Posted 7/12/2014 5:33 AM (GMT 0)
And, Canasa: BAD!!!! (At least, for me.)
I kind of knew that before, having taken all the 5-ASAs during my first year with UC and not improving. When I went off them and onto some dietary modification, I thought I had figured out the answer.
However, eating a pizza put me into a bad flare, the first in years (though I had been low-level flaring for a good bit of that time). Back to the doc. Doc put me on Cortifoam (my request) plus Canasa (despite some objections), at a 2 x daily dosage.
I've posted a lengthier description of my experience, along with some fun graphics, on my shiny new UC blog (https://moderncolitis.wordpress.com), since we can't post images here. This shows my symptoms in all their gory detail, and without any doubt, the fact that the Canasa was making me worse.
Now I'm just on the Cortifoam (1 x daily) and I feel like a million dollars. Seriously, every day I am grateful for how healthy I am. I am running again, will be going for a long hike this Sunday, and generally have my energy back. Heck, I have my life back!
Unfortunately, I know that Cortifoam isn't a long-term solution. My *hope* is that it's kicked me into a real remission; one that a little questionable food won't completely destroy again. In reality, of course, I won't know until I start tapering. I'm really kind of worried that the Dr. will want me to go on more "serious" meds, like 6MP, and I don't think I'm ready for that. ... but will cross that bridge when I reach it. For now, I'm just enjoying my symptom-free life!