Test treatments
Hello everyone!
I'm interested in chatting with other msers who have been, or are currently involved in clinical study trials. I've been in study since the beginning of my diagnosis in 2012 and I have been EXTREMELY happy with treatments! Also, I love knowing that I'm helping pave the way for new treatments, while simultaneously treating my rrms. It's definitely a win win situation! Anyways, would love to hear from others who have experienced trial studies, hope to hear from you all soon! !
@emz46 , getting to see the Neurologist always takes time. They're very much in demand. What you could do is contact your local MS Nurse and have a chat with them. You can locate your MS Nurse here :- https://www.mstrust.org.uk/understanding-ms/who-can-help/map-ms-services
@emz46 - do you have an MS nurse you could speak to? my own was the one to speak me through treatments and different medications etc, my neurologist wasn't really involved until I needed a prescription