Before I get all involved with the post. I just want to reassure my family and friends that this blog is only seen by those who I have invited. I am in no way going to exploit our family. But, I will be spreading the word about JIA to all those who will listen!
So, with that said. Friday...We took Isabella to see a really great Maxiofacial Doc. He saw the Arthritis in Isabella's jaw. He is following the Rheumatologist concerns. She is scheduled to recieve injections of steroids in her jaw. We are worried aout the imflammation in her jaw, and joint destruction. BUT BEFORE we do that I am researching to see if there is another way we can go.
We are still batteling her virus. She had to have several breathing treatments last night. Congetion, and cough. She is on so much Naproxen that she can't get a real fever. So, outlook for today....Dr's office again!
All About Us!
- Larry, Samantha, Devon and Isabella
- Adventureous! We are a family that is not only fighting for our childrens health but for a cure! JIA not only affects Devon and Isabella but also our family. It is a journey that we are all choosing to be on together. We alone can not make a better world for her but with the help of family and friends and our GOD, helping them live will help others too. Knowing more about JIA will make us all a little less scared and whole lot closer as a family! Cuz' baby, that is what IT IS ALL about!
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