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Growing Up Blind | in a rare LCA world

Eme has been robbed of her sight by LCA-CRB1, a very rare genetic disease. By age 3, she was already blind. LCA-CRB1 has no treatment. A gene therapy clinical trial is being conducted for LCA-RPE65 right now that is working and is giving blind kids like Eme their sight back! By replacing the mutated/broken gene…

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Eme has been robbed of her sight by LCA-CRB1, a very rare genetic disease. By age 3, she was already blind. LCA-CRB1 has no treatment. A gene therapy clinical trial is being conducted for LCA-RPE65 right now that is working and is giving blind kids like Eme their sight back! By replacing the mutated/broken gene…
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Growing Up Blind | in a rare LCA world | growingupblindwitheme.wordpress.com Reviews

https://growingupblindwitheme.wordpress.com

Eme has been robbed of her sight by LCA-CRB1, a very rare genetic disease. By age 3, she was already blind. LCA-CRB1 has no treatment. A gene therapy clinical trial is being conducted for LCA-RPE65 right now that is working and is giving blind kids like Eme their sight back! By replacing the mutated/broken gene…

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Blog | Growing Up Blind | in a rare LCA world

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In a rare LCA world. May 22, 2016. It’s a rainy Sunday and Eme has been cleaning her room. Yes, blind kids can clean. Yes, you should be teaching your blind kids to clean their room and do chores around the house just like everyone else. We’ll come back to that another day…. Today, I wanted to show you this. Pretty isn’t it? Not much better, huh? This folder screams inclusion! But today, we are sharing this folder. This act of inclusion. To a third grader that is blind and clearly very different from mos...

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March | 2014 | Growing Up Blind

https://growingupblindwitheme.wordpress.com/2014/03

In a rare LCA world. Monthly Archives: March 2014. March 21, 2014. Eme’s Rainbow Jars. Eme’s Rainbow Jars are now available for shipment! Shipping is $10 sent USPS Priority Mail anywhere in US! Pls add it into your donation.). Order multiple jars for shipment to one address and pay actual shipping only! Contact us directly to arrange shipment of BIG orders! Here’s the backstory🙂 to Eme’s Rainbow Jars…. Eme can’t see a rainbow. She’s never seen one. We’ve tried over and over. Her family organized EmesArm...

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NEW Blog! | EmesArmy | fighting childhood blindness | kids fighting blindness from RARE disease LCA

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EmesArmy fighting childhood blindness. Kids fighting blindness from RARE disease LCA. Valentines for Veterans 2016. June 11, 2016. I 💛 LOVE the Timehop app. I 💙 LOVE faceBook. Mom and 3 yr old newly diagnosed Eme in Colorado. Together, they remind me just how far we have come through the darkness that comes with LCA, Lebers Congenital Amaurosis. Mom and Eme on Mt. Evans in Colorado. She couldn’t see the mountains. The retinal cells, which consist of way more than just rods and cones, use light to captu...

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Valentines for Veterans 2016 | EmesArmy | fighting childhood blindness

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EmesArmy fighting childhood blindness. Kids fighting blindness from RARE disease LCA. Valentines for Veterans 2016. Valentines for Veterans 2016. Valentines for Veterans 2016. Just $10 sponsors 1 dozen COOKIE VALENTINES decorated and delivered to our wounded. Warriors spending Valentine’s Day at Walter Reed National Military Medical Center by the kids of EmesArmy! Any remaining funds will be donated to fighting childhood blindness through the EmesArmy LCA Research Fund. AND in 2012, 2013 AND 2014. Create...

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Rainbow Jars 2016 | EmesArmy | fighting childhood blindness

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EmesArmy fighting childhood blindness. Kids fighting blindness from RARE disease LCA. Valentines for Veterans 2016. Eme’s Rainbow Jars are now available for shipment! Order now for Easter Baskets! Email any Questions EmesArmy@gmail.com. They make fantastic teacher and co-worker gifts! Here’s the backstory. Eme can’t see a rainbow. She’s never seen one. We’ve tried over and over. Last year, mom found this craft on Pinterest (of all places, right? 13 comments on “ Rainbow Jars 2016. April 9, 2014 at 2:23 pm.

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In a rare LCA world. Eme has been robbed of her sight by LCA-CRB1, a very rare genetic disease. By age 3, she was already blind. LCA-CRB1 has no treatment. A gene therapy clinical trial is being conducted for LCA-RPE65 right now that is working and is giving blind kids like Eme their sight back! By replacing the mutated/broken gene with a good copy of the gene, blind kids can see again! Join us and help raise awareness of childhood blindness from LCA (Lebers Congenital Amaurosis). Join in the conversation.

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