I have recently had diagnosis of coeliac confirmed by blood test and endoscopy/biopsy but have yet to see a consultant or dietician or have anything explained to me properly. I saw my GP but she just said to look online for help. This forum is great but I'm still pretty confused. I only got tested as I was looking for something that might help with my psoriasis and did not have many GI symptoms, so I am struggling to know how careful I need to be.
I have obviously cut out all gluten, am reading labels etc, but is it ok to eat something that "may contain traces"? And do I need to use separate pans, spreads etc than the rest of my family? Ive read lots of posts but everyone else seems to get sick from CC whereas I'm not sure if I would notice? But it could still be doing damage. I appreciate how lucky I am not to have been as ill as some of you and to not get gut symptoms from CC, but I am aware that I could be doing hidden damage. Any advice would be much appreciated.
I only know one other coeliac and his philosophy seems to be eat gluten free most of the time and have the occasional binge on pizza and beer.
Had my daughter tested this week, awaiting results...
Thanks for reading. x







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