Ischemic Colitis caused by ET: After having ET for... - MPN Voice

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Ischemic Colitis caused by ET

MacDWild profile image
9 Replies

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?

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MacDWild profile image
MacDWild
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9 Replies
MazCorcoran profile image
MazCorcoran

Hello

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.

Wyebird profile image
Wyebird

Goodness , I be never heard of this.

Ovingite profile image
Ovingite

Hi MacDWild,

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.

All the best

John

MacDWild profile image
MacDWild in reply to Ovingite

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.

mhos61 profile image
mhos61

A poster on the forum (jerrymohler) has discussed this happening to him too.

MacDWild profile image
MacDWild in reply to mhos61

Thanks. I will look that up!

catkinspolymer profile image
catkinspolymer

I have diveticulitus

lizzziep profile image
lizzziep in reply to catkinspolymer

SO HAVE I !

jon1972 profile image
jon1972

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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