i took methotrexate for my psoraisis a few years back and when i was on it, i got the worst flare of my entire life that lasted a painful hospital ridden year and half long flare.
was told it wasnt the methotrexate as they use that for crohns, but it is and was the only new and different thing i was on in ages and bam, UC like never before.
so im pretty much no help but for that little story.
steph - 33 - female - gold coast australia - UC since 2000
was in remission until i quit smoking 5 weeks ago o.O now im flaring like a solar flare!
waiting for blood test to see if i can start imuran
mesalazine granules 3g x1 a day (much nicer than a million tablets a day)
just finished 3 months of prednisolone (worked) and now back on 40mg a day (ick)
quercertin tablets, tumeric capsules, vitamin d3, enteric coated fish oil
pre-conception vitamins and minerals (cuz we trying to make a baby)
oxycontin for pain every 4 hours. plastic bags in the loo from the involuntary puking.
i still eat what i want, when i want, if i feel like eating at all ... diet doesn't affect my UC.