ICO
993365909
Web
americanlipedemaassociation.org
Address
Yukon
Empowering Lipedema Patients Through Advocacy Empowering Lipedema Patients Through Advocacy Empowering Lipedema Patients Through Advocacy ALA Home Who We Are The American Lipedema Association is a 501c3 nonprofit organization dedicated to empowering lipedema patients in the United States. We are a community of individuals affected by lipedema along with medical professionals researchers and advocates united in raising awareness and understanding of this underdiagnosed loose connective tissue disorder. Our mission is to provide support resources and a collective voice for those impacted by lipedema while promoting research efforts to advance treatment options and improve quality of life. Together we strive to foster a compassionate environment where lipedema patients feel heard validated and empowered on their journey.
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Together, we can make a real impact in communities around the world. Help us bring hope and support.
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Discussions
Odpovědí v diskuzi
1
What strategies can we implement to raise awareness about lipedema in communities that may not be familiar with the condition?
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Brooklyn Simmons
2 days ago
Odpovědí v diskuzi
1
How can we better support lipedema patients in navigating the healthcare system to ensure they receive proper diagnosis and treatment?
View
Brooklyn Simmons
2 days ago
Latest reviews
Together, we can make a real impact in communities around the world. Help us bring hope and support.
So grateful for the work the American Lipedema Association is doing! Your advocacy and support are making a real difference in the lives of so many. 💜 #LipedemaAwareness
Brooklyn Simmons
Product Manager
Thank you for being a voice for those affected by lipedema! Together, we can raise awareness and push for better treatment options. Keep up the amazing work! 🙌 #EmpowerLipedemaPatients
Brooklyn Simmons
Product Manager
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