Wednesday, April 25, 2012

Praise Report

I have been hesitant about sharing much about Mia's medical needs. On one hand I want to be very respectful and protective of her. I have been praying about what I should and shouldn't share with others. The reason we share her story at all is that first of all we want the Lord to be glorified in the way He is working in her precious life. Secondly, I want to encourage others who are considering adopting a child with special needs.

When we accepted Mia's referral we knew that she had a history of seizures and developmental delays. At the time she was 2 and a half and standing with support. She could crawl quickly and walk with help. There were many unknowns about her condition. We talked with doctors and were given the best and worst case scenarios. It was scary to think about all of the "what ifs." I remember telling Justin that I could not say "no" to a list of maybes and what ifs." We knew she was our daughter and that we would do whatever it took to get her home and get her the help she needed when she got here.

We knew that she would need an EEG and MRI when she got home. Last week we got the results and we are praising the Lord that they were both normal!!! Mia has not had a seizure in at least 8 months, maybe longer.  She has been on seizure medication since she was a baby. Since she is doing so well and her EEG looked normal we are going to attempt to wean her off of the medication. This makes me happy and fearful at the same time. We are praying that she will remain seizure free without her medication.

The MRI also looked good and for that we are so thankful!! Her neurologist does believe she has a mild case of cerebral palsy, but he is very optimistic that she will thrive and bloom now that she has a family and will soon be starting therapy. We will have her evaluated soon for physical, occupational, and speech therapy. We are going to focus on PT first and will probably have a pretty full therapy schedule by next fall.

She has come so far since she first came home almost 7 weeks ago and she is a totally different child than the one we were referred 7 months ago. God is so good!! We know there may still be tough days ahead, but for now we are choosing to be thankful and focus on the amazing progress she is making.




 I praise you because I am fearfully and wonderfully made; 
   your works are wonderful, 
   I know that full well.
Psalm 139:14

9 comments:

  1. Love this update Meredith!!! Your Mia is truly a miracle girl!!! And isn't all the hard stuff totally worth it when you see her light up! Oh man, we are so blessed to be the mamas to these kiddos!!!!!

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    1. Yes, those sweet smiles make it all worth it!! We are blessed indeed!

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  2. She is so beautiful and no doubt will flourish now that she is home! We can relate to everything you have been through with her as we are walking the same path. God has been SO faithful to these sweet little ones!!

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  3. AWESOME!!! Our new little man is doing really well and he too has mild CP. They totally expect him to walk. He is also 2 right now, and has been with us for about 10 weeks :)

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    1. I have seen him on your blog and he is so precious! I am glad he is doing so well!

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  4. Wow! Awesome, awesome news! I so LOVE your perspective and following your journey. :)

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  5. Praise God for good test results and good medical care! :) Glad to hear this! And orange is one great color on Mia!! I love her smile!
    Kylene

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  6. Go Mia! Charlie smiled seeing her picture. Praying your PT, OT, DT, etc evaluation goes well. We start DT today and speech/feeding next week.

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  7. Oh thank you so much for the update! God is working miracles in that girl's life!! I just adore how she LIGHTS UP in every picture! What a blessing it is to have a family to call your own! And I also just want to thank you for your optimistic attitude towards this! I'm sure some days are more difficult than others but I am so encouraged by those like you who bring glory to God even in the hard times!

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