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Found this today.....

On Dying, Mothers, and

Fighting for Your Ideas

by Morrow <http://www.copyblogger.com/author/jonmorrow/>

[image: image of mother and baby's hand]

The doctor cleared his throat. “I’m sorry, but I have bad news.”

He paused, looking down at the floor. He looked back up at her. He started

to say something and then stopped, looking back down at the floor.

That’s when Pat began to cry.

She’d argued with herself about even coming to the doctor’s office. Her baby

was a year old, and he hadn’t started crawling yet. He tried, yes, dragging

his legs behind him as he struggled to make it just a few feet on the floor,

but it didn’t look right. Everyone told her that she was worrying over

nothing, and maybe she was, but she told herself that she would take him to

the doctor, just to be safe . . .

“Your son has a neuromuscular disorder called Spinal Muscular Atrophy,” the

doctor said. “It’s a form of muscular dystrophy that primarily affects

children.”

Pat was speechless. Everyone had told her she was silly. She had hoped she

was wrong, *prayed* she was wrong, but still . . . she knew.

“What’s going to happen to him?” she managed to say.

“Where most children grow stronger as they get older, your son is going to

get weaker. He’ll lose the ability to move. He’ll lose the ability to

breathe on his own. And one day, he’ll catch an infection that will spread

into his respiratory system, giving him severe pneumonia . . .”

She held up her hand to stop him. “You’re saying he is going to die?”

He nodded. “There are three types of SMA. Caught this early, your son almost

certainly has Type I. Most children with Type I die of pneumonia before the

age of two.” He paused. “I’m sorry.”

Pat looked up into his face and saw that he really *was* sorry. It made her

angry. Not because of his pity, but because in this man’s eyes, her baby was

already dead.

“Don’t be sorry,” Pat said, wiping tears away from her face. Her voice was

suddenly very calm.”He isn’t going to die.”

“It’s important you understand the situation, Mrs. Morrow. The pneumonia . .

.. he won’t be able to fight it.”

“He won’t have to,” she said. “I’ll fight it for him.”

The miracle of mothers

Over the next 16 years, I had pneumonia 16 times. But I never died. It

sounds strange to say it, but my mother wouldn’t let it happen.

She orchestrated a team of more than a dozen doctors. She slept in a chair

beside me in the hospital, sometimes for as many as 30 days in a row. She

pounded my chest and back every two hours to loosen the mucus, covering my

chest and back with bruises.

Today, at 27 years old, I’m one of the oldest people in the world with my

type of SMA, and people tell me it’s a miracle. And I agree, it is. But the

miracle isn’t just me. It’s a mother who fought like only a mother can to

keep me alive.

By “alive,” I don’t mean just “not dead,” either. You’d think my mother

would have been satisfied for me to live at home, tucked away from the world

where she could protect me, but for her, that wasn’t *living*. She insisted

that I be great.

When my elementary school principal decided that disabled children didn’t

have a place in her school, my mom appealed to the school board and turned

every board member’s life into a living hell for two years.

She won.

When I wanted to play basketball, she forced an astounded coach to reinvent

the rules of the game so that I could be the “ball carrier” for the team,

and no one could take the ball away. Not surprisingly, everyone wanted me on

their team.

When I could no longer pick up a pencil, she arranged for honors students at

local colleges to help me with my homework after school. I graduated at the

age of 16, not only near the top of my class, but with college credit.

If you’re a mother, none of these things surprise you. Some mothers are

weak, sure, but the vast majority *fight* for their children, especially

when those children are defenseless. It’s not because they’re trying to be

heroes. It’s because that’s their job.

And I think we can learn something from them. Not to minimize what mothers

do, but I’ve come to believe that our job as writers is not all that

different.

Fighting for your ideas

Growing up, I always had to fight to get people to listen to me.

The worst part about being disabled isn’t the pain or the struggle but how

the world tries to shove you into a corner and pretend that you don’t exist.

After all, what could you possibly have to contribute? You’re going to die

soon, poor thing. Here’s a nice, quiet room and some morphine to ease the

pain.

They don’t *proactively* hold you back, no, but they don’t expect you to

succeed either. I’ve spent my entire life fighting against the weight of

those expectations.

Like when university professors were flabbergasted when, on the first day, I

asked my attendant to raise his hand, so I could answer the question that no

one else could.

Or the vaguely constipated look on the face of a venture capitalist when I

asked for $500,000 of startup capital for my first software company.

Or the disbelieving stares of people at a real estate conference when I gave

a talk about buying million-dollar homes without even being able to get up

the stairs to see the inside of them.

Their disbelief has never stopped me, of course. It’s not a matter of

persistence or strength or attitude, as some people think. It’s a matter of

shame.

How could I possibly look my mother and father and all of the others who

have sacrificed so much for me in the eye and tell them, “I can’t?” I

couldn’t bear it. The shame of dishonoring their sacrifice by giving up

would poison my soul.

And so I fight

If my mother could ignore a doctor who would condemn me to death, then I can

ignore my inner demons who tell me I’ll never make it as a writer.

If my mother could demand that I achieve straight As in school, then I can

demand greatness from every blog post I publish.

If my mother could lobby school administrators and government agencies to

get me the help I needed, then I can lobby bloggers and social media power

users to get my idea the attention it deserves.

Not to imply that I’m unique, because I’m not. Yes, I’ve had to overcome a

lot of adversity, but so does every creative person who wants their ideas to

see the light of day.

If you want to succeed, you can’t wait for the world to give you attention

the way a cripple waits for food stamps to arrive in the mail. You have to

be a warrior. You have to attack with the madness of a mother whose child is

surrounded by an army of predators.

Because, let’s face it, your ideas *are* your children. Their future is as

tender and delicate as that of any newborn.

You can’t just write them down and expect them to succeed. Writing isn’t

about putting words on the page, any more than being a parent is about the

act of conception. It’s about breathing life into something and then working

to make sure that life becomes something beautiful.

That means spending ten hours on a post, instead of 30 minutes.

That means writing a guest post every week, instead of one every few months.

That means asking for links without any shame or reservation, not because

you lack humility, but because you know down to the depths of your soul that

what you’ve done is *good*.

You have to realize that your blog is more than just a collection of ones

and zeros floating through cyberspace. It’s more than the words on the page.

Your blog is a launchpad for your ideas, and *you* are the rocket fuel that

lifts them off the ground.

So burn it up, baby.

Your ideas are counting on you.

*About the Author: Jon Morrow is Associate Editor of Copyblogger and

Cofounder of Partnering Profits <http://www.partneringprofits.com/>. Get

more from Jon on twitter <http://twitter.com/JonMorrow>.*

What's The News On ne & Latte? www.our-sma-angels.com/neRose

TV Story 2-14-10

http://www.wxyz.com/content/news/seenon7priority/story/Home-Makeover-Rally-Held-\

for-Student/3YgIKMHVak-6AoPwhYG37Q.cspx

Newspaper Story 2-18-10:

http://www.hometownlife.com/article/20100218/NEWS03/2180605/1020/Positive-influe\

nce-Canton-girl-won-t-let-muscular-disease-slow-her-down

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