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Progressive Supranuclear Palsy
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Progressive Supranuclear Palsy
Advice
Advice of Progressive Supranuclear Palsy
Often feels dizzy/light headed and has headaches/stiff neck
by Ian
Botox injections in the forearm to combat rigidity in the hand
by syrilynt
Being excepted into the clinical trial
by Chickie
Seeing people be opening up on what I have
by Roger Coburn
no communication
by Stephanie
Alguns sintomas diferenciadores foram muito importantes no diagnóstico
by monicasalgado
Sharing experiences and knowledge
by PSP Warwickshire
None
by Charles Dunn
My Friends
by Ken
Having my family taking care of me and supporting me.
by Dale Perry
Exercise
by Tim Brown
Really think about the patient having the peg
by Caroline bill
Conntacting early on in thr late stage
by
[email protected]
staying positive
by Kathleen Labadie
The Facebook Group "Corticobasal Degeneration: find a cure, support for family & caregivers"
by Michael Fleming
Realize that 'independence' can't be the goal. The goal has got to be to do as much as you can for as long as you can with as much help as you need. It's the only goal anyone with PSP and their families/caregivers can achieve!
by Sue
Keeping my mind busy.
by Thelys
Scopolamine patch has helped with the secretions.
by James Rea
doctor
by SCDaly
Meine kleine Pension mit meinen lieben Gäste, das bedeutet Abwechslung und Freude
by Rita
palliative vare being introduced near the end and understanding an from other health care professionals when things were getting bad
by Helen Henderson
Loving care
by Maureen
physical therapy
by Dona
television
by jeffrey merchant
Wife, friends
by Jim
CurePSP an international non-profit organization- what helps the most is participating in physical therapy and speech and language therapy
by Alex Klein (CurePSP)
Support of family and friends
by Kerryn
Exercise and massage
by Ladd
i am watchng what i eat. notghing drastic,just good food.
by jeannie tubich
Sleeping with a heating blanket
by Karen
Ongoing exercise and physical therapy kept him active and more flexible as his joints stiffened.
by Luebbem
Albuterol in nebulizer has helped with some of choking on food.
by kja811
Speech Pathologist might help someone communicate longer
by Steve
Shes had it a year, and she can no longer pronounce words clearly
by Alisha
Friends who support me
by SAM
Since a few months we've help of an au-pair
by Marrianne
Tratamiento y seguimiento
by Roberto
su forma de ser
by Yolanda
Palliative Care
by Samantha
Also diagnosed with Dementia Associated with PSP
by Ian
Physical therapy (leg exercises, esp) have improved balance and talking
by syrilynt
All the support groups
by Chickie
Moving here me to a more relaxed country community, out of the city busy-ness.
by Roger Coburn
CBD helps sleep
by Stephanie
Ongentys ajudou bastante durante algum tempo
by monicasalgado
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