@Hollys 

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Hollys

Think that was a diagnosis ..

I think this morning's letter with an appointment to a MS clinic might be my neurologist's way of informing me that my 2nd MRI has more of less confirmed it - he did say someone would contact me with the MRI results but never did - they just sent me this instead. I feel OK, I have said to my GP a few times 'think it might be MS' and they've said it wouldn't be (now I feel quite clever that I was spot on!) Anyway moan over - just wanted to say hello. I've been lingering for a while and the posts have got me through a few months of limbo (I even thought if it does turn out to be a B12 deficiency I'd be relieved but I'd really miss these people)
@Schnecke

Hallo well, that would indeed be a slightly awkward way to communicate a diagnosis. 🙄 Did you talk with your neuro about the possibility of MS? In any case, s/he is not wasting time by calling you in again and instead has booked you to see people who know MS well to look into this further. Great mix of efficiency and awkwardness indeed... The MS experts will know more, and if it is indeed MS, this is the team to talk to. 😊 All best and welcome here! 😊

@Hollys

@Schnecke yes I'd had conversations with my neuro about MS as one of a number of possibilities to eliminate so it's not a shock - he just missed out the part where he said someone would phone me to talk about my last MRI - he did say there was a 'big pile' to get through (id never moan about the NHS though) .. but like you say at least I'm going to get to an expert .. finally!

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