Hi, I’M Amy Rivera
Lymphedema NINJA
Winning The Fight Against Lymphedema Together
Hi, I’M Amy Rivera
Lymphedema NINJA
Winning The Fight Against Lymphedema Together
Our Story...
We are Ninjas Fighting Lymphedema — we are the strong ones.
We no longer hide in the shadow of Lymphedema...
Frequently Asked Questions...
You have questions... we have answers!
Our Story...
We are Ninjas Fighting Lymphedema — we are the strong ones.
We no longer hide in the shadow of Lymphedema...
Frequently Asked Questions...
You have questions... we have answers!
Mission
To educate our lymphatic community and medical professionals concerning the importance of early diagnosis, compliance, and resources needed to reduce the medical costs epidemic.
Vision
To bring awareness about the prevalence and devastating effects of lymphedema in our communities and inspire patients to stay compliant with treatments offered.
Mission
To educate our lymphatic community and medical professionals concerning the importance of early diagnosis, compliance, and resources needed to reduce the medical costs epidemic.
Vision
To bring awareness about the prevalence and devastating effects of lymphedema in our communities and inspire patients to stay compliant with treatments offered.
The Ninjas Foundation Story
Ninjas Fighting Lymphedema Foundation is a 501 (c) 3 founded by a lymphedema patient and spokesperson Amy Rivera. Amy was born with primary lymphedema but was misdiagnosed for over 30 years, leaving her disabled and isolated. She truly thought she was the only one who was suffering in silence. Amy realized that this community needed a voice and she established this foundation with clear goals in mind.
Testimonials
Follow Our Journey On Instagram!
You are not alone. Let's make a change together.
Here at Ninjas Fighting Lymphedema, we partner with you to help you navigate this difficult path, making living with your condition easier and more manageable.
Winning Our Fight All Around The World!
With the exponential growth of technology and support, we are reaching the unreached lymphedema community one pin at a time.
