The PSP Association

General Organizational Information
Organization Name: 
The PSP Association
Year Established: 
1994
Mission Statement: 
The mission of the PSP Association is the conquest of PSP, through effective research, education, welfare and communication.
Status of organization: 
Incorporated non-profit
Professional/Medical Board?: 
Yes
501(c)3 Status?: 
No
Paid staff?: 
Yes
Board of Directors?: 
Yes
Serves the following conditions
Diseases: 
Progressive supranuclear palsy
Organizational Contact Information
Title: 
Mrs.
Degree: 
BA (Hons), FCIB
First Name: 
Jane
Middle Initial: 
M
Last Name: 
Hardy
Address: 
PSP House 167 Watling Street West
Towcester, NN12 6BX
Phone: 
+1 1327 322410
Fax: 
+1 1327 322412
Email: 
psp@pspeur.org
Resources and Services Provided
Languages spoken: 
English
Printed materials available in: 
English
Information provided for: 
Affected individuals
Health care professionals
Care providers
Families of affected individuals
The public
Teachers
Legislators
Media
Students
Researchers
Other
Range of services include: 
Referrals to local chapter or group
Referrals to research studies
Referrals to matching individuals/families
Medical referrals
Grief counseling
Referrals for non-medical services
Non-medical services
Crisis intervention
Other
Awareness programs
Political action
E-mail list
Telephone helpline
Clinical or treatment centers
Speakers
Training
Advocacy
Other
Educational materials include: 
Fact sheet(s)
Magazine
Video(s)/Movie(s)
Slides
Journal articles on condition
Pamphlet(s)
Booklet(s)
CD Roms
Research updates
Newsletter
Bibliography
Resource guide
Website
Other
Conferences/workshops for: 
Affected individuals and/or families
Researchers
Professionals
Other
Financial assistance for: 
Other
Combined Federal Campaign (CFC)
#80146
4301 Connecticut Avenue NW - Suite 404
Washington, DC 20008-2369
Tel: 202.966.5557 Fax: 202.966.8553
info@geneticalliance.org