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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
00:51
03:39
04:25
Kelly Vance
09:53
Grazyna Beata -
05:47
Lucy Falconer
05:03
Lucy Falconer