It Is Much Difficult To Eat When At The Eve Of My Dialysis

I do not have the least of appetite now, in fact I am having these hiccups already which is a sign that my body doesn't like to get food on my tummy much less with Cinacalcet in my stomach. So I am just planning not to eat anymore unless I get the low blood sugar symptoms so at that point I have to at least eat some because I might pass-out due to low blood sugar although I am not diabetic.

My dialysis is not in the earliest time tomorrow so I have to wait until I am hooked-up at around 9:30 AM. It would be better if I am dialyzed at 4:30 AM since I am still okay with that schedule as myself and my parents had gotten used to it already. The only issue was it is just hard to take a bath when the water is very cold in the wee hours of the morning.

Near my dialysis schedule was the most difficult times for me. It is because at that point like right noow too much toxins, extra fluids, and Parathyroid medicine is already circulating in my system. Actually the Cinacalcet is the one that makes it worse for me so I am just a bit tortured in that regard and is indeed very hard to cope and I am enduring this kind of situation for more than two years already and it does suck to live this way.

That is why I am contemplating in having a frequent dialysis or even getting that other type of dialysis that is called a peritoneal dialysis which in itself had some drawbacks like a delayed health insurance approval in the first months and infection to access site in the tummy.

One issue for me regarding taking that kind of option is that I already had an operation in my tummy so it might affect my qualification plus I already had a squeezed internal organs so additional one to two liters of water in my tummy might make my breathing difficult considering that it is near the amount of extra water that is taken out from my system during my dialysis although peritoneal dialysis cleans your system 24/7 and it might do me better with regards with my appetiteloss issue.