The Parker Reese Foundation

New Hope For Congenital Diaphragmatic Hernia

Archive for August, 2009

Ireland Rose is Now An Angel.

Posted by Jessica Singletary on August 30, 2009

Please pray for Ireland’s family as she lost a very courageous battle to CDH today.  I am truly at a loss for words as there are too many babies dying from CDH.

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New PRF Fundraiser Website!

Posted by Jessica Singletary on August 29, 2009

Please check out our new website  just for our fundraisers! 

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Change CDH!

Posted by Jessica Singletary on August 29, 2009

Maxton’s mom, Ashley, joined PRF as a board of director last month.  We were thrilled to have her join our team and this month Ashley has started a fundraiser called “CHANGE CDH“. 

Change CDH involves collecting your loose change to help PRF! Simply put, I would like everyone to collect their change until October 31st (or you can keep it going forever!) and take the change to the bank and then write PRF a check for that amount. Pretty simple. If you would like to get others involved you can put a jar on your desk at work or anywhere for that matter. You may think that change doesn’t matter, but my family has collected over $100 in the past couple of months! $16 sponsors one family per night, so change can definitely make a difference!

Whoever collects the most change will win a free t-shirt from PRF!  Every cent counts toward helping families diagnosed with CDH.  If you have any questions please feel free to email Ashley at ashley@theparkerreesefoundation.com.  Thanks for supporting our mission and heling us CHANGE CDH!

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Addison’s Angel Run – February 2010

Posted by Jessica Singletary on August 28, 2009

If you are interested in an individual sponsorship for Addison’s Angel Run benefitting The Parker Reese Foundation please email Marion Acord at marion@theparkerreesefoundation.com.  The levels range from $500 to $50! 

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Miss North Carolina Joins “Heels for Hope” as Guest Judge!

Posted by Jessica Singletary on August 27, 2009

Miss NC, Katherine Southard, has agreed to participate in Heels for Hope as a guest judge.  We are super excited to have such an amazing woman on our team helping us spread awareness for CDH! 

norris full body

We are finalizing the details of this event and will soon post information for those interested in participating!

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Max Needs Us.

Posted by Jessica Singletary on August 26, 2009

Max is in desperate need of some extra prayers tonight.  Monday night his parents, Claire and Jordan, got the call that he would be going on ECMO.  This little man has proved time and time again what a warrior he  truly is but he really needs us now.  Please take a minute tonight to pray for him and his parents.  They are very special people! 

Claire and Jordan- if you are reading this please know that we are praying and are here if you need anything.  I do hope that you feel God’s love and see His mercy in every step of Max’s care.  We are literally a phone call away.  We love you all three very much!

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