In 2017 a home hemodialysis nurse told me that the home dialysis machines were gentler than the machines that are in the clinics. My interpretation of that statement was that the patients who do not have the option to do their treatments at home have to suffer more than patients (clients is probably more fitting) who can treat themselves in their homes.
Because if you know that one machine is less aggressive than the other, why not “only” use the one that is less aggressive? I’ll assume that it is based on time and money. Money makes mans world go around.
A kidney doctor (nephrologist) who knew nothing about my mother, was meeting her for the first time, told me that she would probably live five years being on dialysis. I felt he was a donkey for saying that. Later, I understood why he did. Solely, in their hands, you are less likely to survive. Most of the time you will have to manipulate their recommended treatment to benefit from a treatment that will be customed for you and not set for the majority. We are individuals and have individual needs.
The centers are staffed with technicians who are trained to get as many people in the chairs as possible and to get them out as fast as possible. That’s why many clients look like they have ran a marathon after being dialyzed. Their bodies literally have. My mother has had several hospital visits from orders of pulling too much fluid, and a flow rate that was too high. There seems to be an obsession with pulling fluid, even when it’s not there.
Most times the blood pressure will drop from pulling too much or the body will start cramping, letting you know that it’s too much for the body. I instructed clinics to never go beyond a certain amount during treatments for my mother.
I saw a lady yesterday that I met in one of the clinics last year. She was with her husband and looked like she could barely make it and worse. It troubled me because I know that her treatment doesn’t have to be so harsh. I guess enough people haven’t died or complained to cause changes to be made.
I try to help the patients feel as comfortable as possible when I’m allowed to cross their paths by giving them special hoods or sweatshirts with openings for their accesses so they’ll be warm during treatment, getting snacks that they can tolerate after the treatment, hard candy during treatment for dry mouth, calling to check on their transportation and anything else that is appropriate, but it’s not enough.
These are people who need better care at the core. My trying to help after the damage has been done, isn’t help at all.
From experience I would request peritoneal dialysis as the mode for dialyzing before hemodialysis. Facilities may try to discourage you by talking of sterile techniques. Being sanitary and careful should get the job done.
I did hemodialysis at home with my mother for a year with no incidents whatsoever, with the exception of a few cases of prolonged bleeding after pulling her needles that blood pressure medication and a cold compress took care of.