Symptoms: I am sleeping only 6 hours so my... - Kidney Disease

Kidney Disease

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Symptoms

KGsrKGsr profile image
4 Replies

I am sleeping only 6 hours so my fatigue is all day every day. I can’t stand the feel of the shower on my hair or skin. Most food and drink has lost its taste. I am always hungry because I never feel satisfied. I am cold almost all the time. Can anyone relate?

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KGsrKGsr profile image
KGsrKGsr
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RoxanneKidney profile image
RoxanneKidney

Sorry that this CKD is taking a toll on you physically and mentally. I honestly wish I had something to say to make you feel better. When i get to the point that my hair is falling out, I will do what my mom did when she had cancer...shave it all off. I"ll look like a pea head but it is what it is. I think that the part of the disease that I fear is the water retention and not being able to drink much water. It is like it slowly starves you. I really hope that this hair loss is all you are experiencing. And I am sorry that you are struggling. But you don't have to wash your hair. I hardly ever wash my hair...and that was before I had CKD.

jodaer profile image
jodaer

I generally sleep 8-9 hours a night and am still fatigued every day. The amount of sleep we get doesn't always equate to how fatigued we are. It comes with a chronic condition. I also have very little sense of taste or smell. I wish I could tell you something to help you but I don't have any answers but do understand what you are going through. I wish you well.

ntsgls11 profile image
ntsgls11

Unfortunately this is my life with CKD. My eGFR is steady for now at 34 but my quality of life is sadly not. There is a constant array of new challenges. My sleep is measured in multiple naps of exhaustion. I have a hard time putting meals together. My itchy skin drives me crazy. My hair is thinning fast. I live alone without support. It's hard to have conversations without dragging all this ckd garbage into it and no one wants to hear it. There are times I want to stop all the dr visits, food plans, and pretend the last 8 months since my diagnosis were just a nightmare. I'm just so tired.

Appolonia profile image
Appolonia in reply to ntsgls11

I hear you & sympathize with you, I also have hair loss, itchy skin &live alone & have no support from family members even tho they know I have CKD. They don't understand this chronic disease & I really can't blame them for being disinterested as it's not their issue. Only my one son is sympathetic to my condition. I am not looking for sympathy just some understanding & compassion. I am also just so tired of eating plant based every day.

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