Abby's Army: Some Good News

Tuesday, July 21, 2009

Some Good News

Morgan, Jason, Abby and Lyla are at St. Jude now. The results of the latest MRI show the tumor has not spread since the last MRI. They will not have to begin any treatment at this time and will be able to go home for three months then they will return to St. Jude for her next MRI. They will be in Memphis until tomorrow afternoon and then will be headed home. This is very good news and such an answer to prayer. Thank you for your faithfulness to pray for Abby.

4 comments:

AnonymousJuly 21, 2009 at 8:55 PM
Thank God!!! I am SO SO SO Happy!!
-Whitney
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AnonymousJuly 21, 2009 at 10:18 PM
God continues to bless! I'm very happy too!
Carrie
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AnonymousJuly 22, 2009 at 12:41 PM
Abby, and the entire Conner family, we miss yall and love you bunches!

Mrs. Christy and Mrs. Linda
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Melissa L. ThompsonJuly 27, 2009 at 10:28 AM
What FANTASTIC news!! GOD is good!!
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How We Got to Here-Updated August 2010

It all started with very small seizures. We are not sure how long she had been having them but they were getting more frequent. On April 23, 2009, we took her to Dr. Baker who sent us to the ER at Arkansas Children's Hospital. An MRI revealed a large brain lesion and Abby was taken to the ICU for 3 days. She moved out of the ICU and spent a total of 8 days at Children's. We saw several doctors who were all pretty stumped by what they saw. It didn't look like anything-tumor, infection, swelling. They put her on an anti-viral medication in case it was infection. Another MRI showed no changes. Some doctors thought it was gliomatosis cerebri but some didn't agree with that diagnosis so they decided to take some spinal fluid to analyze. They had to take it from the brain though because of possible swelling. We spent another night in ICU.

After she was discharged we contacted MD Anderson in Houston and St. Jude's. We flew to Houston where another MRI was performed. They informed us that it was gliomatosis cerebri. St. Jude's called later that day and informed us that they felt it was gliomatosis cerebri. That was not what we wanted to hear-gliomatosis cerebri has a 5% survival rate. However, St. Jude's neurosurgeon, Dr. Boop, wanted to try to remove some of the tumor. This allowed for a biopsy of multiple pieces of the tumor. On May 22, 2009, Abby underwent brain surgery. Almost all of her right temporal lobe was removed. Abby had to spend another night in ICU, this time at LeBonheur in Memphis.

The biopsy results surprised us all, it was not gliomatosis cerebri, it was a low grade glioma! God had answered everyone's prayers! The plan was to begin chemotherapy to stop the tumor from growing but our neuro oncologist, Dr. Armstrong, wanted to wait a few weeks to see how this tumor was going to act. We were once again surprised-the tumor wasn't growing. No need for treatment!! And that is where we are today. It has been over a year, and the tumor still has not grown. It's still there, big and nasty, but it is quiet right now. We go to St. Jude's every 3 months for an MRI and other appointments to monitor the tumor.

Abby's Army

Tuesday, July 21, 2009

Some Good News

4 comments:

Abby Summer 2010

How We Got to Here-Updated August 2010

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