This post is for those who have experienced (or are currently experiencing) caring for someone with FTD/ALS. I am hoping to maybe gain some insight and direction from those of you who have been down this road before. I'll give you a quick rundown of our situation: After exhibiting...
advice
age
als
ball
children
clinic
dementia
diagnosed
documents
feeding
food
frustrated
ftd
life
love
peg
please help
please help me
questions
respiratory
swallowing
worry
young