does anyone know of a hospitol or doctor ... - Cure Parkinson's

Cure Parkinson's

25,855 members27,162 posts

does anyone know of a hospitol or doctor that realy knows about PD and can treat it

hawaii profile image
10 Replies
Written by
hawaii profile image
hawaii
To view profiles and participate in discussions please or .
10 Replies
Larryp profile image
Larryp

google Parkinson's association Hawaii and you will find all the support you need

The assoc. can refer you to some other Parkies and they will help

good luck

Drader profile image
Drader

Try the Carolinas Medical Center in Charlotte, N.C. they are wonderful.

There are many good facilities-- it's finding the doctor that works for you. WHen I was diagnosed, my husband got the internet, put in parkinsons and several sites came up. He called the Parkinsons institute and explained my story. It was suggested that I try to get into a study ( there are many out there) then that way I would become a patient of the doctor running th study. I live near New Orleans but travel 6 hours 2x a year to UAB in Birmingham,AL. I am also looking into seeing someone at Baylor University I have been told they have an excellant program. Good luck.

PeggyT profile image
PeggyT

I live an hour and a half away from Baylor College of Medicine Parkinson's Disease Center and Movement Disorders Clinic In Houston, where I go every 6 months. Very fine facility and up-to-date research-oriented doctors.

Antonio_Montolio profile image
Antonio_Montolio

UF Florida center for movement disorder, shands hospital, Gainsville FL.the finest and most up to date Parkinson research and treatment facilities I have ever en counter

Dannny profile image
Dannny in reply to Antonio_Montolio

I agree about 20 doctors on staff........I started treatment 6 months ago

parkey profile image
parkey

i go to booth gardner in everet wa woks very well for me doctors listen and realy care

jillannf6 profile image
jillannf6

i have -PSP- A rare form of parkinsons 4 which there are no meds to help(tried sinemet & amantadine - no use)_bUT I am positive re the condition and i look well given that i have a terminal illness

i am 65 and ws diagnosed in dec 2010 but had had syjmptoms (balance and co od pporblems for 5 years b4 that)

No one inc myself had heard of it: GP/ sOCIAL WORKER/ PHYSIO/eye consultants etc so it it s matrer of tryin g to educate eveyrone i come into contact wiht

Easier said than done as my speech is v garbled now and it is difficult 2 make myself understood and my hadnwirting is non existent ,my typgng dyslexic as one hand is stronger than the other but .......

there are many worse conditions out there and i try to do something each day

jill

Anemone profile image
Anemone

UVA in Charlottesville, where I am lucky enough to have gotten into. As I found out, it isn't easy to find PD specialists, and surely not every neurologist is able to handle PD. Good luck. Understand your problem.

Joealt profile image
Joealt

Northwestern Hospital, on St Clair Street in Chicago Illinois, has a Movement Disorder Center and works with the Michael J Fox Foundation.

You may also like...