Hi, my daughter was diagnosed with PRMS this week. She is bed/wheelchair bound since October. Adding to this she is non verbal and has autism. Communicating is very difficult for her. I really need to understand what her future, and ours caring for her looks like. Information like books I can read, communities to tap into, best beds, things to do/never do, investing in medical devices? There is so much, and I am In the deep end. Any and all info is so very kindly received.