If you didn't get to attend the PSC Partners Conference, you're in luck! All sessions are posted on their website. The research is exciting and progress toward better treatment and a cure is being made!
As part of GLI’s A3 Spring Advocacy Day, I am sharing my story alongside other liver advocates to ensure that liver health is rightfully part of the US public health agenda. https://t.co/4NKqi6EpWd
Thank you for highlighting that the lack of funding of COVID bill "means that millions of vulnerable citizens will be left to fend for themselves. ..But it seems lawmakers are willing to relegate [IC}to continued fear & prolonged isolation." @Dorry_Segev@benryanwriter@SherylNYT
New Episode with @Author_LB! Laura shares about her journey to transplant, healing with her family, and how writing grounded her. https://t.co/EjVwVhWtGr
🚨Don't miss this important date!
🔎PSC is an infrequent disease that may severely impair patients' lives!
🔬There are so many things still to do! Let's work & fight together!
@PSCPartners @PSCSupportUK@EuropeLiver#LiverCancerAwarenessMonth#aeeh4LC
Primary Sclerosing Awareness Day is Oct 29. In this episode, Nicola finds meaning in advocacy after her transplant, post-transplant pregnancy, and surrogacy journey. #pscaware#liver#livertransplant#podcast#surrogacy#patientadvocacy PC: Michelle Kirkby
https://t.co/8SIzD7Bysm
Had a great conversation with @NPR @TonyaMosley this afternoon. 5 full minutes of radio time talking about immunosuppression, organ transplantation, vaccines, and the immune system!
https://t.co/ksl6yMRWWx
The new CDC vaccinated people guidelines do NOT apply to immunosuppressed/transplant patients. The fact that the CDC does not clearly say that is irresponsible. Seems it's our job to spread the word. Please do.
@PSCMami brings you stories at the intersection of primary sclerosing cholangitis (#PSC) and #parenthood. Hosted by Monika Aldarondo, PSC Mami gives perspectives on life with IBD and PSC from parents and caregivers. Find PSC Mami in any podcast app. https://t.co/y0mUiHeTdY
It is such an honor to hear, hold and share each story. Alicia Meyers shared about her experience with PSC and I am so grateful. I hope you are able to find something (or many things) that resonate with your own journey, as I did.
https://t.co/nomStj3XTl
I have loved "moving" across the USA with my team of PSCers and liver transplantees. 200 miles to go so we need 200 donors to finish our Race to the Cure fundraiser! https://t.co/VPt4pTL9pJ