David Andrews

Dave & Gabrielle's Sponsored Walk

Fundraising for LAM Action
£1,107
raised of £1,260 target
by 47 supporters
Donations cannot currently be made to this page
LAM Action

Verified by JustGiving

RCN 1167610
We fund essential medical research to find a cure for Lymphangioleiomyomatosis

Story

Gabrielle is taking part in the 2.6 Challenge by walking 2.6km around our garden on 26 April 2020, to raise funds for LAM ACTION, ably supported by David who will be marshalling the effort. 

LAM ACTION continuously supports ladies like me with Lymphangioleiomyomatosis (LAM) and especially so during this pandemic.

LAM is a rare lung disease almost exclusively affecting women.


MISSION ACCOMPLISHED. I started about 9.15 this morning (Sunday 26th April) before the sun and pollen count were too high.  We are so lucky to have a garden to exercise in.  I enjoyed the smell of the lilac and bluebells and listening to the insects and birds.  The highlights were watching a pair of Canada Geese flying over and hearing my first cuckoos this spring.

Thank you to everyone for your encouragement, messages of support and donations.  Keep safe and well.

29 April 2020
Thank you to Tony, Louise, Suzi and Paul, Ken and Maggie, Niall and Trudi and Sid for your support and online donations.  Also to Janet and Anthony, John and Sylvia and Graham for their encouragement and offline donations.

The text below refers to previous fund raising we did for LAM Action 2018. We raised £957 through Just Giving which is included in the overall total.

Sponsored Head Shave was held on Friday 21st September 2018 at 7pm in Ruspidge Memorial Hall, Ruspidge, Gloucestershire.


Our thanks to Jo from Mel's Top Cutz for shaving the hair and beard and to everyone who came to see Dave loose his locks.

I (David) would like to raise funds for a charity called LAM ACTION. LAM is the shortened version of Lymphangioleiomyomatosis, a very rare disease mainly affecting the lungs. Almost exclusively a female disease, there are currently about 240 women in the UK diagnosed with LAM. This disease is degenerative, causing excessive growth of smooth muscle cells which progressively destroy lung tissue and erode lung function. Although research is ongoing, there is currently no cure for LAM and effective treatment is limited.


My wife Gabrielle has coughed badly ever since I known her and she was incorrectly diagnosed with asthma some years ago. She has now been recently diagnosed with the rare condition of LAM. Since her diagnosis she has felt very isolated. LAM Action has helped to address this.

LAM ACTION has 2
primary aims;

• To provide information and support for those with LAM and their families
• To educate health professionals about LAM and to advance research into LAM

There are so few women diagnosed with LAM that funding for LAM Action is sporadic.  I would like to help and have agreed to do A SPONSORED HEAD SHAVE on FRIDAY 21st SEPTEMBER 2018 and would ask you to donate via JustGiving.

Thank you for your support - Dave


Thank you for taking the time to visit my JustGiving page.


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About the charity

LAM Action

Verified by JustGiving

RCN 1167610
Lymphangioleiomyomatosis (LAM) is a rare lung disease that only occurs in women. It affects just over one woman in a million. We are a self-help group providing support for patients with LAM and raise money for vital research - it is often difficult to obtain money for research into a rare disease.

Donation summary

Total raised
£1,107.00
+ £225.50 Gift Aid
Online donations
£1,107.00
Offline donations
£0.00

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