My 15 y.o. child has been dx with dysautonomia. My understanding is that chronic lyme can be one cause but there can be others and often no one knows. A LLMD believes that she does have chronic lyme but it seems hard to tell. Does anyone have any knowledge or experience of dysautonomia secondary to lyme. Since lyme tests are so inconclusive, are there any other indicators of dysautonomia related to lyme vs. other causes (e.g., in the history and onset of symptoms)?
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