The Parker Reese Foundation

New Hope For Congenital Diaphragmatic Hernia

Posts Tagged ‘Prayers’

Awesome News But Still Need Prayers.

Posted by Jessica Singletary on October 28, 2008

After 18 days, Carter came off ECMO yesterday!  What amazing news this is as now they can start thinking about surgery.  Please pray for Carter and Brad and Kellie as they continue to deal with all that CDH is and means.   This is definitely a step in the right direction!

Ava was extubated yesterday!  Please continue to pray for her that her body heals and she is able to go home soon to be with her family during the holiday season.  She is an amazing little girl with such spunk and fight. 

God is an awesome God.  Please remember to keep these familes in your prayers daily.

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Prayers for Carter.

Posted by Jessica Singletary on October 10, 2008

Please continue to pray for Carter as he was put on ECMO last night.  He and his family need our thoughts and prayers.  Take a peek at their blog and send them some good thoughts! 

They are an amazing family!

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The Dedication.

Posted by Jessica Singletary on September 30, 2008

Went really well.  We had a great time and the turn out was good.  It was so nice to meet Kellie, Brad and Lucy.  And it was awesome to see Russell and April again.  And her parents Debbie and Roy.  There was tons of good food and the best cupcakes in the world!  I think they were the hit of the party!  I’ve used The Cupcake Shppe Bakery before and once again we were not disappointed.  YUMMY!  Below is a picture I took from Kellie’s blog because I haven’t downloaded mine yet.

Thanks for all the prayers and thoughts.  We are so blessed by the foundation and what it is doing for CDH families.  I am constantly amazed at the support we have and the countless emails I receive daily from families affected by CDH.  We will never stop supporting CDH families and with each year we’ll get closer to finding a cause and one day a cure. 

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