the fault in her genes

September 18 approaches and it will be three years since my sister Andrea was diagnosed with Diffuse Large B cell lymphoma (stage 4). Andrea was 42 at the time, a partner, a mother of two

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A mother’s perspective…

“Prepare yourselves for the worst and hope for the best”. These words still echo from Dr Henry Eckhart, the Royal Children’s Hospital senior Haematologist and his team, Dr Keith Waters and Dr Karen Tiedemann as

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We’re shaking things up again!

On Wednesday 15 October from 12.30 – 1.30pm, Snowdome will hold the second ‘Great Shake-Up’ virtual fundraising event. This unique event is streamed live into meeting rooms enabling corporate/business Australia to attend an important fundraising

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New Fellowship award – Dr Jake Shortt

We are delighted to report that Dr Jake Shortt (pictured second from left with Snowdome CEO, Miriam Dexter, the Hon. David Davis and Snowdome Director, Nicky Long) has been awarded the Eva and Les Erdi

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A carer’s perspective …

Reviewing the diary of Gayle’s lymphoma now in its fifth year, I am reminded of the huge range of emotions both from the patient’s and the carer’s experience. Shock and surprise were first, when Gayle

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‘Great Shake-Up’ 2013 Highlights

The inaugural Snowdome Foundation’s ‘Great Shake-Up’ was held in August 2013. It was the first-ever virtual fundraising event held in Australia. Click here to view 2013 highlights video. The ‘Great Shake-Up’ 2013 delivered significant results: Raised

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