31 Days of MS: Laughing My Way Through MS 31 Days of MS: Laughing My Way Through MS by BioNews Staff | March 21, 2021 Share this article: Share article via email Copy article link 31 Days of MS header Photo courtesy of Rebecca Anton Day 21 of 31 This is Rosani Christy’s story: My name is Rosani Christy, and I have been living with MS for over 20 years.Ā I have always been aĀ class clown.Ā Making those around me laugh gave me a high, and it didn’t matter if I forfeited my recesses.Ā I could find the funny in anything except MS. MS was not funny. At least not until I got over the denial of having it. I lived in denial for 10 years. I eventually needed a cane but preferred to walk like a drunkard than use one. I progressed to needing a walker and then a wheelchair. While using a wheelchair, I learned about all the hurdles that people with disabilities have to face. There was a lack of ramps. Automated door buttons only work half the time. The fire exit protocols for people in wheelchairs are horrendous. Those are just a few examples.Ā Then came the comments made by our able-bodiedĀ counterparts. I was called brave at least twice a week for just living my life. My husband would get handshakes or high fives for being such aĀ stand-up guy.Ā At first, these things made me angry, so I took that energy andĀ put it into journaling.Ā When I shared stories with others, I did so in such a way that I made them crouchĀ over in laughter.Ā I eventually took a stand-up course at The Second City because I had so much to share but did not have a platform. I am now a stand-up comedian. Unfortunately, Toronto is not as wheelchair-accessible as one would think. Still, I am part of a committee determined to make the comedy scene in Toronto more accessible. I can only make it to a selected number of venues, and I make sure that I make others laugh and educate them through my stand-up. I get a lot of inspiration from my family life as I am a mother, a wife, a sister, and a daughter brought up by Sri Lankan ‘Tamil’ parents.Ā The culture clash that I experience is enough content for a Netflix special. I can do Zoom open mic nights and comedy shows three days a week from the comfort of my bedroom ā which is a win for me. All I have to do is look presentable from the waist up, which is much easier on my caregivers and me. Multiple Sclerosis News Today’s 31 Days of MS campaign will publish one story per day for Multiple Sclerosis Awareness Month in March. Follow usĀ on Facebook and Instagram for more stories like this, using the hashtag #31DaysofMS, or go here to see 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.
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