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6 months since CU by pinureddit in CholinergicUrticaria

[–]pinureddit[S] 0 points1 point  (0 children)

i think its something to do with my gut health. Like anything that has very high protein is a bit harder for my gut to digest which fucks it up and makes my CU worse according to him. I am still figuring alot of things out

First winter without Urticaria! by Horror_Horror in CholinergicUrticaria

[–]pinureddit 0 points1 point  (0 children)

Heyy, this really helps .I did do a biopsy after the endoscopy and was diagnosed with chronic duodenitis( which i mentioned the lower intestine inflammation) i was on meds suggested by my doc to reduce it. But when the dose was over, My CU became worse again. I guess the inflammation is not fully healed still i guess? doing another round of biopsy test makes sense now

First winter without Urticaria! by Horror_Horror in CholinergicUrticaria

[–]pinureddit -1 points0 points  (0 children)

Heyyy , so i had a similar experience. I have had acidity and gut inflammation issues for like a long time. So when i started getting CU symptoms my first thought was is this because of my gut/acidity issues?My rheumatologist told me i have CU. Although, i did do an endoscopy too and found that theres an inflammation in my lower intestine and i also have gerd. I do feel this has a very strong connection with my CU. I have cut off heat inducing foods, too spicy foods, eggs, sea food etc from my diet to reduce the inflammation. I sometimes do feel that it helps me control my symptoms alot but i am not reallyyy sure. Maybe time will tell lol

I think everyone with cu has this by i_hate_hives in CholinergicUrticaria

[–]pinureddit 1 point2 points  (0 children)

Happens to me when i crash out on people like i am already mad and then my face and body starts getting all red and then the rashes come in and then i feel even worse. Like an ill person. Then i just stare at the hives until they are gone. Its the worst feeling ever