So I went to my MS center appointment. And I complained my little heart out. I had my usual symptoms, and some new ones. I reminded him that I was diagnosed when I was already in Secondary Progressive MS. Therefore I had never really taken any MS drugs except LDN. I suggested we try something new.

He told me that there is no treatment for SPMS. He said that he could give me something for the pain, but that there is nothing more that can be done.

Sigh.

He is, of course, correct. He did order an MRI for me because the pain on the right side of my head is getting worse, and at least I’ll have the peace of mind that I don’t have a brain tumor or something.