where in n.y.and pa.will they test and tre... - PSP Association

PSP Association

9,604 members11,541 posts

where in n.y.and pa.will they test and treat PSP

athlete1 profile image
3 Replies
Written by
athlete1 profile image
athlete1
To view profiles and participate in discussions please or .
3 Replies
PSPA_DebbieB profile image
PSPA_DebbieBPartnerPSPA

Hello, if you contact the US society, CurePSP, I am sure they will be able to help you. Their website is psp.org/

Best wishes, Debbie

Frosty profile image
Frosty

My husband has PSP .We went to a neurologist movement disorder specialist.we took six months of PT,OT and speech.It helped for awhile but now he seems to be getting worse.Check your local hospital for PSP support group meetings.Good luck and stay strong..

judy1962 profile image
judy1962

University of Pennsylvania Dr Murray Grossman in Philadelpia PA

Not what you're looking for?

You may also like...

PSP and "freezing"? PSP in Africa

Hi, my dad has just been diagnosed with PSP. He lives in Zimbabwe. (anyone else out there?) I...
PDDJED profile image

Sweating and coldness in psp

Hi.. My dad was admitted to the hospital a month ago and we had to insert the tube for feeding....
msomaya profile image

Sedation in PSP

Hi ,my Kathy is in hospital level care in a rest home ,todays visit was distressing for me as she...

Psp and cataracts.

Hi friends just wanted to ask if anyone has any experience with a loved one who has psp and has has...

PSP and Sleep

My dad has PSP and we are to the point now where he is having trouble sleeping almost nightly. I...
DaughterSLC profile image

Moderation team

HelenPSPA profile image
HelenPSPAAdministrator

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.