Bit more of an even keel as we are onto night time dialysis.
Posted By Kathleen David on April 15, 2022
The beginning of 2022 seemed to be going okay for us. A few issues that were causing me worry but nothing I could not handle.
The end of January is when our lives came crashing into the unknown.
We knew Peter’s kidneys were not doing well but his numbers were still above the drastic measures zone. This has been going on for five or six years now.
In a three-month period, he went from okay to we have a serious problem as the numbers went all the directions that we didn’t want him to go.
It was around this time that we found out that Peter had been using for approximately eight years might be killing him due to deterioration of the foam they used to both quiet and insulate the machine. The three things that come up most is lung function, heart problems, and kidney problems.
We put a recommended filter on the machine because I don’t think we ae going to see a new one until maybe next year. Every time I exchange the filter the bottom side is grey with black flecks. That was going into my husband’s lungs sover time.
Peter’s kidneys were failing and we had to make some fast choices as to which kind of dialysis he was going to use along with getting onto a transplant list.
We chose preretinal dialysis because it could be done at home and we could still make it to conventions and the like. It takes a lot of materials but we can travel with those and Baxter, our medical supply company that has taken great care of us, will deliver his bags of dialysis fluid because those suckers are heavy.
First Peter had to get a catheter inserted into his gut and it had to heal before the next step. This would allow his preretinal cavity to do what his kidneys aren’t.
Once he was healed, we started training on how to do the process manually or what you had to do before the magic machine. We went to see Peter’s dialysis nurse who is a delight. She took us through the process and gave us time to adjust to all that had happened and would be coming.
Once we were cleared for that, we started living our life in four hour increments with a lot of paper work attached. On the one had, Peter was feeling and looking better. On the other hand, four hours before we had to do something to help keep Peter alive. Made life a little difficult and I was very frustrated by the whole process and tired both physically and mentally.
Once we had done the manual version for a period of time, Peter had a day of testing to see if this form of dialysis was working and if he could go on the overnight machine.
He passed and we trained on the machine.
Last night was our first night with the machine. It worked and the alarms went off twice for very specific reasons. This let us both get a good night sleep and not have to worry about those four-hour increments.
It’s the new normal and we are getting use to it.
I am grateful that we are finally on the evening machine.