We can’t believe its been almost 2 weeks since the kickoff. It was more successful than we imagined and we are humbled by the love and support we continue to get from our friends and family as well as strangers touched by sarcoma. The documentary has been doing its job, telling the story of how we got here. Now we are full steam ahead pursuing research while we also get the word out to educate and find more like sara and Scott. We believe that while this sarcoma is rare it is often misdiagnosed and there are many others out there. We hope everyone that reads our blogs and follows us they will feel like a part of this movement to improve and save the lives of these children and young adults. Every dollar, every shared post and every conversation has an impact that will get us to the cure. Its out there, we believe we have found the puzzle pieces we need everyone on board to complete the puzzle. -Lennie
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An informative video by Sara’s mom, Lennie, recapping our meeting/tour at Memorial Sloan Kettering with leading sarcoma pathologist, Dr. Christine Antonescu, & researchers Drs. Vanoli & Fujisawa.
WATCH VIDEO HERE
POST AND COURIER ARTICLE
Our first mention in the news was a Post & Courier article about our Kick Off to Sara’s Cure Event that was posted on April 23rd, 2018.
POST & COURIER HEALTH ARTICLE
Thank you to Lauren Sausser and The Post & Courier for the health article written in the June 4th, 2018 paper. Your support of our 501(c)3 charitable organization is much appreciated.
LOWCOUNTRY LIVE INTERVIEW
We were thrilled to have had the opportunity to appear on Lowcountry Live to promote our Music Fest and tell people about our mission. Thank you to everyone at Lowcountry Live for the wonderful experience.
Sara’s Cure is a nonprofit 501(c)3 organization. Tax ID# 82-5445706. Copyright © 2018 Sara’s Cure – All Rights Reserved.