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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.
You can be diagnosed and treated early. And there is hope for the future.
With this disease it is so easy to throw in the towel, and that is the worst thing we can do.
There's always going to be somebody worse off than me.
There were symptoms that I saw, and though I went to many doctors and had many tests, no one diagnosed 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.
Take a step back, evaluate what is important, and enjoy life.
Someday they may cure MS, that idiot thing. It gets in there and they can't get it out.
Seventy-five percent of MS sufferers are women.
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.
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.
MS doesn't define who I am.
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.
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