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@YogaLady 

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YogaLady

My Ms 🧡

Feels like I haven’t got Ms anymore 😁😅 as I’ve been really well with it for a long time now 😁. I’ve been keeping very active and fit and looking after myself. doing well with my 4th Ocrevus treatment too 😁😅👍🧡.
Braunton, United Kingdom

@YogaLady 

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YogaLady

Menopause

I haven’t got my Menopause yet 😅 with my Ms! I’m age 40. How many people have it on here? And who hasn’t?
Braunton, United Kingdom

@davesmith71 

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davesmith71

Add Multiple Sclerosis to the NHS medical exemption list for free prescriptions

I want to start a petition – will you sign it? Add Multiple Sclerosis to the NHS medical exemption list for free prescriptions Add Multiple Sclerosis to the NHS medical exemption list for free prescriptions in England. The list has not changed since 1968. MS requires lifelong, expensive medicatio...

@89scott 

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89scott

🤔🤔

Does anyone else find walking in this crappy stormy weather(UK) help clear your head or just me being odd 🤣

Lesion causing pain

Just curious, has anyone had lesions in their lower spine spine, to where when it flairs up, you have a "miscle" pain. Last night it woke me up trying to roll over. Getting checked now, looking for kidney infection, muscle stain, torn scar tissue, or lesions being cranky causing the pain

@JeremiahW 

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JeremiahW

Kegal workouts

Ever since I started working on my kegals, my balance is gotten good. Then it got bad. Any advice?

@ambidexter 

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ambidexter

Self-experimentation

I stopped all treatment six months ago and haven't noticed any changes. I'll have another MRI in six months to see how things are progressing.

@itsemma 

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itsemma

Jewelry and MRIs

I got permanent bracelets and I have to remove them every time. Sometimes they told me that if it’s gold it’s fine but I don’t even know what kind of gold. Any experience with that?

@SoniaG236 

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SoniaG236

Duration of MS

Is MS a long term condition like Parkinson's? I had thought that it was until I saw a few comments recently on here where people said that their Neurologist had said that their MS had gone. Is it to much to hope that it clears up after say 10/15 years? Or is it that MS treats everyone differently?