After having ET for approximately 8 years, last month I ended up with ischemic colitis. A CAT scan and Endoscopy and Colonoscopy (biopsy) determined that blood flow was restricted to the vessels in part of my colon.
It never occurred to me that something like that would happen from ET. I'm taking lovenox injections and just started hydrea.
I'm 42 years old.
Has anyone else had a similar experience?
Written by
MacDWild
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I also have ET (diagnosed last year) and I am 45 years old. I was originally diagnosed with chronic fatigue syndrome and irritable bowek syndrome after a long history of digestive complaints. I suffered with inflammation and was on a very restrictive diet. I think it must have been because of the slower blood flow. I am feeling a lot better since being diagnosed and taking blood thinning medication. I hope this helps.
Was it clinically determined that your colon problem was caused by ET? Is the restriction to blood flow caused by a blood clot or something else? If it is ET related it must be very rare.
Yes. I spent 4 days in the hospital. CAT scan, endoscopy and colonoscopy and saw 2 hematologists. Platelets over 1 million (for first time ever). There is nothing "wrong " with my intestines and they all believe it's ET.
This is an interesting thread. I was hospitalized and had surgery for severe diverticulitis a few years prior to being diagnosed with PV. I have had zero GI problems up till now. I was diagnosed with PV a year ago this month and started on Pegasys 2 months ago. This past weekend I had severe pain, bloody diarrhea, and fever like symptoms that I read to be consistent with colitis. This is a known side-effect of IFN treatment, but now I'm starting to wonder about whether GI issues are also consistent with thick blood. I'll be finding out what my insides look like during my scope next week. Praying that I will not have to discontinue Pegasys.
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