Nemours’ Post

Join us for part 2 as we talk with Casana Fink, who knows she wants to be a living organ donor at some point, but isn't sure on the right timing. In this episode of 🎙 hashtag#TransplantTalks we talk through this decision with Casana. We discuss the differences between living kidney versus liver donation and explore various concerns and considerations for each. Watch https://lnkd.in/e3wKZCAC @american_transplant_foundation 💚💚💚

Can't believe it's been 7 whole weeks since I started 30 Under 30! And 2 weeks since my 27th birthday! While the new friends and professional development are a huge bonus, the most important and fulfilling part of this program is fundraising for Cystic Fibrosis Foundation - Tennessee Chapter. It would mean the world to me to see you at one of my upcoming events (June 18th happy hour at Ole Smoky or the celebration on August 10th!), but I would be especially grateful if you would donate to my campaign and help me reach my $5,000 fundraising goal. Might I suggest $30 to celebrate my Top 30 Under 30 status or $27 for my 27th? Maybe $300 to celebrate the fact that I have 3 more years of being under 30 left? Some more info on CF and the foundation: Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.

The Gift of Life ❤️ In a few short weeks, our second Cardiac Surgical Mission of 2024 is touching down in Ukraine with Global Cardiac Alliance! By donating to CCI, you help ensure that as many children as possible can be treated for life-threatening congenital heart defects, such as 'Chernobyl Heart'. https://lnkd.in/eWV69Y3z

Every journey is unique, and every story holds the potential to inspire, uplift, and connect us all. 💖 Whether you have received blood, are a regular blood donor, or have been touched by organ and tissue donation, your story has the power to touch hearts and change lives. Share your story today: https://bit.ly/3IuHECm

Statistics are not simply numbers, they are lives changed with the chance at a different ending. Learn more about organ eye and tissue donation at lifepassiton.org and register to be a donor.

Join us for part 2 as we talk with Casana Fink, who knows she wants to be a living organ donor at some point, but isn't sure on the right timing. In this episode of 🎙 #TransplantTalks we talk through this decision with Casana. We discuss the differences between living kidney versus liver donation and explore various concerns and considerations for each. Watch https://lnkd.in/e3wKZCAC @american_transplant_foundation 💚💚💚

An unforgettable experience and a complete Institute for Advanced Analytics effort. Watch the video in my blog post below to learn about the adventure!

Show your love this Valentine’s Day by supporting lupus awareness and education! Please consider honoring your loved one affected by lupus by donating. Your gift of $25 or more will help us provide research to ultimately find a cure, educational opportunities for those living with lupus, and spread awareness. As a nonprofit organization, Lupus Foundation of America, North Carolina Chapter relies on the generosity of our community to support those living with lupus by: • Developing safer and more effective treatments for the multiple symptoms of lupus. • Giving those affected by lupus access to educational programs that include pertinent medical, emotional and wellness topics, many led by medical experts. • Providing access to the Lupus Foundation of America, North Carolina Chapter emergency funds, for people living with lupus. Because lupus is a complex disease, it affects people’s daily lives. Many are unable to work and require assistance with paying for things such as durable medical equipment, utilities, housing, medications, and transportation. https://ow.ly/Ankj50QANgv

Every journey is unique, and every story holds the potential to inspire, uplift, and connect us all. 💖 Whether you have received blood, are a regular blood donor, or have been touched by organ and tissue donation, your story has the power to touch hearts and change lives. Share your story today: https://bit.ly/3IuHECm

Every journey is unique, and every story holds the potential to inspire, uplift, and connect us all. 💖 Whether you have received blood, are a regular blood donor, or have been touched by organ and tissue donation, your story has the power to touch hearts and change lives. Share your story today: https://bit.ly/3IuHECm