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@JoyceG. 

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JoyceG.

No DMT at the moment...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

@Demelza 

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Demelza

B12 injections stopped pills instead

Afternoon, Have had MS for 10 years and been having B12 injections for about the same time. Have injections every 8 weeks until Monday when the appt was cancelled. Have been told today that injections are no longer available and it’s pills now which I can get a prescription for in 2 weeks! Anybody...

@Robean 

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Robean

Nurses with MS

<p>Hi all, just wondering if there are any other nurses out there?? </p> <p>Are you still going to work?? </p> <p>I was planning on carrying on going to work and just being extra careful and socially distancing myself in my personal life (aka not going to shops and restaurants etc) but then I spoke...</p>

@Dawson.McWatch 

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Dawson.McWatch

Hand washing is a must

Is anyone worried about the whole coronavirus I’m starting to worry I already have a weak Immune system due to my MS treatment... would that make me variable to the virus because of that or am I just overthinking this?!? Get back to me in the comments what’s your opinion

@poleyjo 

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poleyjo

First Neurology appointment

So after more than 6 months of real struggle with suspected MS symptoms I finally have my first appointment with a neurologist on Sunday. Can anyone please give me insight on what to expect? I have been tracking my symptoms and will condense this list and take it along with me. Is there anything els...

Intermitent fasting Keto diet

Has anyone else with MS been helped following a Keto diet? I've been following this for the past 8 months and finding it very helpful, but am aware that it contravenes so much MS advice about keeping to a low-fat diet. Are there any other people living with MS who have also tried this? I'd so love t...

@lukezni 

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lukezni

Stormy weather

Seems like a bit of a weird question but does stormy weather effect your ms? There is currently a storm hitting here (the first since I've been diagnosed with ms) and my head feels like what could only be described as stuffy/heavy? My ears have a constant feel to them as if they are about to pop

@AMD7L 

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AMD7L

my story

my age is 25. i have MS since 12 years. now i'm adapted with it but it kills everything inside of me. i feel like a zombie. no feelings, no desires, no hops, and no wishes. what i've to do now. help me i wanna be a human again .

Mavenclad anyone else on it

Finally started treatment I thought it was going to be alot worse than it has been so I'm grateful for that. Or they given me placebo. February is always a though month for me it's the last month I got to speak to my mum. She had MS. Died 2018 it feels like longer. It's still strange to me. Anyw...

Watch AWAKE | A film about insomnia &amp; MS

https://www.youtube.com/watch?v=R1RpZtnUrsw&amp;feature=youtu.be Inspired by conversations from right here in the Shift.ms community 💬 'AWAKE' is the latest film that explores the interplay between MS, sleep and mental health 🛌💤😪 THANK YOU so much to all those involved in the filming of AWAKE. A...