It’s been about six months since my initial UC diagnosis, and I wanted to share the story so far and update on the battle with who/what to believe.
One of the most infuriating things about UC is that nobody knows what causes it, or how to cure it (at least not yet). It is commonly believed to be an underlying genetic thing (in the medical community) – so if you’re meant to get it you probably will at some stage or another. I don’t know how much I believe this, and often wonder what life would be like if I hadn’t gotten food poisoning just over a year ago and awakened the beast.

Continue reading “UC and ME – who to believe? #2” →
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