My husband opted for a PEG, or PIG, as his type was called. We were provided with liquid food and I was trained how to feed him.
It extended his life by approximately eight months.
Eventually, he still choked on the liquid food , then later, on water , even though they were given through the tube.
Being tube fed, or not, is an individual's choice. If the choice has been made not to have it, that choice has to be respected.
Looking after someone with PSP, is a big learning curve. We always question ourselves as to whether we are doing, or have done, the right thing, but if we have shown love and kindness, whilst caring for our loved ones, then we have done our best.
PEG tube - our experience
Feeding ideas
PEG Tube
Tube feeding, choking or deep sedation/euthanasia? Your thoughts would help so much, we are quite lost about dad's late PSP stage. 
peg feeding tubes.
