We provide education, community, and advocacy to raise awareness, improve treatment, and uplift those affected by lymphedema—because no one should navigate it alone.
We provide education, community, and advocacy to raise awareness, improve treatment, and uplift those affected by lymphedema—because no one should navigate it alone.
At The Rivera Foundation, we believe no one should face lymphedema alone. Through focused education, compassionate support, and community-driven advocacy, we help individuals not just manage — but thrive.
We know that every journey with lymphedema is unique. Whether you're newly diagnosed, seeking clarity, or supporting a loved one, you don’t have to walk this path alone. Our purpose is to stand beside you with education, support, and unwavering community.
Everyone’s journey is different — but no one has to walk it alone. These voices from our community show the power of education, connection, and healing.
At The Rivera Foundation, we believe no one should face lymphedema alone. Through focused education, compassionate support, and community-driven advocacy, we help individuals not just manage — but thrive.
We know that every journey with lymphedema is unique. Whether you're newly diagnosed, seeking clarity, or supporting a loved one, you don’t have to walk this path alone. Our purpose is to stand beside you with education, support, and unwavering community.
Everyone’s journey is different — but no one has to walk it alone. These voices from our community show the power of education, connection, and healing.
We believe lymphedema should never dim your light. Through education, encouragement, and empowerment, we help you move forward with purpose.
We believe lymphedema should never dim your light. Through education, encouragement, and empowerment, we help you move forward with purpose.
The Rivera Foundation began as Ninjas Fighting Lymphedema Foundation — a movement born from Amy Rivera’s personal journey with lymphedema.
After living undiagnosed for years, Amy turned her struggle into a mission: to educate, advocate, and empower others navigating the same path. What started as a bold effort to raise awareness has grown into a trusted foundation focused on helping individuals not only manage lymphedema — but thrive through it.
Today, The Rivera Foundation continues that work, creating a space where compassion, knowledge, and community meet.
The Rivera Foundation began as Ninjas Fighting Lymphedema Foundation — a movement born from Amy Rivera’s personal journey with lymphedema.
After living undiagnosed for years, Amy turned her struggle into a mission: to educate, advocate, and empower others navigating the same path. What started as a bold effort to raise awareness has grown into a trusted foundation focused on helping individuals not only manage lymphedema — but thrive through it.
Today, The Rivera Foundation continues that work, creating a space where compassion, knowledge, and community meet.
There are many ways to be part of The Rivera Foundation’s mission to win our fight against lymphedema. Whether you're a parent, a provider, a patient, or a passionate advocate — there's a place for you here.
As a member, you’ll receive early access to resources, invitations to special events, exclusive updates, and the opportunity to directly influence our programs and outreach efforts.
Become a volunteer, ambassador, or board chair. Help us grow our movement and raise awareness in your local community.
We collaborate with clinics, nonprofits, and health organizations to expand our reach and impact.
Stay informed with the latest stories, medical advancements, and foundation updates — because awareness fuels action.
Access our growing directory of trusted physicians, certified lymphedema therapists (CLTs), and care teams who understand the unique needs of those living with lymphedema.
The Rivera Foundation is committed to building a world where no one faces lymphedema alone. Through education, advocacy, and community support, we’re creating resources that empower individuals and raise awareness around this often-misunderstood condition.
Your donations help us:
Develop and distribute accessible educational materials
Host support groups and outreach events
Advocate for better care and earlier diagnosis
Expand our reach to underserved and overlooked communities
We may not do this alone — but together, we will win our fight.
No matter how you show up, your support helps us win our fight against lymphedema. Hear the stories, and take your next step today.
Email:[email protected]
Site: www.winourfight.org