I'm not Jewish. There are lots of different forms of dysautonomia though. The particular form I have strikes people of Celtic ancestry and mostly hits females, and one of the main symptoms is gastroparesis and low blood pressure. One of the main reasons it took so long for me to be diagnosed is that few doctors do research into dysautonomia. They are just now naming some forms of the different kinds and giving them ICD codes. Several got codes last year. Mine still remains uncoded, and possibly unnamed, too. You can go look under the ICD 9 codes though and you'll find some that were coded last year.