“Whatever it takes….”

The fundraising group Team Spencer was set up by Rick and Ruth Steven in honour of their son, Spencer who was born in March 2006 with Spinal Muscle Atrophy (SMA) Type 1 and who died just seven months later. SMA Type 1 affects about one in every 6,000 kids and is the most common cause of genetically determined neonatal death. The onset is sudden and most children born with the condition live for less than two years.

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You will need to order a background essay at minimum as soon as to know just exactly how it must appear to be

You will need to order a background essay at minimum as soon as to know just exactly how it must appear to be That is ??? best oriented in age-old contradictions and will objectively inform about reforms, revolutions and wars? That knows the associated weaves of crowned families? For whom it’s not hard to monitor causal relationships on a scale that is global? Individuals
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The Steven Family

Spencer Steven was born in 2006 with Spinal Muscular Atrophy (SMA). Team Spencer was set up by Rick & Ruth Steven in memory of their son Spencer. During Spencer’s amazing life, his parents and sister were aided by fantastic support from PMH and the staff who provided medical and emotional assistance for their journey with Spencer. When Spencer died at 7 months old, Rick and
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Donate

To donate to TEAM Spencer, please contact Lara Marmion on 08 9424 4100 or lara.marmion@amepl.com.au