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General Mast Cell Disorders Discussion >> General Mast Cell Disorder Discussion >> Wet the bed . . . I dread . . . I dread . . . http://mastcelldisorders.wallack.us/yabb/YaBB.pl?num=1391891159 Message started by Ladybug on 02/08/14 at 08:25:59 |
Title: Wet the bed . . . I dread . . . I dread . . . Post by Ladybug on 02/08/14 at 08:25:59 I noticed that the few times that I have wet my bed at night are times when I am totally exhausted. [smiley=embarassed.gif]I recently realized that it might be during the same time when my body temp drops and I am also very cold, can't sleep and crash. I'll have to pay more attention next time. Anyone here having or had the same experience? I would love to know, too, if this would be mast cell related? Thanks again! |
Title: Re: Wet the bed . . . I dread . . . I dread . . . Post by sarahkay1111 on 02/20/14 at 01:49:19 Hi Ladybug--That does not happen to me, but when I am reacting, I have to pee a ton! My last 24-hour urine, I peed over 3 Liters! I would imagine, a combination of our medications and the exhaustion could cause you to pee at night. I hope it gets better! Sarah :) |
Title: Re: Wet the bed . . . I dread . . . I dread . . . Post by Ladybug on 02/22/14 at 17:25:34 Thank you, Sarah. I'm trying everything I can to keep flare-ups down. I'm going to see if I my primary care doctor will refer me to a urologist just to be on the safe side. Hang in there! |
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