Saturday, November 20, 2010
$76.42 more for Quintons grant!
I just raised $76.42 that will soon go to Quintons account! Praying he too might have a full grant soon!
Tuesday, November 2, 2010
Quinton has found his forever family!
I found out just yesterday through an email response that Quinton has a family now! what does this mean for the christmas angel tree? well, quinton no longer is on it cause he found a family but since they already made ornaments with his picture on it you can still get the ornament of Quinton to remind you of this precious child & it will still benefit Quintons fund. I still think I can raise $1000 or more don't you think? With his grant at $127 & with my donation of $56 which would put it at $183, I would need to raise $817 to reach $1000! If I can raise a full grant I would need to raise $19,817. Nothings impossible with God! Adoption costs on average $20,000-$30,000 with a full grant his family would be able to not have to worry about the financial cost! Will you consider donating to Quintons grant fund?
http://reecesrainbow.org/?s=quinton
I will post shortly how you can get an ornament of quinton & help his grant fund grow!
http://reecesrainbow.org/?s=quinton
I will post shortly how you can get an ornament of quinton & help his grant fund grow!
Sunday, October 31, 2010
Christmas Warrior for Quinton
I am excited & proud to have signed up to be a christmas warrior to Quinton for Reeces Rainbow Angel Tree. The goal is to raise $1,000 or more for your childs grant fund! I would love to raise a full grant for Quinton. When you donate $35 or more for a child, you will recieve a beautiful photo ornament (WHEN DONATION MADE BEFORE DECEMBER 15!) of your sponsored child to hang on your tree! This is a very special way to "share Christmas" with an orphaned child, and to make it possible for other American and Canadian families to afford the high cost of rescuing them from orphanages and mental institutions around the world!
So if you would like to donate to Quintons grant fund & receive a lovely ornament with his picture on it (the picture shown to the right)i will have a way to on here tomorrow as thats when the angel tree starts! If you are unable to donate then please keep these children in your prayers!
Thanks!
So if you would like to donate to Quintons grant fund & receive a lovely ornament with his picture on it (the picture shown to the right)i will have a way to on here tomorrow as thats when the angel tree starts! If you are unable to donate then please keep these children in your prayers!
Thanks!
Thursday, October 7, 2010
Its Down Syndrome awareness month!
What is it truely like to have someone special like that in your family whether it be sister, brother, aunt, uncle, etc.?
It is an Honor to have them in your family. I know as I was blessed with an older sister with this extra chromosome! Yes, we siblings do have our struggles as well as parents do but we manage! Can they live a normal life? They most certainly can! My sister loves to dance with my other sister & they perform in front of family, friends, & complete strangers! Did you know that here in the USA their is (or was a few yrs ago-not sure if its changed!) a waiting list for families that want to adopt a child with this extra chromosome?? Yep, Their are those that want to love on these precious kids! Sadly Prenatal testing & misguided information to women plus doctors advice presures them into abortion especially with any type of special needs diagnosis. Overseas in Eastern Europe kids with this chromosome are blessed to be born, but due to it not being socially acceptable & with limited resources they are mostly put into orphanages & if not adopted by age 4 they will be institutionalized & most will live their the rest of their days. Reeces Rainbow helps orphans blessed to be born to find them families as well as their ultimate goal of finding ways to help these families be able to one day accept these kiddos. Please consider helping me in my mission to find Celine a family by donating to her grant fund in honor of down syndrome awareness month! click on her picture to the right or check out my new blog for her http://smiles4celine.blogspot.com/ for the latest contest I am doing to raise funds for her!
It is an Honor to have them in your family. I know as I was blessed with an older sister with this extra chromosome! Yes, we siblings do have our struggles as well as parents do but we manage! Can they live a normal life? They most certainly can! My sister loves to dance with my other sister & they perform in front of family, friends, & complete strangers! Did you know that here in the USA their is (or was a few yrs ago-not sure if its changed!) a waiting list for families that want to adopt a child with this extra chromosome?? Yep, Their are those that want to love on these precious kids! Sadly Prenatal testing & misguided information to women plus doctors advice presures them into abortion especially with any type of special needs diagnosis. Overseas in Eastern Europe kids with this chromosome are blessed to be born, but due to it not being socially acceptable & with limited resources they are mostly put into orphanages & if not adopted by age 4 they will be institutionalized & most will live their the rest of their days. Reeces Rainbow helps orphans blessed to be born to find them families as well as their ultimate goal of finding ways to help these families be able to one day accept these kiddos. Please consider helping me in my mission to find Celine a family by donating to her grant fund in honor of down syndrome awareness month! click on her picture to the right or check out my new blog for her http://smiles4celine.blogspot.com/ for the latest contest I am doing to raise funds for her!
Sunday, September 19, 2010
Better understanding
I wanted to write this since a lot of the time people keep asking me if I am okay when they see my hands shake or ask questions.
Yes, I was born with a rare thing that makes my hands shake at times. Sometimes its nerves as well but most of the time its not. I do take magneisum supplements to help. I know what its like for special needs kids in a way as I too get asked questions about it & it does get tiring answering questions at times but i learn to live with it. I don't remember the exact name of what its called but just wanted to post about it.
Yes, I was born with a rare thing that makes my hands shake at times. Sometimes its nerves as well but most of the time its not. I do take magneisum supplements to help. I know what its like for special needs kids in a way as I too get asked questions about it & it does get tiring answering questions at times but i learn to live with it. I don't remember the exact name of what its called but just wanted to post about it.
Monday, September 6, 2010
Being Joyful
I have heard about being joyful a lot recently including being inspired by my favorite author Karen Kingsbury & fellow friend from church to be more joyful. Well, since this I have become inspired to start my own organzation that will be used as a service project/charity.
PRAISE!!!!!
Celines fund has been raised praise God! This precious little girl has touched 1 or more peoples life now to donate to her fund! Looking forward to seeing how much more I can do to help her find her forever family! Please continue to pray for Celine to find a family! I so wish I could meet her, maybe i will someday!
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