WELCOME TO THE PBCERS!


PBC is NOT a death sentence.....There is LIFE after PBC diagnosis!


BEFORE JOINING PLEASE READ:

To keep in line with our original group mailings, we request all new subscribers set their Yahoo MAIL SETTINGS on "Digest Format", not individual e-mails. NO Webmasters!

Using Yahoo's new "fully featured" e-mail format makes it easier to reply to the group's digest.

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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, quarterly newsletters, 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.

To avoid spam and other unwanted postings, ALL E-MAILS must be approved by one of our moderators (Linie Moore, Linda Lynch, Sandra Stoddard, Diana Watson or Jean Haynes). PBC Daily Digest is usually mailed between 5 - 10am daily.

The PBCers Organization is a tax exempt public charity under section 501 (a) of the Internal Revenue Code as an organization described in section 501 (c) (3).

PBCers Organization
1430 Garden Road
Pearland, TX 77581

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PBCers chatroom & schedule http://pbcers.org/chatroom.htm

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