Join our supportive network of scientists, clinicians, and LAM patients. Receive valuable resources and stay informed on the latest LAM-related news and events. Sign up now: https://t.co/TJ6Mwl6mO9 #Curelam #LAM #lymphangioleiomyomatosis

Join Megan this #GivingTuesday to support women with LAM! 💙 Donate → https://t.co/rx2d66Zxp3 #TheLAMFoundation #CureLAM #RareDisease #GamingForGood #GivingHope

Give a gift that gives back this holiday season! Check out our store for popular “Can you say lymphangioleiomyomatosis” t-shirts, Rosie mugs, and more. A portion of the proceeds supports The LAM Foundation. Spread the word! https://t.co/WsSWKjoIQx

Your support inspires us every day as we work toward a future without LAM. #ICYMI - Please enjoy this video from members of our Board of Directors. https://t.co/3hA0lhFbaA #curelam See less

Recording Now Available Listen as Dr. Henske and Dr. Johnson, share conference highlights, key takeaways, and what has them excited for the future of LAM research. Watch Now: https://t.co/enAXIztvLM #RareDisease

THANK YOU FOR YOUR GRACE, GRIT, AND HEART. Your support inspires us every day as we work toward a future without LAM. Wishing you warmth, hope, and peace this season. THE LAM FOUNDATION P.S. Please enjoy this video from members of our Board of Directors. #curelam

You are invited to a Circle of Hope webinar on 12/15, 7 PM – 8:30 PM ET. Please join us for a discussion with post-transplant patients as they reflect on their experiences and the things they wish they’d known along the way. Register: https://t.co/qMZTFmUcAh #Curelam

Tonight: Join 2025 International LAM Research Conference Co-Chairs, Dr. Henske and Dr. Johnson, as they share conference highlights, key takeaways, and what has them excited for the future of LAM research. Register Now: https://t.co/nLbtBvlXOA #RareDiseaseResearch

Tomorrow: Join 2025 International LAM Research Conference Co-Chairs, Dr. Henske and Dr. Johnson, as they share conference highlights, key takeaways, and what has them excited for the future of LAM research. Register Now: https://t.co/nLbtBvlXOA #RareDiseaseResearch

Join 2025 International LAM Research Conference Co-Chairs, Dr. Elizabeth Henske and Dr. Simon Johnson, as they share conference highlights, key takeaways, and what has them excited for the future of LAM research. Register Now: https://t.co/nLbtBvlXOA #RareDiseaseResearch

Meet Frances, our LAM co-liaison for Region 15: NM, southern, and western TX! Diagnosed in 2013, she offers hope and support to LAM patients, especially in rural areas and to those considering adoption. Find a liaison near you: https://t.co/STSAARhIZD #Curelam

Join 2025 International LAM Research Conference Co-Chairs, Dr. Elizabeth Henske and Dr. Simon Johnson, as they share conference highlights, key takeaways, and what has them excited for the future of LAM research. Register Now: https://t.co/nLbtBvlXOA #RareDiseaseResearch

🎉 Shoutout to The LAMinators, Chowchilla Champs, Team Denver, and Team Love my Lungs! Together, they exceeded their combined Laps for LAM goal of $10k! We are grateful to everyone who fundraised, donated, or shared a post. Your support is vital to the LAM community. #curelam

Join us for Rare Disease Week on Capitol Hill, Feb 24–26, 2026! Educate Congress & apply for travel scholarships by Nov 8. Learn More: https://t.co/Ql0An7RskQ #RareDiseaseWeek #LAMFoundation #EveryLifeFoundation #CapitolHill #RareDiseaseAdvocacy

Join 2025 International LAM Research Conference Co-Chairs, Dr. Elizabeth Henske and Dr. Simon Johnson, as they share conference highlights, key takeaways, and what has them excited for the future of LAM research. Register Now: https://t.co/nLbtBvlXOA #RareDiseaseResearch

It's here! The October edition of The LAM Foundation newsletter is now available. Click here to read the latest: https://t.co/qXOOU9JlHj #curelam #LAMposium2025 #raredisease #thelamfoundation

Meet Teri Childs, our LAM Liaison for Quebec! She is here to provide support to fellow LAM patients. Learn more: https://t.co/STSAARhIZD #TheLAMFoundation #LAMAwareness #RareDiseaseSupport #curelam

Join our supportive network of scientists, clinicians, and LAM patients. Receive valuable resources and stay informed on the latest LAM-related news and events. https://t.co/2DU9modRmA #Curelam #LAM #lymphangioleiomyomatosis

A Promising Breakthrough in Lung Testing for LAM Patients: Introducing Oscillometry We’re excited to share a promising new development that could transform how lung health is monitored in LAM patients. Read the whole story: https://t.co/zivlxaCHtm #PulmonaryResearch

Join us for Rare Disease Week on Capitol Hill, Feb 24–26, 2026! Educate Congress & apply for travel scholarships by Nov 8. Learn More: https://t.co/Ql0An7RskQ #RareDiseaseWeek #LAMFoundation #EveryLifeFoundation #CapitolHill #RareDiseaseAdvocacy