#community - Shift.ms

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community

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First posted on the Shift.ms app

@EleanorAdmin

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Community poll results are in! What age were you at diagnosis?

We love it when our community comes together to share their experiences. Not too long ago, @Eylem7990 asked how old you were at dx, and we were thrilled to see so many responses flood in. We decided to crunch the numbers and turn it into a handy little graphic so you can visualise the numbers. Are...

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@DatWelderwithMS

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MS gaming Community

I know it's a long shot but anyone here game? Since my diagnosis gaming has been an escape for me, has helped me keep my mind of certain things and helps me relax. I'd like to maybe start a MS gaming community. Play some video games with people that we can talk to and relate to. Let me know if you a...

@SeanDarling1989

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Greetings everyone, I am a 63 year old mom to a 36 year old son diagnosed with MS in May of this year. In July my son lost all his abilities to function in every way. He was in the hospital for three months and now he's in rehab learning to walk, talk, and everything else that this demon disease took from him. We have a long road ahead of us and I have so much to learn about MS I'm terrified but I know that everything is possible with God. In July I was told that my son would never speak or walk again, but now he's speaking clear enough to understand him and walking plus feeding himself. I'm praying for everyone in this community and looking forward to making new friends. God Bless you all.🙏♥️🙏⚘️👌🏻

Sacramento, United States

First posted on the Shift.ms app

@UCMS_organization

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Ukrainisn community of MS

Good evening! It is a great pleasure for us to know about your activity in multiple sclerosis in your country! We are new community of MS in Ukraine and want to get information about this problem from abroad. “Sanofi” company recommend us to discover your activity in this sphere. Now we have more ...

Treatment

@Subra

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Hello everyone. I’m new to this site. I guess I’ve never wanted to be part of MS community because that would involve acknowledging my diagnosis. This is despite me being diagnosed five years ago I struggled with walking. Never thought that one would have to think about every step that one takes . Does anybody ever feel this way with the walking?

First posted on the Shift.ms app

@CoreyR

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New to the community

Hello, everyone, I'm new to this community and just wanted to say hi.My name's Corey. I'm from michigan, and it's a pleasure to meet you all.

First posted on the Shift.ms app

@ajpedersen

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New to the community.

Is anyone out there treating their RMS Naturally? I have been on this journey since 2021 with out meds but this year has been the toughest year to date. Stress it definitely my enemy. How are all dealing with stress? And how do deal with work stress?

First posted on the Shift.ms app

@Stephlouise

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Such a refreshing community 🩷

Hi Everyone, Im Steph and was diagnosed with RRMS back in April and saw my consultant for the first time yesterday. I've struggled with dealing with the diagnosis since April, not wanting to discuss it/ bury the subject completely, so when I heard about this community I was reluctant. I was so ...

Newcastle upon Tyne, United Kingdom

@Debbiewoods1974

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Incontact community

Hi I am starting treatment on Monday . Put in the login details to the incontact community and nothing happens . Can someone tell me how do I register . thanks

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