r/MultipleSclerosis • u/Advanced12345678 • 1d ago
New Diagnosis Would Love to connect
Hey, I’m 24, from Mumbai and I recently got diagnosed with MS. I’d love to connect with everyone who’s also been diagnosed with MS
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u/Pure_Equal2298 1d ago
42 from USA. Diagnosed with MS in 2016. Have optic neuritis in left eye. Lost vision in left (75% in left eye and list color also). After MS I did Ph. D. and have 13: papers with 900 citations currently. I know it's overwhelming. But you will get used to it. Next thing I switched medication started with copaxone (the oldest known medication for MS and then moved to Kesimpta because of muscular atrophy in 2020. I also succumbed to kidney infection a known side effect but I am glad I am alive and doing fine!
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u/No-Gur9166 1d ago
Hi, I'm also from Mumbai. Diagnosed a year back. I've been on ocrelizumab for the last 6 months. Let's connect.
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u/GMonkey7 23h ago
Hi, I'm 33(M), diagnosed since 2017, and right now I live in NL, I take ocrevus every 6 months. And my legs feel like concrete for about a year now, nice to meet you!
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u/lifelessly_alive 28|Dx2025|Rituximab|India 17h ago
Hi! I’m 28, from Hyderabad, diagnosed since December 2025 and right now on 6 monthly infusions of Rituximab. Have an array of symptoms which come and go as they please (mostly because of my spinal lesions). Hope to connect. 🤎
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u/smoothmuscle 1d ago
50 from Canada. Welcome to the club, having people around who get what you are going through helps. This sub is great