Posts - PSP Association | HealthUnlocked

PSP Association

9,345 members • 11,394 posts

All posts for June 2014

Change of medication.

I mentioned sometime ago I would let you all know after my husband was tried on Sinemet. Well it made no difference to his symptoms and hence it has now been...

I mentioned sometime ago I would let you all know after my husband was tried on ...

Peter3

•10 years ago

17 Replies

New design for the site?

Heady, it seems that the new design is going to happen. I hope they have ironed out the problems you noted. Keeping it simple should be the first imperative...

Heady, it seems that the new design is going to happen. I hope they have ironed...

easterncedar

•10 years ago

13 Replies

Hello everyone , please has anybody had any experience of a psp sufferer constantly picking at their skin? Arms,legs and now head. love p

pollyannajo

•10 years ago

12 Replies

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My hubby is 52 and has been diagnosed with CBD...he is not aware of what happens in time , should I keep it that way? Still in shock myself

wilma3960

•10 years ago

10 Replies

Does anyone know if having PSP brings with it a compromised immune system?

JudyJ

•10 years ago

31 Replies

One thing that really bugs me is time and again I read "PSP is usually diagnosed in people with low intelligence" what rot

My husband is Cambridge educated an MA BA and just the cleverest man I have ever met.even Dr. Golbe said this about lack of intelegence

My husband is Cambridge educated an MA BA and just the cleverest man I have ever...

Hidden

•10 years ago

21 Replies

My husband was diagnosed with CBD a month ago. I am reading that the life expectancy is 6-8 years. Anyone out there have better news?

cbsmom1

•10 years ago

13 Replies

My father has been diagnosed with CBD, he can no longer walk. Does anyone know what stage he is at in this illness?

Dollyat11

•10 years ago

9 Replies

3 days ago dad had his girlfriend break up with him. Today he thinks I'm his girlfriend not Dtr keeps calling me her name Will this change

rlb_mo

•10 years ago

4 Replies

My wife has PSP and we were wondering if there are respite places in Norfolk that specialise in PSP so as I can get things done in the home

better for her

BarryB6912

•10 years ago

7 Replies

HEALTHUNLOCKED responded!

I feel as if I got my life line back. HEALTHUNLOCKED have restored my page back to the original one. So I thank them with all my heart, the new one just was...

I feel as if I got my life line back. HEALTHUNLOCKED have restored my page back...

Heady

•10 years ago

7 Replies

Hi, My aunt is suffering from PSP. How can we donate her body for R&D purpose?

priyankmalkan

•10 years ago

20 Replies

Going to miss you mum

Mum past away 10.50 am 3rd June peacefully at home so glad I was with mum at the end of mum's journey it's been a rollercoaster , but I miss seeing mum as my...

Mum past away 10.50 am 3rd June peacefully at home so glad I was with mum at the...

blackcushion

•10 years ago

16 Replies

Regarding anesthesia

For those who so helpfully answered my question about the possible danger in using anesthesia for a minor procedure, Heady, Strelley, Goldcap, Alana,...

For those who so helpfully answered my question about the possible danger in usi...

easterncedar

•10 years ago

28 Replies

Position of the chin when aiming the eyes?

If you ask your person with PSP to look and concentrate on something straight ahead, do they raise their chin up to focus? I know we have discussed normal...

If you ask your person with PSP to look and concentrate on something straight ah...

mcfly

•10 years ago

3 Replies

Any one else trying out the new layout?

Hi all, is anyone else trying out the new layout? Really don't like it. The reply box is far too small, so it's difficult to see what you have typed. It...

Hi all, is anyone else trying out the new layout? Really don't like it. The r...

Heady

•10 years ago

17 Replies

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Posts - PSP Association | HealthUnlocked

PSP Association

All posts for June 2014

Change of medication.

New design for the site?

Hello everyone , please has anybody had any experience of a psp sufferer constantly picking at their skin? Arms,legs and now head. love p

My hubby is 52 and has been diagnosed with CBD...he is not aware of what happens in time , should I keep it that way? Still in shock myself

Does anyone know if having PSP brings with it a compromised immune system?

One thing that really bugs me is time and again I read "PSP is usually diagnosed in people with low intelligence" what rot

My husband was diagnosed with CBD a month ago. I am reading that the life expectancy is 6-8 years. Anyone out there have better news?

My father has been diagnosed with CBD, he can no longer walk. Does anyone know what stage he is at in this illness?

3 days ago dad had his girlfriend break up with him. Today he thinks I'm his girlfriend not Dtr keeps calling me her name Will this change

My wife has PSP and we were wondering if there are respite places in Norfolk that specialise in PSP so as I can get things done in the home

HEALTHUNLOCKED responded!

Hi, My aunt is suffering from PSP. How can we donate her body for R&D purpose?

Going to miss you mum

Regarding anesthesia

Position of the chin when aiming the eyes?

Any one else trying out the new layout?

Search posts

Latest poll

What are your main concerns as a carer?

Topics

Archive