Category: MS Monday
MS Monday
Depression
Multiple Sclerosis is a tough disease. It has many common symptoms, vision problems, balance issues, cognitive difficulties. But one that isn’t mentioned, but should be, is depression. Depression is one of the most common symptoms of MS, but one of the least talked about. Prevalence The numbers can vary from study to study, but around […]
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Emotional Changes
That word. Those words. Multiple Sclerosis. Diagnosis. I can’t understand what is happening, or why it’s happening. “But I’m so young. But it’s not fair”. I guess it’s too late for those now. “What will I do? Will I be able to walk next year?” That is what floods my mind, as I walk down […]
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MRI Progression vs. Activity- What does it all mean?
When you have Multiple Sclerosis, going for a yearly (or whatever your schedule is) MRI is one of the ways to keep tabs on your disease. It gives an almost full picture of your brain and spinal cord, and lets you, the radiologist and your doctor see what is going on in terms of progression […]
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Gadolinium
If you’ve ever had an MRI you might be familiar with the name Gadolinium. It’s the technical name for contrast. Contrast is used to get sharper MRI images. In the case of Multiple Sclerosis, it’s how active lesions can be seen. Until recently, contrast was thought to be safe. But latest research is showing a […]
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Surviving MRI’s
If you’ve ever been so fortunate to visit the hospital for specialized testing, MRI/CAT scan/CT scan etc, you know it is not something to be thankful for. Hospitals can evoke extreme anxiety for many people, just by their atmosphere alone. Not to mention the reason for being there in the first place. I’ve had my […]
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The Best Thing(s) I’ve Done For My MS
When I was first diagnosed with MS, I thought the best thing I could do for my MS was take medication. Boy have I come to realize this is so far from the truth. Since then, I’ve realized that living well with MS means so many things. To me, that means eating in a way […]
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What I wish I knew when I was diagnosed with Multiple Sclerosis
When I was diagnosed with Multiple Sclerosis I was only 24 years old. Nearing the end of graduate school, about to set out and find a “real job”, MS didn’t quite fit into that life picture I had envisioned for myself. But I guess that’s how that works, right? You’re never expecting anything that blindsides […]
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Selma Blair
When Selma Blair announced her diagnosis of Multiple Sclerosis in October, I was saddened but very inspired. Her Instagram post that announced her diagnosis was incredibly honest and courageous, in my opinion. She has since gone on to continue posting on Instagram, multiple times a day about her experience with the disease. Good or Bad? […]
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MS Awareness Month
Happy MS Awareness Month? Still seems weird to say. To be happy about a month that brings awareness for a disease that I am acutely aware of everyday. But I’ve learned over the years that this month isn’t for me. It is for everyone else that DOESN’T have this. My thoughts and feelings about this […]
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Strength in Food review
My Review of the Strength in Food AIP subscription box service. Strength in Food is an AIP subscription box service, founded by the owners of One Stop Paleo Shop. It was created to get AIP products and food into the hands of who need it most, in the quickest and easiest way. The creators state […]
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