OUR STORY BEGINS WITH AMY…

Amy Rivera created the Ninjas Fighting Lymphedema Foundation to provide support, education, and advocacy for individuals affected by lymphedema. After her own diagnosis with lymphedema, Amy turned her personal challenges into a catalyst for advocacy and education.

She recognized the need for more resources and a community that could empower those living with lymphedema, helping them to not only manage their condition but also thrive despite it.

The mission of Ninjas Fighting Lymphedema Foundation is to empower individuals affected by lymphedema through education, advocacy, and community support. We strive to raise awareness about this often misunderstood condition, promote early diagnosis and effective treatment, and provide essential resources to improve the quality of life for those living with lymphedema.

Through our initiatives, we aim to create a connected and informed community where no one has to face lymphedema alone.

The foundation serves multiple purposes:

Support and Community: It offers a space where individuals with lymphedema can connect, share experiences, and receive emotional and practical support.

Education: By providing educational resources and programs, the foundation helps both patients and healthcare providers understand the complexities of lymphedema, promoting better management strategies.

Advocacy: Amy’s foundation also advocates for greater awareness and research into lymphedema, pushing for better treatment options and insurance coverage.

Through these efforts, Amy aims to enhance the quality of life for those dealing with lymphedema and to foster a supportive community where members can find encouragement and information.