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The next online Wobble (chat) is the 11th July at 11am UK time, more details to follow closer to the time

Hi everyone! I'm just coming back to check in as I realise I've not been around for a while. I had NEDA (No Evidence of Disease Activity) on my last MRI and have been feeling fine since then *touch wood* I became friends with an amazing woman who also has MS and hosts a podcast about living with a...

Hey Guys🤸🏾‍♂️ Im hoping to meet any females, late 30s, mothers. Who are driven with the belief that Dis-Ease can be cured holistical, through diet, mindset and life style. And are currently not relying on prescribed Pharmaceuticals. I am not discriminating im just hoping to connect with likeminded...

Long story..had mri Feb 2 non specific liasions on my brain and 2 non specific liasions on spine. My left leg and foot numb since Jan. My right leg and foot and my right toes numb last 4 weeks..so my mobilty gradually deteriorating last 14months..dreadful burning night pain in legs and feet burning ...

Hi all, Can anybody recommend a diet they feel is helping? I read/see a lot of different things, basically most just recommend cutting out all the so called bad things we westerners eat, days,meat etc ??? I have had some recent issues with having a few items cooked in fat! Stomach aches etc and...

Mywife and I have reached the difficult decision that we do not want children. If anybody does, please just send me your contact details and we can drop them off tomorrow.

I'd like to hear first or at most second hand an account of what it's like for a PwMS to go through COVID. I'm surprised and a bit concerned that I've not seen one here yet. Either we're very good at shielding, or we tend to die of COVID, or both. Or it's just a quirk of stats, and the rate of inf...

<p>I used to be a keen cyclist prior to getting MS. From losing my balance (and ability to walk unaided for long distances) to today, I haven’t rode a bike for 10 years. Now that my young son has learned how to cycle, he wants me to join him on a short bike rides around our block of streets.</p> <p>...</p>

I've looked it up and apparently, it's a rare effect of MS only 6%. And doctors prefer to say that is probably caused by another factor. I've just lost hearing in my second ear, the first went 12 years ago in very similar sudden onset. I'm on steroids but I have to say this has really knocked all h...

Hi, I'm just wondering what other people in the UK think about the change of advice for the vulnerable from tomorrow. It was only Thursday that it was too early to alter the guidelines for the vulnerable. But now from tomorrow we can go out as long as we practice social distancing. What's changed in...