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@Claire_Juliet_Woon 

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Claire_Juliet_Woon

Tecfidera

I have been on Tec just over three weeks and third week on two tablets of 240. Last four days extreme diarrhea also nausea and stomach cramping. Spoke with MS nurse who said was probably at stomach bug. Everything I have read in the booklet and on here suggests could be a side effect which I told h...

@DominicS 

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DominicS

Can you help Prof G? Got MS, Had Covid?

He says, "I am interested to know if any of you who have COVID-19 are suffering from a persistent loss of smell and taste and how has it affected your life? Please let us know if smell training makes a difference." - Here is the full post: https://multiple-sclerosis-research.org/2020/06/mscovid19-lo...

@Erika_Rosas 

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Erika_Rosas

Pregnancy and MS

Hi my name is Erika Iam 32 years old, I was diagnosed in 2012, am taking tysabri. I got married two years ago( I have a 14 year old son now, doctor said am stable and am good to start planning on having a baby but for that I would have to change my treatment to Ritaxon, I’ve read it’s good to start ...

@dam205 

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dam205

Primary Progressive MS - A touch Lost

Hello all, Well I don't know where to begin!? Guess I should start here. Joined this site nearly 4 years ago just after I was diagnosed. I have had this thing approximately 20 years. Not on any medication, not that there seems to be much, the same as help with this - not much. I suppose when I w...

@AmyS 

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AmyS

MS, Covid and Work

Hi, hoping for some advice - I have emailed my neurologist but waiting a while to hear back so thought I'd see what people on here think. I work as a secondary school teacher. Have been teaching remotely but deciding about returning. This week there is a training day (staggered in small groups) the...

@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...