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@DrLisa 

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DrLisa

Hair loss

Anyone dealing with hair loss? I don’t know if it’s because of MS or a medication, but about half my hair is gone.

@DesN 

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DesN

Sleep.... I really miss you!

Hi all...... I had a really good friend once called sleep... however since MS came along we seem to have grown apart! Share your miracle cures to get us back together again! Pleeeease...... I really miss him

What diet is best for ms

I'm recently diagnosed with rrms, I'm not on any treatment yet. Just wondering what diet is best to follow?

@daveserjeant 

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daveserjeant

Welcome to new MSers

I've recently been talking to someone at work who's newly diagnosed. He remarked about the support he's getting from other MSers Going to test an @ and # by saying @Sclerobro #ocrelizumab
Nottingham, United Kingdom

Welcome to Shift.ms

Hello, I'm the Community Intern here at Shift.ms! I'm here to listen to your stories and share them across the site in the hope that they'll be helpful to other MSers. #MSstories Just testing the @ function by tagging @poleyjo :)
Leeds, England, United Kingdom

@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...

@Sue_Ashton 

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Sue_Ashton

New to group. Experienced with MS!

Hello there. I have just joined the group as I have MS. I was diagnosed in 1994 and it's been a rollercoaster journey since. I'm feeling a bit miserable at the moment as my memory has gone on a go slow. I thought that things would improve when the heat reduced but I'm so forgetful. I went to an opt...

@Henrietta 

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Henrietta

Diagnosis - the long and winding road

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...

@NicolaJinks 

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NicolaJinks

Vaping and MS

Looking for some advice please. Before I was diagnosed with MS I smoked for almost 10 years. I did stop about a year before I was diagnosed and was using a vape which I stopped using after diagnosis. My question is most of the people I live with still vape and regularly do so indoors. Could this s...