Guest guest Posted July 3, 2003 Report Share Posted July 3, 2003 ka, Ask your doc to explain your EMG/NCV results in language you can understand and based on those results, what type of CMT do you have. Ask for the DNA blood test then - the complete CMT evaluation one, here's a link http://athenadiagnostics.com/site/product_search/test_description_template.asp?i\ d=190 your doc may not be aware of the testing for neurofilament light types (some of the type 2s, plus periaxin.) You have every right as a patient to have your tests explained and questions answered even if it has to be explained twice. Also ask for a written report of your EMG/NCV, like the one I shared with the group a few days ago. You also have a right to have copies of all other tests. Seems sometimes docs don't like to " commit " unless they are sure...just keep on with the questions. I am assuming your doc has done the manual tests and taken your family history. You might also want to discuss a nerve biopsy at some point (it is invasive however) If your doc doesn't answer questions or says no to genetic testing, find another doc. It is your right as a patient to ask questions, suggest further testing and have copies of medical records. Other questions might be your need for orthotics, AFOs or other aids if you need them. ~ Gretchen ~ Gretchen Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.