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@madsr 

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madsr

Music lovers?

I’ve only recently been diagnosed, and have found throughout the journey that music has really helped me process, grieve and find strength. Do you have any songs that may have helped you, or mean a lot with your illness? I’d love to give them a listen! ☺️

Cheeky wink about surviving life’s daily chaos!

Nobody warns you that adulting is basically just managing a series of unexpected plot twists, rationing your patience like fine whiskey, and occasionally wondering if the cat is actually running the whole household. What is your go-to survival tactic when life decides to script a comedy of errors?

@rooneyleoni 

Last reply

rooneyleoni

If chronic illness came with an instruction manual, page one would probably say:

“Try turning yourself off and on again, but don't be surprised if it doesn't fix anything.” Humor is my favorite survival tool at this point. What's your go-to coping mechanism when things get frustrating? 🤭

@Terry85 

Last reply

Terry85

Attention

Just got contacted by someone on here trying to basically use this app as a dating site. When I asked him if he had MS he said no then asked for my snap after that I blocked him.

@alipooh66 

Last reply

alipooh66

Crap gap

I’ve been on Ocrevus for three years ( 5 infusions) one coming up in December This time feels different weak legs , weak arms , numb feet & hands. Eyes unfocused , Constantly falling and tripping over own feet and exhaustion!!!!my mris came back and dr say leasons appear stable hmmmmm why do I feel ...

@louisaanker 

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louisaanker

DMT

Has anyone swapped from Ocrevus to Kesimpta?

@Dustinclaire 

Last reply

Dustinclaire

Deep life reflection

People spend half their lives wishing they had a rewind button. If you could press play on a director's cut of your own past, would you actually change your worst mistakes, or are those the exact scars that made you who you are today? Let's hear it.

@Treesa52 

Last reply

Treesa52

Disability

I’m looking for advice on applying for SSDI. Long story, starting from 2006. They said I had MS by a spinal tap, after a third opinion… I was given the diagnosis of CIS. Years later, in 2022 I got the full diagnosis. Because of the years that has past, now I have PPMS, on a slow decline. I’m pushi...

@Beadburk1 

Last reply

Beadburk1

So excited

I decided to write down some of my thoughts about living with MS. It turns out I had loads to say. It turned into a book. I published it today! I just wanted to gush. I’m sure you understand lol 😎✊👨‍🦽

@Jake1886 

Last reply

Jake1886

Ms footwear

I always thought light weight trainers is best but was recently told a firm sole with them being ankle . What are peoples thoughts and findings?