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2
Jul
Brittany Williams’s determination to get treatment for her daughter’s lymphedema sparked the creation of a pediatric lymphedema nonprofit, summer camp, and for-profit.
Published: 2 July, 2024
25
Mar
Mother-daughter duo Sonja and Tayler have a unique bond: they both live with chronic conditions. From the quest for a diagnosis to navigating treatment, going through the process together has allowed lipedema patient Sonja and lymphedema patient Tayler to learn from — and lean on — one another.
Published: 25 March, 2022
2
Jun
Diagnosed with lymphedema as a baby, Blanche Pepitone had her first surgery at 18 months old. Her parents and siblings raised her to live life fully, regardless of her condition, and that has been Blanche's lifelong credo: "You've got to decide how much living you want to do and do what it takes to live that ...
Published: 2 June, 2021
20
Apr
Amy Rivera is a powerful voice in the lymphedema community. Her Ninjas Fighting Lymphedema Foundation offers help and support that she wished for on the journey to a lymphedema diagnosis.
Published: 20 April, 2021
8
Mar
It took 30 doctor's visits before Amy Beaith was diagnosed with primary lymphedema. Lympha Press helps her manage her condition effectively.
Published: 8 March, 2021
23
Feb
In this article, learn how Cam Ayala suffered in silence since his lymphedema diagnosis at age eleven. Enduring over 13 surgical procedures, seven serious infections, lost professional opportunities and broken relationships, discover how he became not only a person who fights back, but also one who gives back.
Published: 23 February, 2021
12

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