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Monday, November, 23, 2009
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Stress and IBD

Ali
Ali
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Ali is married and a homeowner - ack!

I'm a newlywed and a new homeowner living in Alexandria, VA (goodbye...

Ali

Tuesday, November 04, 2008
View All of Ali 's Posts
My doctor (and many others) have told me multiple times that stress will make my UC symptoms worse... I wouldn't say I didn't believe them before, but I never really could tell first-hand.  For the past year and a half, I have been battling a flare that really seemed to come out of the blue; I r...
  1. I REALLY NEEDED THAT!
    Gena
    Thursday, November 06, 2008 at 04:45 PM

    I am so thankful for what I just read, I'd been wondering if stress was a true factor to flares and so forth. It's just seems that I stress so easily that it's out of my control but I am working on some things to do and getting myself involved in new activities that will help me to keep more relaxed. I feel like that story was a confirmation for me so once again thanks. 

    Reply
    re: I REALLY NEEDED THAT!
    Ali
    Friday, November 07, 2008 at 09:59 AM

    I'm glad you could relate!  Good luck with everything - if you find something that really makes you feel good and de-stressed, please share! :)

    Reply
  2. Untitled Comment
    Laura
    Thursday, November 06, 2008 at 05:37 PM

    Hi Ali, 

     

    Congrats on the wedding! You're dress is gorgeous!!

     

    Glad you've been feeling better Smile

    Reply
  3. My last flare was brought on by stress I think
    sally
    Thursday, November 06, 2008 at 10:23 PM

    my son graduated from high school and I had a big bash planned for him. I had tables set up around my pool (which never looked better that early in June - I was busy) and other tables in separate locations. His father and I divorced years ago and the separate families would be coming together. The wind blew 25 mph and it was 99 degrees, which meant no

    one went outside (I live on a hill in the country). I had to come up with plan b and thank god it was my house and I have a bathroom upstairs. This was my first and last flare until

    the dr. diagnosed my uc, but now i live with the asacol and wonder if pills are the only way. I am so glad to read about someone else who shares UC and I can not imagine what getting married with this would be like. I worry about everything and am high strung any way. I am trying to destress my life also. Can it be done?? Did you make any dietary changes? You are a lovely bride and I guarantee stress has something to do with flares.

    Reply
    re: My last flare was brought on by stress I think
    Ali
    Friday, November 07, 2008 at 09:57 AM

    I'm glad some people heard my story and can relate!  I hope you can de-stress your lives too and get/keep your UC under control.  I completely agree, I would love to be able to find another way off of medicine, but I don't know if that will work for me... I think first I have to really get my flare completely under control, and then hopefully we can lower some of my doses.

     

    As far as diet, I'm really bad about that.  I have tried to eat a "Mediterrean" diet, which my doctor recommended - light food, lots of grilled or baked chicken and fish - and avoid dairy, but I LOVE chocolate and cheese.  I have also read about the Specific Carbohydrate Diet and kind of attempted to try that once, but it's so restrictive that I really didn't stick with it.  But I'm sure that if I were to really commit to eating better and staying away from problem foods, then I would be much better off!

     

    For stress relief, I have tried yoga and really enjoy it.  I got a book that is supposed to be like a 6-week program and started going through day by day... it's very relaxing and only takes about 45 minutes.  I love that I can feel my body stretching out and relaxing as the session goes on.  Sometimes I think the meditation part at the end is cheesy, but if you can sit still for an extra 5 minutes, it can clear your head.

     

    Reply
  4. Your Story Takes Me Back.....
    BunnyMomma
    Thursday, November 13, 2008 at 05:51 AM

    "But even on days that I didn't FEEL stressed, I still felt crappy."

     

    When you wrote that it was very comforting. Stress has such a lasting effect on our bodies it's amazing! Our bodies will identify what our minds may not acknowledge.  I would bet money that my present flare has been caused by job stress and I received the "de-stress" chat from my doctor as well, which always makes me chuckle because I know this already.  Sometimes I think having IBD helps to remind me what's really important and keep my priorities in check. It forces me to put myself first whereas I would never do that before.

     

    Congrats on your wedding! Reading your story reminds me how I was flaring when I got married as well!  Worried that my dress wouldn't fit because I was bloated and afraid it would show in the photos, (thank goodness I had a large bouquet, I took it with me everywhere Lol!)  I flared pretty badly throughout our honeymoon too (Bermuda), but managed to make it through all our excursions and my new hubby was very supportive always rubbing my back or legs when needed and still does God Bless him!

     

    Good Luck with your new home! Blessings and happiness!

    Reply
    re: Your Story Takes Me Back.....
    Ali
    Thursday, November 13, 2008 at 02:37 PM

    Thank you so much!!  I'm sorry to hear that you were flaring through your honeymoon too, but glad to hear that your husband is so understanding and helpful.  Mine is too - we're lucky! 

     

    I hope you start feeling better from your current flare, and definitely listen to your body!!  Work is not more important than your health, no matter what kind of deadline you have - just remember that Smile

    Reply
    re: re: Your Story Takes Me Back.....
    joyce
    Tuesday, April 07, 2009 at 06:09 AM

    Hi....my crohns started with marriage problems...I contribute my crohns from all the stress.  it seems like my husb had an 7 yr affair, and i got so sick, and my social worker told me to leave him, which I didn't, and then came the crohns...I have crohns approx 3-4 yrs, I was diagnosed 2 yrs ago, before that I took a lot of bentyl..The primary dr didn't even have a clue as to why I had pains, just labled me as a hypocondric.  Even the GI didn't know at first...I had to call up everyday his office, and tell them about the pain, and finally he did a colonosophy...anyway, I was feeling alot better with pentasa, now I feel sick again.....I take citrate magnesium to have a bowl movement and I think that is the problems....

     

    help!

     

    joyce123

    Reply
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