Ulcerative Colitis Tips

One of the 15,000 ulcerative colitis folks using the site adds:
"Like many UCers I have spent many hours trawling the internet googling the condition and came across your website a few years ago. I read your ebook and really liked your honesty and humour. As everyone says your positivity is so encouraging and now this is my go to website when I'm thinking about UC. Thankfully my symptoms are pretty much under control at the moment but just wanted to say thanks." Kate

Super SCD Me- The Great Experiment


Have been diagnosed with Crohn’s, with Colitis, and to this day, they’re still not sure which one it is- just that I have “one flamin’ colon.” Have been in the IBD club since Jan of 2010.

My Story:

Have been reading this site every day now for the last two months and there are a lot of people who are facing what I’m facing. I want to let you know that I have had RAPID RECOVERY from a flare after only a month of being on the SCD diet. I’m chronicling my experiences, as well as inflammation results, to help folks that are struggling with treatment options, just as I was. (You can see more at www.thescdexperiment.com).

Situation: Diagnosed with IBD in April 2010. Went on 60 mgs/ prednisone for 4 months. Poopin 5-10x a day, all “The Big D”. Could barely get to work.

Went to a different GI to get off the preds. He prescribed me with Humira, which worked for about a year. BUT THEN… hello antibodies! Humira no longer worked and gave me a huge infection, sticking me in the hospital for a week, and out of work for 2 months after losing 14% of my body weight.crohns and colitis patient

HERE’S THE CROSSROAD- Went to a different GI, one of the best in the Midwest. He wanted to put me on Remicade. After my horrendous experience with Humira, I did a lot more research during my 1 week stint in the hospital.

Remicade does the same thing Humira does- it’s a TnF blocker. I do NOT want to get another infection- I’m scared to death. This has sucked big time.

SO after researching Imuran, Remicade, Antibiotics- the route I chose was SCD. After a month anniversary, I can honestly say that I feel the best I’ve felt in 6 months. It’s changing my life.

If you want to click around (seriously not trying to solicit- just share the success metrics that I’ve published online) please do so at www.thescdexperiment.com.

Submitted by “Jo Colitis” in the Colitis Venting Area

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