So, When I was diagnosed 2 years ago, the neurologist kept trying to push anti-depressants on me right away, saying “everyone that’s newly diagnosed gets depressed”. I hated that attitude so I switched Drs. I thought the new one was great, but after a year, she started only “ seeing” patients via video chat…even after I had a new lesion appear and she switched me to Tysabri. Then she suddenly decided not to be a neurologist anymore. She literally emailed me my record, with no MRIs, and said good luck. I lost my insurance at the same time and moved. I haven’t had Tysabri since April and I’m pretty sure I had a massive relapse while off it. I finally saw the new neurologist (the only one close that insurance covers) today, and I fear this one is gong to be a mess as well! She straight up told me she doesn’t know much beyond basic MS care because she specializes in epilepsy. I’m so frustrated…Having this is hard enoug and we aren’t supposed to stress, but most of my stress has come from the damn Drs! I can’t win. I feel as though no treatment and Drs would be better for my mental health.
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