#grateful - Shift.ms

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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

@MarindaBrent

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Grateful

Great evening everyone how’s you all day going ??❤️❤️

First posted on the Shift.ms app

@nicholas97

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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

@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...

@HerStrength

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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!!

@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 ...

@Irene_Kostyk

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Grateful

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

Work and play

@Erusha

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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 🙂

@well well well

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Hello. I’m sort of new to this forum, have been posting away like an uninvited party guest. I’m very grateful for this app and the people here. My post: Someone had a question about loss of conditioning. I’ve been in and out of this too and wanted to say just keep trying and try not be be freaked out. All we can domis try at the various ways we try tomlive with MS. I used to be very fit, that’s no longer possible somInjust keep trying to move when I can even if it’s stretching, it all matters. Cheers to folks here, I’m glad to be among you. Very glad to read all these voices.

First posted on the Shift.ms app

@LEWISHAVERLY

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Living with MS has taught me that strength doesn’t always look like fighting. Sometimes, strength is resting, asking for help, and simply choosing to keep going. 💙There are days when my body doesn’t cooperate and moments when the journey feels heavy, but I remind myself that I am more than my diagnosis. I’m still here, still hopeful, and still grateful for every little victory.MS is part of my story, but it will never be the whole story. 💙🦋

First posted on the Shift.ms app

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