My body, my dialysis choice

stories-single-blob

Unwittingly thrust into the renal world with CKD back in the 1950s, I never really had any control over the treatment options until I was informed that my kidney function had reached a point where dialysis had to be considered for my future treatment.

Fortunately, with the proactive support of my CKD team, I was able to make an informed choice and finally take control of my treatment options. Up until the time that I was being considered for a transplant, my world was constantly upside down, with changes in medication adjusted in accordance with repeated blood tests.

The community team were very helpful in visiting me and my family at home to discuss the different dialysis options. These days, patients and their partners and families are asked to attend a pre-dialysis education class, which I can highly recommend as it gives you access to the entire team and the renal support group.

Having been on a lifelong journey feeling totally helpless, now was my chance to make a decision that would not only affect my life but impact the rest of my family and work life.

Whether it be CAPD, APD or HD, all of which can be carried out at home, I had to take into consideration the practicalities of each option. Coming from an engineering background, I was able to take a practical approach to my decision-making.

First and foremost, I am a primary carer for my wife, so when I wasn’t working, I was shopping, cooking, washing and ironing. I had a son of school age to take care of whilst managing my own health and diet as best as I could; so whilst I wasn’t afraid of needles, I chose not to go down the Haemodialysis route owing to its time-consuming limitations affecting my time at work and at home. The work attitude of the day was that if I couldn’t be at work when I was needed, then I shouldn’t be there at all.

That left me with the choice of either CAPD or APD. I found this to be very appealing as whichever of these I chose gave me the freedom to travel and work and have a reasonable home life. Both of these required that I have a lot of room to store the boxes of fluid. I also considered the time taken to perform the dialysis and whether both options would allow me to work. Another consideration was the risks of peritonitis, and as the CAPD required a clean environment to perform the fluid exchanges up to four times a day and I couldn’t guarantee where I was going to be during the normal working day. I was working quite a heavy duty amount of on-call hours, which left me with a no-brainer APD or Automated Peritoneal Dialysis. While it did place a restriction upon my on-call coverage, it left me a full day to go about my normal daily activities.

Having used the APD system over several years, I have enjoyed a good family life with many holidays around the UK as well a two week cruise around the Mediterranean. Alas, I had to give the work life a miss as I was offered voluntary redundancy after an extended leave due to sickness and just one month prior to starting dialysis. As stated earlier, if I couldn’t be there when needed then I was no use at all.

APD was an excellent choice for me as I was able to dialyse whilst I slept. At last my life was back in my control.

If offered to you, I can highly recommend that you attend the pre-dialysis classes as they are an excellent opportunity to help you in making your decision.

Submit Your Story

We value what you’ve learned from your real-life experience of chronic kidney disease. We’d love it if you could share your story to help other patients, carers, and clinicians.

Recent Stories