Quick Video of an important part of my diet. Actually it’s about 33% of my diet any day of the week, so that’s pretty impressive. After 4 plus years on smoothies to help control colitis and then a year and half off them, I’m back on the smoothie train and loving it.
The doctor tells me stress can make the UC act up more. What I would really like to know is how am I not suppose to be stressed? I work and go to college and I pay my bills like I’m suppose to but it’s hard sometimes. Any tips on dealing with the stress and the pain?
Gastro says it’s NOT UC…symptoms are:
Feeling generally unwell/nauseous, bad gas (really foul-smelling), some bloating with stomach cramps, usually diarrhea, followed by small amounts of occasional constipation. Diarrhea sometimes accompanied by urgency. 99% of the time with red blood. Sometimes with mucous.
Meet Haadi: I am in late 20s, male, living in Australia. Diagnosed in October 2013. Getting stronger every day, food diary has been invaluable, Low Fodmap diet with SCD wisdom, honey instead of sugar in baking, EVO oil and antibacterials have paved the way to my remission Some more about Haadi: I like travelling, reading, […]
Intro: Hi – I’m Megan. I have UC – diagnosed in 2012. Currently in my second flare in two months. I am not a happy camper right now. Some more about me: I live in California and have two very rambunctious boys under the age of six. I am fortunate that my husband fishes the […]
Would you be interested in meeting up with other UC’ers who use this website and the iHaveUC Facebook Page???? That is what this post is all about, and I’m betting that there’s quite a few of you who would be thrilled to hang out with some other UC’ers wherever you live, but I need to know for sure.
I really want to find a specialist but one who believes there is a cure or that I can be in “remission” without having to take meds that don’t technically work. I am open to natural remedies.