My husband was just diagnosed with Progressive supranuclear palsy, a rare brain disorder. Anyone here have it? If so are the meds helping at all? I did some research and they said the meds rarely do.
PSP: My husband was just diagnosed with... - Cure Parkinson's
PSP
hi ia m jill and i have PSP AND LIVE IN THE UK
THERE AR ENO MEDS FOR IT A TALL BUT U CAN TRY COCONUT OIL; COQ10 AND TURMERIC WHICH MAY OR MAY NOT HELP
U MEED TO GET A SOCIAL WORKER ON YOUR CASE
ARE YOU SEEIGN A MOVEMENT DISORDERS CONSULTANT? THEY AR E THE BETTER OF HTE NEUROLOGISTS O\
.LOL JI;L;
HI AGAIN
I AM
SORRY ,MY TYPING IS SOOD DYSLEXIC NOW AS IN THE ABOVE POST BUT HOEP YOU CNA UNDERSTAND IT
ARE U IN THE UK OR UJSA?
T MAKES GOOD SENSE TO LOG INTO THE PSP SITE ON HEALTH UNLOCKED AND JOIN THE PSP ASSSOC IN T HE UK OR THE USA EQUIVALENT- THEY ARE V HELPFUL
LOL JILL
You need to go to the psp site on healthunlock as they are separate from Parkinson's. Psp is often under the label of Parkinson's but in reality they are very different conditions. Psp rarely respond to Parkinson's medications and although many Parkinson's nurses look after people with psp the progression and treatments are very different. In tbe UK there is a very active psp society,
we had our hospital bed through the district nurse along with a wheelchair . you might have to wait for quite a while though ,
we love inS Wales
Live and love . Lol
I'm so sorry how terrible. I hope he will not suffer I will kept you all in my prayers.
Much love
Nettiepie