I have been away from the board for a few weeks, but I have checked in from time to time to read posts. I see that we have a lot of new members!
I have been very busy with my new job, teaching, grading, and planning, so I haven't had much time to post. I really enjoy it (most of the time, when I'm not dealing with students' excuses
I realized that it is right around my first anniversary on the board, so I wanted to take a minute to reflect on how much better I am now than I was a year ago. By no means am I in remission, but it doesn't seem as impossible that I will get there as it once did. After I was diagnosed with MC and celiac in July 2008, I cut out gluten completely but got no better. I gave up dairy on my own based on the quick reactions I always had to it, but I stayed pretty sick throughout the fall. In February, I got results back from Enterolab that said I was intolerant to soy. I also had "high normal" levels for eggs and yeast. I cut out all three of those, and all legumes on the basis that people who are intolerant to soy may also be intolerant to other legumes. After that, I got a bit better. The D remained, but the accidents stopped, for the most part. Over the spring I also cut out other foods I suspected, like corn. I finally started cutting everything I knew wasn't being digested. This included whole nuts and avocado.
I didn't start seeing a real improvement, though, until this summer. I cut out all processed foods and have been surviving on proteins, white rice, rice pasta, and very well-cooked veggies. I think the biggest change was that I quit eating tapioca, which is used in a lot of GF mixes, and which I had long suspected. I have not seen Norman yet, but I have seen a few of his close relatives, so I'm pleased with my progress so far. The hardest part, as so many of you know, is the limited diet. It makes meals difficult sometimes, but it also makes a great excuse when I really don't want to deal with a group/family meal.
I am doing so much better than I was this time last year when I was getting five hours of sleep a night due to being in the bathroom all night. I owe you all lots of hugs and a big thank you for being here for me and for so many others who are suffering from this. You truly are a second family.
Love,
Courtney

Visit the Microscopic Colitis Foundation Website






