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 Power Pedal for Rare Diseases

CSS patients are urged to send a message to Congress
CSS Related Research
Research studies from around the world
currently recruiting participants

The CSSA Welcomes New Medical Advisors

Dr. Maria Cid,
Dr. Carol Langford,
Dr. Philip Seo,
Dr. Stuart Levine
Dr. Curry Koenig, and Dr. Paola Sandroni have joined our Board.

 


In Our Own Words
Personal Stories
about CSS

Lynn Corwin and Tricia O'Hare write about their
experiences with this very rare disease.

Vasculitis Foundation funds CSS research
Dr. Jianguo Liu, St Louis University School
of Medicine, conducts new study
Churg Strauss Syndrome
Association Brochures

Free brochures help raise
awareness and explain CSS to
family and friends
Identifying genetic causes of CSS
A wonderful opportunity for CSS patients to participate in research

Mayo Clinic seeking additional patients
for important study


Rituximab in the treatment of Churg Strauss Syndrome
with renal involvement
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.