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What is your MS story? Let's share!
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Katelynn21
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Katelynn21
Last activity on 05/27/2021 at 2:05 AM
Joined in 2019
8 comments posted | 8 in the Living with Multiple Sclerosis group
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Katelynn Verville
Katelynn21
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Katelynn21
Last activity on 05/27/2021 at 2:05 AM
Joined in 2019
8 comments posted | 8 in the Living with Multiple Sclerosis group
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Also in my research, in roughly 5% of all MS patients some lesions have go n undetected for a long time ( not appearing on test etc. ) some people have to live with the disease until further lesions present themselves unless a doctor decides your correlation of symptoms and other factors conclude that you need the definitive diagnosis. Because there is no one test to rule out or diagnose MS, this is where it becomes extremely hard to diagnose when MRI's come back ok but the patient still suffers. Well i hope the docs figure us out and give us some way of relief even if its just mental relief!
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Katelynn Verville
Lovemegalooo
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Lovemegalooo
Last activity on 05/31/2023 at 6:57 AM
Joined in 2019
7 comments posted | 5 in the Living with Multiple Sclerosis group
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It’s all so frustrating and I feel defeated :(
maybe that’s how the world will end, everyone will die from weird diseases caused by the crap in our food and the crap in our air :(
I have an appointment today, hopefully I’ll get some answers from my cervical spine mri. The dr did discover a cervical rib that could explain some of my symptoms but he was unsure,
ive been doing a little bit of research on rarediseases.org. Maybe that could be helpful for you?
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MegaloooMama
Monkey
Monkey
Last activity on 02/20/2021 at 5:59 AM
Joined in 2020
8 comments posted | 8 in the Living with Multiple Sclerosis group
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Hello my name is Marcus I have been diagnosed with Ms since April of last year. It started as a shake in my left hand then a couple weeks later my left hand seized up. Then two weeks after that then my left leg started to shake. Then two weeks later then my leg seized up. Then it became a safety thing at where I was working at. I was also at a hospital getting a MRI. Once I got done and sat up I noticed I had no vision. After 30 minutes of waiting I got worried. I was at the hospital for five days and I can only see the shapes of body's. Now I only have half my vision. But out of all of what I was going through I always kept a smile on my face which surprised a lot of doctors. I'm I'm curious if anyone else has those symptoms and how u deal with it
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Marcus
Monkey
Monkey
Last activity on 02/20/2021 at 5:59 AM
Joined in 2020
8 comments posted | 8 in the Living with Multiple Sclerosis group
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Hello my name is Marcus I have been diagnosed with Ms since April of last year. It started as a shake in my left hand then a couple weeks later my left hand seized up. Then two weeks after that then my left leg started to shake. Then two weeks later then my leg seized up. Then it became a safety thing at where I was working at. I was also at a hospital getting a MRI. Once I got done and sat up I noticed I had no vision. After 30 minutes of waiting I got worried. I was at the hospital for five days and I can only see the shapes of body's. Now I only have half my vision. But out of all of what I was going through I always kept a smile on my face which surprised a lot of doctors. I'm I'm curious if anyone else has those symptoms and how u deal with it
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Marcus
Katelynn21
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Katelynn21
Last activity on 05/27/2021 at 2:05 AM
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8 comments posted | 8 in the Living with Multiple Sclerosis group
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Katelynn Verville
Monkey
Monkey
Last activity on 02/20/2021 at 5:59 AM
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8 comments posted | 8 in the Living with Multiple Sclerosis group
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I use to work at a lumber mill until it became a safety thing
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Marcus
Monkey
Monkey
Last activity on 02/20/2021 at 5:59 AM
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8 comments posted | 8 in the Living with Multiple Sclerosis group
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What kinda job could a Ms patient do?
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Marcus
Marques
Marques
Last activity on 10/15/2024 at 1:07 PM
Joined in 2020
2 comments posted | 2 in the Living with Multiple Sclerosis group
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Hey I would just like to yall about it and your experiences with it. I guess I could start by introducing myself and things that's happened with it I'm marques and I was diagnosed last summerish but I was having symptoms a bit before, my legs went numb I could still walk but I participate in track and field and it screwed with my technique really bad and i could barely throw anymore and then my whole left side went out numbness again and my eye crossed and all. I just want to meet and talk to people that are dealing with the same thing I am I just feel alone in this and I dont have really anyone to turn too because they either dont really care or are unable to relate.
Newtoms
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Newtoms
Last activity on 12/12/2020 at 8:11 PM
Joined in 2020
10 comments posted | 10 in the Living with Multiple Sclerosis group
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Hello I'm new to this. I was diagnosed on the 5th of March. But my symptoms started before that. They started with a slight numbness in my legs and then all of a sudden I didn't want to walk and still don't want to walk but i do walk with a cane now short distance and a wheelchair for long distance. And it's affecting both my legs and my right stomach and chest now. Its also affecting my balance and sleep and my vision a little bit here and there
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Lee__R
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Lee__R
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Last activity on 04/03/2020 at 5:04 PM
Joined in 2018
1,338 comments posted | 84 in the Living with Multiple Sclerosis group
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Hello everyone,
Welcome to the Multiple Sclerosis community!
It is true that it is not easy to know the path / experience of each member with MS and know who to reach out to or experiencing the same as you. Trust is essential to be able to talk and share calmly, especially in a community like this.
Therefore. we encourage all members in this group to introduce themselves.
Share a little about your story, when you were diagnosed, experiences, etc. with MS to introduce yourself to the community!