Today is LEMS Awareness Day! Today, we raise awareness about Lambert-Eaton Myasthenic Syndrome (LEMS), a rare neuromuscular disease. March 30th marks the anniversary of groundbreaking research by Dr. Edward Lambert and Dr. Lee Eaton, whose work first described #LEMS and significantly advanced the understanding of the condition. @CatalystForRare is proud to support the 2nd Annual LEMS Awareness Day, which was established in 2024 by @LEMSFamily. This day is dedicated to spreading awareness, improving diagnoses, and uniting the LEMS community. 🔗 Get involved & learn more: LEMSfamily.org | LEMSaware.com

LEMS Awareness Day is March 30th! How much do you know about Lambert-Eaton Myasthenic Syndrome (LEMS)? Test your knowledge and help spread awareness - did you know all 5 facts? Living with LEMS can be challenging, but no one has to face it alone. There are incredible organizations and resources ready to help: 🔹 @LEMSFamily (lemsfamily.org) – Supporting patients and families through education, advocacy, and community. 🔹 @RareDiseases (rarediseases.org) – Empowering #raredisease patients with resources and advocacy. 🔹@BeLEMSaware (LEMSaware.com) – Your go-to hub for information, resources, and patient stories. Together, we can raise awareness and build a stronger #LEMS community! Share this post to show your support!

Today is the 1st annual LEMS Awareness Day! Created by @LEMSFamily, LEMS Awareness Day will be held every year on March 30th with the goal of bringing together patients, family members, caregivers, doctors, and researchers to promote progress in the #LEMS community! We are proud to support LEMS Awareness Day and encourage you to learn more about LEMS at LEMSfamily.org and LEMSaware.com.

Tomorrow is the first annual LEMS Awareness Day facilitated by @LEMSFamily. To help celebrate this inaugural day, we partnered with NASDAQ to raise awareness in Time Square! Learn more about LEMS at lemsfamily.org or LEMSaware.com.