Another big thing that would be really helpful is education alone. I see a lot of people who don't understand that they are experiencing something that is not a regular occurrence, such as endometriosis, PMDD and things like that. That language and those diagnoses don't often exist for folks in the first place, let alone once they know they have it. The stigma and taboos often take away from anybody taking it seriously it enough to qualify for any sort of supported work environment for those kinds of experiences, extreme pain or other side effect situations.
I was talking about the bleeding alone, but yes, on the pain factors, the behavioural changes and all of those, there's not a lot of education, especially if you come from a less educated...or have a lack of education in your background. Knowing about that, but then also having the follow-up of it being taken seriously and making it accessible for people to be able to work around that to work....