We have a lot of them....but as usual ----- ROHHAD fries my brain and I have taken the summer off from updating this blog. You can only handle so much of this ridiculous syndrome before you become brain mush! So updates will appear this weekend!!!!
Love to all!!!
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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&...
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