Lambert-Eaton Lems Family Association
We advocate for patients, family and caregivers who have the extremely rare neuromuscular disorder, Lambert-Eaton Myasthenic Syndrome. We are developing and administering a LEMS Patient Registry of medical data to encourage research for better treatments and outcomes for LEMS patients. We are working to educate and inform the medial community, other interested parties, and our own group to better understand Lambert-Eaton, its challenges, and impact on quality of life for patients and family. We are advocating for LEMS patients in state and federal legislation.
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Fort Worth
The Lambert-Eaton LEMS Family Association – Awareness from the Heart Join our LEMS Awareness Day Meeting Please welcome our newest board member Tracy Sharp of Kentucky. The LEMS Patient Registry is OPEN. Contact Us The LambertEaton LEMS Family Association2420 Innovation Dr. 612881Dallas TX 75261 Connect with us .
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Fort Worth
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Kateřina
2025-10-23
"🚀 Exciting news from Cameroon! For the first time, they fully sequenced a circulating variant poliovirus type 3. This is a huge leap forward in the fight against polio in Africa! Together, we can create a future free from this disease. 💪🌍 #PolioFree #HealthForAll"
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