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.

Friday, October 2, 2015

Dudley

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About 8 weeks before Reilly was born, Brian and I decided to get a puppy.  It might seem crazy to some, but, we figured with a newborn on th...
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Wednesday, September 23, 2015

The Difference - Happy 4th Birthday Meagan!

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I remember Meagan's birthday last year. I remember her going downhill that day.  I remember coming home and my in laws not knowing what ...
1 comment:
Wednesday, August 12, 2015

Let the Light Shine

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The summer flew by quickly and there were lots of happenings! After we returned from our Nationals trip, we had some time at home to get thi...
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Thursday, July 9, 2015

Independence

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The last few weeks have been filled with such busy times, I realize I haven't updated the blog in a while.  So many people comment about...
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Sunday, June 14, 2015

Words - announcement to the girls and first meeting with the specialist

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Because of the history of my last pregnancy with Meagan, of course I have to re-visit the specialist OB again with this pregnancy.  I had my...
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Friday, May 15, 2015

Life's Melody

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A little time can give you a lot of perspective on things.  A little taste of reality can really wake you up to the perception of other peop...
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Wednesday, May 6, 2015

Sibling Rivalry

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Anyone who knows our girls knows they are happy.  They are giving.  They are caring.  They love being sisters and love spending time togethe...
Friday, April 17, 2015

Proof

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Meagan has been able to do a lot of things her older sisters do at school through her special needs classroom - art, music, playing with fri...
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Tuesday, March 31, 2015

March Updates Part 2 - Walking Together

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Despite our disastrous family dinner out, we had a few good things happen this weekend.  As you all know, Meagan finally got her new AFO...
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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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