Posted by: Susan | January 12, 2011

You gotta see this blog post.


I am writing my blog today by combining mine with some comments and lots of pictures from Kelle Hampton.

This little cutie in the above picture is Nella.  Her mom, Kelle Hampton, has a blog at http://www.kellehampton.com/

I somehow found this blog and have been enjoying it for the last year.  Nella was born just about a year ago and Kelle, who was already blogging, let the world know what it’s like to have a baby born with down syndrome.  She shared it all….the birth story, the tears and the fears.  Several times a week Kelle would post beautiful pictures, insightful words, triumphs and doubts that she had about being a parent and having a child with DS.  My heart would ache for her and I just wanted to reach through the computer and hug her and tell her it would be all right.  I was able to do that through the comment section.  But here is the really cool thing.  Kelle is so open and honest and transparent that she and Nella have impacted the lives of thousands of families with DS.  She is like the rock star of bloggers not only in blogs for special needs but also in the parenting blogs.  Thousands of people read her blog on a daily basis.  I love it because she is young and with it and inspires me (old and trying to be with it).  Read on for a glimpse of her blog.

Kelly...”I have changed. My eyes have been opened to the broad spectrum of beauty, the value of uniqueness and the amazement of the common thread that binds us all regardless of the color of our skin or the makeup of our chromosomes.

How could I not have been aware of their magic?”

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Kelly, “I am grateful for the pain that propelled me forward this year for without it, I wouldn’t have known the joy of this place.”

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Kelly, “When I sat down to write this post earlier this afternoon, I intended to make this about Nella. But, I’ve learned something more this year. I’ve learned to look beyond. While yes, the rawness of loving my own child and imagining her almond eyed, milky-cheeked, tiny-toothed grin on the face of every other child with Down syndrome is what initiated my purpose in this new world, it has become more. I care not just because my daughter personally connects me to this greater world but because I have learned to see their hearts, their capabilities, their spirit, their determination, their love.”

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Kelly, “And I want you to see it too. Beyond Nella. The faces of these children brighten the worlds of so many lucky families every day. And as I checked my e-mail earlier this evening after a quick Facebook photo all-call, tears rolled down my cheeks at the response. My e-mail alert chirped a continuous rhythm as pictures rolled in, and I couldn’t determine what was more powerful–the faces of these beautiful babies or the words you attached to them in a desperate plea to express a fraction of how you feel.

The love of our lives. She changed me. Our joy boy. The heart of our family.”

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Kelly, “So, here’s the deal.

I’m going to ask you for something. And it’s really important to me. To a lot of people.

I’m going to ask you to think about what you’ve taken from this space this year. I have felt incredibly inspired by not only the feeling of community here but by this productive push toward good that arises simply from the understanding of the power of a group of people connected in a small way on the Internet but, more importantly, in a much greater way within this vast world. And so, I’m asking you again, have you gained anything from visiting this space this year? A smile, a thought, a connection, the encouragement to dig deeper or let your own voice speak out. If you have, I’m asking you to give back today. Please, pay it forward.

In honor of our girl’s first year, we are asking you to give back to her. And the 400,000 other individuals living with Down syndrome in the United States alone.”

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The mission of the NDSS is to create a culture that fully accepts and includes individuals with Down syndrome.

Let me say that more clearly. The mission of the NDSS is to create a culture that fully accepts and includes our little girl. Our Nella.

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Last year, the NDSS helped Annie Clancy, a Connecticut high school student, get closer to her dream of becoming a clothing designer when they gave her the once-in-a-lifetime chance to join designer Anya Cole in her studio to learn how to design and produce clothing. Without the NDSS, Annie wouldn’t have known what it felt like to strut her fabulousness down the runway of a fashion show in a posh SoHo loft.

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Or how about Sara Wolff? A skilled motivational speaker, she serves on the NDSS Board of Directors and actively promotes Down syndrome awareness and understanding through personal appearances and inspirational speeches to educators, employers and community professionals. She is loving what she’s doing. She’s doing something amazing with her one wild and precious life. Not to mention, she got to meet Barbara Walters and Meredith Viera which is more than I can say. As Sara says, “I feel good knowing I can inspire people and make a difference.”

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“I want my little girl to have these opportunities, and I’m just one of many mamas who share this dream.”

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I’ve set a scary goal. $15,000, People. (Actually, I’m editing this after 12 hours into the fundraiser, I’m doubling it, yikes! $30,000.) Editing this AGAIN about 2 days into it. $47,000. Yup, $47 grand for 47 grand chromosomes!) Alright, I’m back. 4 days, and our goal is now $63,000. That’s 21 x 3. Three beautiful little 21st chromosomes, that’s what. And I’m a little nervous about it. But, I believe you care. I believe we can make a difference together. If every Follower–a fraction of readers–gave only $5, we could raise $45,000. Forty Five Thousand Dollars to help change the world into a place that sees the beauty and potential of the magic of these amazing individuals.

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“I want this life-changing year to mean more. I want to hold hands with my family in two weeks and know, when we sing “Happy Birthday Dear Nella” and watch her pat her tiny palms into sweet frosting, that something greater is in store.

For everyone.”

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Please. Give Nella a birthday gift. Help her give back to her friends.

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“If a magazine costs $5, think of how you’ll feel if you spent that instead right here.

Pay it forward. Help us give Nella a very happy birthday.”

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Nella’s shirt and sweater used to be dresses. They were her coming-home-from-the-hospital outfit. Sweater, crocheted by my mama

“Giving is easy. Click on any link to Nella’s ONEder Fund on this page (the easiest being the large banner at the top of the blog which will remain until Nella’s birthday.)

Spread the word. E-mail it. Facebook it. Tweet it. Blog it.
Together, I’m certain we can move mountains.

Give $5. Or give more. But know, you are appreciated and you are making a difference.

Thank you for your support, your love, your joining with us to make something grand of our one wild and precious life.”

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Susan:  So there you have it.  If you would like to make a contribution to the National Down Syndrome Society and help make the lives of the 400,000 people who have DS better click on Kelle’s blog or one of the links above.  I am going to donate in support of : April, Jacob and Sam (our 3 kids with DS) and everyone else that has DS too.

Life Lesson:  One person can make a difference.  You are that person.

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