Improve Quality of Life for MND sufferers
Donation protected
On the 24th August 2024, I will be doing a skydive in order to raise money for the Motor Neurone Disease Association - South Lancs Branch.
As many know, in August 2022, my grandad got diagnosed with Motor Neurone Disease. No words will ever explain how truly awful the disease is and what those with the diagnosis go through, physically and mentally. We have watched it first hand with my grandad and many of you have watched it through the journey of rob burrows.
Motor neurone disease is a progressive condition that affects the brain and nerves, leading to muscle weakness and loss of mobility. The South Lancs Branch of the MND Association provide support and resources to individuals and families like us who are affected by MND, helping them navigate the challenges they face daily. Unfortunately, there is no cure as of yet, however, there are still things that can be put into place to improve the quality of life for those suffering with the disease.
I hope to raise both awareness and funds to aid in the association’s mission. Your support will contribute to essential services to help improve lives.
I can not thank The South Lancs Brach of the Motor Neurone Disease Association for the support they have offered my grandad and us as a family and for the love and care they have shown us since his diagnosis. We are forever grateful for such an amazing team.
My Grandad is an inspiration, and I am so proud to be his granddaughter.
As many know, in August 2022, my grandad got diagnosed with Motor Neurone Disease. No words will ever explain how truly awful the disease is and what those with the diagnosis go through, physically and mentally. We have watched it first hand with my grandad and many of you have watched it through the journey of rob burrows.
Motor neurone disease is a progressive condition that affects the brain and nerves, leading to muscle weakness and loss of mobility. The South Lancs Branch of the MND Association provide support and resources to individuals and families like us who are affected by MND, helping them navigate the challenges they face daily. Unfortunately, there is no cure as of yet, however, there are still things that can be put into place to improve the quality of life for those suffering with the disease.
I hope to raise both awareness and funds to aid in the association’s mission. Your support will contribute to essential services to help improve lives.
I can not thank The South Lancs Brach of the Motor Neurone Disease Association for the support they have offered my grandad and us as a family and for the love and care they have shown us since his diagnosis. We are forever grateful for such an amazing team.
My Grandad is an inspiration, and I am so proud to be his granddaughter.
Organizer
Melissa Carr
Organizer
England