After a year, a definitive diagnosis

Hi! I’m Michelle. Not technically a new member because when I joined almost a year ago, I wasn’t diagnosed, only given the possibility of PSC. Fast forward to yesterday and an appointment with a transplant surgeon. She has given the diagnosis. :frowning:

Right now I’m in the early stages, and another round of tests is coming to see the progression (if any) from last year.

I have been keeping up with questions posted here and am grateful to have this group. Thanks to you all! =)


Welcome to the club!

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Hi Michelle. Glad you posted and gave us an update on how you are doing. We are here for you anytime for any question or need we are able to meet. Be assured of our support as you make your way through this PSC journey. Continue to live your life to its fullest, make your plans for the future. Your body will tell you when you need to rest or slow down. Otherwise just ignore the PSC the best you can and be yourself! We will be here when you have a need. Keep in touch.


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