I have previously carried out some online paid MS research for Exafield ltd and have received a link via email to ask if I know anyone else with MS who would like to join for research opportunities. They are specifically looking for people with MS (either on DMDs or not) to shape future medication/talk about side effects/how your MS affects you. The survey I did was around an hour and I believe I was paid £70 to talk about a new way of administering Ocrevus through a stick-on device rather than an IV drip. They showed me photos and asked whether this would make life easier for me without having to spend a day in hospital hooked up to an IV. I believe the device went to market as my neurologist mentioned it about a year later. The research is done by video call. I have had RRMS since 2015, diagnosed at 25. I'm not on any DMDs. Here’s the link to register your interest, specifically to get your thoughts heard by pharmaceutical companies who are developing DMDs: https://survey.zohopublic.eu/zs/YvD6PF I should add I don’t work for the company - just thought it might be helpful if anyone is looking to help with medical research in exchange for some pocket money and for your thoughts on your medication to be heard!