These are my own personal experiences of being on APD (for over 4 years) and in centre HD (for 4 months so far). I’m thinking they might help someone who is currently wondering which one to try.
PD - I felt alone despite having access to online support groups
HD - I don’t feel alone as I share a ward with 9 other patients each session
PD - I had to do everything - setting the machine up daily, disconnecting daily, ordering supplies, troubleshooting when the alarm went off etc
HD - everything is done for me
PD - you have to phone for outside help when needed
HD - help is in the same room
PD - pain on and off all night long, mainly during drains
HD - slight pain when the numbing injection goes in but not when the dialysis needles go in. Slight pain when the needles come out and they press the bandage against it
PD - you have to do it every single night
HD - you only have to do it 2 or 3 times a week
PD - you have to take your machine and supplies everywhere you go
HD - you just have to go to a local hospital for treatment so don’t need to take any supplies
PD - can be done from the comfort of your own home and while you sleep
HD - it’s inconvenient having to keep travelling to the hospital and back
PD - up to 10 hours per session (or 14 hours per session in hospital if you’re unlucky like me and end up with high potassium)
HD - up to 4 hours at a time per session
PD - removes less potassium and you’re more bloated
HD - removes more potassium and bloating disappears
PD - higher blood pressure
HD - lower blood pressure. I’m no longer on high blood pressure medication
PD - more brain fog
HD - less brain fog
PD - used to take off approx 300ml fluid per session
HD - takes off approx 2L fluid per session
PD - have to go to the hospital every 3 months to see the nephrologist and every month for blood tests
HD - the nephrologist visits you every 2 months during your session and blood tests are done once a week during your session
PD - injections and blood tests are done normally
HD - blood tests and injections are done through the fistula
PD - when the machine is set up, you can connect straight away
HD - when the machine is set up, you have to wait to be connected
PD - online support from other patients
HD - offline support from other patients
PD - always waiting for alarms / problems
HD - can sit back, relax and rest for 4 hours
PD - I looked heavily pregnant 24/7 and felt it too
HD - I don’t
PD - you need to take laxatives daily usually
HD - you don’t need to
PD - you have to visit the renal ward every 3 months for dialysis tests
HD - any test is done in centre
PD - can’t leave the area near your machine
HD - stuck in a chair for 4 hours
PD - high risk of peritonitis
HD - no risk of peritonitis My experiences of PD and HD