You can be diagnosed and treated early. And there is hope for the future.

I go to my physical therapist to keep fighting it and one of them told me if you don't use it, you lose it, but I know we're on television so I won't say what I would often say.

I have heard all kinds of stories about telling employers about MS and I really don't know what the answer is. I am a private person, but I have found support by talking to fellow MSrs in the community.

I recently saw the movie about Ray Charles, and there's a scene where he falls down and the mother doesn't help him. She says, I don't want anyone to treat you like a cripple. I've fallen down before, and Molly will say, get up and just go.

I think eventually they're going to find out that MS is like 10 different things. I have a neurological disease something like MS, and it's MS, so let's take medicine for it.

In addition to having a good partnership with a good doctor, you have to do some of the work yourself. Go online, read about it, and find out what you can tolerate.

My doctor said, for want of a better word, now that we've got medicines out here that can help, let's put you on one of them and say we're treating MS.

There are things that you can do today that, years ago, there was nothing. The community today needs to know that with MRI and the current medications the view is good.

You have to find out what's right for you, so it's trial and error. You are going to be all right if you accept realistic goals for yourself.

Take a step back, evaluate what is important, and enjoy life.

Oddly enough, MS has made my life so much better than it was before. I now appreciate what I have and I am not running around like a rat in a maze.

MS doesn't define who I am.

Seventy-five percent of MS sufferers are women.

I have a disease, but I also have a lot of other things.

I have an enormous fondness for delicious food. It's very comforting.

You have to lift your head up out of the mud and just do it.

You can keep it to yourself, but you could also call a support team like the team at MS LifeLines. They are there to support the MS community and give good advice.

I have worked enough and I am happy to be touring the country speaking about living with MS to give people inspiration and motivation to help themselves.

I'm wondering if they haven't reported all the people with MS, because if all of the cases were reported, the government would have to step in and give more financial aid to us.

Any movie I've ever made, the minute you walk on the set they tell you who's the person to buy it from.