Find another patient to speak with, learn about mental health referrals in your area, join a LAM support group or read inspiring stories from other women living with LAM. Their words may provide you with comfort and strength. Email: patientstories@lamtreatmentalliance.org with your story if you would like for us to post it here!
National Organization for Rare Disorders http://www.rarediseases.org
Newly married and starting out on her career, Mara Rezo thought she had the world at her feet. However, at 25 a diagnosis of LAM saw the breakdown of her marriage and shattered her dreams of motherhood. Now working part-time and keeping as fit as she can with yoga, Mara is doing her best to manage the ill effects of the disease.
AELAM: Asociación Española de Linfangioleiomiomatosis (Spain) http://www.aelam.org/
ARDS Foundation http://www.ardsfoundationil.com
Associação LAM Do Brasil (Brazil) http://www.alambra.org.br
Association FLAM - France Lymphangioléiomyomatose (France) http://www.orpha.net/nestasso/FLAM
Associazione Italiana Linfangioleiomiomatosi http://www.ailam.it
The Carol and James Herscot Center for Children and Adults with TSC at Massachusetts General Hospital http://www.massgeneral.org/tsc
J-LAM (Japan) http://www.j-lam.org
Klinik für Pneumologie (Switzerland) http://www.pneumologie.unispital.ch/Seiten/default.aspx
LAM Action (UK) http://www.lamaction.org
LAM Australasia Research Alliance (LARA) http://www.lara.org.au
LAM Canada http://www.lamcanada.org
LAM Foundation (US) http://thelamfoundation.org
LAM Selbsthilfe (Germany) http://lam-info.de
Living with TSC http://www.massgeneral.org/livingwithtsc/affects/lung2.htm
National Home Oxygen Patients Association http://www.homeoxygen.org
New Zealand LAM Charitable Trust http://www.lam.org.nz
Tuberous Sclerosis Alliance http://www.tsalliance.org