via the My Name’5 Doddie Foundation. The Foundation was once arrange via Scottish Rugby legend Doddie Weir. In June 2017 the Scot printed he was once affected by Motor Neurone Disease. From the outset, Doddie has been pushed to assist fellow victims and search techniques to additional analysis into this, as but, incurable illness. In November 2017, Doddie and his trustees introduced the registered charity, My Name’5 Doddie Foundation.
The following knowledge has been supplied via the My Name’5 Doddie Foundation so as to add additional context and readability to the continued analysis and investment the Foundation is offering and championing.
The My Name’5 Doddie Foundation was once established via Doddie and the Trustees in keeping with his frustration on the loss of choices given to MND victims – no efficient remedy, no get entry to to significant scientific trials and no hope.
The Foundation has already donated tens of millions of kilos for focused MND analysis tasks and are dedicated to proceeding to spend money on probably the most promising analysis to assist in finding new therapies, acquire advanced wisdom and in the end discover a remedy.
My Name’5 Doddie Foundation additionally recognises the higher consideration surrounding possible hyperlinks between head harm and neurological illness, however there may be these days no longer sufficient definitive analysis on which to attract conclusions about possible hyperlinks with motor neurone illness (MND).
Whilst the proof round a hyperlink between head trauma and dementia appears to be gaining momentum, the similar can’t be implied for MND; those illnesses have other reasons and underlying elements.
MND is a posh illness and, even though we have now a miles larger figuring out of the genetics concerned, the hyperlink between genes, environmental and way of life elements isn’t neatly understood. Further analysis is significant to unravelling those main points.
My Name’5 Doddie Foundation continues to dedicate important finances into MND analysis that may assist us to grasp its reasons. Understanding the reasons of MND is an important to reaching the imaginative and prescient of the root; an international freed from MND.
For additional info at the paintings of the My Name’5 Doddie Foundation, we might inspire to consult with their web page right here.