
ALT Lipodystrophy United graphic titled “EL-PFDD Summary.” It reports approximately 100 in-person attendees and 400 online attendees. Participant type is listed as CGL 9.4%, FPL 77%, AGL 3.1%, unknown 6.25%, unsure 3.1%, and other 1.56%. Age ranges are 18 or under 3%, ages 18–34 25.4%, 35–49 41.8%, 50–64 25.4%, and 65 or older 4.5%. When asked how much lipodystrophy interfered with daily life in the past 12 months, 43.1% said extremely, 43.1% significantly, 13.8% moderately, and 0% minimally or not at all. Words used to describe living with lipodystrophy include exhausting, lonely, debilitating, frustrating, overwhelming, tiring, and hellish. The graphic also notes that 62% chose fatigue or pain as the one symptom they would remove with a magic wand, and 87% reported that lipodystrophy significantly or extremely interferes with daily life.

ALT Lipodystrophy United graphic titled “What Patients Need From Treatment.” It summarizes five treatment priorities with patient quotes: durability and peace of mind, one treatment for the whole disease, reducing treatment burden just to function at baseline, earlier preventive access before irreversible damage occurs, and treatment that allows for greater quality of life. Quotes emphasize wanting long-lasting treatment, treatment of the disease as a whole, less day-to-day management burden, earlier intervention, and treatment as an “umbrella” to help weather the storms.

ALT Lipodystrophy United graphic summarizing key themes from the EL-PFDD meeting. It explains that the burden of lipodystrophy extends beyond lab results and can include hunger, fatigue, pain, brain fog, temperature regulation challenges, serious health complications, delayed diagnosis, stigma, fertility challenges, financial strain, and fear about the future. It also describes treatment burden from injections, multiple medications, diet and exercise, appointments, monitoring, travel, insurance challenges, and side effects. The text emphasizes that better lab results do not always mean better quality of life and that patients want treatments that reduce symptoms, prevent complications, and lessen the day-to-day burden of managing lipodystrophy. It closes by highlighting the strength and determination of the community and the message: “Real People. Real Lives. A Healthier Tomorrow Is Possible.”

ALT Graphic for a Lipodystrophy United and Give an Hour PFDD Attendee Debrief. Text says everyone is welcome and participants do not need to have attended in person. The event is October 6 at 6 PM CST via Zoom. The graphic notes that this will be a different conversation from the previous debrief and encourages past attendees to join again. Lipodystrophy United logo appears at the top left and Give an Hour logo at the bottom right.

ALT Graphic titled “Burdens of Lipodystrophy” featuring an iceberg. Above the waterline, labeled “Visible Burdens,” are physical changes and lab results. A quote reads, “Laboratory values only scratch the surface.” Below the waterline, labeled “Invisible Burdens,” are unrelenting hunger, severe pain, stigmatization, strain on relationships, extreme fatigue, organ damage, infertility and pregnancy loss, and mental load. The Lipodystrophy United logo appears at the top.

ALT Lipodystrophy United graphic announcing “It’s not too late to leave a comment!” with a large red number 11 and the text “More days to submit.” The background is a blurred photo from an in-person Lipodystrophy United event, with the organization’s logo in the upper left and lipodystrophyunited.org at the bottom.

ALT Graphic for a Lipodystrophy United and Give an Hour virtual debrief. Large text reads, “Give an Hour Debrief.” The event invites community members to join Julie and Ashley with Give an Hour to reflect on the EL-PFDD meeting and discuss tools and tips for carrying the weight of the meeting forward. The event is September 23 at 6 PM CST via Zoom. Lipodystrophy United logo appears at the top left and Give an Hour logo at the bottom right.

ALT Lipodystrophy United “25 Stories for $25K” campaign graphic featuring Meaghan wearing sunglasses and a gray tank top with medical monitoring electrodes visible on her chest. Her quote describes wanting just one good day a week when she can walk her dog, go to the park alone, or leave home without fear of passing out or having another medical emergency. The graphic encourages donations to help send patients to the EL-PFDD.

ALT Lipodystrophy United “25 Stories for $25K” campaign graphic featuring Dena smiling in a white lace dress. Her quote explains that just as her life began to feel like it was improving, she learned she was at risk for serious health complications and that the only approved medication was no longer effective. The graphic encourages donations to help send patients to the EL-PFDD.

ALT Lipodystrophy United “25 Stories for $25K” campaign graphic featuring Kyleigh seated and smiling. Her quote reads: “I want to be independent. I don’t want CGL to define me. But there is always that question in the back of my mind: If something happens, will anyone else know what to do?” The graphic encourages donations to help send patients to the EL-PFDD.

ALT Lipodystrophy United “25 Stories for $25K” campaign graphic featuring Shannon, a woman with shoulder-length gray-brown hair wearing a denim jacket. Her quote explains that the burden of FPLD is cumulative, including cardiomyopathy, metabolic disease, pain, fatigue, brain fog, sleep problems, autonomic dysfunction, reproductive complications, and loss of mobility—all affecting the same person every day. The graphic encourages donations to help send patients to the EL-PFDD.

ALT Lipodystrophy United “25 Stories for $25K” campaign graphic featuring Sonia, a woman with dark hair wearing a light-colored blazer. Her quote reads: “I have now needed three transplanted organs to stay alive. I consider myself incredibly fortunate to be here. But a transplant does not erase lipodystrophy or its impact on my life.” The graphic encourages donations to help send patients to the EL-PFDD.










