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@pinkie100 

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pinkie100

Tysabri - few symptoms but new lesions

I was diagnosed in June 2019 having woken up with pins and needles in my hands in January. No previous symptoms. Pins and needles extended to whole body from chest down and I experienced MS hug a few times. After a couple of months things seemed more or less back to normal and although the pins and ...

@Rosie_Paolo 

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Rosie_Paolo

Feel a bit deflated and stupid

So I’m waiting for a diagnosis of various symptoms. I had an appointment via video link at home with a neurologist and I just feel like I messed it up. I’ve been waiting for 6 months , in pain , and I couldn’t articulate my symptoms . He asked me if it’s there all the time or now and again - I an...

@Claire_Juliet_Woon 

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Claire_Juliet_Woon

Advise on Exercise

Hi I have RRMS, diagnosed September last year and been on Tec since May this year. Anyway to cut long story short started weight training again after a period of not doing anything, the issue I have is after lifting weights I have had NO arm/muscle ache at all the day after, it is like I have not ...

@Erusha 

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Erusha

Life expectancy

Hi guys I just read the average life expectancy of someone with ms is 25 to 35 years after diagosis Anyone with any thoughts?

@SUKHJEET 

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SUKHJEET

Hie All!

recently got diagnosed with RRMS. its hard to digest. i m really keen to make every effort for healthy life. i was wandering if anyone has benefitted from OMS recovery ?

@Rose23 

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Rose23

Difficult diagnosis, am I mad!

Hi I’m so sorry if this is inappropriate but I’m just upset and don’t have anyone I feel will understand to talk to. I have just come off a telephone consultation with my (very nice) GP. I had an MRI as I have been having symptoms that my GP agreed sound like MS for ages - even years. I’m 36yrs old....

@scout 

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scout

Scout

Need to get something off my chest....... so fed up, diagnosed 24th March 2020. Still no communication, phone calls or anything else from any health care professional. I keep reading about asking your ms nurse for advice - think I’m losing it cos I’m still waiting.

@CHARLST0N 

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CHARLST0N

Saying Hello

Hi all, I am seriously new to all of this, My RRMS journey has been a whirlwind. I had the MRI and got diagnosed literally overnight. Multiple MS occurences all at once. After a huge course of steriods Methylprednisolone 1000mg 5 days. My flares have calmed down. Not gone away, I my hands are numb a...

@JamesB 

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JamesB

Time Between Relapses

What is the longest anyone has gone between relapses since they were diagnosed, drug assisted or otherwise?

@Bridgett_Tadel 

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Bridgett_Tadel

Steroids not helping

Ugh! Had burning stabbing nerve pain in my right foot sat, sun, mon, (of course on the weekend, can't get ahold of any doctors). Felt like my foot was on fire!! started steroid infusions Tuesday, Wed, Thurs, then 2 weeks of oral meds. And I still have the numbness with occasional pain. I was only di...