We've got your back.
The goal of our advocacy program is to provide hope, share options, and allow for time for families to be families. A warrior's time should be spent with their people, not on the phone wrangling operators and waiting on hold.
Whether you're in search of a new oncologist, physician, clinician, prosthetist, need assistance in finding clinical trials and better treatment options, or you just need someone to talk to about your journey with sarcoma or amputation, we're here for you.
Our team will never offer our opinion as we are not medical professionals. Our goal is simply to provide warriors with resources, options, and support.
As Jenn fought her battle with sarcoma, she quickly realized how little support there was for people in similar situations. When she and her husband, Miles, started the Move For Jenn Foundation, they knew they wanted to provide resources to other sarcoma warriors.
As our team started to research the best treatment plans for those who reached out to our foundation, we soon started researching clinical trial opportunities because of an incredible little girl named Millie. When Millie's mom Claire, co-founder of the Mighty Millie Foundation, came to our team with the news that Millie's treatment for rhabdomyosarcoma was no longer working, we immediately began researching clinical trial options. From that moment on, in honor of Millie and the Mighty Millie Foundation, clinical trial research has been part of our Advocacy Program.
- Learn more about how our clinical trial support came to be.
Read a testament about our Advocacy Program from Millie's mom, Claire, founder of the Mighty Millie Foundation.