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.

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...
Monday, March 30, 2015

March Updates Part 1 - Walking outside....

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This weekend was a happy time for the family.  The girls got their third quarter report cards.  All A's and lots of great remarks from t...
Wednesday, February 4, 2015

Knots

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In general, knots just aren't a very good thing to have.  Knots in your hair - ow.  Knots in your jewelry - a pain.  Knots in your muscl...
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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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