Welcome to...

the official web site of the Churg Strauss Syndrome Association. We are a nonprofit organization dedicated to supporting and educating patients and their families who are afflicted with Churg Strauss Syndrome.

The CSSA works toward raising public awareness about CSS and provides assistance in understanding the disease and treatment process. We hope to stimulate and support research into the cause and cure of Churg Strauss Syndrome.

The material provided by the Churg Strauss Syndrome Association is for information only and should not take the place of advice or guidance from your own healthcare providers. Be sure to check with your doctor about all aspects of your medical care.

FAQ - here you will find a list of Frequently Asked Questions that might help answer your questions about CSS.


Vasculitis Foundation Symposium

2008 VF Symposium from perspectives of CSSers
Alicia Perkovich and Suzanne DePaolis
CSS Related Research
Research initiatives from around the world
currently recruiting participants

Universtity of Utah Establishes New Vasculitis Center

Dr. Curry Koening appointed to lead
initiative to
create first Vasculitis Center in the western USA.

 


In Our Own Words
Personal Stories
about CSS

Chris Griffin's story, CSS and kids by Suzanne DePaolis
and CSS from Alicia (patient)
and Brian (spouse) Perkovich's perspectives

CSSA and the CSSISG
Reaching out to Patients
All Around the World
Churg Strauss Syndrome
Association Brochures

Free brochures help raise
awareness and explain CSS to
family and friends
VCRC opens Clinical Sites in Canada
Toronto and Hamilton sites enrolling CSS patients in studies
Vasculitis Awareness Week


Awareness week is September 21st - 27th.
Read how you can help!

Membership List
Membership in the CSSA is free and has many benefits.

eXTReMe Tracker


Local contacts for CSS patients
Holland Greece France Belgique Italy Ireland Swiss Germany UK Spain
Norway Sweden Denmark Australia New-Zealand Japan Canada USA Czech-republic Brazil


About the CSSA | About Churg Strauss Syndrome | Research Articles | Helpful Links | VCRC Patient Registry
News Archives |
Patient Story Archives | Focus on Research Archives | Membership and Donations | Contact Us

Questions? support@CSSAssociation.org - Phone: 413-862-3636
CSS Association, PO Box 671 Southampton, Ma 01073-0671
© 2003 - 2006 CSS Association, All Rights Reserved.