Guest guest Posted March 19, 2009 Report Share Posted March 19, 2009 Thank you , I am sure as you know by now it is perfectly normal to research everything about CMT when we are newly diagnosed. The doctor does a good job at poking us, testing us, and making us feel like lab rats lol, but when it comes to explaining that's another thing. I did the same years ago when I was diagnosed. To this day I keep up, because it is me who has to educate the doctor in most cases, make sure they don't give me something I can not take. Or as of now with the change in my medicare D plan that excluded meds I've been on for years, secondary ins, that don't cover the doc that i've seen for years, search for another doc, and equivilent meds they will cover. As if we don't have enough to deal with. Quote Link to comment Share on other sites More sharing options...
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