09/19/2025
What if your child was diagnosed with a chronic medical condition… and you quickly learned there were almost no resources to guide you?
Doctors with limited knowledge.
No treatment protocols designed for kids.
Therapists who can treat lymphedema, but not children.
This has been a scary reality for too many families, but Brylan's Feat Foundation has stepped into the gap—advocating, educating, and creating child-focused care protocols when none existed. We’re conducting our own research to prove the effectiveness of these approaches, with a paper recently published from data collected the past 5 years at Camp Watchme. We’re giving parents tools, knowledge, and hope where before there was only fear and uncertainty.
And we’re not stopping there. From programs like Camp WatchMe to ongoing education for providers, Brylan’s Feat Foundation is tirelessly working to make sure no child with lymphedema is left without care or community.
Brylan's Feat Foundation is not just changing lives, it’s changing the future of pediatric lymphedema care.
Join our mission and support children fighting lymphedema by donating to the Love For Lymphedema Annual Fundraiser.
1. Go to brylansfeat.org/loveforlymphedema
2. Choose a team and click the "donate to" button.
Donations of $50+, $100+, $250+, and $500+ are eligible for the corresponding raffle prizes!
