PSP Association | HealthUnlocked

PSP Association

9,243 members11,343 posts

Sharon has left us

After a month long fight in hospital my wife could not fight any longer. Yesterd...
Zerachiel profile image

Speech and Word finding - a sufferers perspective

My wife first went to hospital in early 2020 with a soft voice and her face look...
Zerachiel profile image

CHC FUNDING

Hello has anyone had CHC funding removed because they see the needs are managed ...
Northstar1 profile image

Choking with psp.

Hi only just joined this group and was hoping for a little information/ advise. ...
Jellybean219 profile image

Mum's PSP

Mum was only diagnosed with PSP last Octobershe is falling alot more now and ,he...
Blitzford72 profile image

Things to do for PSP – sing a PSP country song (badly!)

A bit of fun for a good cause. You have to watch the video - sorry! https://you...
Richard33 profile image

This Morning

Is anyone watching This Morning with the Salt Path couple?!
Old_Hall profile image

Orangetrunk

This is the first time I've posted. I live in California and heard about Health...

Eye sight

My mum has double vision ,one on top of each other not side to side ,she has a ...

Couldn't wake Mum up

Hello everyone. It's not often I post here, however I read lots of the posts and...

CBD diagnosis

After 4 years of pushing him, pushing for tests and watching a 6 foot plus ex Ro...

Urine Retention in PSP

Hi, My husband drinks plenty of fluids and is hydrated but has inconsistent but ...
Millidog profile image

Ensure liquid meals

Please could I ask if anyone has experience of surviving on liquid meals only. ...

One more star in the sky

My mom, who had PsP, is now a star in the sky. The last stage was brutal. her hu...
momme profile image

Recipe book/meal recommendations please

My husband (diagnosed with PSP July 2021) loves his food but lately eating has b...

PSP Spasms

My wife was diagnosed with PSP some 3 years ago and is now suffering regular pai...
Prius1 profile image

Speech production technology

Has anyone tried speech production technology, such as Stephen Hawking used, for...
TourEiffel profile image

struggling with PSP

my husband is 72 and was finally diagnosed with PSP in September 2023 after a st...
Newstead1 profile image

swallowing

my mum is now having to be given fluids using a syringe 😭 drinking from a cup s...

Drooling

Hi Karol has had a dry mouth since having peg fitted and nil by mouth for fluids...
45purple profile image

i hate PSP

my mum was diagnosed with PSP 3.5 years ago, and it has progressed so so quickly...
Hidden profile image

CBD awareness

Hello this is my first post. my brother lives with me and he has always had co...

Lorazepam - New Findings?

Hi, This is my first post. My mum was diagnosed in March 2021 with PSP. I jus...
AmberLucky profile image

Travel Insurance

I meant to say I don’t know if this is because I answered No to the question can...

lack of help

A friend of mine was diagnosed with CBD last year, but started with symptoms abo...
Newsymum profile image

Seizures

Hi everyone, my Dad is in the later stages of PSP, his speech has pretty much go...
jmorrish profile image

medicine

my wife was diagnosed yet, she is meeting next week to discuss different meds, d...
Advocate10 profile image

Travel Insurance

Wife recently diagnosed with CBD. Lost use of 1 arm, other one is less under...
1957spurs profile image

apathy

hi This is my first post, my husband 79 was diagnosed with PSP 18 months ago. M...
Tulipstaffie profile image

Husband with PSP

I am a Carer for my husband who has been diagnosed with this condition in Novemb...
MontyLucy profile image
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PSPA is a national charity offering information, practical and emotional support to people affected by Progres...

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