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@Will_Berard 

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Will_Berard

Has anyone had COVID-19 (yet?)

I'd like to hear first or at most second hand an account of what it's like for a PwMS to go through COVID. I'm surprised and a bit concerned that I've not seen one here yet. Either we're very good at shielding, or we tend to die of COVID, or both. Or it's just a quirk of stats, and the rate of inf...

@Tiffany_Roberts 

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Tiffany_Roberts

Living with MS and alternative lifestyle

I'm sorry if this isn't allowed, please delete...I'm just trying to find someone who understands what I'm going through who can maybe offer some words of advice. I am a woman who has lived with MS for about 15 years, abs and I have recently become involved in a BDSM relationship. Does anyone else in...

@ColettePage 

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ColettePage

Taopatch

Anyone any experience of this? https://www.taopatch.co/ms

@Lindsay_Muir 

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Lindsay_Muir

training during flare up

Hi! I have a question about how everyone manages working out while in a flare up. do you still push through or is it better to keep things calm while my body is sorting itself out? I just started my flare up 5 days ago and I’m having a moment of frustration ( make that many moments ) My fatigue...

@ColettePage 

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ColettePage

Plummeting mobility!

I’m not on medication for my PPMS & only diagnosed mid April. Tbh I feel totally abandoned by my neuro ms nurse & consultant. The ‘advice/ support’ line for them doesn’t even allow messages to be left, you have to wait for a clerk to answer & they give you a tel appt, if no one answers t...

@Natale_J_Berube 

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Natale_J_Berube

I have rr ms

I am getting a new med for my ms and I am wondering what would be a good one to change from copaxone?

A short story

What is it like to have Multiple Sclerosis? MS is a strange disease. It attacks you, from every angle, but some you cannot imagine. If you walked around in a space suit that gave you general MS symptoms you would miss a lot. Basically if you have MS you really should be living on a space station. T...

@TinaM 

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TinaM

Worry Worry

How does one overlook a main family member thinking I faked the diagnosis of MS..?