ive had uc...for 2 yrs now. ive had other issues with gall bladder, which i believe was misdiagnosed as Uc...and irritable bowel syndrome? for 3 yrs straight...
In 2004 ,i had my gall bladder removed..and i felt good for a while then everything started again...everything started to fail after i had that take care of...
thats when they found my uc through the colonoscopy...ive been through 3 colonoscopys, and 1 where the stick the scope down ur throat?..cant remember what that was called..but anyways...to make a long story short..all the drs couldnt help me. even the surgeons...i went to them for 2 yrs..and they finally sent me to a gi dr...
He was my life saver..because he put me on soo many others..i was on asacol for 2 yrs...and it made me lose my hair..in handfuls....brushes, combs...bathtub, sinks were always full of hair...i clean out my hair brushes/combs every day.a nd still have handfuls!..right now im currently taking 2 medications...colazal, 3pills...750 mgs...and Bentyl 10 mgs, 2 capsules 3 times daily,.what are they actually suppose to do?..i cant remember..i mean know they are suppose to help me. but i still lose hair, but it does work
He also put me on a No caffeine, lactose free diet..and it has worked..tremendously...it doesnt leave me much to eat:(...i pretty much live on chicken and rice......and cooked veggies..pastas..with no sauces...bland foods..is their any other recipes for those who cant eat raw veggies, salads...or dairy?
i cant eat raw veggies, or lettuce cus they go through me?..and give me horrible stomach cramps...and pain, diarrhea. i miss eating salads..but i cant have them anymore!
AnnaMarie
Reply posted for stayceladybug.
I'm 22 with uc and I've had a major thinning of hair on the top of my head after a life threatening flare up.
Reply posted for AnnaMarie.
Dipentum made my hair fall out. The others seem okay.
Reply posted for AnnaMarie.
Anna Marie:
It is upseting, one cannot eat as many things as used to. But you know what, eventually, you´ll be able to do it. I have been diagnosed for 6 years now, and on remision for 1. Now I can eat lettuce! and dairy products! Please keep the hope, and just allow your body to heal. You can tell which things are bad or your gut and just avoid them. For example, I cannot eat an apple, or banana. But just take care of yourself untill you are better and you´ll be able to eat the forbidden products every once in a while, eventually. Just keep the hope and remember we have to have guts!
Reply posted for AnnaMarie.
I was diagnosed with Crohn's in 2004, after three years of being sick and not knowing the cause. I have tried Colazol and Asacol which both caused MAJOR! flare ups and I loss a lot of hair and between the time I was diagnosed until 2005 I had six colonoscopies and I was hospitalized five times. The only thing that saved me was pentasa and I found out I was pregnant. Rowasa enemas are also good but for some reason they make me feel sick to my stomach. I also use prednisone daily, prevasid, levsin xl and during flare up's flagil and ciprofloxin. I was on imuran but I couldn't tolorate it. But I think they all pretty much make your hair fall out!
Reply posted for AnnaMarie.
i really miss salads too!! i mean they are so good with chicken or anything...its ironic how many of the 'healthy' foods are bad for UC, like fruits and veggies :(
Reply posted for AnnaMarie.
I went through the lossing hair when i started taking 6MP. i am 32 with CD. it would come out in handfuls as well. i will say the longer i am on the less hair i am loosing. it is like the body has adjusted. as far as what to eat, they are a few really good books on amazon for UC/CD and even a few cook books. if you would like more info feel free to email me at stayceladybug@nc.rr.com
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