WOW !!!!
I just dont know where to start... Lori would read me the posts over the phone but it was totally different to see it my self. I'm in tears... You are ALL so wonderfully. I cannot express to you guys how thankful I am
I am so fortunate to have so many wonderful friends!!!!!
I'm sorry I didn't post last night, they somehow messed up hi prescriptions so we were at the pharmacy for over an hour.
Then the lovely 2 hour ride home
I hate long car rides. When we walked in the door I gave Cayden his medications, took a much needed shower and crashed.
It is so good to be home.
Cayden is not 100% but he was good enough to leave the hospital. He was holding his oxygen on room air at 93-95% which is great compared to before. Without it before it was down to 80%.
All of his test came back negative... thank god!!! well except the allergy one, which we already knew he had allergies.
At home he is still on steroids (50mg Prednisone), an antibiotic (Augmentem for 14 days), and then his regular asthma meds. We are still doing treatments every 4 hours and will continue until next week. We will see his regular Dr. next week to repeat the x rays to see if th pneumonia is gone, at that time we will change the treatment times.
Oh and he has his follow up with the Pulmonologists in 3 weeks, we will go back to Valley Childrens Hospital for that.
I think I covered everything
but i'm still a little out of it... im still sick and very tired
I feel like I have a newborn again... I cant wait to get some real sleep
Thank you guys again for all your prayers...
From Cayden: I love you , I love you
