I think that's a big question. I don't know if anyone really knows the answer to that one, because a lot of them are so invisible. I think it's just having the conversation and then potentially better supports for organizations like the MS Society or any of the other societies that support episodic disabilities. I don't know. It's just building that awareness.
When I applied to the police service, their view of multiple sclerosis was of someone in a wheelchair, basically, or an example of one person someone knew who had multiple sclerosis who was potentially more aggressive.
Yes, I think it's just having those conversations and getting that out there. That's what I am trying to do. I'm really only one person, so I don't know how best to keep going with that.