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@KAWeakland 

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KAWeakland

Welcome / Hello

Hi, I’m Kim ! I’m 48, about to be 49 . I’ve had RRMS for 11 years now . What a blow to be hit with in your 30’s . I was diagnosed the same time I had to get breast surgery . My now , EX husband wasn’t too much of a supportive man during my years of battling meds and seeing which ones helped 🙁 But...

@Martin_Hoole 

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Martin_Hoole

Early retirement

I'm now 55 i was diagnosed in 2013 and i have just carried half disbelieving that i have ms but have got to a stage that i have had to tell work and everyday is a uphill struggle and my neurologist said that it may be time to take early retirement and I havent got a clue where to start.

@Kirstie_Hawkins 

Last reply

Kirstie_Hawkins

Tingling / numb arms hands

Tingling in arms / hands - MS or not Hello. I have been diagnosed with RRMS and wondered about a strange issue with my hands/arms In both arms I can run my finger lightly down my inner edge of my forearm, thumb side, and it is kind of numb and tingly at the same time. It can give me tingly hands too...

@mikki131 

Last reply

mikki131

CCSVI

So, I received CCSVI in Bulgaria, I whole heartily believe that it did work other than that I collapsed.. of course they no longer do it. So here is my question. They reposted that I have a 90% blockage on my jugular and I cannot remember the percentages on others. So take MS out of the equation sho...

@mikki131 

Last reply

mikki131

Thinking in the future

So I was at my Neurologist and her assistant stated to me that I should be a lot worse than what I am! My neurologist agreed.. so this of course got me thinking of the future. I have decided that I do not want to get bad, I know some people r and are happy and that’s their choice and right. I have t...

@Tara_Scully 

Last reply

Tara_Scully

Need some advice

Hi All, I was diagnosed November 2019 with RRMS. I was put on Rebif which the only complaint i have is the red marks it leaves but would have happily gone on with it. Yesterday i met with a new neurologist after my previous one had left. I had an MRI in advance and there was one small new very sma...

@ItsMewithMS 

Last reply

ItsMewithMS

Vestibular Issues and PT options

Hi- with Covid really just passing through my area I have restarted my PT. I left off in December when they shut down. He left me with some good exercise options and I tried some of the other options so readily available on-line. The good news is that I think I have been able to maintain strength p...

@lemtrada-uk 

Last reply

lemtrada-uk

Lost ability to urinate

Need some advice please guys. Has anyone else lost their ability to urinate following an excessive hospital stay due to a physical trauma. Recently I broke my femur so was hospitalised. Whilst in hospital, I was urinating via a long term catheter. My bladder had gone into retention caused by the tra...

@EllieSmith 

Last reply

EllieSmith

Falling, my body just drops no warning?

Love that ms nurse says oh I respond to emails faster... Last time I got no response at all. This time well I'm 4days in not holding much luck. Guess I'll phone tomorrow and see. Legs been giving out multiple times a day for almost three weeks now. Plenty of bruises have been collected and pulled m...

@Shannon_OHara 

Last reply

Shannon_OHara

Shaking inner ear

I know I have sensitive ears, for example I don't like watching things too loud. Other people moan it's too quiet for them to hear at the level I watch stuff. I used to get it every now n then when the TV is too loud or people are rasing their voices. It feels like the thin part of your inner ear i...