The end of 2012 has been a little bumpy. And in addition Noah has indeed caught his brother's croup. But no matter what lies before us or behind us we are blessed because we have Noah in our lives. Thank you to all that have continue to pray so hard for Noah. Wishing you all a New Year filled with lots of love, memories and blessings.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Sunday, December 30, 2012
Friday, December 28, 2012
Nana Goes to Heaven
Noah's great-grandmother passed away yesterday. The loss of a family member is especially difficult as we don't really have a lot of family and friends who love us enough to be able to cope with our circumstances. She had a short battle with an illness that she got right before the holidays and she just couldn't fight it. I had really thought she'd be okay so it was rather sudden as death sometimes is. You always want that one last goodbye. That one last chance to say I love you. That one last Christmas card to each of the boys that didn't come this year because she was ill... she was a good great-grandma. She was just as proud of Noah as if he had been born without a disability. She even braved the butterfly pavilion with us when she visited last. Something that I'm sure was hard for her to do because she had such a big phobia about moths and bugs that fly. But she did it anyway and was a really good sport about it to be with Noah and doing something that he loved to do.
Noah meets his great-grandmother for the 1st time |
Butterfly Pavilion Bliss |
though you don’t see.
I’m right by your side each night and day
And within your heart I long to stay.
My body is gone but I’m always near,
I’m everything you feel, see or hear.
My spirit is free, but I’ll never depart.
As long as you keep me alive in your heart.
I’ll never wander out of your sight,
I’m the brightest star on a summer night.
I’ll never be beyond your reach,
I’m the warm moist sand when you’re at the beach.
I’m the colorful leaves when Autumn’s around,
And the pure white snow that blankets the ground.
I’m the beautiful flowers of which you’re so fond,
The clear cool water in a quiet pond.
I’m the first bright blossom you’ll see in the spring,
The first warm raindrop that April will bring.
I’m the first ray of light when the sun starts to shine,
And you’ll see that the face in the moon is mine.
When you start thinking there’s no one to love you,
You can talk to Grandma through the Lord above you.
I’ll whisper my answer through the leaves on the trees,
And you’ll feel my presence in the soft summer breeze.
I’m the hot salty tears that flow when you weep,
And the beautiful dreams that come while you sleep.
I’m the smile you see on a baby’s face.
Just look for me, Grandchild, I’m every place!
Love,
Nana
Nana, you'll forever be in our hearts, and please look out for Noah; he needs all the angels he can get.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Wednesday, December 26, 2012
Noah's Big Gift
Noah's 4th birthday was just as beautiful as his first. He had a Shrek
Birthday themed cheesecake and his Service Dog in training arrived.
Meet Samson!
Samson immediately responded well to Noah - it is
truly a perfect match. Samson is very easy going, gentle, loving and
wants to be where Noah is. They are off to a beautiful start. We
weren't sure how our other two dogs would adjust but we're so happy to
report that within less than 24 hours everyone are best friends. Samson
has a lot of training ahead of him in the first year and then he'll
leave home after a year old for extensive skill training, which I am
sure will be hard on the entire family - especially Noah when he leaves
home for a while. But in the end the reward will be so great. Noah had
a really great day. He loved his balloons and loved his cheesecake.
It was a day full of lots of love, laughter and smiles. We remain so
thankful for all the help and kindness that made Noah's Service Dog
possible - and it couldn't have been more perfect for him to arrive on
his birthday.
We were so touched by all the birthday cards Noah received. Especially from Cole's Foundation. They are the most loving group of people ever. They continuously lift us up in love and prayer in lots of caringbridge guestbook posts, and they love our Noah tremendously. He received the most precious birthday cards from other little children from the Cole's Foundation and they are so sweet that they bring tears to your eyes. I save each one in a hope chest for Noah. So he knows someday how many people love him and cheer him on everyday of the year! They are so special to us. It's tiny things like a card that we hold so dear to us, just to know that he's loved and that we're not alone. We're so thankful for our friends at Cole's Foundation!
Noah had an equally wonderful Christmas. He loved alternating sitting in his daddy and grandmother's lap to open presents. He was full of excitement and joy. And he finally was able to open all those presents he had been trying to get to for several weeks. I don't know that Noah has a favorite present. He seems to be enjoying looking at everything that is so new to him. I think he had grown bored of his toys all year so it was nice to be able to pack away his older ones to make room for newer ones for him to play with. And his interests are changing. He's no longer a baby so some baby toys just bore him. That's the tough balance you find when you have a special needs child is finding somewhat age appropriate gifts but gifts that Noah can also find a way to play with at the same time. But it's great that they make so many neat toys these days like cars that drive themselves. Noah loves that kind of thing - any 4 year old would.
Noah
also dodged the Christmas Croup that his little brother contracted
shortly before Christmas. Thankfully Noah remained healthy, although I
worked very hard to keep the two boys apart for many days. Something
that wasn't easy since they have become like peanut butter and jelly to
each other.
And now we look forward to another year full of lots of blessings and continued miracles in Noah's life. He continues to do great things and we are so proud of him. We have a feeling the new year will bring even more amazing things!
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Samson - Noah's Service Dog in Training |
A Happy Birthday Boy |
Noah's Shrek Cheesecake |
We were so touched by all the birthday cards Noah received. Especially from Cole's Foundation. They are the most loving group of people ever. They continuously lift us up in love and prayer in lots of caringbridge guestbook posts, and they love our Noah tremendously. He received the most precious birthday cards from other little children from the Cole's Foundation and they are so sweet that they bring tears to your eyes. I save each one in a hope chest for Noah. So he knows someday how many people love him and cheer him on everyday of the year! They are so special to us. It's tiny things like a card that we hold so dear to us, just to know that he's loved and that we're not alone. We're so thankful for our friends at Cole's Foundation!
Noah had an equally wonderful Christmas. He loved alternating sitting in his daddy and grandmother's lap to open presents. He was full of excitement and joy. And he finally was able to open all those presents he had been trying to get to for several weeks. I don't know that Noah has a favorite present. He seems to be enjoying looking at everything that is so new to him. I think he had grown bored of his toys all year so it was nice to be able to pack away his older ones to make room for newer ones for him to play with. And his interests are changing. He's no longer a baby so some baby toys just bore him. That's the tough balance you find when you have a special needs child is finding somewhat age appropriate gifts but gifts that Noah can also find a way to play with at the same time. But it's great that they make so many neat toys these days like cars that drive themselves. Noah loves that kind of thing - any 4 year old would.
Excited that Santa Came! |
And now we look forward to another year full of lots of blessings and continued miracles in Noah's life. He continues to do great things and we are so proud of him. We have a feeling the new year will bring even more amazing things!
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Sunday, December 23, 2012
Happy 4th Birthday Noah!
Dear Sweet Noah,
4 Years have gone so quickly. You continue to be one of the biggest blessings we've ever received in life. Your laughter warms my heart and makes me smile. Wishing you the best and most beautiful birthday a child could ever have. We love you to the moon and back. May all your dreams and wishes come true.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
4 Years have gone so quickly. You continue to be one of the biggest blessings we've ever received in life. Your laughter warms my heart and makes me smile. Wishing you the best and most beautiful birthday a child could ever have. We love you to the moon and back. May all your dreams and wishes come true.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Friday, December 21, 2012
Merry Christmas from the Warden Family
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Thursday, December 20, 2012
Forgiveness
And Jesus said, “Father, forgive them, for they know not what they do.” Luke 23:34
That could apply to many things in our life. Forgiveness is an interesting thing. You often have to humble yourself to understand that others may unknowingly cast hurt in your direction. In the world of special needs our pain can be intensified by others... but only if we let it be.
In the beginning I was rather taken back that parents with able-bodied children who openly bragged in front of me about how smart their children were, how fast they learned to walk and talk. How they were the best in spelling B's, dance recitals, and soccer games. You wondered why they just didn't know how much you wanted all those things for your child too. And at times it did feel like many were rubbing salt in my wounds. They had what I wanted. An able-bodied, typical child. But jealousy and envy are dangerous feelings. They can feed hate and resentment and nothing at all that promotes or helps cultivate the strength and courage needed for this journey. It can be so self-destructing to always wonder what life on the other side of the fence is like. You should only be tending to the flowers in your own garden, not trying to see what your neighbor is growing.
Likewise, one day I was stunned that a family who had lost the the father called themselves a special needs family, or a mother who had a child who was in the NICU for seven days, but has a healthy typical child but still claims to be a special needs parent. While extremely tragic, the death of a parent doesn't make you special needs family any more than a healthy child who had a rough start. I wondered why they would even want to be like me... there is nothing glamorous about his journey. It's hard. But when I sat back and truly digested their situations I think they were doing their best to relate to me. To try to make me feel not so alone with life's bumps and bruises - or at least I'd like to believe those were their intentions.
I did have to change my expectations of people or I found myself continually disappointed. I expected this friend to pick up the phone to see how I was doing, another friend to know I needed a hug, to have family members know that I needed simply a listening ear. People just don't know what to do with you when you have a tragic thing happen to you. Many simply withdraw innocently because they lack the know how on how to approach you, what to say, how to act. After all it's our lives that have changed - not theirs. While it certainly doesn't let everyone off the hook as to say that it takes a special person to change with you and what happened to your life. Not everyone can make that transition with you. They don't know how. You can't expect them to as it hasn't happened to them.
Just because your life is now swallowed up with endless handicapped equipment, new routines, and a medically fragile child doesn't mean their lives can slow down to incorporate yours. Does it burn? Absolutely so. You crave to be included, thought of... you want that invite to birthday parties, to summer bar-b-ques. But when you really sit back and think even if you were to get an invite you'd likely not be able to RSVP because your child has so many medical and sensory needs and you don't have respite care. Is it the gesture that we're looking for? Sometimes. Everyone wants to feel included even if we can't play reindeer games with the other reindeer.
But back to forgiveness - there is so much frees your heart in that one simple word. Forgiveness. You forgive the mom that boasts that her oxygen deprived child is normal in every way when yours is not, the school teacher that says your child won't ever amount to anything, the stranger who looks at your child and calls him a "cripple." Because as the good Lord says, "they know not what they do." Forgiving doesn't mean you are better than them; it just means you are freeing up your heart to incorporate more love for not only your special needs children but all those around you as you travel this road. We have to be the endless guiding light for our special blessings, we don't have time to hold grudges. It's has no place in the journey.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
That could apply to many things in our life. Forgiveness is an interesting thing. You often have to humble yourself to understand that others may unknowingly cast hurt in your direction. In the world of special needs our pain can be intensified by others... but only if we let it be.
In the beginning I was rather taken back that parents with able-bodied children who openly bragged in front of me about how smart their children were, how fast they learned to walk and talk. How they were the best in spelling B's, dance recitals, and soccer games. You wondered why they just didn't know how much you wanted all those things for your child too. And at times it did feel like many were rubbing salt in my wounds. They had what I wanted. An able-bodied, typical child. But jealousy and envy are dangerous feelings. They can feed hate and resentment and nothing at all that promotes or helps cultivate the strength and courage needed for this journey. It can be so self-destructing to always wonder what life on the other side of the fence is like. You should only be tending to the flowers in your own garden, not trying to see what your neighbor is growing.
Likewise, one day I was stunned that a family who had lost the the father called themselves a special needs family, or a mother who had a child who was in the NICU for seven days, but has a healthy typical child but still claims to be a special needs parent. While extremely tragic, the death of a parent doesn't make you special needs family any more than a healthy child who had a rough start. I wondered why they would even want to be like me... there is nothing glamorous about his journey. It's hard. But when I sat back and truly digested their situations I think they were doing their best to relate to me. To try to make me feel not so alone with life's bumps and bruises - or at least I'd like to believe those were their intentions.
I did have to change my expectations of people or I found myself continually disappointed. I expected this friend to pick up the phone to see how I was doing, another friend to know I needed a hug, to have family members know that I needed simply a listening ear. People just don't know what to do with you when you have a tragic thing happen to you. Many simply withdraw innocently because they lack the know how on how to approach you, what to say, how to act. After all it's our lives that have changed - not theirs. While it certainly doesn't let everyone off the hook as to say that it takes a special person to change with you and what happened to your life. Not everyone can make that transition with you. They don't know how. You can't expect them to as it hasn't happened to them.
Just because your life is now swallowed up with endless handicapped equipment, new routines, and a medically fragile child doesn't mean their lives can slow down to incorporate yours. Does it burn? Absolutely so. You crave to be included, thought of... you want that invite to birthday parties, to summer bar-b-ques. But when you really sit back and think even if you were to get an invite you'd likely not be able to RSVP because your child has so many medical and sensory needs and you don't have respite care. Is it the gesture that we're looking for? Sometimes. Everyone wants to feel included even if we can't play reindeer games with the other reindeer.
But back to forgiveness - there is so much frees your heart in that one simple word. Forgiveness. You forgive the mom that boasts that her oxygen deprived child is normal in every way when yours is not, the school teacher that says your child won't ever amount to anything, the stranger who looks at your child and calls him a "cripple." Because as the good Lord says, "they know not what they do." Forgiving doesn't mean you are better than them; it just means you are freeing up your heart to incorporate more love for not only your special needs children but all those around you as you travel this road. We have to be the endless guiding light for our special blessings, we don't have time to hold grudges. It's has no place in the journey.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Tuesday, December 18, 2012
Christmas is Now
It's no secret that Noah's favorite time of year is Christmas time. He spends countless hours in front of his Christmas train and he's grown increasingly fast at rolling to where he wants to go over the course of this year and he make a bee-line for the wrapped presents each time. And before we know it - he's even unwrapped them - and he's got great aim - he only goes for the ones with his name on them. Super smart he is. We keep trying to tape them back together the best we can - but Noah is insistent that Christmas is now and he wants to open those presents! He's so excited about ripping the paper. This is the first time we've ever seen Noah this excited about opening gifts. He truly understands what they are and he wants them. And when I pull him away from them he give me a look like I'm severely disappointing him and aggravating his big attempts to open those gifts.
Noah has also made amazing progress with head control at hippotherapy. The last two weeks have been incredible. He holds his head up on his horse like any other child would. Chris and I kept looking at each other like is that really our Noah on that horse? Because it looked like any able-bodied 4 year old riding. It was enough to take our breath away. It's beyond words. We're so proud of Noah he's working so hard, and we're thrilled with the results of what 14 weeks of hippotherapy has done for him. We are now on a winter break and resuming back up in February. As most of Noah's therapies go, it's very expensive and something we have trouble keeping up with, but when you see the progress Noah is making you continue to do anything and everything to help him.
Noah's service dog is due to arrive on his birthday. We are very excited about our new family member joining us on Noah's birthday. This dog is going to do so many great things for Noah in his life. Noah will be having a Shrek themed birthday cheesecake made of caramel and fudge this year, something he can eat in it's entirety. We're ditching the cake thing and making it completely something he can eat. We're trying to focus on all the joyous parts of the holiday season, and remembering that our little miracle is still here four years later. A tough fight, a tough road, a tough journey for all of us. But we have his life - and that's the greatest gift. Many people argue Noah's not a true miracle because he has yet to be blessed with a full recovery. But people who question a miracle likely have never seen one. They've never held a baby in their arms, wondering if it would take it's last breath. To be told that after thirteen long minutes that your child was revived after having no heartbeat. To bear witness to a December rainbow in a Colorado sky - a forever promise between God and Noah. I live with a miracle each day.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Friday, December 7, 2012
Gingerbread Therapy
Yes there's a new therapy in town... gingerbread therapy. Don't get too excited. Medicaid deems this alternative therapy too!
I went to the store and seen the cutest little gingerbread men cakes. I loved them. The kind of sweet creation that says I'm so lovely, your children would adore me, and buy me now! I picked up two containers without hesitation. I have two boys and I need two gingerbread men cakes. The baker smiled at me acknowledging that I had found these confections quite cute and turned to say "they are just as good as they look." I thanked him and told him that I was hopeful that my oldest child would have a great time as it was going to be Gingerbread Therapy. He looked at me so puzzled until I explained I had a child that couldn't orally eat solids. And that I had a little one that could, but my heart doesn't let me buy just for one child and not the other - even knowing I have one that has significant disabilities. He took my hand and told me I was a good mom and that my son was going to have the best Gingerbread Therapy and that it made his day.
And indeed Noah did have the best time at Gingerbread Therapy. I put his little decorated man in front of him, he gave me a coy smile and then swatted his little gingerbread man. The cake so springy that it just continued to bounce on the tray causing Noah to giggle about his cake dancing. He didn't even mind that he couldn't indulge in it's sweet fun - to him he was playing with his little gingerbread man and that's all that mattered to him. The gingerbread man probably looked a little familiar to him - it did kind or resemble Gingey from Shrek - who he finds completely hilarious. He spent a good hour working on tossing that gingerbread man around, until I think he realized that his little brother was actually inhaling his and he could not. So as a consolation prize Noah had a big spray of whipped cream, something that he could easily enjoy as a mid-afternoon treat. And in the end I had two very happy boys who both loved their gingerbread men in different ways. It's okay, we made it work and it's a beautiful thing.
We have more Gingerbread Therapy scheduled this weekend, Noah's grandmother purchased the boys a very special gingerbread house to build equipped with a snowman for the front lawn, and a gumdrop walk-way. It all doesn't get much more heavenly than that.
“The Gingerbread House has four walls, a roof, a door, a window, and a chimney. It is decorated with many sweet culinary delights on the outside. But on the inside there is nothing—only the bare gingerbread walls. It is not a real house—not until you decide to add a Gingerbread Room. That’s when the stories can move in. They will stay in residence for as long as you abstain from taking the first gingerbread bite.”Vera Nazarian, The Perpetual Calendar of Inspiration
Our Gingerbread room will be filled with lots of love, hope and faith... we hope your Gingerbread house will be too.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Monday, December 3, 2012
Dear Santa
Dear Santa,
You've known me for many years now. When I was just a tender little thing you never disappointed me. You've brought me countless treasures. And you know that I used to ask for a lot of things. My lists were miles long - I wanted the world. Now that I'm all grown my list has grown significantly smaller. I've learned the true importance and meaning of life. I only want to ask for one thing... one thing that I know is way too big for you alone. Yet it remains on my wish list. And I continue to send that wish out to the universe in hopes that someone might catch that wish in their hands like a speck of magic stardust, and find a way to grant it. Please send me that Christmas Miracle that you know my heart aches for.
Noah was so excited tonight waiting on your arrival, he played with his Christmas train around the tree and spent lots of time knocking down his nativity figurines and playing with his snow globe, which had it's last good snow as his little brother Luke broke the plastic ball tonight. (I hope Luke told you he now needs a new unbreakable snow globe). We kept telling Noah that you were on your way and he just kept growing with excitement. He's been watching movies about how you deliver presents and spread holiday cheer for many months. So tonight was a big deal for him. He'll probably be dreaming of sugar plum fairies until Christmas actually comes now.
Noah was so excited to see you come up the driveway. A huge difference from the very first time he met you. Noah looked at you with such awe and beamed with his sweet and loving smiles. You've charmed your way into his heart all season long and gave him the greatest gift when you made a special visit to our home tonight arriving on the fire truck. Thank you for holding his precious little hand and offering him a loving embrace. Your heart is so big that you don't even see a little boy with physical challenges, you see Noah as I wish the world would see him.
Your helpers are always so nice every year, and it's such a gift to meet everyone your bring with you. Hearts as big as gold. And I'm so thankful and blessed that you and your entire team of elves came to listen to all that Noah hopes to get for Christmas. But he's pretty easy to please and I know he'll be super thrilled with whatever you bring him Christmas morning. Thank you for bringing Christmas magic to our home.
With Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
You've known me for many years now. When I was just a tender little thing you never disappointed me. You've brought me countless treasures. And you know that I used to ask for a lot of things. My lists were miles long - I wanted the world. Now that I'm all grown my list has grown significantly smaller. I've learned the true importance and meaning of life. I only want to ask for one thing... one thing that I know is way too big for you alone. Yet it remains on my wish list. And I continue to send that wish out to the universe in hopes that someone might catch that wish in their hands like a speck of magic stardust, and find a way to grant it. Please send me that Christmas Miracle that you know my heart aches for.
Santa's Little Helper |
Santa's Firetruck |
Santa Holding Noah's Hands |
With Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Saturday, December 1, 2012
The Twelve Days Of Christmas Special Needs
On the first day of Christmas, the good Lord gave to me: a child with special needs.
On the second day of Christmas, the good Lord gave to me: a heart full of love for my child with special needs.
On the third day of Christmas, the good Lord gave to me: an ache in my heart and a heart full of love for my child with special needs.
On the fourth day of Christmas, the good Lord gave to me: a tear in my eyes, an ache in my heart and a heart full of love for my child with special needs.
On the fifth day of Christmas, the good Lord gave to me: an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the sixth day of Christmas, the good Lord gave to me: a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the seventh day of Christmas, the good Lord gave to me: a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the eighth day of Christmas, the good Lord gave to me: supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the ninth day of Christmas, the good Lord gave to me: remarkable doctors &; therapists, supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in heart and my heart full of love for my child with a special needs.
On the tenth day of Christmas, the good Lord gave to me: an appreciation of small accomplishments, remarkable doctors &; therapists, supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the eleventh day of Christmas, the good Lord gave to me: a sense of pride and courage, an appreciation of small accomplishments, remarkable doctors &; therapists, supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the twelfth day of Christmas, the good Lord said to me: Reach out and share your sense of pride and courage, your appreciation of small accomplishments, your remarkable doctors &; therapists, your supportive friends, your sense of humor, your ray of hope, your unsuspected strength for the tear in your eyes and the ache in your heart and your heart full of love for your child with special needs.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
On the second day of Christmas, the good Lord gave to me: a heart full of love for my child with special needs.
On the third day of Christmas, the good Lord gave to me: an ache in my heart and a heart full of love for my child with special needs.
On the fourth day of Christmas, the good Lord gave to me: a tear in my eyes, an ache in my heart and a heart full of love for my child with special needs.
On the fifth day of Christmas, the good Lord gave to me: an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the sixth day of Christmas, the good Lord gave to me: a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the seventh day of Christmas, the good Lord gave to me: a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the eighth day of Christmas, the good Lord gave to me: supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the ninth day of Christmas, the good Lord gave to me: remarkable doctors &; therapists, supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in heart and my heart full of love for my child with a special needs.
On the tenth day of Christmas, the good Lord gave to me: an appreciation of small accomplishments, remarkable doctors &; therapists, supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the eleventh day of Christmas, the good Lord gave to me: a sense of pride and courage, an appreciation of small accomplishments, remarkable doctors &; therapists, supportive friends, a sense of humor, a ray of hope, an unsuspected strength for the tear in my eyes and the ache in my heart and my heart full of love for my child with special needs.
On the twelfth day of Christmas, the good Lord said to me: Reach out and share your sense of pride and courage, your appreciation of small accomplishments, your remarkable doctors &; therapists, your supportive friends, your sense of humor, your ray of hope, your unsuspected strength for the tear in your eyes and the ache in your heart and your heart full of love for your child with special needs.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Sunday, November 25, 2012
Bee-Lieve
Noah Releasing a Balloon for Brayden |
Brayden's Bee Balloons |
We released balloons today for our little friend Brayden who passed away ten days ago to participate in Brayden's memorial. I decorated with little bee's for Brayden who always helped us to remember to always Bee-Lieve. The little bee that will keep flying high in our hearts and hopefully will be one of the many angels that will help look in on Noah and guide us from time to time. Somehow I kind of think Noah new exactly that we were doing. I sensed it. He's a very loving and connected soul. One doesn't have to be verbal to understand.
Noah had a beautiful Thanksgiving. He ate lots of food and as always his favorite was the pumpkin cream cheese pie. He's certainly a pie lover. It was a quiet day which was very nice. Sometimes you just need a quiet, loving day and that is exactly what it turned out to be. Nothing was on a time-table, we let the turkey be our guide for dinner hour. It was the first time I decided to brine a turkey. I watched a late night special on PBS promising the most moist turkey one could ever eat and decided I'd take on the task. I must say, PBS was right. It was super moist - hands down the moistest turkey I've cooked. Yet was warned that when you brine a turkey it would cut down the cook time by 1/3 so I watched that bird like a hawk not completely knowing a concrete completed cooking time. So by letting the bird be our guide as when dinner would be served it created a rather relaxed atmosphere. It was kind of like how we exist with Noah. We let time be his guide. And when he's ready then we're all ready.
Noah's daddy was able to install the train around the Christmas tree on Thanksgiving which remains hands down one of Noah's most favorite holiday activities. He finds it especially fun to roll over and continually derail his train. And Luke cautiously guards it as if he knows he must not touch Noah's beloved train. Although I have detected that Luke has contemplated putting a wise man on the track and we certainly need all the wise men we can get, so I'm making sure that no nativity members are run down this year.
Chris temporarily took down a baby gate to the kitchen and dinning room entry way for Thanksgiving which made me feel like I had a little more freedom with Noah's new hi/lo base chair. We were able to go at least between two rooms without being completely stuck in the kitchen. I've quickly grown rather attached to the hi/lo base chair and any initial feelings of sadness that I associated with it have dissipated. For the first time I was able wheel Noah over to the refrigerator and freezer show him the contents inside. Show him what a bottle of milk looked like - where his yogurt was stored. I also put the chair on the highest setting and Noah watched by my side at the counter as I peeled potatoes and stuck them in a pot full of chicken stock. These are activities that he couldn't do without this chair. And for the first time I feel like he's being able to be included in daily activities more than ever. The possibilities seem endless. He can now even come to the counter and watch me make Christmas cookies and goodies. He was even able to watch me unloading the dishwasher and where the silverware goes in the drawers. Having him being able to finally be included in life's smallest moments is doing my heart a world of good.
Each day the excitement over the arrival of Noah's service dog grows. We found him the cutest little birthday bag with a Golden Retriever on it for his birthday at the dollar store. It's perfect and we're just so excited for this new chapter in Noah's life. It's going to be a very sweet 4th year birthday celebration. We've come so far in 4 years from bringing home a little boy that no one said would survive... we have so far to go, but we're doing it.
In loving memory of Brayden we will always keep Bee-Lieving.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Friday, November 23, 2012
I Know Different
A poem: I KNOW DIFFERENT
by Tricia Proefrock
------------------------------------------------------
Dear mommy, I have felt your tears, falling on my face. Someone else might think they are tears of sadness, because of what I can't do...I KNOW DIFFERENT.
I know those tears pour from your heart out of gratitude for me, because of what I CAN do: I can love everyone in the purest form possible. Unconditionally. I can be judged, but will never judge in return. I know different because I feel, in your hugs and kisses, that I'm perfect just the way I am.
I have seen you hang your head down in shame, when we go out on adventures. Someone else might think you are ashamed of having a child like me...I KNOW DIFFERENT.
I know you are ashamed of the grown-ups who ignore me, yet talk happily to all the other children. The grown-ups who won't look you in the eye, but stare at me, when they think you don't see. I know different because I've seen the many, many more times you have raised your head up high, with pride, because I'm yours.
I have heard you whispering desperate prayers at night. Someone else might think you are asking God to make me a typical kid...I KNOW DIFFERENT.
I know you are thanking Him that I got to be here, with you, for another day... exactly how I am. I know different because I have heard you ask me never to leave you. And I have heard you cheer for me, every single day of my life... you tell me I don't need to be typical to be amazing, I just need to be here.
I know you have a big job, taking care of me. I know your body hurts, because I'm getting so big. I know that more than anything, you want to hear me say your name. And I know you worry that you aren't good enough, and that you will fail me...BUT I KNOW DIFFERENT MOMMY.
I know that even on your worst days, you will always be enough for me, and I will always love you more than you know. ♥
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
------------------------------------------------------
Dear mommy, I have felt your tears, falling on my face. Someone else might think they are tears of sadness, because of what I can't do...I KNOW DIFFERENT.
I know those tears pour from your heart out of gratitude for me, because of what I CAN do: I can love everyone in the purest form possible. Unconditionally. I can be judged, but will never judge in return. I know different because I feel, in your hugs and kisses, that I'm perfect just the way I am.
I have seen you hang your head down in shame, when we go out on adventures. Someone else might think you are ashamed of having a child like me...I KNOW DIFFERENT.
I know you are ashamed of the grown-ups who ignore me, yet talk happily to all the other children. The grown-ups who won't look you in the eye, but stare at me, when they think you don't see. I know different because I've seen the many, many more times you have raised your head up high, with pride, because I'm yours.
I have heard you whispering desperate prayers at night. Someone else might think you are asking God to make me a typical kid...I KNOW DIFFERENT.
I know you are thanking Him that I got to be here, with you, for another day... exactly how I am. I know different because I have heard you ask me never to leave you. And I have heard you cheer for me, every single day of my life... you tell me I don't need to be typical to be amazing, I just need to be here.
I know you have a big job, taking care of me. I know your body hurts, because I'm getting so big. I know that more than anything, you want to hear me say your name. And I know you worry that you aren't good enough, and that you will fail me...BUT I KNOW DIFFERENT MOMMY.
I know that even on your worst days, you will always be enough for me, and I will always love you more than you know. ♥
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Wednesday, November 21, 2012
You're a Blessing
Parents of children with special needs know more than most that every child is a gift worthy of thanks, every one, the ones who thrive and the ones who strive, whether they become our legacy or we become theirs. But on those days when there doesn't seem much to be thankful for, or others are suggesting that your child must be just a burden, or well-meaning people suggest giving thanks just for healthy kids. Your blessings will always be fully counted. Other parents may take the gifts that their children bring for granted. Not you. Not ever.
Wishing you all a Happy Thanksgiving filled with lots of love, memories and blessings.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Tuesday, November 20, 2012
A Time of Thanks
Noah in his New Hi/Lo Chair |
Noah's Hi/Lo Chair without Tray |
The equipment vendor also brought Noah a trial walker but it was too big, so we'll have to wait on a smaller model. I remain hopeful that it is still a piece of equipment that might work for him. We're also trying to troubleshoot more recent problem development with his Britax Boulevard car seat that he has now started to get his head out of the headrest blocks and leave his head hanging sideways while I'm driving. Something both scary and a huge safety concern. It sounds like a appointment is likely in our future to explore some options. We don't have a handicapped accessible van and we can't afford one, so a car seat is our only option right now. We will also need to give some thought in the bath chair department for Noah as I think he's really outgrown the First Steps Baby Highchair that I was using in the tub for him.
Our house feels like it is closing in on me - literally. Noah's pieces of equipment are cumbersome and heavy and we lack wide doorways, and hard flooring in our home and even the storage or a place to house all of the things he needs for daily living. It takes two people to lift his feeder chair or stander anywhere which means they are pretty much stuck in a particular room and stay parked there. I need a mudroom for the dogs so I can eliminate the baby gates... we need a ramp... we need a handicapped accessible house and our current home is anything but. Dear Santa please bring me a house stretcher and handicapped accessible home!
We are growing increasingly excited about the arrival of Noah's Service dog. We've think we have a name picked out pending that the company feels that they've chosen the perfect dog to match with Noah. And it still looks like Noah's dog will arrive around his birthday or the week of Christmas. It of course will mean lots more hands on work for me as I work with this dog to pass puppy good citizen weekly training tests until it leaves home for many months for advanced skill training and to pass all testing and obtain certification. Which I am sure will be hard on Noah and the family emotionally as I know we will fall in love only to be a part for many months. But hopefully our love and sacrifice will bring great rewards.
Noah is ready to gobble down a big Thanksgiving dinner in a few days. I got Noah a little shirt that says: "I'm thankful for pie with extra whipped cream, turkey and mashed potatoes, and seconds please." Although Noah still enjoys his Thanksgiving pureed he sure does love this time of year and chows down with the best of them. And now he has a safe chair to enjoy his meals in. Dear Lord, as hard as this all is for me, thank you for answering that prayer.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Friday, November 16, 2012
With Heavy Heart
The last few weeks have been a little hard. I thought I'd start decorating for Christmas a little early this year. In all reality it takes me weeks just to decorate the Christmas tree as I can't just do it all in a day with tending to all of Noah's needs and watching over a very active little brother. So if I started in December the tree likely wouldn't go up until January! I was doing really well with it all until I stumbled on this silly bear that was stashed away in a rubbermaid container - it was a the build a-bear that Noah was gifted with in the NICU. All the children who were in the NICU during Christmas received a build-a-bear. I picked up that bear and it was like a lightening flash of emotions that just ripped through me. It's the pain that never goes away - you live with it each and everyday - you just tuck it away tight so you can keep going. And that darn bear was the key that just happened to unleash the flood gates of emotion and memory. It still smells of the NICU. That somewhat sterile baby smell. But it's not a comforting smell - not the smell of baby lotions and fresh blankets - it's a haunting smell. Yet it's apart of Noah's early story and I can't rid myself of him. So I stuffed him forcefully back into the container as if I was punishing him for the reminder of where we had been nearly four years ago. I went about decorating the tree - it's still a work-in-progress. It's still rather naked with only lights and ribbon - I hope to have it done around Thanksgiving. But I'm placing no expectations on myself given the boys are still recovering from illness and their daddy has now fallen ill with the same cold. Thankfully thus far I'm holding germ free and being able to care for everyone.
I've been trying to keep myself busy to erase the fact that I found that bear. I was doing rather well, until I received the news yesterday that another little boy that we've grown to love over the years in our special needs community passed away very suddenly. Little Brayden was born with Hydranencephaly and has defied all odds since his birth. He also has a pretty amazing mother who not only was one of the strongest special needs mothers I know, but also started the Global Hydranencepahly Foundation in honor of Brayden and those like him. His mother created the Journey of the Bees: Believing in the impossible - with the motto: "Aerodynamically, the bumble bee shouldn't be able to fly, but the bumble bee doesn't know it so it goes on flying anyway." She has been one of the most loving mothers I've had the pleasure of connecting with. Little Brayden was only six months older than Noah, and she was so kind in gifting us with Brayden's thumb splints that he didn't need anymore and mailed them to Noah. Of course learning of Brayden's passing sent me to a very difficult place. I cried on and off for hours for a little boy I never had the opportunity to meet in person, but one that touched my heart in more ways than I could ever tell you. You fall in love with their stories, their parents, their journey. You know it well - you know the pain, the joy, the love, the heartache and worry like no one else could until you experience it each and everyday with a child. You celebrate their small achievements and accomplishments and cheer them on. You comfort each other on the difficult days, and you pray hard for each and every one of them. So it's rather devastating when one flies home to Heaven. And of course people bombard you with a million God quotes and tell you it's all God's plan - and you're suppose to not question it, accept it as some divine plan that He has in store. But you can't help but wonder what this plan is - how can you take a precious life from the arms of a mother? How can you leave her in a million broken pieces trying so desperately to resuscitate her child and keep him here on this earth. I don't understand it. I want to, I try everyday to wrap my head around it all - to accept the life we've all been given - to find purpose in it. To find a reason for the struggle. But I still want to know why. I lack the ability to ever make it okay for Brayden's mom. I can't bring her the comfort of ever holding Brayden in her arms again. I want to. I want to make it all better for her - for all of us.
Sometimes I wonder how different the world would be if everyone knew exactly what it was like to raise a special needs child; if they could feel it - truly appreciate the journey - it would be such a more thankful world, one in which people didn't argue about trivial things, they counted each breath they took as a blessing and gift, they wouldn't worry about the wrong creamer in their coffee, a date that had gone sour, a car that had broken down... you quickly learn the true meaning of "Real Love" and what truly matters.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
I've been trying to keep myself busy to erase the fact that I found that bear. I was doing rather well, until I received the news yesterday that another little boy that we've grown to love over the years in our special needs community passed away very suddenly. Little Brayden was born with Hydranencephaly and has defied all odds since his birth. He also has a pretty amazing mother who not only was one of the strongest special needs mothers I know, but also started the Global Hydranencepahly Foundation in honor of Brayden and those like him. His mother created the Journey of the Bees: Believing in the impossible - with the motto: "Aerodynamically, the bumble bee shouldn't be able to fly, but the bumble bee doesn't know it so it goes on flying anyway." She has been one of the most loving mothers I've had the pleasure of connecting with. Little Brayden was only six months older than Noah, and she was so kind in gifting us with Brayden's thumb splints that he didn't need anymore and mailed them to Noah. Of course learning of Brayden's passing sent me to a very difficult place. I cried on and off for hours for a little boy I never had the opportunity to meet in person, but one that touched my heart in more ways than I could ever tell you. You fall in love with their stories, their parents, their journey. You know it well - you know the pain, the joy, the love, the heartache and worry like no one else could until you experience it each and everyday with a child. You celebrate their small achievements and accomplishments and cheer them on. You comfort each other on the difficult days, and you pray hard for each and every one of them. So it's rather devastating when one flies home to Heaven. And of course people bombard you with a million God quotes and tell you it's all God's plan - and you're suppose to not question it, accept it as some divine plan that He has in store. But you can't help but wonder what this plan is - how can you take a precious life from the arms of a mother? How can you leave her in a million broken pieces trying so desperately to resuscitate her child and keep him here on this earth. I don't understand it. I want to, I try everyday to wrap my head around it all - to accept the life we've all been given - to find purpose in it. To find a reason for the struggle. But I still want to know why. I lack the ability to ever make it okay for Brayden's mom. I can't bring her the comfort of ever holding Brayden in her arms again. I want to. I want to make it all better for her - for all of us.
Sometimes I wonder how different the world would be if everyone knew exactly what it was like to raise a special needs child; if they could feel it - truly appreciate the journey - it would be such a more thankful world, one in which people didn't argue about trivial things, they counted each breath they took as a blessing and gift, they wouldn't worry about the wrong creamer in their coffee, a date that had gone sour, a car that had broken down... you quickly learn the true meaning of "Real Love" and what truly matters.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Friday, November 9, 2012
I Still Would Have Chosen You
"If before you were born, I could have gone to heaven and saw all the beautiful souls, I still would have chosen you...
If God had told me, "This soul would one day need extra care and needs," I still would have chosen you...
If He had told me, "This soul may make your heart bleed," I still would have chosen you...
If He had told me, "This soul would make you question the depth of your faith," I still would have chosen you...
If He had told me "This soul would make tears flow from your eyes that could fill a river," I still would have chosen you...
If He had told me "This soul may one day make you witness overbearing suffering," I still would have chosen you...
If He had told me, "All that you know to be normal would drastically change," I still would have chosen you...
Of course, even though I would have chosen you, I know it was God who chose me for you." Terri Banish.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
If God had told me, "This soul would one day need extra care and needs," I still would have chosen you...
If He had told me, "This soul may make your heart bleed," I still would have chosen you...
If He had told me, "This soul would make you question the depth of your faith," I still would have chosen you...
If He had told me "This soul would make tears flow from your eyes that could fill a river," I still would have chosen you...
If He had told me "This soul may one day make you witness overbearing suffering," I still would have chosen you...
If He had told me, "All that you know to be normal would drastically change," I still would have chosen you...
Of course, even though I would have chosen you, I know it was God who chose me for you." Terri Banish.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Thursday, November 8, 2012
Package Surprise
We are in the middle of battling the second illness of the season with both boys. I'm again frustrated as my lack of leniency with washing your hands upon entry rule is likely what caused this recent bought of sickness in my household. I'm always worried that I'll offend a therapist, professional or visitor by asking them to wash hands or make a point to remind them we don't accept ill visitors - but not anymore my backbone just got super tough after this last time. If you're offended then you don't have respect for me as a special needs parent who's working really hard to take the very best care of Noah. Surprisingly Noah is coming through this rather well, while his little brother hasn't been as lucky.
Yesterday was filled with some really great news, Noah's Hi-Lo Base chair was approved. I had all but almost thrown in the towel thinking it would either be flat out denied, and that I'd be unsuccessful in appealing. It will still take some time as it's now on order - but it's in the near future, and Chris and I are so relieved. Finally more feeding safety for Noah - we might even be able to progress to eating solids with better positioning. And he can now be on Luke's level since he'll now have seating that will lower to the ground. Which is going to be so nice for him. It's almost so exciting that I feel like I need to make a party cake!
Now for the freaky news:
After a few months of back and forth correspondence with Freedom Concepts and one of Noah's therapists to try to trouble shoot how to make his bike actually fit him and be customized to his needs without having about to fork over a few more thousand to do so, Freedom agreed to give Noah a smaller seat. There are still items like a neoprene lap belt and other accessories that I feel Noah needs but we simply don't have the money they want out of pocket to get those things for Noah. I was hopeful this might be a band-aid fix, although I know we have a long way to go to get this bike where Noah needs it to be for him, until the parts arrived today. Imagine my surprise when I answered the door to UPS to find that Noah's seat part was shipped in a box used to ship herbicide/poison. No joke.
It's unbelievable that Freedom Concepts would think it was appropriate to ship anything to a medically fragile child using a herbicide/poison box. Shoot it's inappropriate to send anything to a any child in a poison box. With all I've been through with this company over the past year I'm not sure I can recommend them to any special needs family. Very bad judgement on their part. To say the least the box remains unopened in my foyer because I really don't want to go near it. There never seems to be a dull moment in the land of special needs. Just when you think you've seen and dealt with it all. I of course have contacted the company but I'm not sure what their response or correction to this new problem will be. But this simply is not okay.
"What gives me the most hope everyday is God's grace; knowing that his grace is going to give me the strength for whatever I face, knowing that nothing is a surprise to God." Rick Warren
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Yesterday was filled with some really great news, Noah's Hi-Lo Base chair was approved. I had all but almost thrown in the towel thinking it would either be flat out denied, and that I'd be unsuccessful in appealing. It will still take some time as it's now on order - but it's in the near future, and Chris and I are so relieved. Finally more feeding safety for Noah - we might even be able to progress to eating solids with better positioning. And he can now be on Luke's level since he'll now have seating that will lower to the ground. Which is going to be so nice for him. It's almost so exciting that I feel like I need to make a party cake!
Now for the freaky news:
After a few months of back and forth correspondence with Freedom Concepts and one of Noah's therapists to try to trouble shoot how to make his bike actually fit him and be customized to his needs without having about to fork over a few more thousand to do so, Freedom agreed to give Noah a smaller seat. There are still items like a neoprene lap belt and other accessories that I feel Noah needs but we simply don't have the money they want out of pocket to get those things for Noah. I was hopeful this might be a band-aid fix, although I know we have a long way to go to get this bike where Noah needs it to be for him, until the parts arrived today. Imagine my surprise when I answered the door to UPS to find that Noah's seat part was shipped in a box used to ship herbicide/poison. No joke.
Herbicide/Poison Box Used to Ship Spare Parts |
It's unbelievable that Freedom Concepts would think it was appropriate to ship anything to a medically fragile child using a herbicide/poison box. Shoot it's inappropriate to send anything to a any child in a poison box. With all I've been through with this company over the past year I'm not sure I can recommend them to any special needs family. Very bad judgement on their part. To say the least the box remains unopened in my foyer because I really don't want to go near it. There never seems to be a dull moment in the land of special needs. Just when you think you've seen and dealt with it all. I of course have contacted the company but I'm not sure what their response or correction to this new problem will be. But this simply is not okay.
"What gives me the most hope everyday is God's grace; knowing that his grace is going to give me the strength for whatever I face, knowing that nothing is a surprise to God." Rick Warren
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Thursday, November 1, 2012
Three Treats
Little Shrek with A Big Shrek that we found Trick or Treating |
Elmo and Hummingbird Pumpkins |
Yoda and Darth Vader Pumpkins |
Noah (AKA Shrek) |
Then we trick or treated for the second time in Noah's grandma's neighborhood because they have more accessible homes to the front door in a stroller. Noah ran into some little friends who gave him some glow bracelets and he was in awe. He got lots of goodies, that I'm sure he will share with his daddy. Then our third stop was our neighborhood. We went to only a handful of special neighbors on our block as it's all we can do to get the stroller up some of the stairs in our area. We got some interesting "treats" this year from pennies in a little purse to a nail file. Gives new meaning to make sure your check your children's candy. People were more than generous with the boys and I don't think I've seen so much candy in our house...ever. We carved two pumpkins this year - a Elmo Pumpkin and a Hummingbird Pumpkin, and Chris of course couldn't help himself with his Star Wars Yoda and Darth Vader pumpkins. They were having a war in our garage for a week with their light sabers. Sometimes you have to really bathe in the simple laughs to get through the day.
And now we get to look forward to Noah's favorite times of year, Thanksgiving and the most important his birthday followed right by Christmas. We also received news that Noah's service dog will likely arrive around his birthday or Christmas. We still owe a balance of $800, and are continuing fundraising efforts for the balance and the continued costs associated like vests, patches, leashes, vet visits including spay/neuter. We are really excited that we are fast approaching this beautiful goal of obtaining a very special dog that will help Noah with his daily activities and alert us to Noah's individual needs. It sounds like that blessing is right around the corner for him. And we are excited about this new adventure in Noah's life. It comes with so many possibilities even down to helping Noah with communication. My biggest hope is that people will be more likely to actually "see" Noah and not look past him. That they'll see a little sweet boy with a dog and turn just to smile at us. Noah needs to know he's accepted into the world just like any other little boy. Thank you all for your continued prayers and thoughts for Noah. It means so much to him and our family.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Subscribe to:
Posts (Atom)