Hi, am Lydia and my mom has PSP from 2015. I have been reading about this illness and can see the changes in my mom's condition as described. I would like to know what kind of food can be given to her knowing that she has difficulty in swallowing. She is also a heart and diabetes patient. She hardly eats much when it comes to homemade food but loves eating pizza's and burgers(she hardly coughs when she consumes this kind of food) so wanna know what can be given so that nutrients go into her body. Off lately she has started coughing a lot on any kind of food.
PEG tube had been recommended by her doc few months ago but we are not too keen.