Anyone have the issues with night sweats. I don't know what to do and it is so annoying waking up in the middle of the night every night with you and your bed wet. I was first diagnosed with Crohns in 1998 and now with a new doctor he has diagnosed me with Colitis instead of Crohns now. I am on Penetasa about 12 pills a day at 500mg. I refuse to do steroids ( side effects are to rapid for me) after I was on it 8 yrs ago. In addition, my stools seem to not be very solid and I have more mucus than anything, does anyone know if this is the point I need to alarm the doctor.
Reply posted for magonza8279.
I had no idea that my night sweats might be related to this condition. Thanks.
Reply posted for magonza8279.
Amazing to me that 3 years ago they diagnosed me with Mono due to the elevated EBV and the night sweats, fatigue, etc. To find out 3 years later that it has been Crohn's all along seems absurd. I guess it seems like they could find it earlier on with a little more thinking outside of the box....or education...
Reply posted for Rwandap.
sleeping on a towel and keeping an extra pair of jammies on the end of the bed. This way when you wake up you just get rid of the towel and change jammies without really having to get up. also using an ice pack on your neck helps too. Good luck
Reply posted for Rwandap.
I think if you are having any issues you should alert your doctor. As far as the night sweats I have been having them for a long time, before and after diagnosis. It just may be another thing that comes along with the condition.
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