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Ride London-Surrey 100 is a fantastic cycle ride starting at the Olympic Park and heading through the Surrey Hills area of outstanding natural beauty before finishing on the Mall. Ride for LAM Action and help find a cure for a rare lung disease which affects only 350 women in the UK. Date: Sunday 16th August […]
It will be here before you know it! Support our fundraising for LAM research this Christmas by purchasing your cards from LAM Action. Printed on high-quality board, the cards come in packs of 10 and cost £3.75 per pack + postage. All cards are 14 cm x 14 cm and bear the message ‘With Best […]
Alice Walker will need no introduction to anyone who has been following our Facebook page as she has taken part in several fundraisers already for LAM Action, including the Great North Swim and the Great North Run. Alice also recently appeared on BBC Radio Nottingham alongside Prof. Simon Johnson, talking about her fundraising for the […]
A new study is planned to investigate a possible inhaled treatment, called LAM-001 for women with LAM. The study is planned to begin very soon and will be conducted at sites in Nottingham, Manchester and London. Women aged between 18 and 70 years with LAM, who are not being treated with sirolimus (also called rapamycin), may be […]
The European Lung Foundation’s new LAM Patient Priorities website is now live! www.europeanlunginfo.org/lam Some of the key features on the site are: Information about LAM – trusted information developed with LAM health professionals and women with LAM. Support in your language: LAM factsheet to download in 9 languages. Map of LAM patient organisations in Europe […]
Every year LAM Action aims to raise £75,000 to support women with LAM and their families and to continue to fund much needed research into the condition. Fundraising through sponsored events is a central part of achieving this goal and we now offer places in more events than ever before, but we need your help […]
Please have a look at the poster here that explains in a nutshell what LAM Action does to support women with LAM in the UK and why it is so important that we get as many members as possible!
LAM affects women differently, from their reaction to the diagnosis to the progression of the disease. We have produced this video, in which several women share their own personal thoughts and feelings about having LAM. Thank you to everybody who took part and to David Mercer for the production.
Professor Simon Johnson was presented with the LAM Foundation Award for Scientific Advancement at the LAMposium in Chicago last night (March 28th). The award was presented by Frank McCormack who also summarised and acknowledged Simon’s work and achievements in the world of LAM over the past 15 years and how much that work was valued […]
RareConnect, an initiative of EURORDIS, is a growing online network for rare disease communities, bringing together thousands of patients, families, and groups who might otherwise be isolated. Through RareConnect, patients and those who care for them can communicate, sharing experiences and information in a safe, moderated online forum. With human translation available at no cost […]