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13
Aug
"We are more than our swelling." This affirmation was the heartbeat of the August Lymphedema Patient Roundtable as our panelists talked about body image, coping skills, and how to be your own best advocate while living with lymphedema.
Published: 13 August, 2021
1
Aug
Thanks to a post on Instagram, Amber Grainger realized she had lipedema and was fortunate enough to connect with Dr. Lindy McHutchison of Carolina Vein Center. For the first time, Amber felt validated.
Published: 1 August, 2021
26
Jul
From the physical pain of living with lipedema to the emotional pain of being objectified for their size, conversation at the July Lipedema Patient Roundtable seemed to cover it all.
Published: 26 July, 2021
19
Jul
Kelly Maynard offers insights into why lipedema patients should address their full body, how her upper extremities have changed, and that the "constant ache" she used to live with is now gone.
Published: 19 July, 2021
15
Jul
It's summertime, and the living is — well, not so easy when you have lymphedema. The July Lymphedema Patient Roundtable focused on all things summer, from hot tips for traveling with your compression pump to cool facts about swimming and the natural compression it offers.
Published: 15 July, 2021
2
Jul
Lipedema symptoms of pain and swelling, as well as progressive fibrotic changes, can be managed. We’ll discuss clinical evidence for conservative treatment of lipedema, and how Lympha Press® pneumatic compression therapy systems can be used as part of a comprehensive home treatment plan.
Published: 2 July, 2021

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