Info on the CLiC Database

CLiC Site Online
         The Web site of the Cholestatic Liver Disease Consortium   (CLiC) is up
and running, so now is the time to click on CLiC!   CLiC is a team of doctors,
researchers, and patient advocates   working together to improve the lives of
children and families   dealing with five rare liver diseases including AGS(!!!!).
CLiC exists to provide a way for patients and families to partner with   the doctors,
researchers, and patient advocates by participating in   research studies. The
greater collaboration that exists, the more   can be learned about cholestatic
liver diseases and the closer we   will be to finding new and better treatments.

         On the CLiC Web site, you will be asked whether you want to
  join the CLiC Patient Contact Registry. Please click YES!. Once
  you sign up, you will be informed of clinical research studies being
  conducted by CLiC and can decide which research studies you
  want to learn more about and whether you want to participate.
  The Contact Registry is free of charge and completely confidential.
  This is a fantastic way for CLiC to increase the patient research
  pool for AGS and for everyone with AGS to stay informed and
  contribute to research. Don't miss this opportunity to be involved!

  Go to the CLiC website now: CLiC Website Link

  The information presented on this web site is provided for information purposes
  only. This information does not constitute medical advice and it should not be
  relied upon as such. The Alagille Syndrome Alliance does not engage in the
  practice of medicine. Under no circumstances, does the Alagille Syndrome
  Alliance recommend particular treatments for specific individuals, and
  in all cases recommends that you consult your physician before pursuing
  any course of treatment.

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