It took panelist Jenny Beaujean 45 years to get a lipedema diagnosis. May it never take anyone that long again!
The Lipedema Patient Roundtable made good on its 2023 resolution by bringing in special guests to add leading-edge information to the monthly conversations. Guy Eakin, Chief Science Officer for Lipedema Foundation, answered questions about research initiatives and the Lipedema Patient Registry. His colleague, Kathy Doherty, informed the audience about the newly released Lipedema Patient Bill of Rights, which can be found at lipedema.org. And guest April Sluder, who leads the group The Lipedema Journey, spoke about her Mindful Movement collaboration with Pattie Cornute. Cara Cruz‘s healing journey after her final surgery, ways to boost your mood with color, and the mind/body/brain connection added to the invigorating conversation.
Thanks to our regular panelists as well as the record number of attendees!
- Pattie Cornute (@LipedemaFitness)
- Cara Cruz (@PaleGingerPear)
- Angelique Charles (@TheLippyButterfly)
- Siouxie Boshoff (@Lipedema.Living)
- Jenny Beaujean (Facebook: Lipedema & Food Sensitivities)
- Linda-Anne Kahn (@LindaAnneKahn)
The Lipedema Channel on YouTube is where each month’s Roundtable and excellent one-on-one interviews “live.” This channel celebrated 1,000 subscribers in January! These initiatives are all part of Lympha Press’ commitment to support the lipedema community. Lympha Press provides the Optimal Plus, which is pneumatic compression therapy specifically indicated by the FDA for the treatment of lipedema. To find out more, reach out to marketing@lymphapress.com.
