Neurodegenative Disease Support

I should think about it. I've heard he's like that with a lot of patients but they didn't expect him to do it to me because I had so many notes from other doctors backing up what I said. He told me I never had Lyme disease, I just had a stroke and laid around for a year for apparently no reason. I asked why I was in pain for three months before the stroke, so much that I couldn't get out of bed. He said he didn't know, but it wasn't Lyme disease. I told him my blood test for Lyme was positive and he said it was not, it was sort of borderline and he didn't know why my PCP said it was, even though the test was done at the Mayo Clinic and they literally tell you what the numbers mean and it was QUITE positive. Unfortunately I didn't know there was a tick and I didn't get tested until 2 months after it started so it was too late but we still tried antibiotics anyway. If you don't do it early it's not enough to kill it, just weakens it. You still suffer for a solid year straight.

He lectured me about opioids not being appropriate for chronic pain, even though I never once mentioned painkillers. The only thing I said was that if there is a medical issue causing my symptoms I'd like to treat that, because I'd rather live without the daily pain and fatigue if possible and lower the other drugs I'm on to treat that. I don't like the side effects. I've been sick for 6 years now and the only controlled drugs I have are Lyrica for nerve pain, and a strong muscle relaxer for my migraines. Still no opioids even though all my doctors have said they will give them to me if I want them, except for that one guy.