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The Linn Family
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The Linn Family
Praise the lord, we are home. Since April 27th we have spent 35 nights in the hospital. Thankfully, this round did not include any time in the ICU which is a blessing. Here’s a recap of some of the main events from this hospital stay:
- lots of tears from pokes for blood work and IVs
- surgery to drain and wash out the collection of abdominal fluid
- chest tube placement for draining lung fluid
- removing chest tube and belly drain (more tears with taking off bandages)
- l0 days worth of multiple IV antibiotics
- multiple chest X-rays
- an abdominal ultrasound with a false read for a pseudo aneurysm, leading to an emergent CT scan that revealed it was a false alarm (after mommy had a full out panic attack)
- many wagon rides around Dukes campus and daily visits to the gift shop :)
Phew.
We were discharged on Wednesday and as of now the fluid in Hollis’s lung has improved significantly and there are no current signs of infection. We were discharged on her current medication regime along with two added oral antibiotics. In total, Hollis takes around 15 medications, some multiple times a day. I will say she is an absolute champion when it comes to taking meds and I am so grateful for that.
We saw nephrology before being discharged since Hollis’s kidneys have not yet returned to their pre-transplant function. We learned that it is possible they might not return to where they were prior due to the amount of damaged sustained after her first transplant. The plan for now is to continue to watch her numbers over time and see how they trend while trying to get her to drink as much water as possible and keep her blood pressure in a good place. She had labs drawn today which will help us determine their true current status. These results should be back by Monday. Please pray for improved kidney function-- my brain can't even go to worst case scenario (though we are very far from there).
Being home always feels good, but it’s hard not to worry about when we might be rushing back to the hospital. Fearing the unknowns along the way is overwhelming to say the least, but we are doing our best to not let this control our lives. On Wednesday when we were being discharged I asked our provider if she thinks there will come a time I am not constantly living in fear for my child’s life. She was very genuine in her reply and said with everything Hollis has been through it is going to take A LOT of time and the fear will always be there, it will just become lessened with time. She said before you know it she will be celebrating her liver-anniversary and you will look back at this time and wonder how you made it through it.
I am ready for that day. Please continue to pray for Hollis and her journey. She is such a brave little fighter.
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Alexa Middlesworth
Michele Levy
Lauren Haynes
Sally Elpers
Treatdenise
Claudia
Mimi Rohrbach
Becky Callihan
Meriehalcomb
You are always in our prayers and deeply in our hearts.
With so much love always,
Aunt Merie
Beth Mclean
“Hear my cry, O God, listen to my prayer; from the end of the earth I call to you when my heart is faint. Lead me to the rock that is higher than I, for you have been my refuge, a strong tower against the enemy.”
Psalm 61:1-3 ESV
https://bible.com/bible/59/psa.61.1-3.ESV
Kablockley
Karen Blockley