Meagan

Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life.

Saturday, November 10, 2012

God and Country

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As we all know, Veteran's Day is November 11th.  This is a day we recognize and thank those who have served and are serving our country ...
Wednesday, October 31, 2012

PUMPKIN!

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One year ago, I was at the Pumpkin Patch with my older girls and my parents.  We had a lovely day exploring the farm, picking out pumpkins, ...
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Yum Yum - Update #1

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We have had quite a breakthrough these last few weeks.  I didn't want to write anything about it because last time I did, Meagan stalled...
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Sunday, October 21, 2012

Infusion #3..and good news!

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Meagan went for her third stem cell infusion at Duke Children's Hospital last week.  It was a crazy hectic week leading up to the trip, ...
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Wednesday, October 10, 2012

Put Your Hands Together

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Meagan's hospital stay 2 weeks ago took a lot out of her.  She has obviously been more tired than usual and in some ways, even still see...
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Saturday, October 6, 2012

Time To Par-tay! (Finally!)

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We finally had Meagan's "official" 1st Birthday party today! We put it on hold for 3 weeks after her 'real' birthday j...
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Wednesday, October 3, 2012

Checkin Out!

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This morning, Meagan woke up with no fever. And we held off giving any Motrin last night, so I knew for sure that the fever was probably gon...
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Monday, October 1, 2012

Improvements and Questions

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Well, first the good news. - Meagan is having more wet diapers. - It seems (knock on wood) Meagan's fever has broken... it is hoverin...
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Sunday, September 30, 2012

Back We Go

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Saturday morning started off pretty normal.  For once, we had NOTHING to do the entire day.  It was awesome.  I was looking forward to final...
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About Me

Molly and Brian
We have 8 beautiful daughters. Our 5th daughter was diagnosed with severe congenital Hydrocephalus at 20 weeks gestation. Although we've been through pregnancy before, this journey was quite different. Reading about other families dealing with Hydrocephalus helped us immensely, and we hope one day, this blog can help families who may have to deal with this condition in the future. We have had a gap with updates as life got busy, but we will try to pick up and post more often to talk about amazing Meagan and her life :)
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