In-flight entertainment
Jeff and I started this blog to share pictures of Leah and the story of her birth with all of the family and friends across the country who prayed so diligently for us. We received our miracle when Leah survived labor and spent forty-five minutes with us. We also included posts on Leah’s conditions and what we went through, in order to share our experience with others who may be dealing with a similar loss. When we received Leah’s diagnosis one of the first things we did was hit Google, but we had a difficult time finding anyone writing about their experience with Leah’s type of skeletal dysplasia; we wrote this to fill the void.
As our lives moved forward we continued to blog about the adoption of our precious son Tommy from Uganda, his homecoming, and the everyday moments that now compose our lives. Now we find ourselves on yet another adoption journey to bring home another son from Africa. Thank you for reading and walking this road with us.
Please feel free to contact us at lovinglittleleah@gmail.com.
As our lives moved forward we continued to blog about the adoption of our precious son Tommy from Uganda, his homecoming, and the everyday moments that now compose our lives. Now we find ourselves on yet another adoption journey to bring home another son from Africa. Thank you for reading and walking this road with us.
Please feel free to contact us at lovinglittleleah@gmail.com.
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1 comment:
He would make an awesome pilot and you could get flight benefits :)
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