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LAM Action
LAM Action is the UK charity for those with Lymphangioleiomyomatosis (LAM), their families and doctors caring for them. LAM is a rare, progressive disorder of the lungs and lymphatic system, generally diagnosed in women of childbearing age. Here, patients with LAM and their families talk about their personal experience of the disease.

• In order to record and upload your story here, please register with Web of Stories and contact Gill or Jan for an Access Code.

• Once you have registered and have an access code please go to the LAM Action minisite and follow the online instructions to upload your story.
Carole Ann Grist
Kelly Vance
Grazyna Beata -
Lucy Falconer
Lucy Falconer