31 Days of MS: Facing my worst with my best 31 Days of MS: Facing my worst with my best by BioNews Staff | March 11, 2023 Share this article: Share article via email Copy article link Photo courtesy of Julie Wigley Day 11 of 31 This is Julie Wigley‘s story: In 2010, I started having numbness in my legs, specifically when I’d look down. I didnāt think much of it, but mentioned it to my primary care doctor during a routine visit. Her face changed and after that moment I officially started my journey of āWe have no idea whatās wrong with you.ā After tests, scans, and more tests, I was diagnosed with an autoimmune disease called transverse myelitis, which can sometimes be the first sign of multiple sclerosis (MS). I lived with this diagnosis, my numb legs, and the fear that there was more around the corner for seven years. In August 2017, at my yearly MRI, new lesions appeared on my scans, and I was officially diagnosed with relapsing-remitting MS. Finally getting the right diagnosis was a blessing in disguise. I was able to start a treatment plan and totally look this thing in the face. First thing I did, even before my official diagnosis, was to make a promise to myself. I’d take care of my body. I’d work to become the strongest version of myself within my limitations. I wanted to be at my best in case I had to face my worst. I’ve been fortunate to have very mild symptoms. I believe the treatment I’m getting is helping stop any further progression. I got to know my āforever symptoms,ā which for me are leg numbness, slight dizziness, and on hot days, numbness on one side of my mouth. They come and go, and I know this. Knowing has helped me control my anxiety and be more aware when something new occurs that I may need to alert my doctor about. I always get asked, āHow can you be so positive?ā Whatās the alternative? You keep your head up. You push when you can push. You rest when you need to rest. MS is not a death sentence. For anyone just getting diagnosed, my advice is to just keep moving anyway you can. Find a strong support system. Learn and listen to your body. Always be an advocate for your health. Ask your doctor, not Google, when youāre confused. Multiple Sclerosis News Todayās 31 Days of MS campaign will publish one story per day for MS Awareness Month in March. Follow us on Facebook and Instagram for more stories like this, using the hashtag #31DaysofMS, or read the full series. Print This Page About the Author BioNews Staff BioNews, the owner and publisher of this site, employs science writers and editors, most of whom have PhDs in the life sciences, as well as veteran journalists, who ensure stories are well-written and easy to understand. Our stories undergo a comprehensive fact-checking and editing process to confirm accuracy, objectiveness, and thoroughness in order to best serve our audience of patients and caregivers. Tags 31 Days of MS 2023
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