Ms Doesn't Define Who I Am.

When You Hear The Word 'disabled,' People Immediately Think About People Who Can't Walk Or Talk Or Do Everything That People Take For Granted. Now, I Take Nothing For Granted. But I Find The Real Disability Is People Who Can't Find Joy In Life And Are Bitter.

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.

Going To Dancing School, Or Being In A Play, Is A Very Familial Feeling. You're Around Friends.

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

You Can Be Diagnosed And Treated Early. And There Is Hope For The Future.