Combined Total: $

updated 12:00 am MST 10/16/26

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Team Legacy | Total: $100

3% Cover the Fee

Team Legacy is raising money in honor our of BFF warriors that unfortunately lost their lives battling lymphedema. They were gone too soon, but will never be forgotten.

Team Camp Watchme | Total: $100

3% Cover the Fee

Team Camp Watchme: "This team is made up of CLT's, patient advocates, campers, company reps, and camper families that have seen the incredible benefits of Camp Watchme and all the resources it provides. Join us by making a contribution to our towards this life changing Camp!"

Team Brylan | Total: $250

3% Cover the Fee

Team Brylan is fundraising to ensure the continuation of life changing treatment and education. Our goal is to give more families access to the proper care needed to fight lymphedema and help create an even bigger community for a brighter future for all pediatric lymphedema warriors.

Team Kate | Total: $100

3% Cover the Fee

Team Jeffrey’s Army | Total: $100

3% Cover the Fee

Team Jeffrey's Army: "This team honors Jeffrey Serro, a 6 year old with primary lymphedema. Jeffrey became a recipient of Brylan's Feat Foundation in September 2020, at 6 weeks old. BFF provided a CLT that taught his mom how to apply short stretch bandages and MLD therapy. His family is excited to raise awareness of Lymphedema, and fundraise to support Jeffrey and lymphie kids all around the world. He has attended Camp Watchme in the past and is excited to attend next summer."

Team Amiya| Total: $100

3% Cover the Fee

Team Amiya: "We have had life changing experiences at camp and want to continue to contribute to furthering BFF's mission in any way we can."

Team Super Sangers| Total: $100

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Team Super Sangers: "The Super Sangers are part of three generations of men with primary lymphedema. BFF is important to us as it has helped give us resources and assistance while we continue to navigate this lifelong management of this disease."

Team Dad Jokes| Total: $100

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Team Tratar| Total: $100

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Team Tratar: "We are supporting Brylan's Feat Foundation because Brylan is our niece and we have seen first hand how difficult living with lymphedema as a child can be, even with the advantage of good medical care. Seeing the kids all over the world that are unable to have access to necessary treatment fuels our teams fundraising efforts!"

Team Sid & Kyle| Total: $100

3% Cover the Fee

Team Universal Lymphies| Total: $100

3% Cover the Fee

Team Universal Lymphies: "Ally, Sandra and Nina are teaming up again! I can explain more...but 2 words sums it up pretty well: Doggy Delights. Ally pours her heart and soul into baking dog treats in order to advocate and raise money all summer long."

Team Drew’s Crew| Total: $100

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Team Drew's Crew: "Brylan's Feat Foundation is incredibly important to our family, especially Drew. We would be lost without their guidance, support, and treatment options over the years since Drew's diagnosis. Not only have we learned so much about her chronic illness, and management, but also have a community we with total support behind one another. She has built lasting friendships at the age of 9. Please consider donating in support of their mission to provide direction, treatment, and support to children with lymphedema..."

Team For The Love Of Camp| Total: $100

3% Cover the Fee

Team For The Love Of Camp: "We're teaming up to raise funds for Bryan's Feat Foundation and Camp WatchMe, two organizations that have made a lasting difference for many kids living with lymphedema, especially for us personally. Why this matters to us: Arianna is 15 and lives with lymphedema. For her, Bryan's Feat Foundation and Camp WatchMe have been so much more than a program. They've been a source of support, understanding, and community, a place where she can be herself and feel less alone in managing a condition that many people have never heard of. Lindz represents Thuasne and visits Camp WatchMe to introduce new products designed to help kids with lymphedema. She has seen firsthand how the right tools and a supportive community can make a real difference in a child's confidence and daily life. Our paths crossed at camp, and we decided to join forces. Every dollar we raised will: Help Bryan's Feat Foundation and Camp WatchMe Provide products and resources for children with lymphedema Support camp programming that brings kids and families together Continue giving children a place where they feel understood and encouraged How you can help Please consider donating, no matter the amount. Every gift makes a difference. If you can't give right now, sharing this page with friends, family, and coworkers helps just as much. Thank you for being part of Team Arianna & Lindz. Together, we can help kids with lymphedema feel supported, confident, and strong."

Team To Wisconsin & Beyond| Total: $100

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Team To Wisconsin & Beyond: "Brylan's Feat Foundation and Camp WatchMe provide support for kids with lymphedema across North America and around the world, connecting patients, parents and therapists with garments, equipment and education. As a CLT in the Midwest and 3 time Camp volunteer, I have seen first-hand the benefits that Camp and BFF bring to families. Donations to the Foundation help provide garments and equipment, advance standards of care and spread the word about pediatric lymphedema."

Diego’s Team| Total: $100

3% Cover the Fee

Diego's Team: "Hi i’m Diego mother, my name is Elena. Diego has lymphedema on leg. I am with your association for help and support this condition. In Italy its bad for this problem and support. Thank you! Elena"

Team Sophers| Total: $100

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Team StopMySwelling| Total: $100

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Team Madelyn’s Warriors| Total: $100

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Team Madelyn's Warriors: "My daughter was a first attendee for attending for camp watch me, this year and it has changed our lives tremendously in such a good way and has brought so much positive light when it comes to our daughter Madelyn. I have learned so much as a mother on how to help her, I’ve always had so many questions about this disease and just how to do it, and taking what I learned to help my daughter for her future has made a huge impact in progress with her lymphedema."

Team ILWTI | Total: $100

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Team ILWTI: "We are International Lymphedema and Wound Training Institute and Lymphedema is our world! I love these kids and foundation so much and want to encourage them to lymphedema community to support and love them as well!!!"

Team Lucie| Total: $100

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Team Lucie: "Lucie has been going to Camp WatchMe for two years, and it has completely changed her life. She went from struggling everyday to accept her diagnosis to taking responsibility for all aspects of her care thanks to camp. She even has a goal to become a Certified Lymphatic Therapist so she can help kids with the same diagnosis."

Team Lymphie Life| Total: $100

3% Cover the Fee

Team Lymphie Life: "I love the BFF and Camp Watchme community, and want to support their efforts in improving the lymphie lives of children around the world."

Team Hippie Guy | Total: $500

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Team Hippie Guy: "I am fundraising to support my granddaughter, Bry, and make sure that all her lymphedema friends get the treatment and community they deserve. Bev and I have been to Camp Watchme for the past two years and it was an experience of a lifetime."

Team Charlotte’s Army | Total: $300

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Team Charlotte's Army: "Brylan’s Feat Foundation has provided immeasurable support and knowledge along our lymphedema journey! BFF has been a blessing to so many and we are passionate to help it continue to bless many more primary lymphedema warriors!"

Team Superhero | Total: $100

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Team Superhero: "We have fundraiser for Brylan’s Feat since we found out about my son’s rare condition in his leg-present at birth. We have navigated many similar obstacles and hurdles and faced similar triumphs as I am sure many families impacted by pediatric lymphedema. It is challenging finding a related community for my son so this is a wonderful cause that is close to the path we are currently on."

Team Lucille | Total: $100

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Team Lucille: "We want to help raise money for this awesome organization, who are making such a difference in the lymphedema community especially for kids!"

Team Positive Purpose | Total: $100

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Team Positive Purpose: "I am Brylan's grandmother. Supporting her in the fight for lymphedema gives me a sense of purpose and pride, knowing I'm helping her create a positive impact on other children suffering from lymphedema."

Team Hero Huddy | Total: $100

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Team Hero Huddy: "Both my son and I were born with a rare genetic lymphedema disorder, we face life and all things lymph together! We are strong, able, and confident!"