redroseart in Parkinson's Movement5 years ago
does anyone have cbgd?
Corticobasal degeneration - A personal story
pamela2103 in PSP Association6 years agoPOPULAR
I am new to this website, but thought I would share my story.
My mum has recently been diagnosed with Corticobasal Degeneration at the age ...
Corticobasal ganglionic degeneration anyone?
Patmimi in PSP Association3 months ago
My husband has been diagnosed with CBD and I do t seem to be seeing posts regarding it specifically. Does anyone have or know much about ...
Corticobasal degeneration and sleepiness
Irenephm in PSP Association2 years ago
It seems my husband, whose cbd has been diagnosed several years ago, is suddenly sleeping much more during the daytime than only a week ago....
CBD CorticoBasal Degeneration Support Group
Martina12 in PSP Association3 years agoPOPULAR
I would like to start a CBD support group which is an off shoot to the PSP support group.
I have never started a support group like t...
FLASHPOLL 4B*: (*for patients who take levodopa BUT DO NOT take dopamine agonists): Do you use recreational cannabis...
JonStamford in Parkinson's Movement4 years ago
Recruiting Clinical trial
Christine47 in PSP Associationa year ago
This was just posted by CurePSP. Sites are in the US and Canada.
The goal of this study is to build a clinical research c...
Check out this news about psp AbbVie study
Jpc1335 in PSP Association6 months ago
FTD Disorders Registry is now live
rriddle in PSP Association2 years ago
The FTD Disorders Registry is an online database to collect information from those affected by all types of Frontotemporal Degeneration: beh...
Be the first to reply
crypto14 in PSP Association2 months ago
Hi Crypto 14 I too am interested in crypto currencies. Iam trying to leave my grand kids and Son and daughter in law money for university an...
Trying to get the lingo
Price69-pat_ in Parkinson's Movement2 years ago
Hi, I am new . I have been following you all for the last month or so.
I need to know what some of the anagrams and abbreviations mean for i...
Save the date - Saturday, October 28th, PSP/CBD Research Update and Family Conference, Foster City (San Francisco Bay Area)
rriddle in PSP Associationa year ago
Save the Date! Saturday, October 28, PSP/CBD Research Update and Family Conference, Foster City (San Francisco Bay Area)
Brain Support Networ...
Does anyone with PSP also have Essential thrombocytosis?
CateT in PSP Association6 years ago
We have just been told that my mum has this and requires a chemotherapy drug. Essentially she has too many platelets in her blood and is at ...
Hidden in Parkinson's Movement6 years ago
Would someone please answer a question for me? All these abbreviations; what do they mean? PSP,PWP,MSA,LBD etc....when posting I would thin...
CBD help, very early stages
AnnieD1749 in Parkinson's Movement3 years agoPOPULAR
My husband was diagnosed last year with Parkinson's Plus / CBD. It's in the very early stages and symptoms seem to come and go. Right now h...
PSP medical articles
GmaDeb in PSP Association2 months agoPOPULAR
Found a great site for information on PSP. Many articles written by post-graduates. Most is fairly easy to understand. I found it through th...
Diagnosing PSP, Wed, Aug 30, 2-3pm PT (Calif time), Webinar - Register Now
Brain Support Network is kicking off a webinar series with Stanford Movement Disorders Center.
Join us for a free, one-hour webinar on diagn...
Atypical Parkinsonian Disorders (Is your PD 'typical'? Depends on proteins involved)
PDConscience in Parkinson's Movementa year ago
For those uncertain about their precise form of PD, this update may provide some clarity:
\"Diagnosis of Parkinson disease (PD) — by far the...
Lacey23 in PSP Associationa year ago
I've been to my husband' medical appointments and watched our neurologist do his series of tests, but watching Paul in PT/OT I can see a def...
Palmarloop in Parkinson's Movement2 years ago
I read recently that this substance is a whizz at producing new brain cells as well as protecting those already in place. Has anyone tried i...
R8360V in Parkinson's Movement2 years ago
Hi All, hope everyone is keeping okay. Its a long time since i havent written, truthfully im doing so now because after 8 years ive finally...
Register now - Sat, Oct 28, PSP/CBD Research Update + Family Conference, San Francisco Bay Area
Registration is now open!
Brain Support Network will host the:
PSP/CBD Research Update and Family Conference
Saturday, October 28, 2017
Gallstones and nafld
Andy6666 in PSP Association4 years ago
Merry Xmas to all and hoping you all have the bestest Christmass ever.
I am new here nervous scared and confused lol.
Just found out I ...
Hionarock1 in PSP Association2 months ago
Where did you get diagnosed?
Hidden in Parkinson's Movement4 years agoPOPULAR
pagf, psp, pwp : Please explain what the acronyms used on this site mean. thanks
Stages of psp
nannygoon in PSP Association5 years ago
Sister in nursing home with parkinsons plus quering psp. My sister over the past 2/3 weeks she has become very very unresponsive and not com...
GAILINGRAM in PSP Association5 years ago
Not many people from the south seem to have PSP I have many questions and would like to hear PSP pt and caregivers response. My mom had weak...
Getting the right diagnosis
ray-wiffen-1958 in PSP Association7 years ago
hi i was 49 when i was diagnosed with corticobasal ganglionic
degeneration i throught thats it ill be dead before my kids have
grown up but i ...
CBC vs PSP
Karynleitner in PSP Associationa year ago
My husband is declining rapidly . He still does not have a final diagnosis and his movement specialist made a referral to Mayo Clinic in M...
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