No specific call-to-action just a story from someone close to me about someone dear to my family. As I get older these programs that were so hollow and faceless to me growing up are starting to become more and more real by the day. Perhaps I should have feared that they were in jeapordy much much sooner, but I guess like a lot of people the issue didn't become real to me until it did. Anyway This is an edited version (to eliminate personal information) of a letter from a close relative about her spouse of 50 years. I should mention that Bill suffers from Alzheimers and Parkinsons. Those who know the combo know that Parkinsons meds aggrevate the alzheimers and vice versa. Getting old is truly a bitch. Anyway here goes:
The owner of the home is a Certified Nursing Assistant but she is a lady and the only one to take care of the residents (right now there are only 4). But she can't manage Bill by herself. Bill is 6'3" tall (I'll add that he is probably closer to 300 lbs than 200) and stiff as a board. She is only about 5'2" tall. The Hospice aide is a man and strong as a horse. He has to crank up Bill's bed till he is in a sitting position, then take hold of his feet and swing them around to the side of the bed. Then he puts a "gait belt" around Bill's chest, puts Bill's hands on his (the aide's) shoulders, pulls Bill to a standing position using the belt, pivots Bill a quarter turn, and sits him in the wheel chair. Then he takes the belt off and puts it on again to strap him to the chair. Bill is not able to stand on his own, keep his balance, or help with the turn. Bill is not able to pick his feet up so Jason pulls the wheel chair backwards and lets Bill's feet drag in order to move him into the living room. If Jason can come back later, Bill will stay up for about two or three hours. Otherwise, he is up only for as long as Jason can stay there at the home. Jason usually does his paperwork for his job there so Bill can have time sitting up. Jason is so good with Bill. He bathes him, cuts his hair, cleans out his ears, trims his eyebrows, shaves him, brushes his teeth, cleans his nails, even trims his nose hairs. It costs us $1175.34 a month for Bill to stay there and the state and Medicaid pay the balance and pay for his HMO. Hospice pays for the aide, his equipment, supplies, and all of his medicine except Plavix, which is a blood thinner. If we had more money we would not be eligible for help from the state and Medicaid and I am thankful that we are getting this help.
Anyone with action related info RE: Medicaid would be much appreciated