Roundtables

Two new hashtags were birthed following the July Lipedema Patient Roundtable's riveting discussion: #DoTheThing and #WearTheThing. The message? Don't talk yourself out of trying something new for fear of what other people will think.

With thirty-six episodes in the vault, the Lipedema Patient Roundtable celebrated its third anniversary with some trips down memory lane.

The May Lipedema Patient Roundtable covered everything from Ehlers-Danlos syndrome and inflammation to mental health and the upcoming Lipedema Awareness Month.

Joining our regular panelists were patient speakers from the Fat Disorders Resource Society (FDRS) Conference, including Wyckham Avery, Sarah Bramblette, Hiba Hamati, Beth Rylaarsdam, and Jenn Sephton.

The April Lipedema Patient Roundtable was jam-packed with information and inspiration as each anchor panelist shared their biggest takeaway from the recent Fat Disorders Resource Society Conference.

The Roundtablers were honored to welcome William Repicci, President and CEO of the Lymphatic Education & Research Network, to the virtual table as part of Lymphedema Awareness Month.