Love is always in the air at the Lipedema Patient Roundtable, but the feeling was palpable as the group shared what community means to them in this February “Galentines” episode. With representatives from the Lipedema Foundation and Fat Disorders Resource Society (FDRS) welcomed as guests, questions and answers abound. The Foundation unveiled new materials intended for patients to bring to their medical team, including their Clinician’s Guide to Lipedema and Research Roadmap, and discussions surrounding how to participate in the organization’s research database were discussed.
Angelique Charles encouraged the audience to “not give up on themselves” and Siouxie Boshoff shared how “Vitamin G – gratitude” made a difference in her month. An East Coast virtual watch party for the FDRS Conference may be in the works, spearheaded by Pattie Cornute and Jenny Beaujean. And Cara Cruz cautioned all to be prepared for the post-conference letdown after spending days with people who truly understand lipedema.
The following questions were asked about the live research opportunity, with the Lipedema Foundation promising to provide answers in the coming days. So, here they are:
1. Is it advisable/helpful for people to stop compression and/or other conservative therapies a few days before they participate?
We do not advise or recommend removing compression any earlier than coming to the research study without compression (expedites the changing room process). We are stating the following for participants on our Live Research landing page: “Participants will need to disrobe prior to participating in the study, and changing areas will be available. To expedite the process, please come to your assigned time slot without compression if possible.”
2. Are we interested in participation from people who have undergone surgery?
Yes. Having undergone liposuction in the past does not prohibit your ability to participate in this study.
Special thanks to special guests Jonathan Kartt, CEO, and Courtney Mascio Henderson, Professional Education Manager, from The Lipedema Foundation (@lipedema_fndn). The Roundtable truly appreciates the participation of Cheyenne Brinson, President, and Polly Armour, Research Coordinator, for the Fat Disorders Resource Society (@fatdisorders).
And everyone’s favorite Galentines? Our anchor panelists and moderator:
- Jenny Beaujean (@Jenny_Beaujean)
- Siouxie Boshoff (@Lipedema.Living)
- Angelique Charles (@TheLippyButterfly)
- Pattie Cornute (@LipedemaFitness)
- Cara Cruz (@PaleGingerPear)
- Brenda Viola (@brendaviola_vicicommunications)
Lympha Press is committed to supporting lipedema patients and helping them manage their condition with the Optimal Plus, indicated by the FDA for the treatment of lipedema. To find out more, visit www.lymphapress.com.