Home > Engage > Roundtables

Roundtables

Virtual connection. Real support.

Explore
  • Clear Filters

Lymphedema Patient Roundtable

Lymphedema can be challenging, but you don’t have to face it alone. Join us live as our panel of patients and experts answer your questions and talk about life with lymphedema.

Second Tuesday of Every Month
@ 8:00 PM EST

Lipedema Patient Roundtable

Be inspired by some of the top social influencers and clinical minds in the lipedema world! Our monthly Roundtables offer candid talk, real-life advice, and lots of encouragement.

Third Wednesday of Every Month
@ 8:00 PM EST

Let's get social!

We’d love to connect with you.

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.

20
Sep
Does lipedema affect fertility? How about the ability to sweat? And why does lipedema light up on airport scanners? These are just some of the questions that popped up during the September Lipedema Patient Roundtable for our panel of patients and medical professionals.
Published: 20 September, 2021
17
Sep
It's Fall, y'all, and lymphedema patients in the Northern Hemisphere are rejoicing at the transition to cooler weather! From compliance to clothes to circulatory changes, panelists at the September Lymphedema Patient Roundtable shared the different ways the Fall season can affect life with lymphedema.
Published: 17 September, 2021
20
Aug
Living with lipedema can be painful. But one of the beautiful things about living with lipedema is the community and the wealth of information and support it offers. A big theme during the August Roundtable was pain relief, with panelists and attendees discussing everything from cold laser therapy and far-infrared ...
Published: 20 August, 2021
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
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
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

Lymphedema Patient Roundtable

Lymphedema can be challenging, but you don’t have to face it alone. Join us live as our panel of patients and experts answer your questions and talk about life with lymphedema.

Second Tuesday of Every Month
@ 8:00 PM EST

Lipedema Patient Roundtable

Be inspired by some of the top social influencers and clinical minds in the lipedema world! Our monthly Roundtables offer candid talk, real-life advice, and lots of encouragement.

Third Wednesday of Every Month
@ 8:00 PM EST

Let's get social!

We’d love to connect with you.

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.