If you have visited here before, you can probably see that I have changed the name of the blog again. I started blogging at 4URuthie to tell the story of our journey to adopt our 1st daughter. I changed it to Mountains for Maggie when we were praying for God to move mountains on behalf of our 2nd daughter. Well now it is no longer just Ruthie’s or Maggie’s stories. It is now our family's story, and the stories of those we share life with, as we Conquer Mountains together. Both ConqueringMountains.net and 4URuthie.blogspot will lead here.

About Me

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I am a pastor's wife, mother of 4 kids (2 adopted and 3 with special needs), physical therapist, and photography junky. This is where it all comes together for me. Feel free to join along as I process life out loud.

Sunday, September 27, 2009

No Excuses

I was walking up the stairs with Ruthie the other day and just had one of those powerful moments where I was in awe of her ability to do anything she puts her mind to. I teared up because I quickly thought of all the adults I know who are paralyzed in life because of either something that happened to them in their past or because of a diagnosis they have been given. The cool thing about Ruthie is that she doesn't see herself as limited. I ask her to do hard things all the time like put on her shoes or feed herself and not once has she held up her little hand to say "but mom don't you see I have limitations". She is a no excuses kinda girl and I love that about her.

I have been thinking on this for several days as I have pondered the next steps in raising both she and Jack and how do I raise them to be people who see their "disabilities" as part of their story and not as their identity. I really believe that is the difference in people who succeed beyond their experiences/limitations and those who are forever strapped by them. I believe one way I do this is to give them an eternal perspective. Paul says in 2 Cor 4:17
"For our light and momentary troubles are achieving for us an eternal glory that far outweighs them all"

Now you may be thinking, "but Ginny my experience (or diagnosis) is hardly light and momentary." Well, neither was Paul's from that standpoint. He was beaten, rejected, and imprisoned but still had this to say in light of eternity with Christ. Again, it is all in how you view it and I believe we must look at all of our experiences with an eternal perspective.

Finally, I think we can't be strapped by the world's definition of normal and the need to fit within that. Some of the most influential people in the world would qualify as abnormal by the world's standards, but it is what they did with that title that made them special. Where would Oprah be if it wasn't for her childhood experiences, Bill Gates if he wasn't borderline autistic, Jennifer Rothschild if she wasn't blind? It was the perspective that their abnormal life experiences or disability gave them that made them who they are.

One day Ruthie and Jack will be faced with the harsh reality that by the world's standards they are "different", but my hope is that they will take this as just part of their story and with an eternal perspective in their grasp, they will change the world.



Sam had his first soccer game Saturday. Here are a few pictures. He plays until the middle of November for anyone who wants to make a Saturday game.





3 comments:

TanyaLea said...

Very good post!

And Sam is so cute in his little soccer gear! :) I love that Ruthie is on the field cheering him on!!

Have a blessed week! <><
~Tanya

Natalie said...

I read this and heard my mom's voice in your words, Ginny. She has raised me the same way...And because of that I know that my disability DOES NOT define me, and the only way it ever will is if I let it! I've often said that my disability may be the forst thing people notice, but I hope it's one of the first things they forget!

Jack and Ruthie are amazing kids that will be known for being kind hearted, determined, God loving people that God is already using for His glory in AMAZING ways! :)

Cheri said...

Beautiful stated! I have had doctors tell me that Lia will never do ...... (fill in the blank). That only makes us strive for that achievement even more. I do hope that my older children are now looking past some of their school mates "disabilities" and see that they too are very much like them.

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