Share your views and experiences of LAM in our online survey
ELF and the European LAM Federation will be holding a patient priority setting workshop at ERS Congress this year.
It will be an opportunity for people affected by lymphangioleiomyomatosis (LAM) to come together with LAM experts, researchers and industry to identify their shared priorities and learn from one another. The priorities identified during the workshop will then be presented in a symposium as part of the scientific programme of the Congress.
We invite people with experience of LAM to share their views and priorities via our online survey.
Complete the survey and we will share your views during the workshop. The survey is available in 7 languages:
Visit the LAM RareConnect page to find out more about the event, or read the interview with Iris Bassi of LAM Europe Federation.