Thanks for visiting Gabriel's website. Here are some of our favorite pictures of the past year...enjoying the simple things that have come to mean so much to us. Love, Gabriel's family
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About Gabriel
He was the baby that doctors said we would never be able to have on our own.
From the moment I was told that I was pregnant, my husband and I knew we had a special little miracle that would steal our hearts forever. Afterall, our first 2 children (which are also special "little" boys) were born by invitro-fertilization. What a wonderful surprise for our family. A third little "Little" and a perfect name for him "Gabriel".
Our family has always felt so blessed and as strange as one may think, we still feel this way. But it was that one day in May 2004 when our whole life was turned upside down and the phrase "Ignorance is Bliss" could have been our motto.
Gabriel, was diagnosed with Duchenne Muscular Dystrophy just days before his 3rd birthday. We will never forget this day. It changed the way we feel each day, the way we will live the rest of our lives, the way we breathe every minute, and the way we appreciate even the simplest of things every second.
We are constantly pursuing many avenues in search of a cure for this horrible disease. Although a cure has still gone undiscovered, we have put our faith in God, and are dedicated to and active in the support of organizations to find the cure.
This website is a dedication to the life of Gabriel, and in recognition of our friends and family, and how much they mean to us.
Please take time to send us your thoughts and prayers. It is these words of encouragement that help keep us going strong.
From the moment I was told that I was pregnant, my husband and I knew we had a special little miracle that would steal our hearts forever. Afterall, our first 2 children (which are also special "little" boys) were born by invitro-fertilization. What a wonderful surprise for our family. A third little "Little" and a perfect name for him "Gabriel".
Our family has always felt so blessed and as strange as one may think, we still feel this way. But it was that one day in May 2004 when our whole life was turned upside down and the phrase "Ignorance is Bliss" could have been our motto.
Gabriel, was diagnosed with Duchenne Muscular Dystrophy just days before his 3rd birthday. We will never forget this day. It changed the way we feel each day, the way we will live the rest of our lives, the way we breathe every minute, and the way we appreciate even the simplest of things every second.
We are constantly pursuing many avenues in search of a cure for this horrible disease. Although a cure has still gone undiscovered, we have put our faith in God, and are dedicated to and active in the support of organizations to find the cure.
This website is a dedication to the life of Gabriel, and in recognition of our friends and family, and how much they mean to us.
Please take time to send us your thoughts and prayers. It is these words of encouragement that help keep us going strong.
23 comments:
Good Morning Little Family,
Just taking a few minutes here to check out Gabriel's blogspot. He looks mighty handsome in his picture.
Wendy and John, stay strong in your faith and we will continue to lift your family up in prayer.
Hugs to you!
Hello,
What a beautiful son you have!! As I was reading Gabriel's story, God reminded me that we, as parents, have the awesome privilege of taking care of His precious little ones. God specifically gave you Gabriel, because He knew you would lift Gabriel up as a testimony for His glory. While your struggles may seem overwhelming at times, God is right there with you - to lift you up and carry you through the tough times. May God bless you and your family. Please continue to let the Women of Purpose Class know how we can best pray for you.
Blessings,
Shelley Wise
Hi Wendy,
I'm so glad you visited the Women of Purpose class yesterday and shared this website with us. I just popped in to check it out and have enjoyed reading your story and looking at the pictures of Gabriel and the rest of your family.
You've been given a special gift, and I know God is using him, as well as you and John, to accomplish great things to His glory. Your faith and courage as you make this journey are an example to us all.
I pray God will continually provide the strength, peace, wisdom and love you daily require.
Have a great week!
Janet
Wendy et al...
What a neat thing to do for Gabriel. I knew that he had special needs but was unaware of exactly what they were. I am hopeing to be for helpful to him in Sunday School at 11 now that I know more about him. He is always such a sweet spirit to have in the class and I am blessed to have in this year. If there are specific things that you know that I can do to include him in the class time please let me know. I was also interested in the brochuer that I saw that was labled help for educators.
By the way did you know that the name Gabriel means "Hero of God".
Blessing on the Little Family,
Kaylene
Hi! Wendy and John,
AJ and I just finished watching the video. (AJ is home from school because he has a headache!) It was nice to see how much Gabriel's grown since we've seen him last. AJ is 11 1/2 and in 5th grade this year. He also has Duchenne's. He is doing well. Remember God gave special children to special parents and without our faith and the support of family and friends, this would be a very difficult journey. God bless you and your family. I look forward to catching up with you sometime soon. Call me.
Lora
Hi Guys: I am so happy to see this website. As we all know sometimes there are so many demands that we don't get to stay in touch on a regular basis. I just want to let you know you that you are always in my thoughts and prayers. I was there on the awful day with you and I want to tell you from one mom to another how proud I am of you for the strength you and your family have shown. You and I know how special it is to have three sons!! Lots of love, the Paradiso Family!!
Wendy & John,
Thank you for sharing Gabriel's story with us. I checked out the links to better understand DMD.
I miss seeing you, but I do think of you often; you and your family are in my prayers.
Hugs and Love!
Linda Flint
Wendy,
What a blessing Gabriel is to all of us. He is so handsome. I can see how God has answered our many prayers over the years. You are such an example for me as you stand firm on God's promises. As I stand with my friends who are hurting over their little one in the NICU; I know God is faithful and He never fails. Thank you for your example of faith. We will have the 'Victory'. God bless you and your family. I love you.
Hello Everybody,
I just wanted to let you know that i read the website that you have posted for my "little" cousin, and it made me think about and miss all of you very much. I hope that everything with Gabriel, and everything with my family is going well... I know that "the hero of God" will amaze us all... i miss and love you all very much!! And i cant wait to come home and see my Little Family...
~Adam~ xoxo
Hi Wendy,
Thank you so much for sharing your website! It's wonderful! I love the video- Gabriel's such a beautiful boy! I will enjoy checking in on his progress.
It's not easy having a sick baby. Stay strong and know that our prayers are with you always.
Cynthia
Hi Little Family!
Every time I see you interact with Gabriel is a strong encouragement. You guys show the love of Jesus always even when life seems to be tough. Thanks for being such an encouragement!
Hey Guys. :]
my dad just told me about this, so i thought id say hello. :]
i would just like to start off saying, Aunt Wendy, you are my godmother, and always will be. You and your family will always have a special place in my heart. By bringing Gabriel into this world, it has shown that miracles can happen, no matter how hard it might seem. This family has had hard times with cancer, divorce, sickness, but it seems like we can work our ways through it, and still stick together. To me, Gabriel is the glue that seems to make it all stick together. I know that when you brought Gabriel in while I was working, he brought a smile to my face all the time, and i was going around to people going "isnt this the cutest kid youve ever seen?" Your such a ladies man, Gabriel. Whenever I see him, all i can do is smile, i could never be sad or frown when hes around. Im really looking forward to the holidays this year, and I look forward to seeing you all soon, because i havent seen you guys in a while.
give everyone hugs from me.
:]
Kaitlin.
Dear Ms. Wendy,
Thank you so much for the website. When I watched the video I started to cry. Maybe I could come and see Gabriel sometime. Tell him I miss him. I hope to see him soon.
Love Brianna Cech
John and Wendy-
While I do not have a google account, I did go on and read and visit the site. WOW. It is so so awesome. I sat and cried. Simple beautiful. I thought of Psalm 139:13-16. THat would have been the verse I would have typed in the blog and ROmans 12:12. He is so beautiful. ANd what a nice family. The brothers are so big too.
Blessing to you all-
In love,
SUZI
What an amazing website. Michael and I watched the YOUTUBE clip together and were touched by the video. Gab and your family are always in our prayers. Thank you for sending this to me!!!
Sherry
God has blest our family with a special 'angel', our Gabriel. His sweet eyes that twinkle when he sees you and his soft little cheeks can just melt your heart. His smile and giggle lets one know how happy he is to see you. Just to hug this little guy is truly a special moment in one's life. I thank God every day for our miracle child, our Gabe.
Luv, hugs and kisses
Mom aka 'Grandee'
Wendy,
I was finally able to log on to the web-site. I had to "Google" in order to bring it up. I am standing here at work and the tears won't stop. We attempt to make everything as normal as possible in order to keep our sanity, but it is at times like this that we are reminded how precious life is. I truly believe that Gabriel's mission here on earth is to remind us of this. Our families have weathered tremendous storms, and yet we continue to faith. Faith shows itself differently in each of us, but I truly believe that without it we would not have a purpose for being.
Hug your precious "little" gifts from God for me.
I love you, and I am so proud of you!
Shelley
Hi Little Family,
I just wanted to say what a fantastic website you put together. The photos were just great, and reminded me how much Gabriel's spirit touches us also. Throughout our baseball season, his presence at the games always put a smile on our faces. I really love when that little guy is around us, he changes our entire outlook on our day (even our lives). You guys are an inspiration to everyone you meet. Tell Gabe I'm going to eat his feet!!
Talk to you soon--Don
What a beautiful thing to do--such a creative act of love for Gabriel and others who can know him better.
He is a gorgeous child as are all of your children!
Love to you all.
Gabriel,
There are not enough words that I can say to explain how great you are. Ever since your mom and dad brought you home from the hospital I knew that you were one special baby and that you would change my life forever. You have given me hope, hope to find a cure for this sickness that you have. You have given me courage, courage to do what is right even though how hard it may be. You have also gien me love, love for my cousin that will never leave me heart. Gabriel you have showed me and given me all of these characteristics because each and every day you express them through your loving self. You may not be able to express them verbally but you express through your actions and actions are all you need. I love you with all my heart Gabriel!!! Cousins for LIFE!!!
Love your Cuz
Kyle
Mr. and Mrs. Little,
What a privelege to work with the "Middle Little" and by doing so meet the smallest Little and be blessed by both of them, (and Tyler too!) Gabriel brings joy to my day everytime I see him.He is so beautiful and his smile can light up a room! He is the highlight of car duty each day! Wendy, your faithfulness to your children and to the Lord through it all, has been a wondeful blessing and encouragement to me! Though I have only known your family for a few months, you have made an eternal impact on me. Keep trusting Him with your Little ones and I know you will stand back in amazement at the wonders He will work in each of their lives! Thank you for being such a testimony!
Praying for you,
Miss Johnson
Ephesians 3:20
John and Wendy..
Rod Parsley is having a world wide prayer event all day tomorrow praying over these piles of requests and will send an annointed cloth to each person...When I saw the miracles that took place last year on TBN I felt moved to send a request on behalf of your precious family...You are a blessing to so many and I feel in my heart when I pray that I needed to do this...
My Prayer Request is for my friends John and Wendy Littles young son Gabriel.
http://gabrieljohnlittle.blogspot.com/
Gabriel, was diagnosed with Duchenne Muscular Dystrophy just days before his 3rd birthday. His parents will never forget this day. It changed the way they feel each day, the way they will live the rest of their lives, the way they breathe every minute, and the way they appreciate even the simplest of things every second.
They are constantly pursuing many avenues in search of a cure for this horrible disease. Although a cure has still gone undiscovered, they have put our faith in God, and are dedicated to and active in the support of organizations to find the cure. Our entire church Loves Gabriel and is praying for him.
Please PRAY for healing of Gabriel! He is having Surgery on Tuesday Dec 4th at the Childrens Hospital in DC. I pray and feel as if GOD is going to heal him through someone placing their hands on him.... I pray that someone is you!!!Thank you so much for what you are doing...May GOD BLESS YOU!
Ok Wendy, now that you made us all cry.......
What a wonderful way show the wonder that the good Lord offers us every day.
Anyone that has met Gabriel will realize that pictures only offer part of what this young guy offers up. Without words, his eyes will steer you to his heart and soul.
What a joy to have him leave his fingerprints on your big screen! Only Gabriel can get away with that.
Gabriel, you bring out the best in people and God gave you the best when he chose your Mom and Dad.
We love you.
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