It isn't supposed to be this way is it? You are the parent and have children to take care of. Yet now you are faced with this disease and you wonder if in time your kids will be taking care of you. I think what breaks my heart more than the firsthand stories of what this disease is like from a patient's perspective are those stories told by the kids who have parents who have MS.
When I was first diagnosed with MS I went to the internet for information and support. There was a video...


