Reply To: Newly Diagnosed.. I think

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1 month ago

@cwe33, shame you haven’t appealed during covid cos my assessment was over the phone. They may still be operating like this too, might be worth giving it another go if you feel up to it. I think ms nurses can advise or someone at your local CAB (if you can get an appointment with someone there!) I’m PPMS & diagnosed during lockdown following an urgent mri & getting the result over the phone wasn’t great but that’s how it was. I’ve pretty much had to fumble my way around everything & almost fight for advice cos my neuro centre ‘closed shop’! I did however on my pip form describe my ms as everyday is my worst, that I don’t have good & bad days & that its progressive – clue is in the title! Colette