We are excited to share that the Fat Disorders Resource Society (FDRS), a volunteer patient-led organization, is hosting its annual conference (FDRS 2024 Annual Conference) in St. Louis on April 19-21. The Lipedema Foundation will be attending the event, which gathers patients, clinicians, therapists, and researchers for education, networking, and listening. There are many wonderful aspects of FDRS, and LF has compiled 5 compelling ones we hope will encourage you to attend in 2024!
Find Your Community
Immerse yourself in a positive and empowering atmosphere. Connect with others who understand the challenges of living with Lipedema, share experiences, offer inspiration, and build a robust support network. Past attendees attest that these connections have helped them better understand the condition and treatment options.
Be Part of Research & Awareness
Would you like to contribute to research efforts? On April 18 & 19, before the FDRS 2024 conference, LF will be partnering with LymphaTech to collect 3-D digital measurements of people with Lipedema. The goal is to gather data that could contribute to a better understanding of the disease. Participants should receive a copy of their measurements.
You can also help our awareness efforts! A professional photographer will be present to capture additional photos for our LF SmugMug Photo Library, which currently features over 500 anonymized photos showing people with Lipedema, including signs and symptoms. These pictures are used to support education efforts by and beyond LF, such as clinician presentations and news articles. We welcome all individuals who are living with Lipedema to participate.
Learn more and sign up here!
Connect with the Lipedema Foundation
Learn more about the Lipedema Research Roadmap from our CEO, hear about resources designed to support clinician engagement from our Professional Education Manager, and discover what the last year in Lipedema research uncovered with our Chief Science Officer. LF is thrilled to be presenting three sessions at FDRS 2024.
Make sure to stop by the LF booth. Our whole team will be in attendance at FDRS. Come meet the team, learn more about our new resources, and grab LF brochures, copies of the Clinician’s Guide, and a variety of other materials to help you educate healthcare providers and your community about Lipedema.
Hear from Clinical Experts & Researchers
Interact with leading experts, including healthcare professionals and researchers dedicated to and invested in Lipedema. Attendees will have the opportunity to gain insight into the latest research and perspectives on patient care.
Empowerment through Knowledge and Resources
FDRS 2024 will prepare you with the latest information in Lipedema research, education, knowledge, and a variety of resources. Better manage your Lipedema journey, make informed health decisions, and advocate for your well-being with what you learn, the people you meet, and the bonds you form with other patients.
Don’t just take our word for it. Past patients have called the conference “energizing” and “life-changing.” If you have attended FDRS in the past, share this blog post and your story about why others should consider joining FDRS this year.
Don’t wait! Register here for FDRS 2024.
