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
Interviews
Every person's story is worth telling.
There is no definitive lymphedema or lipedema experience.
From veterans and athletes to college students and parents, life with these conditions is as varied as the people who live with them. Hear from real patients as they share their stories, in their own words.
Explore
Contact Us.
We're ready to help.
Looking for more information, or to be connected with your local representative?
We can help. Fill out our contact form to get started.
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
25
Jan
Appearances can be deceiving. To look at Amanda Sobey today, surrounded by gym equipment and the picture of health, you'd never know she once had to crawl to the bathroom and was bedridden for an extended period of time.
After receiving her lymphedema diagnosis, she found her way back to health step by step starting ...
Published: 25 January, 2021
25
Jan
An accident while playing basketball at age 15 left him with an unusually swollen leg and, eventually, a lymphedema diagnosis.
Dominique's mother also had lymphedema, and they learned to encourage each other to stay compliant to manage this chronic condition. Dominique's mom was a great source of inspiration ...
Published: 25 January, 2021
12
Jan
Bethany Davis was on a trip to Disney at age 11 when she first realized she couldn't feel her ankle bones. A primary lymphedema diagnosis followed along with a lifelong quest to manage this chronic condition. From feeling shame about her condition to choosing NOT to manage it for a period, Bethany's candor is ...
Published: 12 January, 2021
12
Jan
For a decade, Alexa Ercolano has used her successful blog, www.TheLymphieLife.com, to educate and inspire her fellow lymphedema patients. She wondered for years what was wrong with her leg and finally, at age 14, was diagnosed with primary lymphedema.
Her candor in sharing challenges with an eating disorder and ...
Published: 12 January, 2021
Contact Us.
We're ready to help.
Looking for more information, or to be connected with your local representative?
We can help. Fill out our contact form to get started.
