Journal - These are all the Things My Son's disabilities Robbed from Me

Dear Duchenne Muscular Dystrophy,

I’ve been meaning to write to you for quite some time, but thanks to you two, I’ve been pretty busy (as you can imagine).

Over the years I’ve cursed at you, yelled at you, cried at you and tried my best to understand you. The more I’ve learned about you, the more I realize how little I know.

But there’s one thing I haven’t done. I’ve never stopped to thank you. That’s right. I need to stop and thank you for a few things today. You probably don’t get a lot of thank you notes mixed in with all your hate mail, so let me try to explain why I’m writing.

You see, you robbed my son of his ability to use his feet, leg,  arms and hands & eventually lungs. Because of you, he became non verbal due to his breathing on a ventilator, even when he was 24 years old. But when you robbed Timothy's ability to do things, I believe God decided to give him a voice and a platform still.

My son may not been able to speak out loudly, but I believe God uses his life to inspire, bless and teach others around him.

Hey DMD, do you remember that cave you tried to lure Tim in, and other DMD families into for the rest of our lives? You know, the isolated dreary cave where you want us all to live in without hope? We tried it. It just wasn’t for us. So now we do search and rescue, returning to the cave over and over to show others the way out to a better place.

There are so many other things you’ve robbed from me, for which I need to thank you.

  • You’ve robbed me of my own pride, selfishness and greed. 
  • You’ve robbed me of my tendency to put my work above my family. 
  • You’ve robbed me of living for myself instead of in service to others. 
  • You’ve robbed me of only caring about those who are just like me. 
  • You’ve robbed me of believing there are some struggles just too big for us. 
  • You robbed me of never finding out what God’s plan and purpose is for my life. 

Since you came into my life, I’ve met some amazing people because of our common association with you. Therapists, teachers, assistants, service providers — dedicated and passionate people who have crossed our path and have become part of our story — people I might never have met if it weren’t for you.

Thanks to you, I’ve also met some amazing parents raising their own heroes with special needs who inspire and encourage me.


What you don’t know, Duchenne Muscular Dystrophy, is that I believe God didn’t take away the struggles, the pain or the challenges; He just simply used them in ways I never dreamed. He’s used them to teach me unconditional love. He’s used them to teach me the essence of grace. He has used them to teach me to find joy in all things. He’s used them to show me how to be content in the little things. Really, I believe He’s simply used them to draw me closer to Him, help me understand Him, and make me stronger through Him. In trying to destroy us, we believe all you did was prepare a stage for God to show his glory.

You really helped me take my relationship with God to a much higher and deeper level — so thank you so much! I’m so grateful! I rely and lean on Him now more than ever. I asked God to change and heal my son, and instead He used my son to change and heal me.

 I also want to thank you for drawing my son and I closer together in our relationship. We’ve learned to cry together, laugh together, grieve together and stand strong together because of you.

So you see, Duchenne Muscular Dystrophy, I have quite a bit of gratitude for you. Of all the things I’ve said to you and about you, I’ve never thanked you. Who knew that out of my seeds of hate for you, could grow such love for my son?

So consider this my thanks to you. But let’s be clear, just so you know. I still loathe and despise you with everything in me.

Regards,
Dee Bird


Written mostly by: Jeff Davidson (Whose son had Celebray Palsy & Autism)
... & Dee Bird (whose son had Muscular Dystrophy) 
Thank you Jeff for hitting it right on the nail!!!!


REST IN PEACE 
TIMOTHY M. BIRD
4/89-3/2014


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