Original
The average life expectancy of a PSP patient is seven years from the onset, however my mother lived 9 from the onset, 4 from the time she was diagnosed. The last years however, were spent in a wheelchair or in bed. Complications and risks are from falling and aspiration of the lungs from the difficulty in swallowing food and choking.
I am reading everyday about new studies and new drugs being tested and believe there is now much more awareness of this disease. It seems of new drugs being tested for Parkinsons and Alzheimers may possibly have a positive effect on PSP symptoms. I am optimistic that there will soon be something to improve the quality of life for those with PSP.