Friday, November 11, 2016

Long overdue update


Wednesday night 11/9/16
First, thank you to everyone that has messaged and called.  I apologize for not responding to all.  It is difficult to communicate with Matt, let alone everyone else.  There have been providers in our room all the time.  It is difficult to catch a breath.  Also, jet lag + hospital life = SO TIRED!!!!  With that said, here is what is going on so far.

We have shared previously that Maelee has lower limb paralysis.  During our time together (just over 2 weeks!), she did not have any bowel movements.  Upon our return to the US we contacted our pediatrician with our concern.  She directed us to the ER for evaluation of constipation.  Since Maelee’s medical history is unknown, the ER made the decision to admit Maelee to the hospital late Monday night.  We have been in investigation mode ever since. 

In addition to figuring out her constipation issues, the team is investigating her paralysis and bladder.  Many tests have been ordered and specialists consulted.  The major test that would provide many answers is a MRI of her brain and spine.  During a very frustrating trip down to the MRI unit, it was determined that x-rays would be required prior to the MRI.  The x-rays needed to rule out any potential metal in Maelee’s body since metal is not allowed in a MRI machine.  She does not have any surgical incisions, so there was no major concern.  To our surprise, Maelee has an implant in her heart.  The conclusion is that she had heart surgery as an infant.  Since there are no surgical records, we do not know if the implant is metal.  Therefore, a MRI cannot be performed at this time.  This is very disappointing because it is the best tool to assess her brain and spine.  This news came late Wednesday afternoon, so we are waiting to hear the new plan from the neurosurgery team.  We also requested that cardiology be involved to assess her heart.

Maelee has a very severe bladder infection.  It is believed that she is unable to fully empty her bladder due to her paralysis.  She has bacteria that are resistant to most antibiotics.  The infectious disease team has found one antibiotic that may kill this type of bacteria.  The new antibiotic was started Wednesday afternoon.  In addition, urology was consulted to discuss bladder management.  There will be testing tomorrow to test Maelee’s kidneys and bladder function in addition to assessing any damage.

Maelee continues to eat and drink very little.  Speech and dietary have been consulted to aid with these issues.  Also, physical therapy has been consulted to work on her core strength and maintain muscle flexibility.

One of Maelee’s x-rays suggests that she has hip dysplasia.  Additional imaging was done today and we are waiting to see orthopedics to discuss this issue.  It is likely that it will be a minimal issue for her because she does not bear any weight.

I may be forgetting something right now, but as you can see, there is a lot going on.  Please pray for wisdom for doctors.  Pray for Maelee to continue to build trust with us and her caregivers.  Pray that she will be less fearful with caregivers.  Pray the antibiotic will be effective to treat Maelee’s bladder infection.  Pray for Matt as he holds down the fort at home.  Pray for the kids as life is a bit crazy right now, and no schedule causes difficult behavior.  Pray for Deanna as she navigates and comprehends all of the issues at hand.  Also pray for rest and stamina for all.  

We are thankful that God has us here.  We expected Maelee’s medical evaluation to take months.  It is a blessing to have all of these specialties working together to care for our girl.  We are thankful for the opportunity to get her medical care as soon as possible.  God knows every hair on her head and all of her medical issues.  We pray that we will receive clarity with her diagnoses and be able to give her the best care possible.

Thank you for praying.  Thank you to everyone who is helping with our kids.  Thank you to everyone who has been checking in.  Thank you for blessing our family.  We are so grateful for all of you!




Thursday 11/10/16
At one point today there were 12 doctors in the room discussing Maelee’s plan of care.  What a blessing to have so many specialties coordinate together!  We have added neurology and neuro ophthalmology to her team.  These specialties were added because there is concern that her eyes are not tracking properly.  This may be the result of a brain abnormality.  Tomorrow, Maelee will have CT scans of her brain and spine under sedation.

Today she had ultrasounds of her kidneys, bladder and spine.  She also had an abdominal xray, echocardiogram and kidney function test. 

Cardiology came by today and discussed their findings.  Maelee does indeed have a PDA closure device in her heart.  The cardiologist was able to find the smallest, faintest, finest incision on her leg as the point of entry.  Right now the device is doing its job.  Her heart looks good currently.  The problem is that the device is in the right place but the wrong angle.  There is a chance that over time it may cause blockage of her aorta artery.  This is something that will be watched over time with routine visits to cardiology.  We are praying that no surgical intervention will be required. 

All of the testing on Maelee’s bladder and kidneys came back today.  She does have bladder damage and reflux from her bladder to kidneys.  This will be treated with medications and catheterization.  These are issues that we anticipated with her paralysis.  These issues can be managed at home and prayerfully will resolve.

Maelee is still not drinking at all since Tuesday and eating very little.  She needs to eat and drink for us to leave!  Tomorrow while she is sedated, she will receive a feeding tube. Pray she starts drinking!  Nothing has enticed her: straws, sippy cups, regular cups, bottles, milk, juice, water, Gatorade. The list goes on!

Infectious Disease stopped by.  Maelee will also have blood work drawn during her sedation tomorrow.

Maelee still has not had a bowel movement on her own.  The team is hoping that if she increases her nutrition, then she will eventually have a bowel movement.  If not, we will need to investigate further and implement a bowel management routine.

It was a busy day here today!  I may be forgetting something.  Thanks again for all the well wishes, texts and calls.  Thank you for understanding if I don’t answer.  Continue to pray for our sweet girl.  She has been through so much! For those wondering about discharge…”hopefully by the end of next week,” says our favorite resident.  Womp, womp!  Prayerfully sooner!!!

Friday 11/11/2016
This morning started with a trip to have Maelee’s CT scans.  The plan was to do these scans under sedation.  Unfortunately, Maelee’s IV was no longer working.  The team was not able to start a new IV.  Thankfully they were able to give her some medication through her nose to relax her.  She laid still to complete the scans.  Praise God!

When we returned to her room she had her NG tube placed while she was still loopy.  She is currently receiving medication through the NG tube to help clean out her bowels.  After her bowels are clear, they will begin to feed her through the tube since she is not eating or drinking for us.

There was still the problem that she needed to have an IV after it was blown this morning.  The team came back and was able to place an IV using ultrasound for guidance.  She is a very hard stick!  It was determined that a PICC line should be placed in order to have reliable access.  Shortly after the IV placement, Maelee was able to be sedated for the PICC line placement. 

During her procedure, neurosurgery stopped by to review the CT scans.  There are no gross abnormalities present that would explain Maelee’s paralysis.  As we have shared, the MRI is really the best tool to assess the brain.  Neurosurgery would like one more CT scan view for completeness, but they do not have any surgical concerns.  They have requested that GI be consulted.  Add another specialty to the list!

This afternoon Maelee has been sleeping.  She is completely off her schedule because of jet lag and hospital life.  Last night we had play time from 1am-430am.  Girlie needs to get on US time!

Thanks again for praying and checking in!

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