I have included pictures of a normal brain scan as well as Rayden's scans from Jan. and March. I know these may not be exactly the same level of scans but I thought it would help make my point. ![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEi7nPcurBPBoQxU23sOPXueUx0hYG5kIxQCfhtmwMrX_368V03kfh6a4pKUFc_GZZckCXSTFIYMmyTvsTQAOo-mMxc3NriaoI3ZwLGQ-nEORFbrkcXPrccp0USLPNXGecMdAxP_mKvXgO5N/s1600-rw/normal+brain.jpg)
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEi7nPcurBPBoQxU23sOPXueUx0hYG5kIxQCfhtmwMrX_368V03kfh6a4pKUFc_GZZckCXSTFIYMmyTvsTQAOo-mMxc3NriaoI3ZwLGQ-nEORFbrkcXPrccp0USLPNXGecMdAxP_mKvXgO5N/s1600-rw/normal+brain.jpg)
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhGF3lWeJ6UCaenfWYXlSFu25wzECecu_D9s7z3sk0c-QPP-25WcgReUwy6NX_TvBJGA-6M3y9J3lU39rLmv8VwaLWJi4tBfMViAS-FgvlxyQAaum-CeM9k0M4xojV_O_XWH9rw4Csq7_Ty/s1600-rw/brain+2+text.png)
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgc8Ju3-KApX_auFbO4vN831FV1ZG_T_LKdXhl1w4X8K9IS8GhziwvA0luqUmH8fdOSQyGemv1PH6JIDlFvTOSLcB2RxUxJl2NZ0_mezGcIo7naMXSJr_nQuQG4D5Jz-v4kxkZigLpUAHFQ/s1600-rw/brain+1+text.png)
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhajS2PKWjvMAiWuP-YuTh1yunVpfPoLgKL81SGTFsPiDGo4N9X1OLCZis021eOCKIbEzpm31trmPZZh7HXCbP1z2Pht7EXqpS7c-8_h7aTk2BnQyNoHEVwk5Ipu7hHGN9VzrVk_vyUExhN/s1600-rw/brain+3+text.png)
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhv5m47WDcSiux8laFbNRUY3E33I61fHRFMeKyndu3gem0mrLO3y0SdsWMhDsyYxvpukwKy2CACvKd1Slao26GawQMQWvSbkQQ2l-tdo2guToHCi_WFqCXNm-q-oBSEN_EdLWmG0Gyfyb2e/s1600-rw/brain+4+text.png)
still see so much fluid that it scares me to death. I wonder how he will ever have enough room for his brain to grow if his head is FULL of fluid? Will he be able to function on such a small amount of brain? Will there be a time where he stops learning/maturing because his brain doesn't have any room to grow? I'm just super worried. Dr. Elton stated that he may not need a lot of brain to function normally. That most people don't use 95% of their brain anyway! But I worry... What kind of future will he have? I know he is already a miracle and I should be grateful and just let it go at that. But I worry...
I sit in awe of how wonderfully made he is. His precious little smile just melts my heart. The way he wraps his tiny little fingers around mine, and looks at us with those gorgeous blue eyes. The adorable way he smacks his lips and sticks out his tongue to tell us he's hungry. How he rocks himself in his bouncy seat by kicking his legs. His sweet little grunts and snores. The most adorable way he folds his little hands in prayer when he sleeps. Yes, I am reminded that he is wonderfully made...
God never ceases to amaze me!! As I was typing this blog post this scripture came across my mind. Then this song just appeared on my computer!!! Please take the time to listen to it.
https://youtu.be/GhzlI5KGTno
2 comments:
This is a beautiful post. Thank you for sharing it. I went through the same process with my son and it was a difficult and trying one. I think the thing that made the difference was the community around us. We had a big group of people who just seemed dedicated to making our life easier. I will be praying.
Kacey @ Glendale MRI
Thank you Kacey. Now (April 15, 2016) a full year later, Rayden's brain has filled in and looks NORMAL!! His ventricles have decompressed to normal size with hardly any fluid at all. Isn't God amazing? Even Rayden's Neurosurgeon is amazed!!!!!!
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