Posts - PSP Association | HealthUnlocked

PSP Association

9,252 members11,349 posts

All posts for May 2014

Hi. Just joined here as my husband now diagnosed with CBD not PD as first thought.

He is now in a care home but to be honest they have little experience of his con...
FeeBee profile image

We've been informed today that my partner may well have psp, further tests will be undertaken soon.

My question is, is there such a thing as assisted or adaptive living properties ...
Gadgetgeek profile image

My wife experiences a feeling like she is walking on air,no dizziness but a feeling like she will fall because there is no floor HELP

Sera1956 profile image
Want to take advantage of all our features? Just log in!
or

Can anyone help with advice or anything on this one, my husband is going through another dementia episode at the moment, and it has been

going on for nearly 3 hours. He is refusing to eat, drink or anything, he will...

THE PARTY IS FINISHED BUT THE NEXT ONE WILL BE ON.

When would suit you all? a Sunday lunchtime for all the folks in the UK? that w...
jillannf6 profile image

Who put that brick wall there?

Having a really bad day today! Been going along nicely for quite a while. S se...
Heady profile image

Another hurdle

Seems to be another hurdle every day mum in bed till midday as finding the hoist...
blackcushion profile image

New Diagnosis

Hello, I have just recieved the news my father has PSP. We thought he had stage ...
AJJG76 profile image

Do you use the "pull-up" pant style incontinence pads?

We have a quantity of these products which are now surplus to our requirements a...
Kathy profile image

At a loss as to how to support and protect my parents without hurting them

My siblings and I have recently been made power of attorney over my father's aff...
Didalju profile image

Is there anything to help with the explosive cough my husband has. We thought it was a cold but the cough is not going away it is constant

My husband has PSP and since he had a UTI things seem to be progressing faster.
Hidden profile image

Help for my Mum - Parkinsons, PSP or MSA? Help and advice please

I'm hoping someone can help with advice in respect of my Mother. She was diagno...
YipYapStaam profile image

Firstly, I must say thank you to this community for all the advise and words of wisdom. My dad was diagnosed with psp for seven years and I

Have a feeling we are reaching the end. His salvia has thickened that he is now ...
emmaapanah profile image

THE PARTY IS STARTING

AR EYOU READY/IT SI COOL IN THE UK THIS EVENIGN SO NO BBQ I SHALLS TA RTWITH A G...
jillannf6 profile image

To Think I Tell My Boys To Never HATE !

Google this: /give.psp.org/i-hate-psp-t-shirt-donation-page
edkor profile image

Someone May Have Already Posted This : Bristo Myers Squibb Acquires iPierian, inc.

GOODLE THIS ; IPN007
edkor profile image

Does anyone have any idea of the incubation period of PSP?

My first wife had CJD which is another rare brain disease. The neurologist and ...

Please can anyone help. What is the difference between Psp and MSA ... Is it possible to have both as my mum has the symptom s of both...

Brighteyesxxx profile image

Infection

My mum has urine infection she hasn't past urine for nearly three days.
blackcushion profile image

online party tonight sunday 25 may 6pm UK time SO PLEAS E BE THERE!

hi all do not forget the party tonight no particular protocol wear what you wa...
jillannf6 profile image

Are sweats common in the more advance stages of PSP?

My dad has been getting sweats day and night with or without fever. How normal i...
jessybx19 profile image

TPI-287 20 mg/m2 SOMETHING BETTER HELP!!!!!!

Something better help I cant hang on much longer. Please!!!!
edkor profile image

DRUG TRIALS PHASEII

TPI-287 20 mg/m2
edkor profile image

Can anyone on this blog tell me anything about MSA-P? My husband was just diagnosed with this disease by the doctors at Mayo's.

My husband now has been diagnosed with MSA-P. First it was PSP then CBD now the...
Hidden profile image

Will this poem help? I hope so. I couldn't say what I'm feeling better having lost my dear wife May 4, 2014

This is for all those who have lost loved ones to PSP recently Fingerprints Not...

Does anybody know what medication a PSP patient should be getting in the final stages? thanks

llangton profile image

Mum

This morning at 9am Mum breathed her last in the arms of the man she loved and w...
hmfsli profile image

Hi My husband diagnosed with psp recently. He is going to Walton centre next week. We haven't had much info so far,( told to check Internet)

Does anyone else suffer pins and needles in hands and arms? Also loud,sharp soun...
knitter13 profile image

Possible confusing antidepressant medication implications for PSP?

We all know that gait and postural instability problems are major symptoms of PS...
Hidden profile image

At this moment....

I am scared. My dad is not looking good. He is slowly slipping away (due to PSP)...
jessybx19 profile image

Search posts

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.