Welcome to my mommy blog of our journey with Cyclical Vomiting Syndrome!
My son is a second generation CVS kiddo. He earned the diagnosis in June of 2012 after 3 years of "bad stomach bugs". Since then we have come to learn a lot about the condition and life in general.
He has had over 20 hospital admissions since Dx. Hoping 2014 will be better! We know it will in many ways and in others not....BUT... we know what to do and it goes smoothly anyway. There is no cure for CVS, but through education and treatment we can dramatically change the lives of hundreds of kids who suffer from this thought to be rare migraine variant. We do all we can to minimize his episodes, take med, homeschool, take preventives, pretreat etc.. but still life goes on it just happens to include CVS!
Welcome to my personal blog about life with a child with Cyclic Vomiting Syndrome (CVS) a rare migraine variant. Its fun, exciting, and a little bit crazy...and a lot of puke!
Wednesday, January 8, 2014
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