It seems the more I learn about this disease (UC) the more I am recognizing things that have been going on. (just diagnosed in October). I wake up during the night and early AM just unbelieveably thirsty---- anyone else have this?
Reply posted for wannabeucfree.
I rarely drank water up until my diagnosis (Crohn's) two years ago. Now I drink about 6-8 bottles of water a day. I can't drink anything else. I notice that when I wake up in the morning, I reach automatically for the bottle of water at the side of my bed on the stand. And before I go to bed, I drink a half of a bottle automatically also.
Keeping hydrated while passing so much diarrhea is critical.
Reply posted for izzymovielover.
Hi:
I always have water with me when I go out. A sippy cup works great in the car because I can take a drink while driving without having to uncap it.I also freeze bottles of water to take in the car so I'm never without. Especially since we do have a hydration problem. I'm also one of those people who can handle ice water. This is good because I live in the desert. 9 PM and I just took off my shorts and put on sweats until I go to bed. No heat in the house yet except I set it at 74 through the nite. When I go to bed I fix a glass of ice cubes so when I get up to go potty I have a drink. I read a long time ago that everyone should drink if they get up at nite to replenish the liquid you just put out. Makes sense when you think about it. Marilyn
Reply posted for izzymovielover.
I like that "the JOY of UC..."... could be a comedy show, for we who suffer!!!!!
Reply posted for bellaboo.
Hi Joanne-
Things are somewhat better--- not bleeding much at all. I still have pretty bad diarreah (you'd think I could spell it, as often as I live with it!)
I have always wanted to lose weight, and now, because I am being really careful about what I eat I am .. That is a sad funny!!! I am writing it down, although I could easily lose more, I want to stay reasonably healthy!
The other thing happening, is that I have a constant bloated feeling. I used to think it was from overeating, but I think it is the UC, since overeating hasn't been an issue at all.
But, better. Discomfort, not pain, and no fountains of blood--- progress to be sure! What about you? Progress? Lynn (basslynn1@gmail.com)
Reply posted for wannabeucfree.
Hi Lynn,
I get thirsty at night too. Partially due to the colder weather now. I want a warm tea when I get home and don't drink enough water at night. (Been home 2 hours without a sip.) I also read that our inflamed bowels can't absorb water as well, so that would explain it too. I drink mine at room temperature...more likely to drink it if it doesn't give me the chills. I also started to drink Gatorade if I've had a bad bout of diarrhea. How goes the battle otherwise?
Joanne
Reply posted for wannabeucfree.
I have UC. I also get incredably thirsty.... I sleep with 2 water bottles so that as I am winding down for the night watching some tv I can sip at my leasure. I've also been taking to carrying around a waterbottle during the day most days while in my classes.
When you are getting diarreha as often as people with UC and Crohns do your body loses a TON of water and water is not something your body stores so its a daily battle to be hydrated. Most people as it is don't drink enough water it is particularly important we do so that our body can get SOME of the water it needs dispite it being lost so readily.
It could also be a sign of diabetes, but more likely its just another Joy of UC to learn to cope with. ;-)
Reply posted for wannabeucfree.
While I don't have the UC (my mom does, and maybe my son) it may be a sign of diabetes. Or it may be natures way of getting you to drink more water. I have been obsessive with reading everything I can lately, because of my son, and I've learned that you are supposed to drink a lot of water.
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