Wendy is resting at Ronald Mcdonald house with the other kids. If you have never checked them out, please do so. They have been wonderful beyond anything I expected. Not just a room, but really like a home. I am with Naomi.
Naomi was put on a regular ventilator last night. The nurses and techs have been able to further clear her lungs. The EEG tells us that seizures are continuing in a disjointed manner. All of her vitals remain stable with the support she is recieving. She is currently off the Insulin drip. HUGE shout out to Jesus there! We will get past today with the swelling on her brain, and then we will see where we need to go. One minute at a time. hour by hour, day by day, then we will be walking out of here. Together. Waiting is hard. I don’t think I have ever done anything that is this hard. My thinking has become a little disjointed, little grace please. Wendy is finally eating a little more. We are just waiting right now for her little body to heal up. Thank you all for the prayers. Please go harder. Thanks for the many many words of encouragement from others that have been in our position. Please keep lifting Naomi’s name. I told one of her nurses that I don’t cry for what I fear is coming, I cry because I see the process. The process of healing. We stand and believe. I invite all of you to do the same.