Wednesday, December 31, 2014

Christmas 2014

This season was filled with joy and wonder as our little ladies soaked up their second Christmas as Fertigs. 





Emma is thoroughly engaged when she listens to stories these days and almost daily this month she would ask me to tell the Christmas story.  I tried to be enthusiastic each time.  It is a beautiful wonder that God became man. 


Christmas Eve


Christmas Day (in our matching aprons that Nana made!) 


We are so incredibly blessed! Merry Christmas!!!! 




Saturday, December 20, 2014

Happy Birthday, Bella!

Two years ago, we gathered with dear friends to celebrate the life of our foster daughter (on this blog, we called her Bella). We played games and ate cake, but also had a special moment to pray and to surrender her life to the Lord, to His purposes and plans for her.  

Bella, you are in our hearts forever and rarely far from our thoughts.  We are so thankful for the godly family Jesus chose for you. We love seeing pictures of your beautiful face and sweet smile! Happy Birthday, little one! We love you. 

Wednesday, December 10, 2014

Good news!

The curvature in Emma's spine hasn't changed from a year and a half ago.  We need to continue to monitor her growth process.  But for now, no treatment is necessary.  





We are breathing a sigh of relief and this family can rest and recoup for a while.  Praise the Lord!!! 



Pray for Emma today

It's 5 am and we're on the road again.  Just one week ago we left Florida to drive back to Ohio.  We've basically just started to feel settled at home.  This time it's not the whole family traveling, it's just Emma and I.  This time were riding, not driving.  This time we're not leaving for two months, we're just making a long trip in one day.

We're headed to the Shriners hospital in Chicago.  I know, another hospital visit when we've just been through so much with Elsie.  Today Emma has an appointment to see an orthopedic specialist.  It's our initial appointment so, I don't know much about this hospital yet.  I've just been told, "they take care of everything." Including transportation and money for lunch in the hospital cafeteria.  

You'd never know it from looking at her and watching her run and jump around, but our little lady has spina bifida, congenital abnormalities in her spine and spinal cord.  Last year we tackled the issue of her spinal cord...neurosurgery.  Today we begin to understand more of the issues with the bone structure of her spine...orthopedics.  She briefly saw an orthopedic surgeon while in the hospital last year.  He explained that the curvature of her spine needs to be monitored.  If it's too severe, her rib cage won't have enough capacity for the growth of her lungs.  Growth at her age is a slow and steady rate, so it hasn't been an ugent issue.  But it's also time to find out more.  

Again, please pray.  Pray that whatever the doctors have to tell us today, we would walk in faith and trust that God is good and providing for us.  Pray that her spine is growing straight enough and no major surgery is necessary.  Pray that even though this is another hospital and another big appointment, that we'd still be able to rest and enjoy this day.  And pray for Mark as he's home with Elsie all day!