Support Multiple System Atrophy Trust (MSA)

Denise’s Dad, Denis O’Connor was diagnosed with Multiple System Atrophy (MSA) in 2020.

https://www.msatrust.org.uk/what-is-msa/

MSA is a rare neurological disorder that affects adult men and women. It is caused by degeneration or atrophy of nerve cells in several areas of the brain. This can result in problems with movement, balance and functions of the body such as bladder and blood pressure control.

The symptoms are wide-ranging and include muscle control problems, similar to those of Parkinson’s Disease. There is currently no cure for MSA and no way of slowing its progression.

We wish to raise money for the Multiple System Atrophy (MSA) Trust charity who are one of the few organisations providing free services for people with MSA, carers, friends and family members – in fact, anybody whose life is affected by MSA. We are thankful for their help and support as Dad battles this awful disease.

Thank you so much for your generosity.

Denise & Kevin