Delivering facts about #LAM #RareDisease and The LAM Foundation. We're dedicated to funding research, advocacy and awareness to improve the QoL for all LAM pts.
Cincinnati Ohio
Joined April 2010
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Join our supportive network of scientists, clinicians, and LAM patients. Receive valuable resources and stay informed on the latest LAM-related news and events.
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#Curelam #LAM #lymphangioleiomyomatosis
ALT Group of individuals standing together at an event, with the text 'Join Our Community! Get the latest from The LAM Foundation.' in the background.
For Dr. Ildikó Krencz, LAM research began in the lab and grew into a decade-long passion. Read her story: ow.ly/GvVu50ZYBvn
#LAM #RareDisease #WomenInScience #LungHealth #MedicalResearch #LAMCommunity #ResearchMatters #ScienceForHope
It's World Oxygen Day! Participate by learning more WorldOxygenDay.org, taking action Thelamfoundation.org/soar, and sharing to raise awareness about oxygen access challenges. #WorldOxygenDay
It's here! Your peek at progress and more in this month's newsletter.
Don't miss out—read the September issue of Currents today! us12.campaign-archive.com/?u…
#CureLAM
Join The LAM Foundation Community today!
Sign up to become a part of our supportive network of women with LAM, their loved ones, scientists, and clinicians. Receive valuable resources and stay informed on the latest LAM-related news and events.
Visit Thelamfoundation.org/join
#ICYMI Watch last week's Day of Giving live event recording for inspiring LAM updates and help us reach our $300,000 goal! thelamfoundation.org/videos/… #CureLAM
We’re thrilled to nearly reach our $300,000 goal! Thanks to all who supported our Day of Giving. Help us cross the finish line by Sept 30. Give Now: thelamfoundation.org/donate
BREAKING NEWS: Every gift matched up to $10,000! Donate now to help us reach $300,000 and fund a cure. thelamfoundation.org/donate #CureLAM #IbelieveinaworldwithoutLAM
Countdown to our Day of Giving live event! RSVP: thelamfoundation.org/celebra… LAM updates, contests, special announcement, and match grant: thelamfoundation.org/donate #CureLAM #IbelieveinaworldwithoutLAM
WATCH: A special message from our Scientific Director, Dr. Vera Krymskaya.
youtube.com/watch?v=jFfWzajN…
#CureLAM #IbelieveinaworldwithoutLAM
UPDATE: We still need: 7 gifts of $5,000, 6 of $2,500, 15 of $1,000 & 9 of $500 to hit our matching challenges. Every gift is doubled — help us reach our $300,000 goal. Donate now: thelamfoundation.org/donate
#CureLAM #IbelieveinaworldwithoutLAM
Today's the day! It's our Day of Giving. Donations at $500, $1,000, $2,500 & $5,000 are being matched by generous LAM families — doubling your impact toward our $300,000 goal. Every gift counts. Donate now: [link]
We can't wait! Join us TOMORROW for 2026 Day of Giving: virtual event, research, stories & special announcements! RSVP thelamfoundation.org/event/d… #CureLAM
The LAM Foundation celebrates new publication by Mary Beth Brown, PT, PhD, and collaborators at the University of Washington. Read More: thelamfoundation.org/new-dis… #CureLAM
Excited to share progress from Dr. Roya Babaei Jadidi's Foundation-funded study at University of Nottingham on IL-6 signaling's role in lung repair in LAM.
Read more: ow.ly/fLOm50ZFT4J
#CureLAM
It was great to see our rare disease friends at the TSC World Conference in Aurora, CO earlier this month. Thank you for allowing us to advance research on behalf of our communities.
@tscalliance
Every gift brings us closer to $350K for the people, programs and progress that will lead us to a cure.
What does a world without LAM mean to you?
Make a gift today that reflects your answer.
thelamfoundation.org/donate
#CureLAM
The LAM Foundation and advocates met Congress to push the SOAR Act, connecting lived LAM experience to policy. Learn more: thelamfoundation.org/soar/
#SOARAct #RareDiseaseAdvocacy
1.5 million Americans rely on supplemental oxygen. Cindy is one of them — and even she couldn't get the equipment her doctor prescribed. Here's why the SOAR Act matters:
ow.ly/AnY150ZFnnj
#SOARAct #SupplementalOxygen #PatientAdvocacy
A gift on September 3rd will support the people programs and progress that will lead to a cure for LAM.
Swipe through the graphics to see three examples of the impact your gift will make.
Give now: thelamfoundation.org/donate
For more than 25 years, Dr. Marina Holz has been looking for answers as a scientist. For the past 15 years, she has dedicated that curiosity to the LAM community.
Read the full story: ow.ly/lb8s50ZCuCi
@Holz_lab
#CureLAM #RareDisease #WomenInScience #LAMResearch
