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@Lauren_Evans 

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Lauren_Evans

Netflix project!!

Calling all aspiring actors! I am casting the third series of a very successful Netflix show. Please do take a look at the brief below and get in touch if you are interested: Roland is in his 40s. Warm, cheeky, sharp, witty. He has MS with mobility and fatigue symptoms. He lives on his own with ...

@Feloreena 

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Feloreena

Slow recovery from Optic Neuritis?

Hi everyone, hope you are all doing well. :) I am interested to hear about people's experiences with Optic Neuritis, and in particular those who have had a slow recovery from it. My own story - I got an attack of Optic Neuritis in my left eye in June this year. It started off with some mild pain a...

@Laura_Martin 

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Laura_Martin

Hello All

Good morning all, My name is Laura and I’m 30 years old. This morning I’m sitting waiting to take my first Tecfidera tablet which was delivered yesterday. I genuinely thought I just had damaged nerves in my back from pushing myself at an exercise class, falling over as my leg stopped working and no...

@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...

@Miranda_McNair 

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Miranda_McNair

Newly Diagnosed: 6-29-20

Hi Everyone, Monday, June 29, 2020. 3:00pm. Dr. Mark Skeen, Chief Clinical Neurologist of Duke Health in Durham, NC looks at me and said, "Yes, today's two MRI's confirm my suspicions. Now, let's focus on medicine over the next weeks, so that we can attack this!" For nearly two years, I have been ...

@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...

@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...

@cwright17 

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cwright17

HELP! Am I depressed?

I don't know if anyone else feels like this, but over the past couple of months I feel lethargic, down and very teary. It's like everything I do, I hit a brick wall and don't want to continue. I've had suicidal ideation, stopped only by the thought of the impact on my family and my partner. I've cri...

@ColettePage 

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ColettePage

Shielding

Hi everyone, especially those with PPMS, I watched a video of Prof G via ms society & im sure one of his slides said progressive ms patients should shield. Is that correct? Colette

@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...