So I've had my colonoscopy clear, CT scan showed an abnormal growth on my pancreas.  Within a week I've been referred from general surgery to Upper GI to Neuroendocrine teams and gut hormone test taken. 

My results are back...my upper GI nurse told me the figures but couldn't explain them.  She is surprised the neuroendocrine team havent called, not even to  introduce themselves. I need them to call me to explain next steps yet after searching for numbers and leaving 3 answerphone messages noone is talking to me. They've not even opened the email from the GI nurse. This is a week after my results have been returned.. unfortunately it's two different health boards so they can't read each others notes.:angry:

is it normal to wait for so long for a specialist team to contact someone?  Im now understanding why my mum was so annoyed at times..