Is it PMS or the MS?
To recap, I was diagnosed with MS in March of 2016. It wasn’t a surprise because I had suspected it for years. I had the tingling, the weakness, the drop foot, etc.
I’ve had a theory that I’ve been suffering from exaggerated PMS symptoms ever since I stopped taking the birth control pill (post hysterectomy). Every month there’s about a week and a half when I feel like I have a mild flu. I need to sleep a lot, my lower back hurts, and my hip flexors tighten. I think these symptoms couple with or exaggerate my MS symptoms and generally make my life difficult.
I’m currently experiencing that phase of the month, but I think things are slightly better because I’ve been working on improving the health of my legs. I do strengh training for the leg muscles twice a week, and I try to walk 30 minutes on the treadmill on most days. The trick is to make sure I work out during these “fluish” times of the month so I can continue to improve my fitness level. I’ve been drinking a lot more water these days which I think is making a difference too.
I’m not doing great on the diet side of the equation. I haven’t been eating enough food because of the anxiety I’ve been feeling. Thus, I haven’t been getting those five fruits and vegetables every day. The increased Fluoxetine dosage seems to be working now that three weeks has passed. I’m hoping things will continue to improve.
Making art helps ease the anxiety. I’m trying to keep my art blog going as I create. I’m starting to think of myself as an artist. I’ve got two canvases going now. The art journal work has ceased for the moment. I’m sure I’d be more productive if I cleaned off my table. That might happen someday.