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BE A PART OF THE CURE!

Cystic Fibrosis Research

What Are Clinical Trials?
Why Volunteer for Research?
Frequently Asked Questions

Research on the cause, biological mechanisms, new and better forms of therapy and, ultimately, the cure for CF is an important part of our CF Center activities. You can be an important part of that research! To find out how, call a research coordinator today!

Phone 650-736-0388 or email us to join the team!

Cystic Fibrosis ( CF ) is one of the most common genetic ( inherited ) diseases in America. It is also one of the most serious. It mainly affects the lungs and the digestive systems in the body, causing breathing problems and problems digesting foods. It is a chronic disease that currently has no cure.
Lucile Packard Children's Hospital The CF Center at Stanford, located at the Lucile Packard Children's Hospital, is an integrated disease management program that follows patients from diagnosis through adulthood.
With the current longer life expectancy for patients with Cystic Fibrosis, our clinic population includes patients of all ages. More than half the patients followed by the Stanford CF Center are adults aged 18 years or older.

For more information or an appointment please call    
650-723-5191
LPCH sign
CF Clinic Hours:
Adult Clinic: Tuesday, Wednesday, and Friday
      Adult Clinic Coordinator 736-1358

Pediatric Clinic: All day Tuesday and Friday
      Pediatric Clinic Coordinator 736-1359

Brian Burks
Nanotechnology

Brian Burks

KidArt KidArt
Children's art
reveals attitudes toward illness
Stenzels
Transplant Winners
Remember CF.DOC?
Read about the final results.

For those interested in donating to the CF Center at Stanford: checks should be made out to LPCH with notation on the memo line of the check "CF Research" or "CF Center". The check should be mailed to our office at 770 Welch, suite 350, Palo Alto, CA 94304.

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URL: http://cfcenter.stanford.edu    Sponsored by the Cystic Fibrosis Center At Stanford    Content from the CF Center staff
Last modified 07/21/2009