Hi Wat,
Nice to meet you, welcome to the site here
I'm doing really well on dialysis and I have PKD. I have very little fluid removal. They usually take about a half kilo of fluid off of me at my treatments. I am on the morning shift and prefer it as opposed to the evening shifts, when I first started. I'm on the Tues, Thurs, Sat morning shifts.
Yes, you'll find in the beginning its extremely overwhelming-I found the very same. I go to in center. Are you in center also?
In my unit, we get to decide how much fluid we want removed. Even though I don't needle myself, I do have some control even though I do in center dialysis.
What kind of access do you have right now? Do you have a chest catheter?
Everybody is different when it comes to fluid removal and time for dialysis. I started off doing 4 hours of dialysis and now I'm down to 3.5 hours sitting in the chair.
I found I was pretty washed out after dilaysis for the first whole year, I think that's pretty normal to feel tired after dialysis.
I started dialysis in an emergency too, I almost died, I was stage 5....kidney function at about 12 per cent at the time of starting dialysis. I was extremely sick, vomitted a lot, severely itchy......became an insomniac and had severe muscle cramps and had no appetite. My neph said I was less than 2 hours away from kicking the bucket. .....Oh, and I had the major brain fog, I could not think clearly if my lfie depended on it.....
I'm much better now and have been doing well on dialysis, awaiting transplant....is a transplant something you're considering?
to you!