In a retrospective chart review, how many providers do patients go to with reports of MS types of symptoms before they are formally diagnosed? What is the average time from the first time that “possible MS” is noted until treatment?
How does a diagnosis of Multiple Sclerosis interact with pre-existing neurodivergent traits (such as those found in Autism and ADHD)?
What help can Physicians provide to someone who is diagnosed with CIS in those who have MS without just treating the symptoms as they appear?
What are the most effective medications for relieving leg and calf pain, particularly pain that is worsened by exertion, for people with MS?
