I went to my PCP today and asked some questions (about my skin, oddly enough) that only amounted to the answer that it's probably because of being immunosuppressed, and that because I'm immunosuppressed, it isn't likely to resolve. Just feeling a little down today. Anyone ever have those moments before? I remember when my MS was really acting up,I went to my PCP today and asked some questions (about my skin, oddly enough) that only amounted to the answer that it's probably because of being immunosuppressed, and that because I'm immunosuppressed, it isn't likely to resolve. Just feeling a little down today. Anyone ever have those moments before? I remember when my MS was really acting up,I went to my PCP today and asked some questions (about my skin, oddly enough) that only amounted to the answer that it's probably because of being immunosuppressed, and that because I'm immunosuppressed, it isn't likely to resolve. Just feeling a little down today. Anyone ever have those moments before? I remember when my MS was really acting up,I went to my PCP today and asked some questions (about my skin, oddly enough) that only amounted to the answer that it's probably because of being immunosuppressed, and that because I'm immunosuppressed, it isn't likely to resolve. Just feeling a little down today. Anyone ever have those moments before? I remember when my MS was really acting up, I had a really hard time going to my neurologist because I figured I'm just going to see how fast my body is declining, and I couldn't fathom how doctors couldn't "fix" it, but now this has become my new norm. Still, it kind of stings to know that MS has ruined other parts of my life that I didn't expect to be affected.