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@crunchyfriends 

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crunchyfriends

Sudden onset of weakness in left leg

Hi all, The last couple of days I have been experiencing some weakness in my left leg, going from the area around the base of my spine all the way down to my foot. Sometimes it extends upwards into my left arm and shoulder. This is a totally new symptom for me and otherwise I feel well but this co...

@Lisamarie@6 

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Lisamarie@6

Recently diagnosed

Hi , I was diagnosed last nov with MS . I have been on Copazone since jan but after a second relapse I was told it’s not working . I’m starting Tysabri on the 17th July . Just wondering if there’s many side effects . I’m still getting my head around the diagnosis. Sorry just another question , I’m ...

@twiggy3 

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twiggy3

What's happening

Had rrms 22 years last relapse 16 yrs ago. Symptom free really so very lucky. A month ago all symptoms came back just like when diagnosed. Mri showed no relapse . Don't know when this will subside . Any info much appreciated. Thanks

Hello :)

Hello everybody. I just found out about this forum and looking forward to connect and share our experience 🙂 I've been diagnosed a year ago and still learning on how to " collaborate" better with my new friend MS. I am based in Romania, Bucharest. I hope all of you are safe during this hard period!

@Sabina_Frunza 

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Sabina_Frunza

Hello :)

Hello everybody. I just found out about this forum and looking forward to connect and share our experience :) I've been diagnosed a year ago and still learning on how to " collaborate" better with my new friend MS. I hope all of you are safe during this hard period!

@Randilla 

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Randilla

Leaning towards Tecfidera

I was diagnosed with RRMS last week. The neuro gave me some options in regards to treatment; I'm to take a week to educate myself and hopefully come to a decision. Tomorrow will be one week. I'm leaning towards Tecfidera, but I'm absolutely terrified. I'm terrified about all of this, but in regards ...

Hi, I'm new to the group

I'm newly diagnosed with RRMS. I'm rather young and frightened... can anyone give me advice and support? Thanks

@AndyG 

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AndyG

New to the group.

Hi all I'm new to the group having only been told I have MS last Thursday although haven't been officially diagnosed but the MS consultant is pretty sure. Bit of a whirlwind following the news bit being as positive as I can. I have an appointment with my specialist nurse in a couple weeks where trea...

@Aiga_Akmentina 

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Aiga_Akmentina

MS everyday support/ opinion

Years ago I needed to change my life completely! Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. After 17 years living with MS I feel that there is something more I can do. I`m thinking of creating MS mom needs serving, supportive, a...

@ncm22 

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ncm22

RRMS TO SPMS

Hi, I was just thinking they say rrms progresses to spms. And it usually is 10 to 15 years after being diagnosed. I would like to know other peoples experiences, if they would like to share. I have been diagnosed since 2010 with rrms, but had symptoms since 2007. Main symptoms numbness from wais...