Does Fasting Help?

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Regular Member

Date Joined Feb 2008
Total Posts : 298
   Posted 3/2/2008 10:19 AM (GMT -6)   
I am going through a flare and was wondering if it is "ok" to fast for breakfast and lunch but then eat a small dinner (of low residual foods)?

I speak to my doc on Tuesday and am going to get some peptamin (thanx Writer!) but need something to help me out until then. Any and all comments would help! :-)
Battling w/ CD for 2 years...
Osteopenia in the spine caused by prednisone
Currently on Remicade

Forum Moderator

Date Joined Apr 2007
Total Posts : 32602
   Posted 3/2/2008 1:28 PM (GMT -6)   
I am not a believer in fasting but that is my opinion.  I do not think it is a healthy way to deal with your CD.  Others may have better advice.
Take care
Kitt, Moderator: Anxiety ~ Panic  ~ Crohn's
*~* *~*
It is health that is real wealth and not pieces of gold and silver.~Mahatma Gandhi~

Regular Member

Date Joined Jan 2006
Total Posts : 355
   Posted 3/2/2008 1:40 PM (GMT -6)   
I don't think it is a good idea to fast to help with a flare either.  Maybe drink Ensure or Boost as a meal for breakfast and lunch instead.  When my Crohn's was really bad and I was working, I could not eat anything for breakfast or lunch at all or I'd be in the bathroom all day.  I am a teacher, so it is not possible to be in the bathroom many times a day. I'd just skip those meals and wait for dinner.  I am not saying it is a good or healthy thing to do at all, but I felt I had to with my work situation.  On the weekends, I would just eat and know I'd be in the bathroom all day.   

Veteran Member

Date Joined Apr 2005
Total Posts : 3763
   Posted 3/2/2008 1:56 PM (GMT -6)   
The way I deal with it is to not eat until I get to work. That way, when the run to the bathroom starts, at least I am not in my car. I would keep to liquids or very soft easy to digest foods. I tend to do the bland, full liquid diet with some slight changes. I seem to be able to tolerate rice, pasta, fish, mashed potato, and some chicken. So I make lots of custard and pudding with lactaid milk and end up packing a small cooler that I can keep under my desk with my food for the day. I find if I don't eat all day, I end up eating things I shouldn't just because I'm starving, and then I've really messed myself up.

CD 19 years offically, 29 unofficially. 3 resections '93, '95 '97
Symptoms constantly but all tests show only minor ulcerations. Currently having multiple episodes of gastritis with no known cause.

Prednisone, 6MP,Prevacid, B12 shots, Bentyl, Xifaxan.....

Elite Member

Date Joined Feb 2004
Total Posts : 20558
   Posted 3/2/2008 2:41 PM (GMT -6)   
I don't eat my first actual meal until suppertime, I have a fruit smoothy with yogurt and chamomile tea (first thing in the am when I get up) before supper and then in the early eve after supper I snack on one or 2 snacks, it's all in how you condition yourself...for most of my life I've never really eaten food for breakfast it started during my teen years.

My bum is broken....there's a big crack down the middle of it!  LOL  :)

Regular Member

Date Joined Feb 2008
Total Posts : 298
   Posted 3/2/2008 2:49 PM (GMT -6)   
Thank you all so much for your advice! =-)
Battling w/ CD for 2 years...
Osteopenia in the spine caused by prednisone
Currently on Remicade

Regular Member

Date Joined Aug 2006
Total Posts : 443
   Posted 3/2/2008 7:58 PM (GMT -6)   
I think potatoqun has a good idea with drinking Ensure or Boost for breakfast and lunch, if you can't stomach regular food. (They aren't very different from Peptamen.) I don't know about you, but I have a really hard time concentrating if I skip meals entirely, and not getting the nutrients isn't a good thing either with Crohn's.
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