UC my experience
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Hi, I am 48 and was diagnosed with UC 2yrs ago, at this time my husband was suffering with terminal cancer and i thought my problems were the last thing anyone wished to hear about, but looking back on this now i feel it was probably brought on by the STRESS eventhough my hospital consultants maintain UC is not a stress related condition.
I have tried various drugs to try to control this but now 2yrs on i was told on Friday that there is poss no alternative but surgery. As my UC is till active and i have had no quality of life for two years. I do feel for anyone with this disease it rules your life, i don't go anywhere, unless i know the precise location of the loo, not even the local shops, sorry to depress you if you suffer, but unless anyone knows what this is like you can't explain.
rie
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Guest
Posted
Surgery is a big step that obviously can not be reversed!
Good luck x
Guest
Posted
I was finally diagnosed with UC 11 years ago although I have suffered with it since teens, now in my 50's.
It is a nightmare disease and it totally ruins everyday life, I feel I have missed out on so much.
Anyway I have been taking Asacol ( now only 1 tab a day ) for the past 11 years and I can honestly say I have not had a flare up since, very minor blips occasionaly but a slight increase in meds for a couple of days sorts it.
I realise I am one of the lucky ones who responds well to the medication, I dread having a problem again but would happily go for surgery if it meant the end of it. I am also lucky in that I have a very good consultant who I totally trust.
Good luck, I hope it all works out for you.
:lol:
Guest
Posted