Miracle Morgan: More advocates on our side

Wednesday, January 15, 2014

More advocates on our side

On Monday, I took Morgan to the pediatrician she had seen as a baby. He is actually the one that initially referred Morgan to a neurologist when she was 18 months old. For various reasons, she has not seen this pediatrician in about three years. I felt The Lord was leading us back to him. He referred Morgan to a pediatric developmental specialist who can evaluate her more specifically and recommend what she needs. I am thinking Morgan needs more therapy and have not pushed for it before because we were just so concerned with the seizures before. Now she is showing potential for learning and I want her to get all that she can to have the best quality of life. This pediatrician is so compassionate and so I am so glad I have one more advocate to help us out. When I went to pick Morgan up early at school on Monday, they were outside. I was expecting to find Morgan in the wagon with one of the teachers. However, it was so awesome to see that she was on the playscape with all the other children! She didn't want to leave so I let her slide one more time. It was just so amazing to see her being right up there with the other children, having fun. When a year ago, she was sitting on the ground in her own world. Praise The Lord for all He has done in Morgans life so far!

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Morgan's Story

Our daughter Morgan turned five in December. She was born healthy and developed normally, at first. She began having seizures at the age of two. Since then, her development has halted, even regressed. She now cannot talk. She walks, but is uncoordinated which causes her to fall multiple times a day. She rarely smiles or laughs, since she doesn't feel good.
She is an intelligent little girl that just seems to be trapped in her body right now. Doctors said that the seizures and the medicine were likely holding her back from progressing. She has been on seven to eight different seizure medicines and continues to have multiple seizures daily and nightly mostly during her sleep. The medicines were also affecting her negatively. Some of them made her hyper, some made her so lethargic she couldn't function, and some made her kind of crazy. We tried multiple treatments to try and help her such as diet, supplements, and therapy. We would see fluctuating results. All the while, she just wasn't developing or learning and continued to have daily frequent seizures.
She has undergone multiple testing and seen multiple doctors. Last year, after three days of being in the hospital with video monitoring of her seizures, she was just put on some more medication. At that time, we were told she was not a candidate for surgery as her seizures were coming from different parts of the brain.
In the last couple of months, Morgan's seizures had worsened so much, that we were having to give her the emergency treatments and even called EMS. It was no quality of life for her. We had to do something. We had been so against surgery before, but finally my husband and I had decided we were ok with it and were going to ask the doctors if it was an option now. Well, we didn't even have to ask them because when we got to the appointment, the doctors had looked over her MRI again. After studying her case with a panel of specialists, they had decided that she was now a candidate for surgery. They said they thought they could remove or disconnect most of the areas that were causing the problems.
We are praying and believing that the doctors will be able to get ALL of these problem causing areas. We are believing that ALL seizures will be gone and never return, and medication will no longer be needed. We pray for a speedy recovery with no initial temporary regression( which doctors said was possible). We also pray for total restoration and the ability for her brain to catch up and to learn and develop.

With God ALL things are possible

Thank you all so much for your prayers.
Jeananne, Billy, Will and Morgan Johnson