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Hi everyone, I hope you’re all well! I’m feeling a little lost at the moment. I gave birth to my beautiful baby boy 9 weeks ago - unfortunately my epidural was placed in the wrong spot and wasn’t picked up until I went completely numb from the waist down and needed to be moved with a sliding she...

Lockdown is taking it's toll with dire consequences leading to unimaginable fatigue and pain. I can't wait to be making appointments again with the freedom of attending them without the thought of Covid-19 in the background.

Hi all, just looking for some advice... Has anyone experiened pelvic and leg pain after their tysabri infusion?? I started my first infusion nearly 2 wks ago and since then the pain in my leg is driving me crazy

does anyone ever feel really alone in their relationship??? I do it seems that my partner either doesn't listen or just doesn't want to acknowledge how things are. Having a tough time at the moment, don't feel great MS wise. I work full time- from at the moment, they have retired. Having a bad weeke...

I am one of those people who has all MS symptoms, but especially loss of eyesight. Anyhow I got a jpb. mostly home work, translation, etc. I told them I have MS but did not tell them I am registered blind. I have done this job for about 4 months. In face to face situations I can fake it, and mostly...

Hi everyone. Does anyone else suffer with pains in eyelids? Is this normal? Is there anything to help with this?

I hate this disease (and I'm trying hard not to fill this with expletives). I have been with my partner 4 years after 16 years in a pretty miserable relationship. We are very much in love and had (and that really hurts me to say) a fantastic sex life. However, my interest in sex had been declining ...

Over the past 15 years or so I have taken a host of drugs (ending with ‘in’) without success. Even the last course of lidocaine infusions failed to have the same affect that they originally did. The pain management consultant informed me that the only other way to go was Morphine patches. My GP was...

Hi Everyone, Hope everyone is ok. I am just wondering what individuals experiences and advice with trigeminal neuralgia is. I was diagnosed with MS in October and TN was my first symptom starting back in September. My TN is a constant pain on the right hand side of my face/head and has been for jus...

Hi there I’m from Australia, moved to the UK in 2018. In 2009, following a bout of extended vertigo (originally suspected to be labrynthitis) an MRI found a number of MS like lesions. Neurological examination was normal, and a follow up MRI several months later found no changes. Neurologist recomme...