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Finley's Fighters

Welcome to our site! Finley's Fighters was organized after our youngest daughter, Finley, was diagnosed with a rare genetic eye disorder called Lebers Congenital Amaurosis (LCA) in 2009. This eye disorder is progressive and will cause her to go totally blind without a cure. Finley's particular LCA is from a mutation on the RDH12 gene. This is one of the rarest forms of LCA, and, for now, there is no cure. All of the money raised by Finley's Fighters is going to the RDH12 Fund for Sight. For more informat...

http://www.finleyfighters.com/

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Welcome to our site! Finley's Fighters was organized after our youngest daughter, Finley, was diagnosed with a rare genetic eye disorder called Lebers Congenital Amaurosis (LCA) in 2009. This eye disorder is progressive and will cause her to go totally blind without a cure. Finley's particular LCA is from a mutation on the RDH12 gene. This is one of the rarest forms of LCA, and, for now, there is no cure. All of the money raised by Finley's Fighters is going to the RDH12 Fund for Sight. For more informat...
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Finley's Fighters | finleyfighters.com Reviews

https://finleyfighters.com

Welcome to our site! Finley's Fighters was organized after our youngest daughter, Finley, was diagnosed with a rare genetic eye disorder called Lebers Congenital Amaurosis (LCA) in 2009. This eye disorder is progressive and will cause her to go totally blind without a cure. Finley's particular LCA is from a mutation on the RDH12 gene. This is one of the rarest forms of LCA, and, for now, there is no cure. All of the money raised by Finley's Fighters is going to the RDH12 Fund for Sight. For more informat...

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1

Finley's Fighters

http://www.finleyfighters.com/Products.html

We will have several products with the Finley's Fighters logo for sale, plus custom braille shirts. All profit will go to the RDH12 Fund For Sight. That we established. This money will be used for sight saving research for Finley and other children with the RDH12 mutation. We are so excited about our new Fund. We are going to make every effort to save Finley's sight, but we need your help! BUY YOUR FINLEY'S FIGHTERS BRACELET HERE. Will read "Finley's Fighters - Knocking Out Blindness". To the right you w...

2

Finley's Fighters

http://www.finleyfighters.com/Pictures.html

The Real Finley's Fighters. Highly Paid Finley's Fighters Bracelet Models. Using Braille To Support Those That Have To Use It. This is what it is all about. You can see the before and after videos of young Corey Haas before and after he received gene therapy his RPE65-caused LCA. This is possible for almost all children with LCA. The thing standing between Finley and this is the money to fund the development of an RDH12 gene therapy.

3

Finley's Fighters

http://www.finleyfighters.com/Links.html

This page will allow you to read some various information about Lebers Congenital Amaurosis, and other things associated with blindness. We hope you find the information informative. Our foundation website will be a link on here soon! I was bold in the pursuit of knowledge, never fearing to follow truth and reason to whatever results they led, and bearding every authority which stood in their way. " - Thomas Jefferson. Connecticut Board of Education and Services for the Blind (BESB). Finley in the News.

4

Finley's Fighters

http://www.finleyfighters.com/Story.html

Soon family members were also noticing that something was a little off about Finley's behaviors. They would comment that she wouldn't look them directly in the eye when she talked to them. They said they noticed how close she needed to get to books when looking at them. We maintain a family blog ( www.pletcher5journey.blogspot.com. Our family will never be the same. But Finley's diagnosis has changed us for the better. Would we have wanted this for her? No But can some good come from it? We are thankful ...

5

Finley's Fighters

http://www.finleyfighters.com/home.html

Welcome to our site! Finley's Fighters was organized after our youngest daughter, Finley, was diagnosed with a rare genetic eye disorder called Lebers Congenital Amaurosis (LCA) in 2009. This eye disorder is progressive and will cause her to go totally blind without a cure. Finley's particular LCA is from a mutation on the RDH12 gene. This is one of the rarest forms of LCA, and, for now, there is no cure. All of the money raised by Finley's Fighters is going to the RDH12 Fund for Sight. For more informat...

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thetingalings.blogspot.com thetingalings.blogspot.com

The Tings: March 2011

http://thetingalings.blogspot.com/2011_03_01_archive.html

Thursday, March 17, 2011. Many of you know already, but for those of you who don't - I'm pregnant! Frank and I are very excited about enlarging our family and we know that Reese is going to be a GREAT big sister! God's goodness never ceases to amaze me! So far the pregnancy has been going well - except for the all day nausea and lack of energy. :) Keeping up with Reese (who is now walking) takes a little more out of me than it used to! Subscribe to: Posts (Atom). The RDH12 Fund For Sight. When to say what.

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The Tings: July 2010

http://thetingalings.blogspot.com/2010_07_01_archive.html

Sunday, July 4, 2010. Happy 4th of July! From our family to yours, we wish you a very happy 4th of July! Friday, July 2, 2010. Here are two short videos of Reese in the swimming pool for the first time and of her talking to herself in her. Mirror (which doesn't have the best lighting, but it's her talking that's so much fun to hear! Sorry about the quality of the videos - I will work on making them better! Subscribe to: Posts (Atom). Constantly amazed by God's goodness and grace! The RDH12 Fund For Sight.

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The Tings: November 2011

http://thetingalings.blogspot.com/2011_11_01_archive.html

Tuesday, November 29, 2011. Catching up . . . kind of. I know it's been a while since I've posted - things have been a little busy lately. :) Since I last posted, Jet has turned 2 months old, Reese is 23 months old (Where have these last 2 years with her gone? And we're still losing sleep. :) So this post is going to be a little bit of a catch up post. Jet also turned one month old during the month of October - his first month truly flew by! He even had a cake and we all sang happy birthday to him (This ...

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The Tings: September 2011

http://thetingalings.blogspot.com/2011_09_01_archive.html

Friday, September 30, 2011. It is amazing how instantly and totally your heart is captured by such a little person! Frank and I were so blessed to have Reese and now the Lord has given us another blessing. The only feeling I have is utter amazement and gratitude! My prayer is that we never take for granted these gifts that have been given to us! Subscribe to: Posts (Atom). Constantly amazed by God's goodness and grace! The RDH12 Fund For Sight. First Week of School * 2016-2017. Garcias living large 2.

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The Tings: September 2010

http://thetingalings.blogspot.com/2010_09_01_archive.html

Wednesday, September 22, 2010. I just wanted to post some pictures and a couple of videos of Reese over the past month. She's learned how to wave and how to crawl! I can't believe how fast her first year is going! We are enjoying being home together! Subscribe to: Posts (Atom). Constantly amazed by God's goodness and grace! The RDH12 Fund For Sight. First Week of School * 2016-2017. The Pletcher Five Journey Blessings Times Three. Garcias living large 2. Lost Tooth and Other Things. I Am a Little Church.

kovallnews.blogspot.com kovallnews.blogspot.com

Kovall News: December 2013

http://kovallnews.blogspot.com/2013_12_01_archive.html

Sunday, December 29, 2013. You enter the park under a tunnel of red lights. AJ and I met while working at Kennywood in 1997. I had just graduated high school, and he was a cocky undergrad. We started dating in 1999, and we have many fond memories of our time at the park. We still have some wonderful friends we made while working there, so it is always fun to go back and see how things have changed over the years. 14 years later, where it all began! Jack had no interest in riding (which was odd),. But he ...

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Kovall News: Ethan Is Six!

http://kovallnews.blogspot.com/2014/06/ethan-is-six.html

Saturday, June 7, 2014. Last Friday, at the end of a very hectic week, we celebrated Ethan's 6th birthday. Six! I can't believe he is that old. Almost a first grader. I remember every detail of my pregnancy with him (he never stopped moving), every detail of his birth (three weeks early via c-section since all that moving got him stuck sideways - AND he almost had to be delivered on the side of the road since he was in such a hurry.), and every day of his life. E through the years :-). Subscribe to: Post...

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Kovall News: March 2014

http://kovallnews.blogspot.com/2014_03_01_archive.html

Sunday, March 30, 2014. Happy Birthday, AJ! We celebrated AJ's 30-something.birthday this weekend. He already got his 'big' gift from me about a week ago - Mr. Fitness wanted a Fuel Band from Nike, and he has been wearing it since it came in last week. It tracks his steps, calories burned, etc. It's a cool little piece of nonsense, but he's happy with it :-). This picture shows WHY he has become Mr. Fitness ;-). Here's to 37 more :-). Jack was not pleased we were singing. Hilarious. Monday, March 24, 2014.

kovallnews.blogspot.com kovallnews.blogspot.com

Kovall News: Picture Day!

http://kovallnews.blogspot.com/2014/05/picture-day.html

Sunday, May 25, 2014. We are enjoying some glorious summer-like weather. We've spent a ton of time outside this weekend, which is getting us in the yard-work frame of mind. The boys are in their glory - playing in the sandbox, swinging on the swing set, and coloring all over our driveway with chalk. We've taken many walks, kicked many balls, and pulled many weeds. We are ready for summer! They were so exhausted on Friday after playing outside. Jack got a 'gentleman's haircut.' Even though,. May 3 - (E!

kovallnews.blogspot.com kovallnews.blogspot.com

Kovall News: August 2013

http://kovallnews.blogspot.com/2013_08_01_archive.html

Tuesday, August 27, 2013. We survived Kindergarten, Day 1! I was so worried that I would be an emotional basket case (I've been crying about it off and on for about two weeks, so…), thus causing Ethan to melt down, but all went smoothly. His teacher sent this home for us to decorate for her classroom. I thought it would be fun to see how his writing changes throughout the year. Ethan was ready to go this morning in his cute outfit. Seriously - just a little man! The kids had a nice picture to color when ...

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Finley's Fighters

Welcome to our site! Finley's Fighters was organized after our youngest daughter, Finley, was diagnosed with a rare genetic eye disorder called Lebers Congenital Amaurosis (LCA) in 2009. This eye disorder is progressive and will cause her to go totally blind without a cure. Finley's particular LCA is from a mutation on the RDH12 gene. This is one of the rarest forms of LCA, and, for now, there is no cure. All of the money raised by Finley's Fighters is going to the RDH12 Fund for Sight. For more informat...

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