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… spectrum …

June 16, 2014 Leave a Comment

 

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Tell me more (about SB) Mondays

 

 

Spina bifida is a SPECTRUM disease.E920F6DA985B354F7C56D9E63E63E_h316_w628_m5_cCvjEnSkD

Now when I think of spectrum, I tend to think of rainbows.  Why?  Because when white light is refracted it splits and disperses into all the colors of the spectrum – a rainbow.

I really really like rainbows.  After a rain, I always look for the rainbow.  🙂

But how does this define spina bifida as being a spectrum disease?  Well, if ‘spina bifida’ is like the white light, when it touches a human being, it reveals itself in so many color patterns … and all of them different.  If the color orange, for example, represents normal pressure of the CSF fluid in the brain and spinal cord, then absence of that color means you have hydrocephalus.   (I wish Amanda had that color.)  And if blue represents the ability to walk, well there are lots of spina bifida people who can walk – they have lots of blue in their rainbow!  No blue means they can’t walk.  So even though yourainbow-partial-lrg may know someone with spina bifida that walks and works at a regular job – well they have got a different array of colors (symptoms) then someone else with spina bifida.

People with spina bifida are born with their own rainbows.  Sometimes, colors are missing or the spectrum of colors (abilities) is arranged a bit different.

It’s okay.  All people have abilities and deficits that set them apart from one another and make them unique.  Maybe that’s what they mean when people talk about ‘showing your true colors’ – showing people what you DO have.

The impressive thing about spina bifida people is that, even though they are born with a different color palate, it rarely stops them.  They tend to take what they CAN do – work with the colors they have – and make the very best of it.image

(Yeah – I get angry when I see colors missing from Amanda’s rainbow – darn that spina bifida – but she still has lots of colors!)

So, spina bifida or not, we all need to be the best we can be with what God has blessed us with.

I never saw a rainbow I didn’t like.  They’re all beautiful.

Just Laurel

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About Laurel

Laurel is a wife and mom to three girls, including Amanda, who has spina bifida. She's a nurse and writer, sharing about her faith and journey as a caregiver

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Hey – it’s me! just Laurel. I am just a 50-something year old mom who lives in southeastern Michigan. Married forever to the love of my life, Ted. We are just like any other family with kids out there: working hard and doing our best to raise great kids and to live as decent, moral people.

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