My dad was diagnosised with PSP (Progressive Supranuclear Palsy) nearly 5 years ago, a rare neurological disease which is caused by the progressive death of nerve cells in the brain. This cruel disease robs people of their ability to walk, talk, see and swallow. Frequent unexpected falls can lead...
My dad was diagnosised with PSP (Progressive Supranuclear Palsy) nearly 5 years ago, a rare neurological disease which is caused by the progressive death of nerve cells in the brain. This cruel disease robs people of their ability to walk, talk, see and swallow. Frequent unexpected falls can lead to serious injury - so it is 24 hour care which can be both physically and emotionally challenging.
It is estimated that there are 280 cases of PSP in Ireland, 4,000 cases in the UK and 20,000 in America as it remains largely undiagnosed and under reported with no known treatment or cure. I would like to raise money for this charity, PSPA Ireland to help raise awareness of this disease, for research and also possible treatment.
Every little helps no matter how big or small and would be greatly appreciated.
PSPA Ireland is a voluntary organisation that is dedicated to providing advice, information and support for people living with or affected by the rare neurological conditions; Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD).
Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD) are neuro-degenerative brain disorders.
The death of nerve cells in the brain leads to difficulty with balance, movement, vision, speech and swallow. The conditions