I understand just how you feel. I like the group of GP's I visit as they are both compassionate and
open minded & will support me in anything I want to try but they do not really know anything about
MS. The MS society here encourages everyone to do their own research & I follow that & also believe that no one knows me better than me. (I love your signature by the way & it says it all!)
Which is why I will not be going back to the last one I saw. Not only did he deny that loss of taste & smell were MS (I told him that I found it on the MS Soc website), he also tried to change my diagnosis to primary progressive from RRMS which became SPMS. I have had attacks for 30 years. Doing that I felt was both destructive & insensitive. Basically he was saying all my earlier attacks were nonsense, made up?.
Its one thing we can do vote with our feet (& our wallets)
Good luck. Keep looking there is a good one out there for you.
Have had relapsing/remitting MS since 10 yrs old. Secondary/progressive since 1995. Baclofen pump since 2008.
"The past is history, the future is a mystery, the present is a gift."