Untitled (Didn't have one)
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Have
you ever thought of how good of a life you had? How many opportunities and
chances you had?
That you had the good life had nothing to worry about, stress free.
Living life as it came. But not for some people, they wished and prayed they could get a life like yours because they couldn’t.
Because they’re already stuck in what they still had to live in.
An illness life lasting, slowly taking. Taking the ability to walk, run and move.
That chance to run wild like a carefree child playing games, all gone at an early age.
The dreams of being rich, driving sports cars will live on.
We all have high hopes that one day he could walk run play alongside us but without the cure, we can never be sure.
But as much as we can fill his life with happiness so that there will always be a smile to bright up the darkness.
To see him every day like that, watching the illness take over, making him more and more weak but his heart is strong.
With all his family around him, he’s determined to live with it,
Every year there’s a walk held to help children living with Muscular Dystrophy. Fundraising money to help find a cure or giving the necessities of living with MD.
After when we are told how much we raise, you get that good feeling when you help make a difference in someone’s life.
Those affected are my inspiration, because I know I have what they don’t and I intend to be thankful each and every day and help them in each and every way.
That you had the good life had nothing to worry about, stress free.
Living life as it came. But not for some people, they wished and prayed they could get a life like yours because they couldn’t.
Because they’re already stuck in what they still had to live in.
An illness life lasting, slowly taking. Taking the ability to walk, run and move.
That chance to run wild like a carefree child playing games, all gone at an early age.
The dreams of being rich, driving sports cars will live on.
We all have high hopes that one day he could walk run play alongside us but without the cure, we can never be sure.
But as much as we can fill his life with happiness so that there will always be a smile to bright up the darkness.
To see him every day like that, watching the illness take over, making him more and more weak but his heart is strong.
With all his family around him, he’s determined to live with it,
Every year there’s a walk held to help children living with Muscular Dystrophy. Fundraising money to help find a cure or giving the necessities of living with MD.
After when we are told how much we raise, you get that good feeling when you help make a difference in someone’s life.
Those affected are my inspiration, because I know I have what they don’t and I intend to be thankful each and every day and help them in each and every way.