Guest guest Posted September 23, 2003 Report Share Posted September 23, 2003 I am extremely happy with my GP. I've been with him for 3 years now and he's extremely cooperative with me. Recently I saw him for prescriptions to help with my symptoms of CMT. I know a neurologist is technically better suited for this - but I have not been able to find a neurologist who (1) truly knows CMT the way they claim and (2) treats me with respect. I've found that the basic knowledge my GP has of CMT is the most knowledge I've found of any doctor. He also (without question) gave me samples of neurotin, welbutrin and ultracet, and when I called his office a few days ago for prescriptions to be called in on all of these he called in the prescriptions written exactly the way I asked (in other words - I told him what dosage I wanted and how often and he did not question my judgment). My pain management doctor/back doctor is less knowledgeable, but equally courteous to me. I also printed out a folder full of information on CMT (since he had never heard of it before) and he actually told me that he was reading through it at our last appointment. I found that to be very encouraging to me. When looking/keeping a doctor I personally find that the way they treat me is the most important. I really need to have a kind/courteous doctor that treats me with respect. I'm sure knowledge and skill should be first (and when it comes to surgery and such it is) but for " regular " doctors I'd much rather see a kind one with less knowledge then a knowledgeable one who treats me like dirt. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2003 Report Share Posted September 24, 2003 --- I am not very satisfied with the technical and interpersonal aspects of my healthcare. Maybe because I was subjected to so many tests (many of them extremely painful/tortuous)? My doctors (including my neurologist) don't seem to know much about this disease and my prognosis for the future and/or how to be of help. It is frustrating! And now that I've been turned down for disability, I feel like I don't have anywhere to turn to someone who understands/sympathizes (except, of course, fellow-CMTers). Colleen Quote Link to comment Share on other sites More sharing options...
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