Selma Blair explains why the diagnosis of multiple sclerosis caused tears of relief and help from Michael J Fox



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After an inspiring appearance at the Vanity Fair Oscar's post-party party, Selma Blair uses this lighting to draw attention to life with multiple sclerosis.

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"I'm fine," she says Hello AmericaRobin Roberts through his difficulty speaking. "I'm very happy to see you just said what it's like to be in the middle of an aggressive form of multiple sclerosis."

The actress, whose career spans over more than two decades and includes movies like Cruel Intentions and The revenge of a blonde, began talking about his diagnosis last October.

Talk to GMA In an interview broadcast Tuesday, Blair explained that his speech was different due to spasmodic dysphonia, a neurological condition. She said that she believed that it was important to talk when she was in the midst of an outbreak.

"I was a little afraid to talk, and even my neurologist said," No, it will raise a lot of awareness. Because no one has the energy to speak when they are in crisis, "she said with a laugh," But I do. Because I like a camera. "

MS is an unpredictable disease of the central nervous system, according to the National Institute of Neurological Disorders and Stroke. It affects vision, balance and muscle control. It seems different in every patient and every moment, and can range from mild symptoms to a loss of ability to write, speak or walk.

For Blair, she had trouble before her diagnosis. She said she sought advice from actor Michael J. Fox, thinking that she might also be suffering from Parkinson's disease.

"I said," I do not know who to say, but I drop things, I do strange things, "Blair remembered. "He made contact with me and we started conversations, he really helped me … he gives me hope."

She said that some days she could not even drop her son to school a mile away without needing a nap on the way home.

"Since my son was born, I was in a MS crisis and I did not know it, and I gave him everything to look normal," she said. "And I cared for myself when he was not with me, I drank, I had pain, I did not drink always, but there were times when I could not take it."

Blair said the doctors would not take her seriously, accusing her symptoms of being an exhausted single mom. When she was diagnosed, she said that she was crying with tears of relief.

"I had tears in my eyes.These were not tears of panic," she said. "It was tears to know that I now had to give in to a body in loss of control, and that relieved somewhat."

Blair said she was trying not to be too harsh on herself as a working mother who is struggling with MS, especially on hard days.

"I go to bed and I do not move," she says. "You can not do everything, it's good to feel really bad."

She had to explain her diagnosis to her 7-year-old son, who feared the diagnosis would die in her death.

"And I said," No, I mean, we never know what kills us, Arthur, but it's not the doctor who tells me I'm going to die. " She said. "And he was like," Oh, okay, and that was all. "

She said that she would like to come back to GMA again in a year to see if she's better.

"If I'm not, and I can always have a conversation," she says, "that's enough."

Melanie Lawson, News Eyewitness News presenter, talks about her personal journey with MS

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