I've been quietly reading for a few days but I thought I ought to introduce myself. I was diagnosed with mci in 2009 but told it was down to stress and depression. Last year my memory got worse and was fobbed off with 'it's probably menopause'. Then I started to get dizziness, a referral to ENT followed who ran a CT scan in October, suddenly in December foyer someone looked at the results the memory assessment service was involved, I'm up to my neck in doctors talking about the possibility of some form of early onset FTD. I'm only 46. Neuropsychologist this week, neurologist next week.
I'm just trying to remember to breathe but I'm off the scale in stress, terrified at what they are going to find, and wanting to find people who understand what this feels like.
I'm just trying to remember to breathe but I'm off the scale in stress, terrified at what they are going to find, and wanting to find people who understand what this feels like.