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LAM Trust of New Zealand

LAM Trust of New Zealand

If you can’t breathe, nothing else matters

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Category: Uncategorised

by Bronwyn GrayPosted onJune 1, 2015Uncategorised

June 2015 – FDA approves Rapamune to treat LAM

FDA News Release. The U.S. Food and Drug Administration approved Rapamune (sirolimus), to treat lymphangioleiomyomatosis (LAM), a rare, progressive lung disease that primarily affects women…

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by Bronwyn GrayPosted onJanuary 1, 2015Uncategorised

2015 International LAM Annual Conference

The 2015 International LAM Scientific and Patient Conference will take place in Chicago, USA, from March 27th to 29th 2015. Find out more on the LAM…

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by Bronwyn GrayPosted onDecember 1, 2014Uncategorised

December 2014 – LAM Biomarker Innovation Summit

On November 13 -15 an exceptional group of biomarker scientists with diverse expertise gathered in Atlanta, GA, at the LAM Biomarker Innovation Summit. This meeting…

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by Bronwyn GrayPosted onOctober 1, 2014Uncategorised

October 2014 Tonio to run the Auckland Marathon for LAM

For the second year in a row Antoine Salles, Chef and owner of French Bistrot “Touquet” in O’Connell St in Auckland City, will run the Auckland…

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by Bronwyn GrayPosted onOctober 1, 2013June 19, 2019Uncategorised

October 2013 LAM NZ Update

The LAM Trust invites you to the Annual Gift Of Music Charity Concert by the Renowned Concert Pianist Mi-Yeon I. Founded by Mi-Yeon I, the aim is…

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by Bronwyn GrayPosted onSeptember 1, 2013Uncategorised

September 2013 LAM NZ Update

Following on from the very successful Short Course on Rare Lung Disease, hosted by the Australian Lung Foundation on 9 and 10 August in Sydney,…

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by Bronwyn GrayPosted onJune 1, 2013Uncategorised

June 2013 LAM NZ Update

LAM Therapeutics launches operations to develop drugs for rare lung disease, Lymphangioleiomyomatosis (LAM). LAM Therapeutics, the first biopharmaceutical company dedicated to identifying and developing drugs…

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by Bronwyn GrayPosted onMay 1, 2013Uncategorised

May 2013 LAM NZ Update

The Impact of Rare Diseases: in New Zealand and Internationally. Rare Diseases are conditions that affect a small portion of the population but are often…

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by Bronwyn GrayPosted onApril 1, 2013Uncategorised

April-May 2013 LAM NZ update

The Annual LAM patient and scientific meeting was held in Cincinnati, Ohio, USA, April 12/13/14 2013. More than 100 women with LAM from a dozen…

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by Bronwyn GrayPosted onMarch 1, 2013Uncategorised

March 2013 LAM NZ update

Bronwyn Gray, the NZ LAM Trust’s Director met recently in Melbourne with LAM patient, Heather Telford, immediate past president of LARA (LAM Austrlasia Research Alliance)…

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Recent Posts

  • WWLAM21 – LAM World Awareness Month
  • Post transplant patient completes 11km Auckland marathon
  • Lisa 17th year post transplant
  • The LAM Foundation COVID-19 Statement
  • Congratulations to Jess and Ruth

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© Copyright 2022 – LAM Trust of New Zealand
The New Zealand LAM Trust is a Not For Profit organisation, registered with the NZ Charities Commission under the Charities Act 2005.
The Trust is committed to finding a cure for Lymphangioleiomyomatosis by providing support, education, information and raising funds for scientific research.
Charity Registration Number: CC20304
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