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@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 ...

@Aiga_Akmentina 

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Aiga_Akmentina

Does food and drinks effect how we feel?

From positive and active days to a day like this...more slow and feeling tired of everything. Sometimes I`m thinking and trying to understand is it just the case of MS. I somehow start to see correlations between my slow days and days where I feel active and positive! I have read and heard that foo...

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 ...

@cath3203 

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cath3203

Tecfidera and weight loss

Hi I’ve been on Tecfidera for about 6 months after moving from Beta interferon injections once a week for the last 9 years, at the beginning of my journey I weighed around 60 kilos which I know at 5 ft is a little on the heavy side, but I find myself now weighing 48.4 :(, with the onset of Covid 1...

@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...

@chriscoxrox 

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chriscoxrox

Something new

Two musicians with MS One in Texas and the other in New York have made something amazing over the last year and a half and never even met in person. This conceptual album is about to change the game. Not only the music but most of the animation and artwork were done by the two musicians with #multip...

@Thorpee 

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Thorpee

UK car insurance..

Hello everyone, a thought came to me in the dead of last night. Has a diagnosis of MS dramatically affected anyone's car insurance? I presume it has to be declared? Weak legs and twitching eyes are one thing, but if this affects my pocket as well I'll be very unhappy. My car insurance is currently c...