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Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

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Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

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Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

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@nlrt121791 

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nlrt121791

Grateful

Just have to say I’m so glad I came across an ad for this app on social media! It’s so great to have people who get it! Have a blessed day everyone! We are kicking MS butt!
First posted on the Shift.ms app
1

@MarindaBrent 

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MarindaBrent

Grateful

Great evening everyone how’s you all day going ??❤️❤️
First posted on the Shift.ms app
2

@nicholas97 

EditedLast reply

nicholas97

Grateful

This may seem like an odd post but I want to THANK everyone on this page for sharing their experiences good and bad with MS!! Before I found this site I truly felt alone in what I was experiencing with my everyday life with this invader that has demolished my life. I have cried reading several post...
First posted on the Shift.ms app
6

@dkon 

dkon

Grateful

I just received my diagnosis last Friday and even though the news itself is unfortunate I feel so grateful for how the discussion was handled. I was called to the hospital’s immuno-neurology unit and two neurologists and the MS nurse gave me and my partner 1.5 hours — as much time as we needed to ex...
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@HerStrength 

Last reply

HerStrength

Grateful

Hey guys! We go through soooo much having MS and many people can’t relate and it is so frustrating. However, we are still here my loves. WE HAVE LIFE!!
  • Work and play
  • Symptoms
2

@Marz 

Marz

Grateful

Hi everyone, I’ve had RRMS for over 20 years. I was diagnosed during a time when Australian TV was flooded with commercials of young women with MS in wheelchairs. So, when I was diagnosed naturally I assumed this was what my future held. Thankfully, I had a tribe of supporters who would not allow ...
  • Balance
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@Irene_Kostyk 

Last reply

Irene_Kostyk

Grateful

Does anyone suffer from wearing the wrong pee pad? Nothing seems to work. Please, let me know.
  • Work and play
1

@Erusha 

Last reply

Erusha

Grateful

Good day all, Just want to say this site has really helped answer questions others couldn't also just having a platform to share with people who understand. I'm sure I'll have more comments and questions on the future but thanks to everyone for all the help thus far 🙂
2

@Glamluvs5H8MS 

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Glamluvs5H8MS

True story really. I am going to stay with my oldest son, here home my other son is overwhelmed, he doesn’t feel comfortable being too far from me🥹 his other siblings have minimized what he seeing maximally! We talk and I do understand his feelings, they are valid! So I’m me meeting my 2 granddaughters who are both under 4 so I am excited yet I have zero income😫 my flight and thing were gifted to me. I’m am grateful for that. I wanted to get to meet my granddaughters before anything else happens. I have hired counsel to assist me in obtaining Disability, I apply a few times and was denied. I can’t even afford my medication. Not looking for sympathy, I guess, just wanted to be more clear, I ABSOLUTELY hate MS and what it’s done to my confidence, yeah I don’t trust myself,& I before this all I was actually looking forward to turning 50! Yeah made it to 50 but I don’t like how I feel and how unsure I am now about the things I was MOST confident about doing, not so much these days and it makes me ANGRY cuz I didn’t plan this nor have the resources to live with this confidently. Praying for a steady body to keep doing what it HAS been doing for 49 years!! Health care is NOT caring these days and I can only say, timing has been my lack for some time now. I digress have a awesome MS’n day everyone. 💜🫶🏾🤟🏾💪🏾🤞🏾✌🏾

Fort Worth, United States
First posted on the Shift.ms app
9

@ToriB3 

Last reply

ToriB3

I’m Tori :) My head still hurts from all the information I’ve received in the last few days. I went into the MD for a weeklong bout of vertigo(which I’ve never had before) and nausea. She did an MRI as a precautionary scan to make sure it wasn’t a stroke and that is when they found the lesions and such. He is 80% certain MS is what I have, but he has to do blood work to rule out MOG and NMOSD before starting treatment. Why can’t I just KNOW! He said I have textbook MS lesions but there is a larger lesion than typical for MS so he said that is what he wants to check out! I’m very grateful they got me in so quickly but that’s big news to sit with maybe or maybe not :(

First posted on the Shift.ms app
11
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