Posts - PSP Association | HealthUnlocked

PSP Association

9,255 members11,351 posts

All posts for March 2023

Pneumonia in CBD

Hi I’ve just found out my mum is in hospital with pneumonia and I’m on holiday i...

PSP hElp advice

my husband was diagnosed with PSP late January ...back in 2019 he was thought to...
Tubbybru profile image

In response to Troubleandstrife's request the poem I wrote about my husband no longer being crippled by CBD

Niggly (Nigel B) His wicked sense of humour will have now come to the fore ...
AliBee1 profile image
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Getting care

Hi My father in law has psp last 3 years. Up till now he has his wife help getti...
Happysole profile image

End stages of PSP

Because it took so long for Mom to get a diagnosis of PSP, we can only guess how...

Waiting for an ambulance….

My mum is 69, has CBD and as I type we are waiting for an ambulance. The GP has ...

Final stages of CBD

Hi all My dad is in the final stages of CBD and in fact the Palliative Care Con...

Joy 204010

Want to know how you all cope with your PSP journey.. My husband has had PSP fo...
204010 profile image

Psp testing

Hi. I lost my mum in october to this horrible illness. I'm still struggling with...
Beckany profile image

Heavy Breathing through Nose

Just wondering if anyone else has run across this -- my mom (PSP/CBD, near late ...
LARWLSN profile image

Eating problems

My mum has been diagnosed with PSP for 2 years now( though she had a lot of symp...
Walking18 profile image

Hand tremors when eating

My wife was diagnosed with PSP nearly two years ago. Recently she has been havin...
Wombatz profile image

Tomorrow is moving day

Patient here. I’m moving to assisted living tomorrow and I feel like I’m prepar...
Kayelless profile image

Exposure to environmental contaminants and how it relates to increase in Parkinson's disease...

I know that PSP, MSA, and CBD and Parkinsons are not one and the same but this h...

manonfire

hi, Just joined, husband has psp for 9 years +, nice to meet you all.
Manonfire profile image

District nurses

Hi all. I read lots of posts and many of you talk about being supported by dist...
Joluu profile image

Frequent Urinating

My husband has PSP and is constantly waking up at night to use his urinal bottl...
Redjune1 profile image

recently diagnosed with PSP

I’m hoping to connect with others who have this disease. I want to learn more a...
Johno12345 profile image

help re: fast track chc

Hi all. Just wondering if anyone has any experience of the fast track process fo...

Still here ...

Remarkably still here despite some close calls. Mum is very frail, 6 stone 2 at ...

Chc when is the right time to apply?

Hi All,I read a lot on here about CHC funding applications, some successful and ...
Millidog profile image

My dad and PSP

My dad has just recently been diagnosed with PSP. We are wondering if he has ha...
Hidden profile image

My lovely mum has gained her angel wings

my mum passed away on Thursday 9th March after being officially diagnosed with P...
ep12345 profile image

last two weeks

things have been better for the last couple of weeks, however, leg pains and cra...

Blood tests for PSP

Does anyone know what the blood test is called that, I have heard, you can get t...
REOC profile image

Mom-questions

Hello, My mom was diagnosed about a year ago with PSP. She uses a walker and ...

Why I’m moving to assisted living

Patient here. I’m the one who has stopped fighting what can’t be stopped. My pl...
Kayelless profile image

PSPDrugs

hello, I am looking for advice regarding PSP drugs and struggling to swallow the...
Purp23 profile image

severe apnea during sleep day/night

I've been informed by physician this condition is normal in PSP patients. Any ad...
diroca profile image

Imaginary mucus

Hello lovely people, my mam complains about mucus in her throat, however we have...
AvonJane profile image

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