WELCOME TO THE PBCERS!


Primary Biliary Cirrhosis (PBC) is NOT a death sentence.....There is LIFE after PBC diagnosis!


BEFORE JOINING PLEASE READ: NEW subscribers must be approved. Please let us know if you are a PBC/other liver disease patient, family member or friend when subscribing. NO Webmasters!

If you read online, please set to "Special Notices" NOT No Mail.

We are a Moderated Group. E-MAILS to the group and pictures must be approved by one of our moderators. After e-mail is approved it will be added to the next PBC daily digest. Approved pictures will be added to our picture site. The PBC Daily Digest is mailed between 5 - 10am daily.

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"Facebook" PBCers Organization Page
https://www.facebook.com/pages/PBCers-Organization/146541062382

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The Primary Billiary Cirrhosis Organization aka PBCers is a wonderful source of support and education for PBC patients, family members, friends and other autoimmune liver disease patients. Formed in 1996, the PBCers is the largest online PBC support group with almost 3,000 members worldwide.

As a group, we discuss medical information, pain management, medications, research, ask questions, transplantation, vent our anger & fears, speak freely on the ups and downs of daily living, share our personal experiences and build lasting friendships.

The PBCers offers various areas of support such as the PBC daily digests, message board, doctor& chatroom. Our main website is located at http://pbcers.org

We are NOT medical professionals. Please consult a doctor about your medical condition before making any changes in your daily living and or treatment plan.

The PBCers Organization is a tax exempt public charity under section 501 (a) of the Internal Revenue Code.