Anyone have Crohns/IBD...could use some motivation

I don't have Crohns, but I have AI. Friending you now

I do have IBD. I have a lot of food intolerances and triggers. It's a constant struggle in my case, especially lately, to keep weight on. I wanted to put some muscle weight on but I can't bc I can't get enough calories in to maintain, much less gain. I'm looking for a new GI bc my current one is a douche who won't listen to me. I know it's a constant struggle whether you are trying to lose or gain because there are so many other factors in our lives.

I do have Crohn's, and it was a struggle honestly until I added MFP and was able to keep a full diary of what I am eating.

Aside from feeling mixed feelings about food before eating it (huge red flag, just avoid that food at that moment), I use MFP to see what else could have triggered something.

I also have Gastroparesis, which causes the stomach to swell shut and not pass food into the small intestine. As much of a curse as that can be, it stops food that would otherwise trigger my Crohn's in the stomach, and I can get it ...forcibly reversed for 1 night of pain, rather than crazy drugs or the knife.

I have always had a struggle of losing weight, and my body absorbs protein a little poorly, but sucks up fat like there's no tomorrow. I was always the fat kid in school, and Crohn's didn't help me lose weight (I'm one of the few).

All in all, Crohn's is difficult, but keeping a smile on your face will make it easier. And so long as we all have smiles on, they will be contagious (seriously, the dumbest looking smiles are the most contagious!).

Good luck on your journey!

I was diagnosed with UC about 4 years ago. I tried doctors and medication and more medication and regular colonoscopies and scopes. Nothing really made it better. Then my doctor started talking steroids and surgeries. That's when I fired him.

The whole speech about diet having nothing to do with IBD is total BS. I am no longer on any prescription drugs and managing my symptoms better than ever, spending most of my time symptom-free. Diet is the biggest factor. Then it's sleep, stress management, and exercise. I've tried every diet under the sun and finally found what works for me. Over-eating is a huge trigger and when I over-eat and start to feel my stomach hurt, I spend a few days under eating and juicing vegetables to get back to a good place. Eating processed foods is horrible for my UC too so I follow a clean diet (no processed or restaurant foods) as much as possible. Also you should be tested or do an elimination diet to search for food allergies. I know it's a fad right now, but it's trendy for a reason. Cutting out dairy and gluten have completely changed my life as they were major causes of bloat and indigestion and I had no idea! I also limit my caffeine and alcohol as much as possible (drinking none is ideal) and got off birth control to get my body back to basics.

For positivity and motivation I always go to my nutritionista and favorite blogger Meghan Telpner. She has been living 100% symptom free after being diagnosed with Chron's Disease about 10 years ago. She's a great inspiration and has helped me find my own way of dealing with IBD that works for me. She's also just a bright ray of sunshine and positivity which is key when dealing with dark, scary disease things. Check her out:

http://meghantelpner.com/about/meghan-telpner/

my mom has Crohns since 1988. it is bad news. she been through hell but you can lose weight. hang in there

I was diagnosed with UC about 4 years ago. I tried doctors and medication and more medication and regular colonoscopies and scopes. Nothing really made it better. Then my doctor started talking steroids and surgeries. That's when I fired him.

The whole speech about diet having nothing to do with IBD is total BS. I am no longer on any prescription drugs and managing my symptoms better than ever, spending most of my time symptom-free. Diet is the biggest factor. Then it's sleep, stress management, and exercise. I've tried every diet under the sun and finally found what works for me. Over-eating is a huge trigger and when I over-eat and start to feel my stomach hurt, I spend a few days under eating and juicing vegetables to get back to a good place. Eating processed foods is horrible for my UC too so I follow a clean diet (no processed or restaurant foods) as much as possible. Also you should be tested or do an elimination diet to search for food allergies. I know it's a fad right now, but it's trendy for a reason. Cutting out dairy and gluten have completely changed my life as they were major causes of bloat and indigestion and I had no idea! I also limit my caffeine and alcohol as much as possible (drinking none is ideal) and got off birth control to get my body back to basics.

For positivity and motivation I always go to my nutritionista and favorite blogger Meghan Telpner. She has been living 100% symptom free after being diagnosed with Chron's Disease about 10 years ago. She's a great inspiration and has helped me find my own way of dealing with IBD that works for me. She's also just a bright ray of sunshine and positivity which is key when dealing with dark, scary disease things. Check her out:

http://meghantelpner.com/about/meghan-telpner/

I cannot even begin to describe how healing it is for me to know that someone else is symptom free as well.

I have taken similar steps to yours, on my own, and it's comforting to know that someone else's symptoms were helped by similar methods. It's rare to find!

Thank you for the link, and good luck on your MFP journey!

I'll keep it short and sweet.
25 years old and I have had Crohn's since (as my doctors have reported) 7. I was missing many of the symptoms as a kid so I was never fully diagnosed until I was 18. I have failed every medication that has come my way the last 7 years, so I am now prepping for surgery next month.
I have had a lot of yo-yo with my weight depending on what my stomach was deciding to do. Was up to over 200 pounds, and got down to 152 last year after I was admitted in the hospital. I believe that weight fluctuation will always be an issue until you find a medication that will put you into remission (IT IS POSSIBLE! I was in remission for 2 years with Remecade). Like posters below have stated, it really has to do with your diet. I have cut out booze, pork, fried foods, many processed foods, no fast food, reduced garlic. Logging your foods are great because you can see what might have triggered a flare
Wishing all my fellow chronies/ibs'ers much love, and am always up for friends