TESTIMONIALS:
HEAR FROM THE NINJAS COMMUNITY
“I'm so grateful for Ninjas Fighting Lymphedema Foundation. I’ve had lymphedema since 2001, but hadn't had treatment because I couldn't afford the compression sleeves. I finally was able to get lymphedema therapy and my therapist contacted Ninjas about getting the sleeves. It only took a few weeks til I had the sleeve and everything I needed to treat my lymphedema. Amy and Ninjas made sure I had the correct size. The swelling has gone down a lot. Thank you so very much.” - MA
“This is an amazing organization that raises awareness and steps up to the plate for people who need help living their best life fighting something that can be so draining. I appreciate them so very much. And thank them from the bottom of my heart!” - SG
“This organization helped me getting help with my compression garments to aid me with my lymphedema when nobody else would help me.” - FG
“I struggle with primary lymphedema in my lower legs and at one point was struggling financially to the point that I was unable to afford replacement compression wraps and stockings. Amy at Ninjas Fighting Lymphedema, worked closely with me to make sure that I received the compression equipment that I needed as quickly as possible. My legs and body were able to get the care they needed and that also helped my mental health. I am so thankful for Amy and NFLF.” - AH
“I needed a new compression sleeve after having mine for over a year and it was falling apart at the seams. Without a sleeve that fits properly it is impossible to live an active lifestyle much less do daily tasks as simple as washing dishes. Ninjas Fighting Lymphedema Foundation stepped up and quickly purchased a sleeve for me. I am so thankful for their generosity and kindness. I would still be in my old ratted sleeve because I just don't have the money for a sleeve in my budget. They are an amazing organization that raises awareness and steps up to the plate for people who need help living their best life fighting something that can be so draining. I appreciate them so very much. And thank them from the bottom of my heart!” - SG
“I am so grateful for the Ninjas Fighting Lymphedema Foundation and their founder Amy Rivera. Amy goes above and beyond to help those of us struggling with this disease. She is always willing to explain her struggles that she has endured with this as well as provide people like myself who had nowhere to turn to look for the answers I needed regarding this disease. Amy has always been willing to provide me with the resources I have needed for my lymphedema. She is a blessing to us all. Thank you Ninjas for doing all you do for us fellow lymphies. You rock!” - TB
“I’m a single mother of four and I have secondary Lymphedema in my left leg. I have suffered with this condition for over 10 years getting misdiagnosed by doctors and under treated. My leg began to deform in shape and form a lobe that was so swollen it covered my feet and was extremely pain to touch, unbearable to stand or walk. It was also painful to watch. I inboxed Amy and after hearing my story and seeing my leg, Amy and her organization got me the medical help I needed. They got me proper compression, talked to me and cared for me.” - CW
“An amazing organization that has paid for compression stockings that would have been difficult for me to afford. I'm very grateful.” - MR
“This is an incredible foundation with a great purpose. The founder has a huge heart for the patients affected by Lymphedema, and understands first hand what the patient struggles can be like. This is a wonderful foundation to work with, and is providing hope to many!!” - TB
“I was misdiagnosed for 10 years. When finally diagnosed, my lymphedema was out of control. When I priced the wraps that are properly used for lymphedema they were pricey and insurance would not pay for them due to them not being deemed a necessary article. So I had seen where Amy Rivera had fought with it most of her life and started a non-profit to assist with lymphedema and helping to purchase wraps. She and NFLF is a god send, and without them, I would still be struggling.” - AZ
“I saw Amy Rivera's video on YouTube. I researched and found her foundation's website. I made a call and was told Amy would personally call me back. Living in Canada, I was doubtful. Well, a week later - Amy called and is personally helping me. A reduction kit has been ordered by her foundation. After 7 years of no hope, not only is there hope...but possibility of recovery! Thank you Ninjas!” - JD
“I can not express my love and feelings for this organization. I am a senior with limited income and with the unfortunate issues of this disease not being a covered item from Medicare, it has been impossible to get the needed items to maintain the disease of lymphedema. If they did not help me I would be unable to buy the custom compression hose or the pump, I thank Ninjas for their ability to help others with such compassion.” - JK
“I am so grateful that I had a friend introduce me to Amy, the founder of NFLF!!!! I have learned so much from Amy & she is such an inspiration to myself among others. NFLF has helped me out & I am so thankful. This is a great foundation!” - MG
“It's great having a foundation like this spreading not only awareness but providing assistance to people like myself. I went many years without any knowledge about my condition just a general awareness to complications related to it. Finally I met someone who could help me after I was in very bad shape. My sincere hope is an organization like Ninjas can help someone else find out sooner, and get the help they need.” - RB