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McKenzie Rainn - Always in our Hearts - Home

What if you were suddenly faced with the diagnosis of a severe, genetic disease of your newly born child?  On February 17, 2012, a family that is like family to me had to face this question with...

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What if you were suddenly faced with the diagnosis of a severe, genetic disease of your newly born child?  On February 17, 2012, a family that is like family to me had to face this question with...
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McKenzie Rainn - Always in our Hearts - Home | mckenzierainn.weebly.com Reviews

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What if you were suddenly faced with the diagnosis of a severe, genetic disease of your newly born child?  On February 17, 2012, a family that is like family to me had to face this question with...

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McKenzie Rainn - Always in our Hearts - Home

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McKenzie Rainn - Always in our Hearts. A Note From the Family. Helping the fight against SMA. What if you were suddenly faced with the diagnosis of a severe, genetic disease of your newly born child? On February 17, 2012, a family that is like family to me had to face this question with their second daughter, McKenzie Rainn. At just three months old, McKenzie was diagnosed with Type 1 SMA (Spinal Muscular Atrophy). Create a free website. Create your own free website. Start your own free website.

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A Note From the Family - McKenzie Rainn - Always in our Hearts

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McKenzie Rainn - Always in our Hearts. A Note From the Family. A note from the family:. For those of you who were able to meet and hold our little McKenzie Rainn, and for those of you who did not.we know that she will forever be in ALL of your hearts.". Enjoy all the little things in life, for some day you will look back and they will be the big things.". Love and Kisses -Steve, Jenni and Madison Losacco. Please take a moment to stop by and read about McKenzie and her. Create a free website.

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Pictures - McKenzie Rainn - Always in our Hearts

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McKenzie Rainn - Always in our Hearts. A Note From the Family. Create a free website. Create your own free website. Start your own free website. A surprisingly easy drag and drop site creator. Learn more.

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SMA Resources - McKenzie Rainn - Always in our Hearts

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McKenzie Rainn - Always in our Hearts. A Note From the Family. Please visit the following SMA websites for further information and other ways to get involved. Create a free website. Create your own free website. Start your own free website. A surprisingly easy drag and drop site creator. Learn more.

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Donations - McKenzie Rainn - Always in our Hearts

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McKenzie Rainn - Always in our Hearts. A Note From the Family. Please feel free to make a donation below on behalf of McKenzie Rainn. Donations will be used to help her family with any SMA related expenses as well as be a fund for her family to directly reach out and help other families affected by SMA. All donations are considered a gift and are not tax refundable. Create a free website. Create your own free website. Start your own free website.

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Friday, February 3, 2012. This is a cool cursor i found online. Http:/ www.youtube.com/watch? Monday, April 26, 2010. Mckenzie's blog is going private please leave your email if you want to be invited to read her blog. Posted by Danielle Christiansen. Friday, April 23, 2010. My duo at competition. We got a high Gold and a Gold at competition this year. Ignore my mom she screamed the whole time. Posted by Danielle Christiansen. Friday, April 9, 2010. You guys should see our family blog. If you are older t...

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McKenzie Rainn - Always in our Hearts - Home

McKenzie Rainn - Always in our Hearts. A Note From the Family. Helping the fight against SMA. What if you were suddenly faced with the diagnosis of a severe, genetic disease of your newly born child? On February 17, 2012, a family that is like family to me had to face this question with their second daughter, McKenzie Rainn. At just three months old, McKenzie was diagnosed with Type 1 SMA (Spinal Muscular Atrophy). Create a free website.

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