Sleep was available last night but I DID NOT sleep 8 or 9 hours, but 5 hours. I will NOT exclaim in loudly that was NOT a bad sleep because I can function on 4 to 5 hours a sleep at night. I will be on the dialysis machine here at home for 3 hours in the dialysis chair that was provided for me to use. It’s not 100% comfortable to sit in like the clinic chairs are because it does NOT have heat and massage built in with it like the clinic recliner chairs do. That is the downfall of the chair and why it’s uncomfortable some days. Even my power chair is uncomfortable at times, especially when I am in it all day. Some days I would rather sit in my power chair or lay on my bed, but the machine needs a water source to be used from below the sink of the kitchen. Otherwise, when I was not ready to have a my second transplant right away because my first kidney decided to show signs of giving up, the kitchen sink and the living room is where I sit to do my dialysis treatment for, sometimes, an uncomfortable chair. I do dialysis because I am not ready to die and leave family and my fur babies behind yet.