Thanks for replying, I really didnt think there would be anyone out there so I wasnt even going to post. My DD 16.5mths old hasnt been diagnosed as yet but we suspect she has this so I have reduced the amount of fructose in her diet and we have seen a huge difference. I was wondering if you could share your experience with me, in particular how did Ashton come to be diagnosed with it, how did they test for it, what food does he eat (I realise this can vary from person to person) and anything else you can help me with.

I have a paed appointment this week and I am going to ask them about it. Hopefully we can find out for sure if this is what she has, she is also anemic which I have heard can be a symptom of FM.

Thanks
Sal xoxox