Posts - PSP Association | HealthUnlocked

PSP Association

9,266 members11,356 posts

All posts for June 2011

an anxious week

My mum seemed to take a turn for the worse this week. Two posts I've written on...
Fiona_McL profile image

Diary of a Daughter and Carer

Ive been writing a blog for a few months now and thought I would share...This wa...
AmyT profile image

help and support required...

Living with PSP is a challenge for all of us. If it's at all possible, get to a ...
Fiona_McL profile image
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It's odd but...

... until my Mum was diagnosed with osteoporosis in early 2008 she was generally...
hmfsli profile image

How do you cope with dreams and hallucinations?

Mum has experienced really vivid dreams and hallucinations for quite some time n...
hmfsli profile image

Hello

I'm Idris. Obviously this is not my real name. It's a Doctor Who thing. I've be...
Idris profile image

My Dad is a star!

My Dad is an absolute star! I know it is not unusual for daughters to think we...
hmfsli profile image

Getting the right diagnosis

hi i was 49 when i was diagnosed with corticobasal ganglionic degeneration i thr...

Has anyone seen the short film A Short Stay In Switzerland? Julie Walters is in it.

I watched it in 2008/09 and thought it was very hard hitting. Having watched it...
HannahDaykin profile image

Where and when did my Dad go?

2006 and I had just got off the phone to my Mum. Flinging my arms around a frien...
HannahDaykin profile image

How does my Mum do it?

I have no idea how my Mum is so strong to care for my Dad. I suppose she does it...
HannahDaykin profile image

Hospital Survey

Our Hospital Survey has gone live...this survey is about services provided in th...
PSPA_DebbieB profile image
Partner

falling

i have had an exciting morning = taxi to dentist for check up - teeth good desp...
jillannf6 profile image

research trials

is sthere any available research trial in UK ongoing? (apart from the davunetide...
jillannf6 profile image

A Brief Introduction

I thought I would introduce myself before I start sharing my thoughts about and ...
hmfsli profile image

Where we're at

Some personal blog posts describing PSP in my life. I'll update as I do more! :...
Fiona_McL profile image

the lee silverman voice treatment

hi i was just wondering if any body has been refered by there speech and languag...

trouble with social services and local councils

hi after being diagnosed with cbd at the age of 49 was quite a shock to the syst...

Where I am today.

Living in Sheffield (for university), I wish it was easier to cope with my Dad h...
HannahDaykin profile image

getting diagnosed wiTh PSP

Hi I am 65 and was diagnosed with PSP in December 2010 and have felt so much bet...
jillannf6 profile image

When my Dad was first diagnosed..

..I was 18 and was in my first term at Sheffield Hallam University. We had thoug...
HannahDaykin profile image

An article in The Nottingham Post about My Dad during PSP Awareness Week.

http://www.thisisnottingham.co.uk/research-condition-robbing-dad-speech/story-12...
HannahDaykin profile image

Raising awareness for PSP on Facebook

This is a link to my page on Facebook which I am using as a medium to raise awar...
HannahDaykin profile image

Come on in!

HealthUnlocked is in session for PSP! We are so pleased it’s time to load up th...

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