I've mentioned this elsewhere on this site, but I take a no nonsense approach to it all. I've only had to deal with it for 4.5 years, so I'm still fairly new to diagnosis, but here's a few of my everyday ways of dealing with it:
-I don't sweat the small stuff. This means I take everything that happens to me and I put it in a category. I've decided which symptoms I can't live with and which ones I can. If I'm going to the bathroom a lot one day... ehhh not a huge deal. If I'm tired, its not the end of the world. However, if I can't eat... I have to go to the doc and figure it out (Prednisone, something). If I'm in pain, I deal with it... but not if it gets to a certain point.
-I'm currently doing pretty decent and have been for a year and a half. That means I have my days... still have some things that aren't where I want them, but I'm overall between 75%-90% feeling good. I've decided that those are percentages I can deal with.
- I don't let things stress me out as much as I used to. I just let it roll off of me. There's no use in stressing to me anymore, because it directly affects my condition. This also follows the "picking battles" mantra I follow. I decide if certain events or things are life ending or life threatening issues. If they aren't then I go to the next question and I ask myself if I can deal with the thing... if I can then I drop it. If I can't then I think of ways to fix it. If I can't deal with it and I can't fix it, then I seek help from others and put it on top of my priority list.
- Staying busy is a good idea... I feel a lot better on days I go to work than the days I have off.
- Get plenty of sleep. SLEEP SLEEP SLEEP. It's a beautiful thing. I sleep usually anywhere from 8-10 hours a night.
- Take those stupid vitamins and supplements
I have struggled with taking my iron and folic acid pills, but honestly... I need them. And they make me feel better.
- Push yourself out of the house (if you are well enough) Its difficult, but being outside, or spending time with a family member or friends really takes that stale "stuck funk" out. Also, weather permitting, open the windows or the back door. Let the sunlight in. Don't let yourself get stuck in the dark and stuffy.
I dunno, I've had so many times where I finally thought "hey this is remission, maybe I'll do well now for a while" and the next week I'm in a full blown flare. I try to do as much as I can when I can. And I've realized Crohn's isn't the end of the world. Do I still have sad days? Yeah... but I let myself be sad and then I choose to be happy. I feel like a positive attitude has helped me to cope with everything. The major things to control are stress levels, nutrient intake, and sleep. All of these things help make a Crohn's patient happy