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LAM Australia Research Alliance – Seeking a cure for LAM

LAM Australasia Research Alliance (LARA) funds research into lymphangioleiomyomatosis, a rare and devastating lung disease striking women mostly in their 30s.

http://lamaustralia.org.au/

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LAM Australia Research Alliance – Seeking a cure for LAM | lamaustralia.org.au Reviews
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LAM Australasia Research Alliance (LARA) funds research into lymphangioleiomyomatosis, a rare and devastating lung disease striking women mostly in their 30s.
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KEYWORDS
1 Lymphangioleiomyomatosis
2 LAM
3 lung disease
4 lymph
5 asthma
6 Angiomyolipoma
7 Tuberous Sclerosis
8 cyst
9 AML
10 alveoli
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join us,donate today,donate,what is lam,about us,news,research,stories,fundraising,links,lymphangioleio​myomatosis lam,lam diagnosis,find,more news,our supporters,our team,view team,patron,dr linda friedland,dr tamera corte,prof allan glanville,executive
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LAM Australia Research Alliance – Seeking a cure for LAM | lamaustralia.org.au Reviews

https://lamaustralia.org.au

LAM Australasia Research Alliance (LARA) funds research into lymphangioleiomyomatosis, a rare and devastating lung disease striking women mostly in their 30s.

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Stories | LAM Australia Research Alliance – Seeking a cure for LAM

http://lamaustralia.org.au/category/stories

Gai Golder’s Story. Featured in the Australian Women’s Weekly here. Every day opens a new page – I breathe out negative air and breathe in fresh happiness and bright hope. Tracy Hughan’s Story. First symptoms January 1990 (aged 30) / diagnosed 01 September 1997 (aged 37). I had my first pneumothorax when I was 18 weeks pregnant with my third child in January 1990. At the time, I was hospitalised with a draining tube in my chest for a few days. Marion Lang’s Story. WHY AM I SO BREATHLESS? My name is Anna ...

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FAQ | LAM Australia Research Alliance – Seeking a cure for LAM

http://lamaustralia.org.au/faq

How many women have LAM? We have no proven statistics, but as of March 2015 we know of 104 women living with LAM in Australia. The LAM Foundation has 1300 US women on its registrar. As of 2012, 300,000 had been diagnosed with LAM/TS (LAM in association with Tuberous Sclerosis) worldwide and 12,000 with Sporadic LAM. Do men get LAM? Generally no. Only one case we know of has been reported. Can LAM be passed on genetically? How can I find out if my symptoms are LAM? What should I do if I seem to have LAM?

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Donate Today | LAM Australia Research Alliance – Seeking a cure for LAM

http://lamaustralia.org.au/donate-now

Every donation to LAM Australia Research Alliance helps fund LAM research. Four ways to donate. Acc Number: 4926 67193. So we can issue a receipt, please email LAM Australia admin@lamaustralia.org.au. The name/s and postal address of the donor/s. LAM Australia Research Alliance. PO Box 636 Bondi Junction. So we can issue a receipt, please print the name/s of the donor/s on the deposit slip. Email LAM Australia admin@lamaustralia.org.au. Go to the Apple App Store. MEDICAL and SCIENTIFIC ADVISORY PANEL.

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Kate Wingrave’s Story | LAM Australia Research Alliance – Seeking a cure for LAM

http://lamaustralia.org.au/kate-wingraves-story

Kate Wingrave’s Story. November 2010 is a month I will never forget. This was the month when I was rushed to hospital with severe back pain and came home diagnosed with lymphangioleiomyomatosis, a disease I’d never heard of before. November 2010 is a month I will never forget. That was when I was rushed to hospital with severe back pain and came home diagnosed with lymphangioleiomyomatosis, a disease I’d never heard of. Luckily, Steve came across the website of an Australian organisation formed by women ...

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Doctors with LAM expertise | LAM Australia Research Alliance – Seeking a cure for LAM

http://lamaustralia.org.au/doctors-with-lam-expertise

Doctors with LAM expertise. Prof Allan R Glanville. Medical Director Lung Transplantation. T 61 2 8382 3257. F 61 2 8382 3084. E Allan.Glanville@svha.org.au. Interstitial Lung Disease Clinic. Royal Prince Alfred Hospital. T 61 2 9515 6120. E tamera.corte@sswahs.nsw.gov.au. T 61 2 8382 2330. T 61 2 8382 3150 (appointments). T 61 2 9389 1255. E dr claudia@vernonst.com. T 61 2 6244 2066. F 61 2 6244 2604. E mark.hurwitz@act.gov.au. T 61 7 3163 1178. F 61 7 3217 2312. E s bowler@mc.mater.org.au. T 61 8 9346 ...

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Our mission is to improve the health prospects of women living with. LAM Australia Research Alliance is a not-for-profit organisation run wholly by volunteers. Funding research to find a cure for LAM. Raising awareness of LAM. Supporting women living with LAM. DOCTORS WITH LAM EXPERTISE. The new President of LAM Australia Research Alliance, Dr Brian Oliver,. Run or walk for LAM in Sunday Mail City Bay Fun Run in Adelaide, South Australia. RESEARCH GIVES HOPE TO WOMEN WITH LAM. Prof Judith Black AO. WHAT ...

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