Lipodystrophy United (LU) is a non- profit 501 (c)3 organization composed of committed individuals living strong with Lipodystrophy (LD).

Albuquerque, NM
Joined September 2013
What an incredible night! Thank you to everyone who helped make the night so special, and to everyone who showed up exactly as themselves. We’ll be smiling about this one for a long time. #lipodystrophy #prom #lipodystrophyunited
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Next up in our Lipodystrophy United Overview Series with Jessica Muang: Adipokines! In this video, Jessica gives a simple overview of adipokines and why they matter for understanding lipodystrophy. #lipodystrophy #lipodystrophyunited #adipokines
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We’re excited to introduce a new Lipodystrophy Overview Series with Jessica Maung! We’re starting with the basics: What is adipose tissue, and why does it matter? Follow along as we continue the series with more short, accessible overviews on the science behind lipodystrophy.
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Our EL-PFDD made one thing clear: living with lipodystrophy goes far beyond lab results. Patients want treatments that reduce symptoms and daily burden, prevent complications, and improve quality of life. Thank you to everyone who helped! #lipodystrophy #ELPFDD
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If you already have very little fat in some areas, what happens when you take a GLP-1 medication? In this clip, the panel explains that fat loss comes from areas where fat is present—and that weight loss can also include muscle. #Lipodystrophy #LipodystrophyUnited #GLP1
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Join us for another Give an Hour PFDD Attendee Debrief on October 7 at 6 PM CST. Julie and Ashley from Give an Hour will lead our conversation and will help us create a supportive space to process it together. Register here: us06web.zoom.us/meeting/regi…
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A huge thank you to Dr. Stephen Stone for creating this powerful illustration. It captures an important message: laboratory values only scratch the surface of what it means to live with lipodystrophy. Comment submission is still open lipodystrophyunited.org/subm…
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There’s still time to make your voice heard. We have 11 more days to submit comments following our EL-PFDD Meeting. If there was something you didn’t get the chance to say during the meeting, please share it with us. Visit lipodystrophyunited.org/subm…
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Join Give an Hour on September 23 at 6 PM CST for a community debrief following our EL-PFDD. We hope you’ll join us: us06web.zoom.us/meeting/regi…
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If you left the meeting thinking, “I wish I had said one more thing,” please share it now. Your comments can help inform our Voice of the Patient Report. The deadline has been extended to October 11! Comment: lipodystrophyunited.org/subm… Survey: lipodystrophyunited.org/el-p…
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We’re honored that Lipodystrophy United’s Voices of LU has been nominated for the inaugural 2026 Prix Galien Patient First Award in Honor of Michael J. Fox! 💙 This recognition belongs to our entire community. #LipodystrophyUnited #PrixGalien
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A big thank you to Julie and Ashley from Give an Hour! Julie reminds us to think ahead about what brings us comfort; Knowing what helps you feel grounded can make it easier to reach for support when you need it. Zoom registration: us06web.zoom.us/webinar/regi…
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25 Stories for $25K | Story 24: Meaghan Meaningful improvement means feeling safe enough to leave home, walk her dog, or go to the park without fear. Donate to help patients attend the EL-PFDD and check if your employer will match your gift. Donate: lipodystrophyunited.org/form…
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Your experience matters! Take the EL-PFDD Pre-Survey to help us ensure the meeting reflects the real priorities, challenges, and experiences of people living with lipodystrophy and their caregivers, whether you attend virtually or in person. Survey: lipodystrophyunited.org/el-p…
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25 Stories for $25K | Story 23: Dena Dena’s story is a reminder of how quickly hope can be replaced by uncertainty when treatment options stop working. Help us MATCH $25,000 to bring more voices to the EL-PFDD. Donate: lipodystrophyunited.org/form… #ELPFDD #Lipodystrophy
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Mallory has a question… will YOU go to prom with us? September 12, 2026! Whether you dress up, keep it casual, or wear whatever makes you feel most like yourself, we can’t wait to celebrate our community together. Register for our EL-PFDD and symposium: lipodystrophyunited.org/regi…
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Story 22: Kyleigh; Living with CGL means also carrying the uncertainty of whether others will know how to help if something goes wrong. Donate to help patients attend the EL-PFDD and check if your employer will match your gift Donate: lipodystrophyunited.org/form…
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For Shannon, the burden of FPLD is not one symptom or one diagnosis, it is the accumulation of many challenges, day after day, over decades. Help us MATCH $25,000 to bring more patient and caregiver voices to the EL-PFDD. Donate: lipodystrophyunited.org/form… #25StoriesFor25K #ELPFDD
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Sonia’s story is one of survival, resilience, and the lasting impact of lipodystrophy. Even after life-saving transplants, the disease still shapes her daily life. Donate to help patients attend the EL-PFDD—and check if your employer will match your gift lipodystrophyunited.org/form…
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25 Stories for $25K | Story 18: Sydney Understanding her diagnosis has helped Sydney better manage her health, advocate for herself, and navigate questions with confidence. Help us MATCH $25K and check if your employer will match your gift Donate: lipodystrophyunited.org/form…
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