Story
Those of you who know me know I don't dance, so this will be your one and only opportunity ever to laugh at my two left feet! Please make the embarrassment worth it. In aid of my mate Rob and everyone else affected by MND.
Money and sponsorship raised from the Rob Burrow Strictly Ball event go to the Rob Burrow Centre for MND Centre Appeal.
The Rob Burrow Centre will help give people living with MND the best quality of life. With your donations and sponsorship, we can build a state-of-the-art MND Care Centre, to give people with MND and their families the best possible care and support.
Former Leeds Rhinos player and dad of three Rob Burrow has been courageously sharing his story of motor neurone disease with the public since he was diagnosed at the age of 37, and he has raised the profile of the condition beyond all expectations. Since he was diagnosed, Rob has actively campaigned to help raise awareness and raise funds in support of MND charities and having excelled in his sporting career, he now plans to support the creation of a centre of equal standards that will benefit many more people living with this disease. The new centre will be called The Rob Burrow Centre for Motor Neurone Disease and will be the first in the UK to have its design led by the holistic needs of the patient and their family, creating a supportive environment that complements the expert team providing the care.
Thanks for taking the time to visit my JustGiving page.