Blog

Nicole’s story

I became ill 5 years ago and couldn’t get even one doctor to recognize my conditions, despite bringing them printed information from experts, detailing and accurately describing the symptoms I

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Barbara’s story

Everyone is unique, and so, in some ways, is the personal story of everyone who has lymphedema. Mine, however, is more uncommon than most such stories, for I have primary

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Tiffany’s story

I am a 31-year-old single mother of a 6-year-old girl. I have Primary Congenital Lymphedema or Milroy’s Disease. My lymphedema was noticed at birth. My lymphedema not only affects my

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Jessica’s story

I have primary lymphedema in my left leg.  The first time my leg swelled, I was 18 years old. My parents had taken me to Orlando for my college orientation

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Lori’s story

I am a 48 year old mother of one boy 12. In 2004, I became ill with a serious intestinal infection. After months on oral and IV antibiotics, I was

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David’s story

I am a 58-year-old male and have secondary lymphedema in my right leg due to the removal of a lymph node and follow-up radiation after being diagnosed with prostate cancer

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Joann’s story

I became aware that something was wrong in high school when a girlfriend told me that my legs looked like they didn’t belong with my body. At this time, in

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Amy’s Story

After many years of asking my doctor what was wrong with my legs and being told they were just “fat,” I decided to find out why myself. Thankfully with the

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Cindy’s Story

Cindy after-photo   Please support the Lymphedema Treatment Act. The cost of maintenance for patients like me prevents far more costly expenses from serious complications such as infections and even

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