I hope that people with MS (especially newly diagnosed) and the general public, if they watch, will watch to the end and note that Shelley Fabares points out that this is what MS "can be", not what MS "is".

I have mixed feelings. While I want everyone to know how devastating it CAN be, I would hate that someone, especially a young person, sees this and thinks "This is my future".

But I want people who can support research financially, for example, to be reminded of how bad it can be.