I Hate Dialysis Message Board
Dialysis Discussion => Dialysis: General Discussion => Topic started by: jambo101 on March 08, 2019, 11:04:19 AM
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3 hours into my dialysis session today i got cramps in my arms, it was painful and there was nothing that could be done except turn off water extraction.it was a rough session as early on i went hypoglycemic then later on very low Blood Pressure. on the positive side they detached me from the machine 15 minutes early. .The title of this forum is an understatement.
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Maybe next time they'd allow you to have a couple sips of tonic water (the kind with quinine in it). Bring your own bottle and ask them. Tonic water works super fast and you only need small sips of it. My husband sometimes would cramp up when we did home hemo and I not only reduced or stopped fluid removal but he was allowed a small sip of tonic water. I'm not on dialysis but have a history of muscle cramps and when I get those terrible ones that go all the way up the thigh I start swallowing a little tonic water. That stuff is a lifesaver. But of course your neph would need to approve. I don't see why they wouldn't unless you are extremely fluid overloaded. Please ask because there is no need for you to be suffering like that. They should help you out a little more with this...my husband's clinic gives tonic water to those who can have it.
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Hope things are better for you jambo. I know the nights after a session like you describe are often pretty rough.
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I'm surprised to hear of arms cramping. Mine are always my calves.
But last week while in the chair I started cramping in my mid-ribs in the sides. I thought it was because of the way I had turned to look and reach for something that had fallen off my chairside table.
I'vve never figured out why but I sometimes cramp in my hands and fingers. Many times while driving but not always, sometimes just reaching for a glass, or a door knob.
I think I'm weird.
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Nope Charlie, perfectly normal. My hands and feet usually lead the way to cramps. If I don't pay attention to those, the calves are next. One of the worst is the one that wraps around the chest, I suppose its the diaphragm? It seems I am at a point where just one or two tenths below dry weight causes cramps these days.
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My physical maladies almost always happen in that 4th hour ,cramps usually starting in the hands light headedness verging on passing out .
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I take a gulp of Tonic Water before I leave for dialysis. Quinine is a natural muscle relaxer. That why it works.
I also like Gin and Tonic's. It is good for me!!
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Im really coming to hate this whole dialysis process, i think major depression is setting in. :(
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jambo, don't get depressed. I had a lot of these problems starting out, especially the light headedness and passing out. I finally figured out that if I started getting light headed and especially if I suddenly got hot and broke inot a sweat, I needed to get soemone's attention quickly to have some fluid returned. I kept being told that it was a matter of figuring out how fast they could remove fluid, getting a true dry weight, and that it would get easier after I got rid of the catheter. All o fthat proved to be true. Still no day at the beach, but easier than the beginning.
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I agree the closer you are to the start of Dialysys the more it sucks. After 6 years it still sucks but it sucks less. When I started I found the never ending string of Dialysys days depressing. One Friday when I was on my second or third month oh Dialysys on a Friday I turned to the charge nurse and after dialysis I told her that was it I wasn’t coming back anymore this week. She started to argue and I just repeated nope this is it for the week. After several iterations she suddenly put together it was Friday I was a MWF patient and I was done for the week. So she slapped me in the back of the head and walked away laughing. Strangely I felt better when I left and the next week I realized for me Dialysys needed to be dealt on a week by week basis and every Friday I would celebrate being done. I also started collecting dialysis shirts to vent with.
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I like the idea of t shirts to vent. I may steal the idea.
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Feel free my favorites are first I found “Dialysis: Doomed if you do, Dead if you don’t “ and the second is a large shark swimming with its toothy mouth open with bold print “Dialysis Bites” some how they make me feel better.
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Michael,, what you said about the nurse slapping you on the back of the head and laughing with you made me think of something. It is far easier if, as a patient, you are able to forge a connection with the nurses and techs. Thankfully, at our clinic that is not hard as we do not have the "I know what's best" types. If you know you can trust the people who are going to be treating you for four hours, and know they are going to do their best to make you comfertable, except the temperature, and make sure you have a good treatment, it is far easier to face going in three times a week. I can't imagine the agony of some who talk about how they are ignored and not listened to regarding their treatments, and the way some say the nurses or techs make it a point to tell them they do not care.
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I have sciatica and I am ALWAYS in pain in the chair. I get leg spasms with my legs jumping around involuntarily. It is torture for four hours. But, as soon as I get out of the chair and stand up, I am fine.
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Michael,, what you said about the nurse slapping you on the back of the head and laughing with you made me think of something. It is far easier if, as a patient, you are able to forge a connection with the nurses and techs. Thankfully, at our clinic that is not hard as we do not have the "I know what's best" types. If you know you can trust the people who are going to be treating you for four hours, and know they are going to do their best to make you comfertable, except the temperature, and make sure you have a good treatment, it is far easier to face going in three times a week. I can't imagine the agony of some who talk about how they are ignored and not listened to regarding their treatments, and the way some say the nurses or techs make it a point to tell them they do not care.
Very well said!!
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I have sciatica and I am ALWAYS in pain in the chair. I get leg spasms with my legs jumping around involuntarily. It is torture for four hours. But, as soon as I get out of the chair and stand up, I am fine.
i am in a similar position, pain and discomfort 3X a week coupled with nausiating taxi rides to and from the hospital coupled with an inability to walk more than 50ft without having to sit down gasping for breath, im wondering if this is my lot for the rest of my life whats my motivation to continue with this life?
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If you are gasping for air so easily, you should check out your heart and lungs. It is sometimes tricky to determine if breathlessless comes from "here" or "there." I have been unable to breathe because I'm asthmatic and that sometimes kicks up. Other times itI a's because I didn't dialyze enough and I have fluid on board. Finally, I have a bad heart that shows up as shortness of breath.
I agree that it is sometimes hard to decide if life is worth living when you feel crummy all the time. The choice is yours.