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Ruby Steuart
Ruby Steuart
Hi! My name is Ruby Steuart and I’m 24 years old. I'm an emergency medicine physician assistant - a passion that was inspired by my life with cystic fibrosis. The hospital has always been a safe place for me and ever since I can remember I have had a great admiration for my entire care team. I want to help others the way they have helped me.
I am part of the 10%. The 10% who cannot take the life-changing, “miracle drug”, Trikafta, which was approved by the FDA in October 2019. Watching this drug absolutely transform some of my closest CF friends' lives has been an incredible experience! I have watched the hard work of the CF Foundation pour life into fellow CFers. I can’t help but feel overjoyed. I know, without a shadow of doubt, that the CFF will work tirelessly to support the development of a drug for our 10% and ultimately, a cure for all.
Throughout the years, my passion as a cystic fibrosis advocate has grown exponentially. My favorite days are the days in which I get to be deeply involved in advocacy and fundraising for the CF Foundation and the CF community. I love fighting this fight against CF with the most amazing fellow CFers, advocates, physicians, and researchers by my side. We are blessed to have people like you - so eager to support research and advancements in finding a cure for cystic fibrosis. Thank you to the Cystic Fibrosis Foundation and community for everything you have done and continue to do! Now let’s finish this fight!
I am part of the 10%. The 10% who cannot take the life-changing, “miracle drug”, Trikafta, which was approved by the FDA in October 2019. Watching this drug absolutely transform some of my closest CF friends' lives has been an incredible experience! I have watched the hard work of the CF Foundation pour life into fellow CFers. I can’t help but feel overjoyed. I know, without a shadow of doubt, that the CFF will work tirelessly to support the development of a drug for our 10% and ultimately, a cure for all.
Throughout the years, my passion as a cystic fibrosis advocate has grown exponentially. My favorite days are the days in which I get to be deeply involved in advocacy and fundraising for the CF Foundation and the CF community. I love fighting this fight against CF with the most amazing fellow CFers, advocates, physicians, and researchers by my side. We are blessed to have people like you - so eager to support research and advancements in finding a cure for cystic fibrosis. Thank you to the Cystic Fibrosis Foundation and community for everything you have done and continue to do! Now let’s finish this fight!
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