Saw the pcp on Tuesday.
L had the idea to make a comprehensive list of all the symptoms that have come up in the past year or so. It helped tremendously! We were able to give it to Dr. S, and she was able to get a better picture of things. She’s thinking that a lot of it can be related to a potential cervical vertebrae problem; we just have to figure out imaging. I have a chest piercing that had the radiology nurse really uncomfortable last time, enough that she said they would refuse to do further imaging from the waste up unless I had it removed… that would take a surgical procedure, and I’m just not interested in losing it forever if I can find another center that will do the imaging… so I’m waiting to hear back from her office about the next steps around that.
She’s also going to set up a referal for a second opinion on the neurology side of things, but I have to send her a copy of the neuropsych report so she can include it in the referral. I have that pulled together, just need to make it out to the post office to mail it.
I really hope something is figured out around this, and I hope there’s an easy, painless, non-invasive fix for it…
In the mean time, we are trying meloxicam for the pain… I took the first dose tonight, and I’m wired. The first 2 hours after I took it, I felt hyper, as if I’d taken an upper. I hope, if that’s one of the ways my body reacts to it, that it goes away soon. It actually helped the pain for those two hours, but it wore off quickly… it was the lowest dose though, so maybe a higher dose will help longer? I dunno, but it was nice to feel pain-free for those 2 hours or so.
So, we’re have some other things to look into. Hopefully one of them will yield answers.