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Pontocerebellar Hypoplasia support advice and resources - Cody and Dylan Sheppard

ACT Cerebellar Hypoplasia Support Network Incorporated - supporting families with affected children

http://www.codysheppard.com/

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CONTACTS AT CODYSHEPPARD.COM

ACT Cerebellar Hypoplasia Support Networ

Sonia Sheppard

7 Ped●●●●●Place

Ric●●●son , ACT, 2905

au

61 02●●●●●12845
co●●●●●●@homemail.com.au

View this contact

ACT Cerebellar Hypoplasia Support Networ

Sonia Sheppard

7 Ped●●●●●Place

Ric●●●son , ACT, 2905

au

61 02●●●●●12845
co●●●●●●@homemail.com.au

View this contact

ACT Cerebellar Hypoplasia Support Networ

Sonia Sheppard

7 Ped●●●●●Place

Ric●●●son , ACT, 2905

au

61 02●●●●●12845
co●●●●●●@homemail.com.au

View this contact

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Pontocerebellar Hypoplasia support advice and resources - Cody and Dylan Sheppard | codysheppard.com Reviews
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ACT Cerebellar Hypoplasia Support Network Incorporated - supporting families with affected children
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Pontocerebellar Hypoplasia support advice and resources - Cody and Dylan Sheppard | codysheppard.com Reviews

https://codysheppard.com

ACT Cerebellar Hypoplasia Support Network Incorporated - supporting families with affected children

INTERNAL PAGES

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1

Dylan's Funeral

http://www.codysheppard.com/dylan/funeral.html

Dylan in the News. Cody in the News. Dylan and Cody's Special Places. What can we say? What an emotional and amazing day. We didn t realise until this day how many lives Dylan had touched. On arriving at the church we couldn t believe our eyes. There were cars everywhere on the side streets, in the church car park and in the oval car park behind the church. The service at the Cemetery was extremely special. Everyone gathered around and blew bubbles to Cody. A massive number of helium coloured bal...Our h...

2

Cody Sheppard's story

http://www.codysheppard.com/stories/cody.html

Raquo; Cody Sheppard. Dylan in the News. Cody in the News. Dylan and Cody's Special Places. Stories of affected children and families. Cody Darren, our first child was born on the 28th April 2004. A day after Cody was born he was admitted to the intensive care unit for further assessment due to poor feeding, high muscle tone, and little responsiveness. During the next couple of days we believed that our dream of having a family was no longer a dream, and spent days questioning our faith and asking why us?

3

ACT Cerebellar Hypoplasia Support - Fundraising events finance

http://www.codysheppard.com/funding

Dylan in the News. Cody in the News. Dylan and Cody's Special Places. How have the profits and donations been spent? As a result of the various fundraising events and donations from organizations, family and friends, the Sheppard family have been able to provide the following equipment and support to Cody to allow him to have the best quality of life, and to provide him with the best send off:. Specialized bath chair;. Tumble form chair;. Big Mac Communicator and specialized toys;. Darren and Sonia will ...

4

Dylan Sheppard's story

http://www.codysheppard.com/stories

Raquo; Dylan Sheppard. Dylan in the News. Cody in the News. Dylan and Cody's Special Places. Stories of affected children and families. Dylan Darren, our third son was born on the 4th of May 2010. Throughout the pregnancy he was closely monitored by the Fetal Medicine Unit. We were reassured for the whole of the pregnancy that the brain was perfect. Ldquo;I tried to convince myself that there is no way that Dylan could have the same condition as Cody”. Links to other stories. The Joshua Deeth Foundation.

5

Dylan Sheppard - In the News

http://www.codysheppard.com/inthenews/dylan.html

Dylan in the News. Cody in the News. Dylan and Cody's Special Places. Dylan in the News. Paliative Care Australia launch of Journeys. Palliative Care Australia held a morning tea at Parliament House, Canberra, on Thursday 18 August 2011 for the launch of. Journeys – palliative care for children and teenagers. And Palliative Care supports us. Journeys Launch – Agenda. Our Family Journey – Presentaion. Photos of Journeys Launch. Click photos for larger view. Story published in The Chronicle, August 23 2011.

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Pontocerebellar Hypoplasia support advice and resources - Cody and Dylan Sheppard

Dylan in the News. Cody in the News. Dylan and Cody's Special Places. The purpose of this website is to share information about the condition, and to support other families who have children that have been diagnosed with the condition. This website is dedicated to Cody and Dylan. It is in memory of Darren and Sonia's two beautiful boys who were faced with many challenges during their short life. They will never forget how brave their boys were and their gorgeous smile. Darren and Sonia Sheppard.

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