Guest guest Posted February 4, 2006 Report Share Posted February 4, 2006 I am just wondering about what sort of insurance you all speak about about. Is it health insurance ie to cover costs of tests, hospitals, therapy etc, or are you talking about disability type of insurance to cover loss of income down the track? I am just trying to fathom out what sort of insurance my children (young adults) might need in case they have mito (also do not live in the US so am not familiar with some of the terms). They haven't been diagnosed yet but are going for tests shortly, since there are some suspicious symptoms. pamela Re: : MS The dilemma is that none of those individuals are mito experts. That seems to make all of the difference in the world. I do fully understand about the insurance challenges though. Insurance issues are my worst nightmare. MitomomX3@... wrote: I tried to go that route earlier and the insurance refused an out of state opinion when there were neuro's and neurosurgeons here that looked at it. these films have been read by several radiologists, a neuroradiologist and then transported to another facility and re read by a neurosurgeon and neuroradiologist. the insurance said no more.. karen Quote Link to comment Share on other sites More sharing options...
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