One of my dear local friends and fellow blogger needs our help! Erin, from Gabriel Updates, and her family are in need of some support. In a few weeks Gabriel their 3 year old will be in an Intensive Feeding Program to teach him to eat and enjoy food. They have been waiting for a very long time to get into this great program and are thrilled that Gabriel will be getting the help that he needs. The problem is that Erin will be missing 8 weeks of work while Gabriel attends long hours each day at therapy. So to ease the financial stress a few of us have started a fund for the family to help out with bills, their mortgage, Isabella's childcare, and any other expenses that arise during this time. I am asking for your help. Please make a donation this holiday season to this amazing family...no amount is to small! You can make a donation by clicking on the Chip In link on the right of the screen! Thank you so much!
Happy Thanksgiving!
Dearest Erin, we love you and help is on the way :)
(To my fellow bloggers please help me rally around this family and share their story and the chip in on your blog)
Go to the Facebook link on the top right of this blog to get entered in our first giveaway. If you are selected you will receive a custom made hat of your choice.
Read the instructions below!
Okay Fans it's GIVEAWAY time, here is how it works! For the next 48 hours everyone will have a chance to leave a comment on F & F's Facebook wall (this will be your entry), it will close Wednesday morning at 10:30 EST. In that post please let me know which hat you love and would like to receive if you win. Also please share our page on your wall mentioning the giveaway. If we can reach 150 'likes' by the close time on Wednesday, there will be 2 lucky winners instead of 1! I will then comment on each post and assign you a number. The drawing will be held Wednesday and the winner(s) will be announced! Ready. Set. Go.
Please make sure you click on ALL photos to see all the hats available, there are more than initially show up!
Thank you to all the awesome supporters of our little business!
P.S. If you are a blogger and you mention this giveaway in a post you can get a second entry!!!
Make sure you mention this on the F & F facebook wall so you get credit for the 2nd entry!
Oh my goodness! I can't believe how long it has been since I posted last. In all honesty we are busy! Very busy!
We have some new exciting things we are working on. My husband is officially launching a photography business. Below you will find several pictures taken by him of our babies! So proud of him!
I am currently working on also launching a business with my Mom. Freckles and Firecrackers will be an online children's boutique (inspired by my red-headed-babies). Featuring handmade crocheted hats by my Mom along with several other essential children's item! Below you will find several of our hats!
All of these things combined with all the activity that comes with raising four young children keeps us running. We are so excited for things to come. I promise to TRY to get to the blog more. The Tennessee Grandpa is NOT pleased with the lack of activity on Kaitlyn's Korner. Sorry Dad!
To stay in touch with us on a daily basis find me on facebook, Jenee Skocelas Ross.
Hope you enjoy the pictures! Kaitlyn at 19 months and Ty at 7 months! I would love to hear your thoughts!
This is a portion of a letter written to Sarah Palin asking her to take full advantage of her platform and become an advocate and educator for Down syndrome and all intellectual and physical disabilities. The reason I am sharing it is because I feel it truly explains why we as a society really need to think before we speak, and more specifically why we need to remove the "R" word (retarded) from our vocabulary. I've been trying for a couple weeks now to find the words to write on this issue. I think the letter to Sarah Palin written by leaders of the Oz Squad hit the nail on the head. So with their permission I'm sharing a portion of the letter. Please read on, change your thinking, and become a voice and help end the use of the "R" word....
Everybody knows and agrees that the word "retarded" used in a clinical setting defines a group of individuals as having limited cognitive abilities. In this respect, the term carries similar effects as racial or sexual orientation categorizations, in that it invokes a specific class of individuals with immutable characteristics.
But what not everybody seems to realize is that the current, common definitions of the word "retarded" as stupid, wrong, ineffective... the catch-all for anything that is annoyingly deficient, are steeped in our cultural view of people with mental retardation.
So whether one is using the term as an insult or to raise laughs through satire, the speaker is tapping into our common cultural understanding and belief that people with mental retardation are characterized by those negative definitions listed above. The speaker references a group of individuals defined solely by their cognitive limitations, denying them their individual personalities, and by extension their essential humanity. He agrees that this group is inferior and worthy of our scorn. This use of the word "retarded" has become so deeply ingrained in our society that the user probably doesn’t even realize that he has done this.
Many people, when called out on their use of the word, insist that they meant no harm to the mentally retarded community, that their use of the word had nothing to do with this minority group. These people must be made aware that there is no separating the insult/joke from its basis for understanding it.
No one believes that Rahm Emanuel or Rush Limbaugh thought that they were insulting those with true mental retardation when they called people whose ideas they objected to "retarded." But we do believe that both men were making the point that their targets' ideas were of so little merit that they deserve to be grouped with an undesirable category of people. Both the direct target of the insult, and the class of people it refers to, are indisputably demeaned by such a slur. You cannot have one without the other.
Put a simpler way, if people with mental retardation were generally well-respected and thought highly of, the insult "retarded" would not exist.
Having the government remove the term retarded from the books, and having the medical community change the diagnosis terminology to "a person with intellectual disabilities," is not enough to eradicate the insult. The public must be made aware of how the insult relates to and hurts an entire group of people. This is not a word police PC thing, rather it is a matter of common decency.
Some argue that the insult "retarded" will simply be replaced by another word that is just as hurtful to the intellectually disabled community. But just because some group of the population will always turn clinical or descriptive terms into epithets does not mean that we should condone it. Such a standard would condone the use of virtually any racial, ethnic, or sexual orientation slur.
Thanks for reading, and please help Spread the Word to End the "R" Word.
Watch this video, it shows just how overused that word is in our society, and how so many people don't think before they talk! It makes me ill!
My best friends were there, my sisters, bonded by that extra special chromosome.
We had an amazing time. The occasion was to celebrate life, the life of our special almond eyed wonders who have enhanced our lives in countless ways. One of them being the new family that was created along the way of this extra special journey. These girls have become my rock, it is a sisterhood few understand.
Below is a great picture. For the first time we were all able to be at the same place at the same time.
The host of the party was Erin, many of you know her as mommy to Gabriel over at Gabriel's updates. Her little Bella turned one this past week giving us one of many reasons to have a party. Thank you Erin for inviting us all over!
You also see Dina and her little man Tyce, Tyce is the youngest in our group. He is quite a cutie pie. Dina blogs about their new journey at Entyced.
In the middle is Kaitlyn and I and Angie and her pretty girl Lily. Both our girls have had amazingly similar paths. Our girls are only 5 months apart and we only live a couple miles from each other.
Next over to the right is Cathie and her little guy Ian. He is a doll. He is the oldest in our group of 6 turning 3 this Spring. He was so much fun to watch, he is a smart little guy.
Right below Cathie is Jen and the beautiful Abigail. Abby turns 1 next month. Kaitlyn and Abby are soooo similar. From their chubby little fingers and thighs, to their cute little grins. I love those girls!
Who needs coloring books? We use this ALL the time!
This is the story of our lives as we embark on an unforseen journey. We continue to look to God to guide us through as we live out His plan for us and our little girl Kaitlyn.
Kaitlyn was born August 2009. She has been diagnosed with Down syndrome and a congenital heart defect (AVSD).
We are so excited she's here and can't wait to share our new experiences with everyone!
Welcome to Kaitlyn's Korner!!
If this is your first time visiting we invite you to read "Our Story."
I am 32 years old and a wife and mother. I have been married to an amazing man(Blair) for 8 years now. We have three beautiful boys and an extra special little girl. I created this blog to share our journey through parenthood and the experiences God has in store for us!
Brady is 6 years old. He is gentle, kind, and has a silly sense of humor. He loves letters, super heroes, and playing with his little brother. He is so excited to have his little sister home.
Big Brother Bryce!
Bryce is 4 years old. He is rough, tough, but ever so sweet. He loves trucks, tractors, and the color blue. He loves helping mommy with his baby sister.
Our Angel Kaitlyn
This little girl is the keeper of my heart. She was born in August 2009 with an extra special chromosome, she has Down syndrome. She also is our hero, at 3 1/2 months of age she under went open heart surgery to repair a congenital heart defect (Complete AVSD). She is amazing. This blog is inspired by her!
Baby Brother Ty
At 11 months old little Kaitlyn became a BIG sister. God blessed us this Summer with this little guy. Ty David makes my heart smile. He is growing so fast. He loves Mommy, feeding time, and his silly siblings. He has the best giggle. He is adjusting to life outside the womb and is slowing learning that it really isn't all that bad. His newest milestone is jumping in his jumperoo!