What it's like to have MS and the exploration of clinical research

[@Shiftms]

Great video!

[@TrishnaBharadia]

Fantastic video! Well done everyone and NIHR!

[@Zaz170]

Thanks for your Nice video! I have a MS since 2019 we are feeling less alone 🙏🏽🥰

[@Jumboo364]

I have a friend with ms. Thanks for your work

[@helenhucker346]

Unfortunately there continues to be plenty of MS patients for these researchers to study.

[@vesnakocoski4486]

What pills?

[@anthonygoulet365]

I did not hear anything about Diet.

[@mybachhertzbaud3074]

For me it is a very real pain in the ass 24/7. And of course, legs and feet.😒

[@Heresheis0818]

Those prescriptions save your day!#neurotic degeneration#Cognitive declines

[@mary-vy3mo]

Why do all these people.congratulate themselves....sad.

[@scores718]

Robbie. I was dx ppma about 34vyrs ago. Could you share which drug has helped cont er ol bladder? I failed at every med I've tried. Ending with mybetriq. Thank you. Want my email?