her 4th MRI since February. I really don't like MRI days. Its so
stressful, we've had issues so many times with MRIs. They said it
should be a couple hours and then she can come home.
We won't know anything until next week.
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Hi everyone. It's been a long time since I sat and wrote about our daughter's extremely rare disease diagnosis. Literally 15 years a...
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I received this story in my email today. It still shocks me that my daughter has ROHHAD. It's a horrible disease that destroys a child...
Misty keep us informed; you know I check everyday. I hope you do not have a sick weekend with Havey. I looked at the picture when she was having chemo; what is the purple thing on her head?
ReplyDeleteHaven seems to be doing well; let her know G-GB and Candy are watching her. I noticed she was using the computer; bet she is better than I am:)