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Bradleigh Nicolynn Dowdney

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Monday, October 4, 2010

Brayden's MRI on Friday

Thank you ALL for lifting up our little man on Friday.

Before all this stuff with HCV hit our radar, Brayden was scheduled to have an MRI done on his spinal chord. Brayden has a cyst that is growing on his spinal chord and we have it imaged in order to ensure that it is not putting any pressure or compression on the chord. This would decrease the amount of blood and oxygen carried to the brain and is extremely dangerous. We have had the cyst imaged twice, once in December right before we carried him home and then again last Spring. The MRIs did show that the cyst was developing and giving the spinal chord room to grow, without much compression. THAT IS GOOD!! We are needing this cyst to stay off that spinal chord until Brayden is late teens, due to the nature of the surgery.

When we arrived at the hospital, we were admitted due to the need for anestheia during the proceedure. If his heart rate or breathing fluctuated during the MRI they would keep him overnight for observance. A few hours after we arrived, the anesthiolgist came to talk to us about the proceedure. When she learned of B's recent blood work she said that she did not feel comfortable administering meds during this crucial time for his liver. Anesthesia alter the blood flow to the liver and is hard for the body to metabolize. She said that she would have to contact the Neuro Surgeon who ordered the MRI before she could cancel it and that she would try to contact him. PRAISE GOD..she was able to speak with Dr. Roberts and they did confirm that we were in a position to give his little liver some time before we proceeded with a MRI.

We were so very thankful that the Dr. was protective over our litle son's liver and agreed to give him some time to, LORD WILLING, clear this HCV. The Neuro Surgeon requested that we see him in clinic before we were able to leave and so we did have a very long wait to see him. After his exam of Brayden he discussed, at length, his concerns and projections regarding this cyst. He felt really good about the decision to postpone the MRI for 3 months and then we will see where B is with his blood work.

It was a double edged sword...we were so anxious to see how this cyst was developing however, so very thankful that we waited and gave B this opportunity to fight. So on the front of the spinal cyst, we will have to wait 3 months. In the meantime...that just give us all the time to lay this precious little one at the Father's feet and ask for healing. I would love for the cyst to just disappear! Wouldn't that be a fun conversation with the doctors?

David and I have come to remember one of our very first prayers for this little boy. We prayed that Brayden's life would point people to Christ and glorify the Father. We prayed that all that came into contact with him would hear of the healing, faithful, providing, and merciful Jesus that has worked miracles in this littles life and stand ready to do the same for all.

To God be the glory for all things He has done.....and will do yet again.

Kelli

1 Friends for Coffee:

The Scott Household said...

Kelli,
I've read your blog (through Kelly's Miracle Blog) and am in amazement at the strength of your son.
I am a carrier of HCV (Genotype 1A) and understand how scary it can be. I'm also a mother (new-ish!) to a 9 month old who will soon face her first quanatative test of her HCV levels. Please let me know if I can help in any way :)