Brylan’s Feat Foundation

How One Mom Revolutionized Pediatric Lymphedema Care A mom’s story of creating two foundations and a camp for kids with lymphedema.

Camp Watchme is less than one month away and we truly could not host camp without the support of our incredible sponsors!
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Camp Watchme is the first and only summer camp in North America for children (ages 5-17) with lymphedema. Each child is encouraged to bring a parent or caregiver to join them. Camp Watchme allows children to have the quintessential summer camp experience, meet other children with the same disease as them, learn more about lymphedema, and receive treatment from certified lymphedema therapists. Parents receive invaluable education and emotional support through group sessions and get to see their children thrive.
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It is with great sadness that we share with our community the news that this brave lymphie warrior has passed away. At only a little over 2.5 years old, he has unexpected left us far too soon.
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Lumtha has been a true light and joy to watch grow and beat the odds for the last two years. Brylan’s Feat Foundation is honored to have been a part of his lymphedema fight and journey. Our prayers and condolences are with the Zonke family in South Africa.
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You will forever be in our hearts sweet Lumtha and a continued reminder of why we fight so hard to improve the standard of care for children fighting lymphedema worldwide
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🥳🎉Happy Birthday Betty Westbrook🎉🥳
If you haven’t wished this beautiful soul a very happy birthday, please do so! Not only is she a fierce lymphedema advocate (who never takes no for an answer), but she is also an incredible mom, entrepreneur, current student, the BEST business partner, and overall inspiring, strong, and resilient women! You do it all and BFF would not be the same without you. We love you ❤️
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There is only a few weeks left until our 2nd Annual Charity Golf Tournament benefitting the strongest lymphedema warriors, the kids! Click brylansfeat.org/golf to register your foursome today and check out our sponsorship opportunities!
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We have 3️⃣ foursomes still available❤️
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EARLY BIRD PRICING ENDS MARCH 31st!
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In celebration of lymphedema awareness month, we have discounted the price per player by 20%, only $180! Don’t miss out on this amazing price and sign up today!
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Sponsorships are still available. Please message us with any questions.
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I am looking for some companies who would love to contribute and sponsor our 2nd Annual Golf Tournament Links for Lymphedema located here in Scottsdale, Az.

This tournament help funds Brylan’s Feat Foundation which also puts on CampWatchMe which is the only camp in North America for children and their families who are affected by Lymphedema.

Some of you may know Brylan’s Feat Foundation was started because my daughter Brylan suffers from Primary Lymphedema. Each year we continue to grow and support more families all which cannot be done without our sponsors and donors.

If your company or someone you know might be interested please reach out to me directly.

Lymphedema is estimated to affect 250+ million people worldwide according to WHO data, with one third of those patients being of pediatric age.
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There is currently NO CURE for lymphedema. It will not simply go away and a child cannot grow out of it. Lymphedema is often ignored or neglected because of misinformation.
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Do your research, stick with the facts, and stay consistent with a treatment plan!
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Signs of lymphedema May include :

-swelling or pitting edema
-a feeling of tightness or heaviness in limbs
-restricted range of motion
-recurring infections
-hardening/thickening of the skin (fibrosis)
-aching or discomfort
-severe fatigue
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March 6th is WORLD LYMPHEDEMA DAY!
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March is Lymphedema Awareness Month! Throughout the month, we will be sharing lymphedema facts as well as testimonials from our amazing CLT’s, lymphie parents, and of course a few of our strong, fearless warriors💙
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We will also be raising money this month through social media as we do every March specifically for Camp Watchme, the first and only summer camp for pediatric lymphedema patients in North America.
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If you or someone you know have been affected by pediatric lymphedema and need assistance with treatment and/or education, please contact us. We have recipients in 28 countries and counting!
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1 in 10 Americans Are Living With A Rare Disease
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Lymphedema Is Associated With Over 40 Rare Diseases
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Come out and enjoy a day on the course while supporting a great cause at our 2nd Annual LINKS FOR LYMPHEDEMA Charity Golf Tournament benefitting children fighting lymphedema💚
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Sign up before the end of March to receive *Early Bird Pricing: 20%off*
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⛳️ brylansfeat.org/golf ⛳️
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📣 hey BFFs, this is Betty, and I wanted to tell you a story…

Many of you have experienced yourself what I’m about to say and if that’s you, be sure to leave a comment or send your own heart felt thank you to .

Not only is Brittany the Founder and CEO of this world class nonprofit, my partner in , and a listening ear to parents all over the globe. She’s a fierce advocate for children and their parents to receive education, treatment, and confidence to live the best life possible.

What we don’t see much on this page is how she is a wife to her high school sweetheart, mother to *FOUR* very busy and brilliant kids, she coaches soccer, plays on her own soccer team, continues to be there for her sisters, cousins, parents, and neighbors despite her own growing list of “to-do’s”.

Does she need a vacation? Yes. Will she take one? No, because she’s got priorities that include being at her kids tournaments, producing evidence based treatment for children thriving with Lymphedema, and believing that one day all of this hard work will pay off for generations to come.

In the mean time, if you have experienced her super power of listening, loving, and leading send her a HBD 🎂 message or DM her just how she has personally impacted your life. ♥️

Mark your calendars! We will be back at the YMCA of the Rockies in Estes Park, Co in July, 2024.
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Please visit brylansfeat.org/campwatchme for more info and/or to register on November 13th
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#2024

The 2023 Love For Lymphedema Fundraiser is officially over and we are so incredibly grateful to each one of our donors and sponsors for their generosity!
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This was our first year running the fundraiser completely in-house and we are so excited to have had such great support.
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A huge congratulations to the winning team, LymphieLove! And to the raffle winners as well.
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There is an estimated 80+ million children fighting lymphedema worldwide. As the first and only nonprofit specific to pediatric lymphedema, we strive to provide resources to ensure best management and proper care of lymphedema.
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There is a little over 5 days left to join our efforts by making a contribution to the Love For Lymphedema Fundraiser. Link in Bio or visit brylansfeat.org/loveforlymphedema
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Would you like to support children fighting lymphedema like this cutie? brylansfeat.org/loveforlymphedema
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Brylan’s Feat Foundation is dedicated to providing assistance to pediatric lymphedema patients around the world with invaluable and life changing treatment and education.
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Please join our mission by making a donation to our Love For Lymphedema Fundraiser. We greatly appreciate your contributions, which allow us to continue to reach more children so that they have access to proper care.
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The 5th Annual Love For Lymphedema Fundraiser is LIVE! brylansfeat.org/loveforlymphedema
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This fundraiser is our main funding source to continue providing our two main programs.
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1️⃣TREATMENT RECIPIENTS…
Pediatric patients around the world use Brylan's Feat Foundation as a resource to provide life changing treatment. Including financial assistance and access to custom garments, bandaging supplies, therapy sessions, surgical procedures, and pneumatic pumps.

Lymphedema education is one of the main pillars of Brylan’s Feat Foundation. Recipient caregivers are directed by certified lymphedema therapists virtually to ensure proper care.

2️⃣ CAMP WATCHME…
An event for children with lymphedema to have the quintessential summer camp experience, meet other children with the same disease as them, learn more about lymphedema, and receive treatment from certified lymphedema therapists. Parents receive invaluable education and emotional support through group sessions and get to see their children thrive.

Volunteer certified lymphedema therapists (CLT’s) have the unique opportunity to work with pediatric patients and collaborate with other clinicians from around the country.
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Go to brylansfeat.org/loveforlymphedema and choose a team to donate to. Thank you in advance for your support!
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*START DATE POSTPONED*
We will begin out 5th Annual Love For Lymphedema Virtual Fundraiser on September 25th, 2023 and will close on October 16th, 2023.
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Sign Up To Be A Team Captain 👇🏻
www.brylansfeat.org/loveforlymphedema
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We are excited to host our annual Love For Lymphedema Fundraiser beginning next month.
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This is a virtual fundraiser which means everyone can get involved.
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Sign up to be a team captain today and support the youngest lymphedema warriors ($100 minimum)♥️
brylansfeat.org/loveforlymphedema
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As we reflect back on THREE sessions of Camp Watchme just a few weeks ago, we want to extend a huge thank you to our incredible CLT’s (certified lymphedema therapists) that volunteer their time and truly go above and beyond for our campers! And of course, our fantastic sponsors who partner with us to help this very vital resource for pediatric lymphedema patients continue growing and thriving!
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As we begin our first full day of Camp Watchme 2023 Session 1, we want to thank our AMAZING sponsors who help us bring this wonderful resource to life for pediatric lymphedema patients and their families♥️
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#2023

A smile so contagious it deserves to be beautifully remembered. Please join us as we mourn the passing of Muhammad Abidzar, age 5 from Indonesia.
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Our hearts our heavy and our tears have not stopped since learning of this devastating loss. Brylan’s Feat Foundation appreciates your condolences for his family. It has been our greatest honor to provide ongoing assistance, resources, and support to the Abidzar family. Our team of administrators, CLTs, and community partners have grown to love this family passionately and are taking the news hard.
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“We will continue to put our best feat forward and push for pediatric lymphedema patients in Muhammad’s memory. Muhhamad will be honored and celebrated for his courageous fight against this disease.” -Brittany and Betty
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Two weeks ago, Founder and Medical Advisor had the privilege of speaking at their first international conference, in Nottingham, England.
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The experience was absolutely unforgettable as they were able to share about BFF and our resources while meeting the top leaders in the lymphedema community from around the world.
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But the best part was meeting THREE BFF recipients and their parents! With recipients in 26 countries, it has always been a dream to meet the families our organization supports and BFF is so grateful to have had this opportunity♥️
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A few weeks ago we hosted our Inagural Links For Lymphedema Golf Tournament in Scottsdale, Az and it was absolutely amazing!
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A huge thank you to all our golfers, sponsors, and the wonderful staff at for making it such a fun day supporting children fighting lymphedema.
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Our First Annual Golf Tournament is coming up on May 19th in Scottsdale, Az. Come on out and support the only nonprofit in the world specific to pediatric lymphedema💚 brylansfeat.org/golf
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Come support children fighting lymphedema just like these two Camp Watchme golfers💚
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Starfire Golf Course in Scottsdale, Az
brylansfeat.org/golf
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