Worldwide Resource Links
Tons of great resources and information all in one place!
Click on the logo to visit their website.
*All third-party trademarks, logos, and brand names shown on this website are the property of their respective owners. These brand names, logos, and trademarks are used only for identification purposes and do not imply endorsement.
The first clinic in Canada, fully focused on the diagnosis and management of Progressive Supranuclear Palsy (PSP) and other similar conditions.
Mission MSA is dedicated to supporting individuals and families affected by Multiple System Atrophy (MSA), providing resources, education, and advocacy.
MSA United is an international consortium working to improve the lives of those with Multiple System Atrophy (MSA) through research, support, and global collaboration.
The Lewy Body Dementia Association (LBDA) is a leading organization providing support, education, and resources for Lewy Body Dementia, a condition related to Parkinson's disease.
The Parkinson’s Foundation is focused on improving care and advancing research for Parkinson's disease, including Atypical Parkinsonism conditions.
CurePSP is a USA nonprofit dedicated to awareness, care, and cure for PSP, corticobasal degeneration (CBD), and multiple system atrophy (MSA).
PSPA is the only UK charity dedicated to improving lives for those affected by PSP & CBD through support and research.
Since 1965, Parkinson Canada has provided support services and education for people living with Parkinson’s disease, including PSP/MSA/CBD.
The Michael J. Fox Foundation in the USA is dedicated to finding a cure for Parkinson's disease and improving therapies for those living with Parkinson's and Atypical Parkinsonism.
The Krembil Brain Institute at Toronto Western Hospital (UHN) in Canada is home to one of the world’s largest teams working on brain and spine problems.
Fight Parkinson's in Australia offers specialist support for individuals and families affected by PSP, providing information and advocacy.
NORD provides services for patients, families, and medical professionals dealing with rare diseases like PSP.
NINDS studies PSP as part of its Parkinson's Disease Biomarkers Program to track disease progression and identify at-risk individuals.
Mayo Clinic’s experts are experienced in treating rare conditions like PSP, serving over a million patients annually.
Across the globe, a powerful network stands ready to support those touched by Atypical Parkinsonism. From Canada’s innovative clinics and Australia’s dedicated advocates to the UK’s PSPA and the USA’s research pioneers like CurePSP and NORD, these organizations unite expertise, care, and hope. Whether you’re facing Progressive Supranuclear Palsy (PSP), Multiple System Atrophy (MSA), Corticobasal Degeneration (CBD), or related disorders, you’re not alone—explore these worldwide resources and find the strength you need!
Donate