The PSP Association offers advice, support and information to people living with the degenerative brain diseases, PSP and CBD, and supports research into treatments for those conditions.
Amanda Sutton, venue manager at Broadway House, said: ”There will be a warm welcome awaiting the participants, their families and friends at Broadway House where they can take rest and refreshment after the event and share their experience with us. We will be replenishing their batteries with delicious finger food and plenty of juice and water and there will be rooms set aside for massage areas for the participants.”
Jean Kelly, fundraising manager with The PSP Association commented: “We have 70 supporters running on behalf of the charity in the 2014 Virgin London Marathon. The PSPA is a small charity and the event is its biggest fundraiser. There is no cure for PSP, a degenerative neurological disease, or any effective treatment, but there is still a lot PSPA can do and the money raised will make a huge difference. It will go directly towards helping those living with PSP, be it through funding our Specialist Care Advisers, holding more local Support Groups, or funding research into the causes, treatments, and eventually, a cure for PSP.
“We are looking forward to hosting our post-race reception at Broadway House and greeting our amazing runners and their friends and families. All that is left to say is good luck PSPA runners!”
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