Collette spent almost 20 years going back and forth between different doctors and treatments, before she was finally diagnosed with PBC.<\/p>\n\n\n\n
\u201cIn those days there was no treatment; there was nothing,\u201d she says. \u201cI was told I had five to seven years or the option of a liver transplant.\u201d<\/p>\n\n\n\n
Given the lack of information, she put a listing in a national newspaper to find out if there were others living with PBC. She was inundated with responses from people who suffered personally or who had loved ones living with the disease.<\/p>\n\n\n\n
Determined to spread the word, she founded The PBC Foundation, dedicated to providing support and information to those affected by PBC.<\/p>\n\n\n\n
\u201cTo know that my situation has helped others in their PBC journey, is very precious to me,\u201d she says. \u201cAnd thanks to receiving treatment, I can now live my life.\u201d<\/p>\n","protected":false},"excerpt":{"rendered":"
Collette spent almost 20 years going back and forth between different doctors and treatments, before she was finally diagnosed with<\/p>\n","protected":false},"author":11,"featured_media":3537,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[436],"tags":[],"class_list":["post-3543","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-rare-disease","entry"],"acf":[],"yoast_head":"\n