Tag Archives: PSP

Caring: Feeding Mum

Ma and I have a deal, we both know that PSP is progressive (it is in the name*) and that there will probably be a time when I can’t care for her. When she first got diagnosed, I said that … Continue reading →

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Social Care

Andy Burham has launched or at least speeded up Louise Casey’s look at social care. He said some good things and there’s been lots of things said about care and unpaid carers and the cost of paid care. Here’s what’s … Continue reading →

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Monday Miscellany: Just the worst news

Happy Monday! 1. Last week we finally got Ma an NHS appointment for her brain issues. The dr was lovely and confirmed a progressive supranuclear palsy (PSP) diagnosis. The doctor didn’t sugar coat it for us, movement, balance, vision, speech, … Continue reading →

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