@Want to introduce my self. My names John. I have SPMS. The first event was in 1986, paralyzed On the left side. I was missed diagnosed as something else. In 2019 MS hit me like a bomb! Finally know what I have. Pretty damn awful for the last 39 years, especially curren condition. Looking for connections. on Shift.ms

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@JohnMacV13

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Want to introduce my self. My names John. I have SPMS. The first event was in 1986, paralyzed On the left side. I was missed diagnosed as something else. In 2019 MS hit me like a bomb! Finally know what I have. Pretty damn awful for the last 39 years, especially curren condition. Looking for connections.

First posted on the Shift.ms app

@NisiP1234

Hello John. This is a horrible disease 💯

27 Feb 2026 03:13

@autumnsunset

I have active SPMS. for 40 to 60 years I have had symptoms of MS. I only received a diagnosis in 2025! I too have been misdiagnosed for decades. I have suffered greatly. My symptoms were primarily fatigue and severe pain. Chronic pain. No one believed me. It's been tough.

27 Feb 2026 09:48