ALF NASH Day 2021 Statement
In September 2020, the American Liver Foundation held a virtual NASH roundtable to help address the unmet needs of those living with Nonalcoholic Steatohepatitis. From this discussion, we crafted a NASH Patient Bill of Rights to help patients work with doctors and their medical teams to achieve the best possible health outcomes. In this video, patient advocates read the document out loud.
Thursday, June 10th is International NASH Day, and we don’t want a NASH diagnosis leaving anyone feeling powerless. Although every person’s diagnosis and treatment plan are different, patients deserve the best treatment, and these rights can help one examine the best path forward. We hope that everyone feels inspired and empowered on their NASH journey! To read and download the document, visit our NASH Information Center: http://bit.ly/ALFNASHRIGHTS.
To join global efforts to raise awareness about NASH and take action to address this life-threatening disease worldwide, please visit the official International #NASHday page: https://www.international-nash-day.com/!
Last Updated on June 10, 2021
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