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Donation to the Little and Dependent

1/25/2014

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Eastern Tennessee Children's Hospital is one of the most amazing children's hospital in the country. Not only do they care for a variety of pediatric illnesses and needs, but they have a super special NICU. 

The reason their NICU is so special is because they are one of the hospitals that treat the highest number of drug-dependent newborns in the United States. And we aren't talking street or illegal drugs...these are prescription pain medications and most obtained under normal circumstance.

These babies are weaned off prescription medication, by being given doses of morphine until they are able to tolerate being completely off any kind of opiate. This process can take days and week to accomplish. The unit can hold 49 infants and over half of them are born with neonate abstinence syndrome (drug-dependent), these babies have to be watched around the clock for seizures and even worse, in case they stop breathing.

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When I was in college, this was a topic I was starting to write a research paper on...it is a personal subject as my youngest was born drug-dependent and not because I misused my pain medication, but because I was given excessive amounts of pain medication between all of our admission during pregnancy for pre-term labor and for the amount of pain I was in throughout the entire pregnancy because of the amount of scar tissue I had and two pregnancies very close together and severe anemia issues as well. 

Only problem was, when she was born, we didn't know what was the cause of all the problems we had in the first two months of her life, until I happened to read a forum on drug-dependent babies and all the pieces fell into place. It was scary.

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So when Ellen from Socks 4 Surgery posted the articles published in 2013 about Eastern Tennessee Children's Hospital and what their NICU was doing - we decided that some extra comfort needed to be sent to these precious little ones as well.

Ellen sent out socks and hair bows and in her awesomeness asked if we had any gowns that we could send their way as well. I had to wait until I got back to the house and went through what we already had sewn NICU Smock wise and put together a box that we will be sending out the the hospital this Monday.

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So in total we have twenty-eight gowns headed to the hospital's volunteer services and some of our brochures to be used throughout the hospital for other children that may want a gown of their own as well.

We will keep praying for the hospital's staff and volunteers that are working with and caring for these precious babies and their families. We pray for the babies and their families as well through this rocky start to their journey and lives. 

We hope these gowns find each little doing the best they can and provide them with a little extra comfort.

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Clicking on the picture above will take you to a brochure (PDF Format) the hospital has created on Drug Use during Pregnancy and about Neonatal Abstinence Syndrome.
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Lia Sophia Raffle Tickets on Sale - Raffle the month of February

1/11/2014

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Our Lia Sophia raffle starts on Feburary 1st, 2014!!!

We have lots of really pretty items in our raffle - I will share some with you here, but you can see all of the ones we are posting in our Facebook page's album.

Tickets are on sale now through our website on the events page and cost $2.00/each.
Payments can also be mailed.

For every 100 tickets we sell, Kim will also be giving away an item from the current catalog that is valued at $100.00 or less to a randomly drawn winner from all those that purchase a ticket.

Here was our first special drawing winner (we've sold about 116 tickets as of this posting).
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Kim is the mother of one of the precious little girls we have made a gown for and she has been so gracious in helping us with this raffle. We greatly appreciate all her help, her support and of course giving us the honor to make a gown for Callista.


Below are some of the pieces in the raffle. We really hope you consider buying a ticket or two and sharing our raffle with those you know. There is a Facebook event created for this raffle as well that you can invite them to and all the information is provided there as well.
Thank you to everyone who has purchased tickets, shared our raffle and just helping spread the word about Gracie's Gowns!
I really look forward to this raffle and drawing our winners in February - we will have 3 winners on Valentine's Day too. So fingers crossed everyone who purchases a ticket wins something really pretty.

Jessica

Gracie's Gowns
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Waste Not and Pay it Forward

1/11/2014

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This time last month we were gathering fabric to be sent out to other organizations (which we still have fabric that we can do that with) and we mailed it out just before Christmas - well we're at it again with some more of our remnant pieces of fabric.

So where's it going? Well it is going to a lovely family we know, and many of you may as well - they also take stuffed animals and create companions for children, that are just as unique as they are.

If you guessed Healing Helpers then you are 100% correct!

As I briefly mentioned in our last blog - the kiddos and myself are moving early this summer - so operation clean-up, organize and get ready to start moving is taking place...you wouldn't believe the amount of stuff we manage to accumulate in our tiny little house. So in that - we had some very new stuffies in need of a great home! The kids were more than excited to know they would be going to the place that made David's piggy.

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Here is some of the fabric remnants being sent for pouches, I am of course partial to the Riley Blake fabric from the Pieces of Hope collection (a portion of the sales were donated to Autism Speaks). I thought it was perfect for the kiddos that their heart will represent them being diagnosed on the spectrum.

Below are the other fabrics we finished filling the box with. Once we have the extra shipping funds available we will send this box on its way to Oregon where Healing Helpers is located.

Pretty fabrics right?!
Hope they make some really awesome pouches for Healing Helpers and make some little ones really happy with their new companions!


Have a fabulous day and weekend,
Jessica

Gracie's Gowns
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CureFest 2013 

11/2/2013

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On September 1st, 2013 - Gracie's Gowns participated in CureFest for Childhood Cancer on the National Mall in Washington D.C. with 52 other organizations. We banded together for the day and there on out to advocate for pediatric cancer awareness, research, treatments and cures.
The event was co-hosted by Journey 4 A Cure and theTruth365 - both have done amazing things for children battling and surviving cancer. They not only bring awareness and research funding, but they get to you on a personal level - they tell each child's story, I'm sorry I need to rephrase that - they have each child tell THEIR story, each family share their experience in ALL aspects of the cancer world, the successes and even more heartbreaking, the losses. They show the real statistics of the pediatric cancer world and if you read each of them...it will change your life forever.
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At CureFest they had several speakers - parents, siblings, organization representatives...but the ones that shook you the most were the children.

Gabriella was one of those children - her speech had you laughing at one minutes, inspired throughout and in tears over the reality of what cancer does to children. Her speech was beyond motivational - there was no way you could hear her give "the cold hard facts" without making it your mission to do something to make a difference. 

I am posting her here, because this past weekend, Gabriella lost her battle very suddenly to a brain tumor. She was diagnosed in November of 2012 and passed away October 26, 2013. She made the last year of her life a mission, a legacy even...to show Virginia and the world they HAVE to do something to improve the lives of children battling cancer, to "give them their childhood" to not only treat, but cure the cancers and in a way that doesn't rob them of the life they deserve. She raised funding for the Make-A-Wish foundation after she was granted the wish to go to Paris, France with her family - she knew that other children deserved the chance to have that one lasting memory with their families. She helped raise over $250,000 for Make-A-Wish in just one campaign. 

Gabriella - know that you are deeply missed, but never forgotten! You have impacted and changed so many lives that can only be counted by God. Your parents will continue your work, those that are touched by you have been inspired to do the same as well. We may never do it as great as you did, but we will always try our hardest.

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Throughout the day we gave away 50 goodie bags to those that stopped by our table - here is a collage of the items that were included. Knowing we were headed to this event, simply because it was local enough to us to do so, I invited other organizations and businesses to contribute to our bags and help spread the word about who they are and what they do.

Healing Helpers participated with their Heart Key Chains that they also embroidered a Yellow Ribbon on.

Socks4Surgery participated with their information and magnets.

Pink Door Fabrics sent some quilting bundles of fabric - Chelsea and Charlie have been amazing with donating and letting me purchase fabric at a lesser cost for gowns.

Bee Brave sent their mini stress relievers - which if you remember from our blog on them, they were made from scraps of fabric from our gowns.

We of course included our bracelets and information.

Hollie is a Thirty-One Consultant and contributed her information and nail files from Thirty-One Gifts, she also contributed our raffle item for the day too!

The Hensons contributed their information about Zeal for Life (will update this with their website, once I have it again, it is not with me right now).

Tricia contributed her Pediatric Cancer Awareness bows! One of which was given to Gabriella when we met her. She wanted it so bad and decided it looked great on her dress for the day!

THANK YOU to everyone who contributed to our bags! I know each item was well received!

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One of the best moments was meeting The Beltran family! We had been working on these freckles for his siblings and when I found out that they were going to be at CureFest, I just knew I had to get them done. 

Dominic was a local little guy that passed away from cancer - he loved superman so the fabric was made with superman and each one had a different color for the eyes, arms, legs and stomach and then we embroidered his name in gold.

This is the page they created for Dominic on Facebook and they are continuing their efforts for pediatric cancer research, awareness and advocacy!

https://www.facebook.com/Staystrong4dom

Here are the rest of our photos from CureFest for those who want to see some of them. I hope you enjoy them and check out all the amazing pages and organizations we've posted on the blog.
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Healing Helpers: Comfort, Education and Friendship

11/2/2013

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I have been wanting to spotlight Healing Helpers for a long time now...but as is with life, it gets in the way and well I am finally at the library, without kiddos and can sit down and write out a couple of blogs...so I am starting with them before it closes today.


On a personal level and a professional level I LOVE, LOVE, LOVE...did I mention LOVE? Healing Helpers! Lani-Lee and Michael and all their precious children have become so near and dear to me over the last year and some it isn't funny. 


The idea of using stuffed animals, which ever child has at least one they MUST drag with them everywhere they go, or at least have for naps and bedtime and turning them into a teaching tool for special needs and medically complex children is fantastic! They are practical, functional and beyond all else really help show your child (when and how they can understand) what they have been through in life. This is my son and his Healing Helper piggie (that he calls Piggie or Oinker depending on his mood I suppose). David was the first kiddo to receive one with an Autism heart - because that is his diagnosis and what he battles everyday, he has had surgery and leg braces, but this is what mattered most to me - his heart...the soul of who he is. His diagnosis does not define him, rather he defines it and it helps make him the special little-big man that he is! David loves his piggie and enjoys showing the heart off to others, showing his name and the Thomas the Train pouch inside it (he loves Thomas the Train too) and just snuggling with it at night. It has become his friend when he is hurt or we have to go to specialist we haven't been too before.

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So that was on the personal level - oh plus they are so awesome to talk to on the phone and seriously spent HOURS of time with me on the phone when things went all crazy in July here with Gracie's Gowns. They were my rock, they really helped get me through that week at times!


Now professionally - we have teamed up with Healing Helpers in making smaller "animal sized" hospital gowns. These are ordered through Healing Helpers when someone orders one or just orders the gown if they already have one. This was the first Healing Helpers gown and of course was made for precious Annabelle when she had her most recent open heart surgery. It matched the gown that we made for Annabelle to wear. Since then we have made some others - and have a couple more to make as well. So I am just going to share some of the picture that they've posted of the gowns with and without their Healing Helpers.

To learn more about Healing Helpers or to even inquire and place an order for one, please visit their links below:


Website: http://www.healinghelpers147.com
Facebook Page: https://www.facebook.com/healinghelpers
Etsy Shop: http://www.etsy.com/shop/healinghelpers

They also accept donations of materials, like new or new stuffed animals and monetary donations as well. They have a sponsorship program too and are looking to do so many more great things in the future with Healing Helpers! 
So stop by and see how you can help them out too! That is how I first was connected with them was through donating stuffed animals and fabric scraps from gowns and other projects to be used for their pouches!
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Busy Buddy by Bee Brave

8/18/2013

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This amazing tray with a removable pillow that also becomes an amazing storage keeper is called a Busy Buddy - the amazing mother, daughter team behind it is called Bee Brave!

Our son David, was a recipient of a Busy Buddy - he is autistic (you can read back through the blogs and find his full story) and we spend two hours in the car every trip to therapy, every appointment, every specialist and every testing...which this summer was three days a week...for him, it is boring and frankly he hates it!

I cannot tell you how much he LOVES this - he can use it at home on his lap to color (we don't have much table space, and he can take it away from the girls), he uses it in the car, he can hide his most treasured possessions inside the pouch for the pillow (it has a zipper)...and well it worked great for mommy when I was laid up in bed and I was able to write out the new requests for gowns even.


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David is pretty picky about what he likes - what child isn't right?! I had just made him a special little bean bag seat/ottoman thing...lol. And this was the fabric he picked out for it. The amazing part of his Busy Buddy, was I was able to send in this fabric and her mother made the pillow with it! David was so excited to see his "moo cows," "piggie" and tractor on the fabric.


Melissa went one step farther and matched the painting on the tray to the fabric as well! Once again - he was in HEAVEN! It was so great to see his face light up when it arrived in the mail and it was perfect timing as we had therapy the next day! But he wanted to take it outside to play with his trucks in the sandbox instead...lol.

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So we compromised - he is David with his Busy Buddy!

He was allowed to take it outside with him, but it had to stay with mommy, I wasn't about to have sand start coming out the zipper pocket...lol.



He doesn't always smile, but he wanted to say "mooooo" as his picture was being taken. The boy loves cows, what can I say? He wants to be a cowboy when he grows up.


When I sent in David's fabric for his Busy Buddy we also went a couple steps farther and created a wonderful bond and work relationship on the Gracie's Gowns end with Bee Brave.

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We sent all this amazing fabric over to Bee Brave to help make the pillows for other children, teens and adults that end up being on their sponsorship list!


Of course, it is mostly all scraps from gowns that have been made for children by Gracie's Gowns. Some of our gowns we have lots left over, and this is the case with these fabrics, but we also sent lots of smaller pieces to use as well for their mini stress relievers!


We filled up a diaper box of fabric and mailed it out to Melissa and her mom and something even more amazing is stemming from this too!

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We are participating in CureFest 2013 in Washington D.C. - it is an event sponsored by The Truth 365 to bring awareness and support for Pediatric Cancer.


The event is on September 1st, 2013 and all of the participating organizations, work with children who have cancer, fund pediatric cancer research, promote awareness, etc.


Bee Brave - is sending us 50 mini stress relievers for our goodie bags to distribute throughout the time of the event! We wanted to help promote other organizations that are small like us, but work with children who have cancer, and just chronically ill children as well and let them not only put informational materials in our bags, but include a little item too!


Melissa sent me this picture of some of the ones heading our way here soon! All I can think of when I see this is the precious kiddos that received gowns from the same fabrics and it makes me tear up, knowing they have inspired something so amazing in my own heart and really and truly are the heartbeat that keeps Gracie's Gowns running!

If your organization isn't attending CureFest and would like to include an item and informational materials in our goodie bags, we are putting together 50 bags. The items need to be at my house no later than the 29th of August so I can get them put in the bags.


Direct sales companies are allowed to include an item, but I am only taking one representative per company - and you must include a sample item with your information. Please contact me BEFORE sending anything, just to make sure I don't have another representative already - and that I need to keep my eye out for a package - same with any organization.
To learn more about Bee Brave you can visit their 
Facebook Page at (stop by and send them some love, Gracie's Gowns style of course):
https://www.facebook.com/beebrave2013



And their website is:
http://www.beebrave.org

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The Chartres Cathedral 

8/2/2013

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When I was in high school, I had to opportunity to go to France with my French teacher, friends in my level and students from other French levels as well.

It was an amazing trip - everything I loved all in one place. Music, the history of France, the shopping everyone talked about, the monuments and artwork...it was spectacular.

The cathedrals and castles were probably the most intriguing sites we saw. Of course the Eiffel Tower and the Arc de Triomphe, the Louvre and Versailles were unique and ravishing, but the cathedrals really drew my attention above all else.

Something about the architecture, the amount of work that had to be done my so many people, over years and years of time...and even sometimes having to be redone because of fires, natural disasters and war. And the final project still standing for all future generations to see, it was breath-taking. Most of the cathedrals are still in use for religious services in France (sorry random side note there and memory from touring). Chartres Cathedral was the one that intrigued and amazed me the most. And here is why....

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The Rose Window - look at it, isn't it just beautiful! That is all stain glass. This alone took years to complete...the detail is so intrinsic and most of it is still the original glass that was used when the window was first constructed in 1215. The scene the window depicts is the Last Judgement, and was a gift that at the time cost 80,000 pounds! Now let me share a little story with you as to why I am even blogging about Chartres Catherdral, the Rose Window and why it's detail, the beauty and the work involved mean so much and can really put things into perspective for each parent who reads this.

Once again - this is from a posting on Facebook - though I do not know who originally wrote this, to give them the credit, but I pray one day they see the blog and realize how much of an impact it really has on those who read it.
Invisible Mother

 It all began to make sense, the blank stares, the lack of response, the way
 one of the kids will walk into the room while I'm on the phone and ask to be
 taken to the store. Inside I'm thinking, 'Can't you see I'm on the phone?'
 
 Obviously not; no one can see if I'm on the phone, or cooking, or sweeping
 the floor, or even standing on my head in the corner, because no one can see
 me at all. I'm invisible. The invisible Mom. Some days I am only a pair of
 hands, nothing more! Can you fix this? Can you tie this? Can you open this??

 Some days I'm not a pair of hands; I'm not even a human being. I'm a clock
 to ask, 'What time is it?' I'm a satellite guide to answer, 'What number is
 the Disney Channel?' I'm a car to order, 'Right around 5:30, please.'

 Some days I'm a crystal ball; 'Where's my other sock?, Where's my phone?,
 What's for dinner?'

 I was certain that these were the hands that once held books and the eyes
 that studied history, music and literature -but now, they had disappeared
 into the peanut butter, never to be seen again. She's going, she's
 going, she's gone!

 One night, a group of us were having dinner, celebrating the return of a
 friend from England . She had just gotten back from a fabulous trip, and she
 was going on and on about the hotel she stayed in. I was sitting there,
 looking around at the others all put together so well. It was hard not to
 compare and feel sorry for myself. I was feeling pretty pathetic, when she
 turned to me with a beautifully wrapped package, and said, 'I brought you
 this.' It was a book on the great cathedrals of Europe . I wasn't exactly
 sure why she'd given it to me until I read her inscription: 'With admiration
 for the greatness of what you are building when no one sees.'

 In the days ahead I would read - no, devour - the book. And I would discover
 what would become for me, four life-changing truths, after which I could
 pattern my work:

 1) No one can say who built the great cathedrals - we have no record
 of their names.

 2) These builders gave their whole lives for a work they would never
 see finished.

 3) They made great sacrifices and expected no credit.

 4) The passion of their building was fuelled by their faith that the
 eyes of God saw everything.

 A story of legend in the book told of a rich man who came to visit the
 cathedral while it was being built, and he saw a workman carving a tiny bird
 on the inside of a beam. He was puzzled and asked the man,
 'Why are you spending so much time carving that bird into a beam that
 will be covered by
 the roof. No one will ever see it'

 And the workman replied, 'Because God sees.'

 I closed the book, feeling the missing piece fall into place. It was almost
 as if I heard God whispering to me, 'I see you. I see the sacrifices you
 make every day, even when no one around you does.

 No act of kindness you've done, no sequin you've sewn on, no cupcake you've
 baked, no Cub Scout meeting, no last minute errand is too small for me to
 notice and smile over. You are building a great cathedral, but you can't see
 right now what it will become.

 I keep the right perspective when I see myself as a great builder. As one of
 the people who show up at a job that they will never see finished, to work
 on something that their name will never be on. The writer of the book went
 so far as to say that no cathedrals could ever be built in our lifetime
 because there are so few people willing to sacrifice to that degree.

 When I really think about it, I don't want my son to tell the friend he's
 bringing home from college for Thanksgiving, 'My Mom gets up at 4 in the
 morning and bakes homemade pies, and then she hand bastes a turkey for 3
 hours and presses all the linens for the table.' That would mean I'd built a
 monument to myself. I just want him to want to come home. And then, if there
 is anything more to say to his friend, he'd say, 'You're gonna love it
 there...'

 As mothers, we are building great cathedrals. We cannot be seen if we're
 doing it right. And one day, it is very possible that the world will marvel,
 not only at what we have built, but at the beauty that has been added to the
 world by the sacrifices of invisible mothers.
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Fingers and Toes

8/1/2013

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When I think about fingers and toes - I almost automatically think about being pregnant for the first time and I just couldn't wait to meet our precious little baby and take in all her features, but especially her fingers and toes. My second thought, is the book you see above.

But what I am going to share with you tonight, I have been wanting to share for a while now - I read it on Facebook on a friend's page back towards Mother's Day this year. Something even more special about this friend is that her baby was born with Hypoplastic Left Heart Syndrome...and her precious little boy became an angel watching over her.

This story is so touching and so important - being the mother of a special needs child, allows us to appreciate the little things more in life, but it also forces us to re-evaluate a lot of what we think, believe and say. We also know that we want more for our children than what this life has to offer them.

We know that when a new mom-to-be says they don't care as long as the baby has 10 fingers and 10 toes...they aren't telling the whole truth. This is for all the mothers out there of children with special needs - no matter what their condition may be, we are all connected.
My friend is expecting her first child. People keep asking what she wants. She smiles demurely, shakes her head and gives the answer mothers have given throughout the ages of time. She says it doesn't matter whether it's a boy or a girl. She just wants it to have ten fingers and ten toes. Of course, that's what she says. That's what mothers have always said. Mothers lie.

Truth be told, every mother wants a whole lot more. Every mother wants a perfectly healthy baby with a round head, rosebud lips, button nose, beautiful eyes and satin skin.

Every mother wants a baby so gorgeous that people will pity the Gerber baby for being flat-out ugly.

Every mother wants a baby that will roll over, sit up and take those first steps right on schedule (according to the baby development chart on page 57, column two).

Every mother wants a baby that can see, hear, run, jump and fire neurons by the billions. She wants a kid that can smack the ball out of the park and do toe points that are the envy of the entire ballet class.

Call it greed if you want, but we mothers want what we want. Some mothers get babies with something more.

Some mothers get babies with conditions they can't pronounce, a spine that didn't fuse, a missing chromosome or a palette that didn't close.

Most of those mothers can remember the time, the place, the shoes they were wearing and the color of the walls in the small, suffocating room where the doctor uttered the words that took their breath away. It felt like recess in the fourth grade when you didn't see the kick ball coming and it knocked the wind clean out of you.

Some mothers leave the hospital with a healthy bundle, then, months, even years later, take him in for a routine visit, or schedule her for a well check, and crash head first into a brick wall as they bear the brunt of devastating news. It can't be possible! That doesn't run in our family. Can this really be happening in our lifetime? I am a woman who watches the Olympics for the sheer thrill of seeing finely sculpted bodies. It's not a lust thing; it's a wondrous thing. The athletes appear as specimens without flaw - rippling muscles with nary an ounce of flab or fat, virtual powerhouses of strength with lungs and limbs working in perfect harmony. Then the athlete walks over to a tote bag, rustles through the contents and pulls out an inhaler.

As I've told my own kids, be it on the way to physical therapy after a third knee surgery, or on a trip home from an echo cardiogram, there's no such thing as a perfect body.

Everybody will bear something at some time or another. Maybe the affliction will be apparent to curious eyes, or maybe it will be unseen, quietly treated with trips to the doctor, medication or surgery. The health problems our children have experienced have been minimal and manageable, so I watch with keen interest and great admiration the mothers of children with serious disabilities, and wonder how they do it. Frankly, sometimes you mothers scare me. How you lift that child in and out of a wheelchair 20 times a day.

How you monitor tests, track medications, regulate diet and serve as the gatekeeper to a hundred specialists hammering in your ear.

I wonder how you endure the clichés and the platitudes, well-intentioned souls explaining how God is at work when you've occasionally questioned if God is on strike.

I even wonder how you endure schmaltzy pieces like this one -- saluting you, painting you as hero and saint, when you know you're ordinary. You snap, you bark, you bite. You didn't volunteer for this. You didn't jump up and down in the motherhood line yelling, "Choose me, God! Choose me! I've got what it takes." You're a woman who doesn't have time to step back and put things in perspective, so, please, let me do it for you.

From where I sit, you're way ahead of the pack. You've developed the strength of a draft horse while holding onto the delicacy of a daffodil. You have a heart that melts like chocolate in a glove box in July, carefully counter-balanced against the stubbornness of an Ozark mule.

You can be warm and tender one minute, and when circumstances require intense and aggressive the next. You are the mother, advocate and protector of a child with a disability.

You're a neighbor, a friend, a stranger I pass at the mall. You're the woman I sit next to at church, my cousin and my sister-in-law.

You're a woman who wanted ten fingers and ten toes, and got something more. You're a wonder
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The picture above is a charcoal drawing that I made not too long after David was born - I would never have guessed that I would become a mother to a child with special needs, a child with Autism...a child that has become my hero and the best thing to ever happen to my life. 
Some people get to meet their heroes...but some of us have given birth to ours. 
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Heroes with Grace: William

6/29/2013

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William, or Liam as he is more popularly called is a handsome two year old boy that has been diagnosed with Mucopolysaccharidosis or abbreviated as MPS.

It is a rare disease and one that makes every day a battle, every day unknown and every day full of adventures.

Liam also suffers from conditions related to the MPS. These include: food allergies, an arachnoid cyst in his Right Cerebellopontine Angle Cistern with enlarged space around it, Ataxia, Arthritis, Bilateral Dislocated Hips (with Defective ossification, dysplastic acetabella, & damage to his iliac wings bilaterally), Chronic Regression, finger clinidactyly bilaterally,  Developmental Delay, irregular Gait, Hypersensitivity, Hypotonia, Hearing Loss, Osteoponia, Plagiocephaly, Seizures and he is also nonverbal.

So much for such little ones to go through. Fortunately he has a great family and friend support to help get through each event and make every moment count. It has not been an easy road and there has been lots of obstacles to climb in his two years here on Earth. Liam has been poked and prodded his whole life trying to find answers and find out what's wrong; but he is blessed to only have had 1 surgery so far. He had emergency surgery to repair his inlingual and umbilical cord hernias at 4 months old. He was transported from one children's hospital to another that would be able to handle doing this emergency surgery while he was in ICU battling RSV. His surgery was only supposed to take 30-45 minutes but ended up taking almost 3 hours, as they had to fight to safe his left testicle due to all the fluid buildup cutting off the blood flow to it. Luckily it was saved and he was released after being in the hospital for a month.

In the future Liam will have to have hip surgery on both hips in a few weeks time and a total hip replacement if those surgeries don't fix his problems. There will be many more surgeries in the future, but Liam and his family are just taking them one at a time.

Liam's mom described their most frightening and most exciting moment in their journey with MPS so far like this:

The most frightening moment was June 7th, 2013. Liam didn't sleep really at all the night before and he went to bed fine around 9pm but then at 130 he woke up screaming and rubbing his legs. He stopped when I cradled him, but the moment I put him down he would scream. this went on until 830 when he finally let me put him down. Liam then went on to sleep until 3pm ate lunch and went back to bed. He didn't walk/crawl or even attempt to do anything but sit in the chair I put him in and have me hold him. The doctor says that some days are just bad ones. He didn't even want to see him!

Most exciting moment was the first time he said momma. I was blessed to hear him say it countless times for 3 whole months; before he became non-verbal for no known medical reason.
There was more that Liam's mom went on to say about MPS - which I didn't know, but also a beautiful view of how all our special children, are still children...no matter what they are going through or up against, they still all just want to be the child they were meant to be.
Did you know that MPS is detected by a simple blood or urine test. But it is currently not a test regularly done in pediatric doctor offices. Please at your next doctors appointment ask them to test. Especially if your child has autistic tendencies, developmental delay or is regressing.

There is no cure but through awareness there is hope! 


Liam may have a lot going on but at the end of the day he is just a toddler, who wants to play with his cars, balls & watch star trek. He is the happiest little boy you will ever meet and is such a fighter! He fights everyday just to walk and play. 
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To learn more about and help support Liam and his family you can visit their Facebook Page.
www.facebook.com/fightingforanswers

To help provide financial support to the family you can donate through their gofundme page below. The family is currently trying to move from Texas to Florida because their insurance doesn't cover out of state appointments, but also because the doctors that specialize in MPS are located in Florida.
http://www.gofundme.com/fightingforanswers

To Learn More About Mucopolysaccharidosis view this link:
http://www.mpssociety.org/

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These are the Words I Would Say

3/4/2013

1 Comment

 
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It  has been a while since I blogged here on our page ~ frankly because we have just been SO BUSY with gowns, filing our nonprofit status, the fundraiser, computer issues and oh yeah, more gowns...it is hard to find the time to sit down and blog the stories of our families and take care of my own.

Tonight's blog is partially a test to see if it posts and works, but just my reflections on today, our family and part of the journey we are on and maybe pass along a little advice, tips, hope and inspiration to those who read this. As many of you have followed Gracie's Gowns for a while you know that our son was formally diagnosed on the autism spectrum this past summer. And while it was a diagnosis that we were expecting at that point it was still hard to comprehend, not the diagnosis itself, but what was to come after.

Today we had our 6 month follow-up with the developmental pediatrician that diagnosed David on the autism spectrum, sensory processing disorder, impaired fine and gross motor skills and the list goes on with issues all related to his autism. While waiting for this appointment, I met a mother who was going to be seen before us and was here for their initial evaluation...I knew what she was about to experience, the emotions, stress...the fear. We weren't able to talk much, but I told her this "remember it is just a diagnosis, something that your child is living with...but it is not who your child is." She was called back just after that and I was fighting back tears, remembering everything I felt 6 months ago.

Our appointment today, did not go as well as I was praying it would...it happens, there are ups and downs, but it really hit hard because we have been working so hard with him and trying to give him all the resources his needs to achieve great things in life...and it just didn't seem to matter. All his evaluations came back that he is still mentally and functionally in the same place he was when we first started our journey...despite everything we have done. The progress he has made, doesn't seem to matter as it isn't what they feel is important, but did we get strategies or ideas to work towards what is...not really, do I even know what is right now...no. But on the way back home after being there all day, I started saying the things I wish I had known from the start to help get us through the tough days...so here is my list of things I would say to someone just starting their journey with a special needs child of any condition and maybe some of you will find peace or comfort knowing you aren't alone.

  • There will be troubles ~ it won't be easy and it won't be fun...but it will always be worth it. Those accomplishments no matter how insignificant they are to the "professionals" they were enough to make you smile ear to ear and shed a couple of tears even...they are important not only to you, but to your child.
  • Your child has _________ (insert diagnosis there), but they are not __________ (insert same thing). If you google their diagnosis or look it up in a medical text, you will not find your child's photo there, not even their name. It is something to live with, but not let live their life for them.
  • Researching isn't a bad thing....IN MODERATION. We live in a day and age where you can find hundreds of thousands of articles, papers, blogs, websites and just general opinions about almost anything you can think of and it is great to read and learn as much as you can about your child's condition...but it can also harm you. CREDIBLE resources are key, but sitting in front of a computer for 8 hours straight isn't going to help you either.
  • All the dreams, plans and ideas you had for your child may not happen, but it is okay. They were YOUR dreams for your child, not their dreams. Let them have their own dreams, challenge them to reach their dreams and support them each step of the way...what they end up liking and becoming will amaze you.
  • You will hear the words "never, can't, won't and don't" from therapists, doctors and specialist alike...but as long as you don't use those words towards or about your child (other than protecting their safety of course) they can never be limited in what they can accomplish (learning this one ourselves).
  • Your child will get tired from appointments, therapy and testing...and it is that much more tiring on you. Hang in there and try not to cram too much into one day if possible or schedule a break between appointments even. Down time is necessary to regroup, recharge and take on the next thing.
  • ALWAYS remember if you are not comfortable with something to ASK questions...I call our pediatrician first with all my questions because other than us, she has known and sees David the most and has watched him grow on the medical aspect. She is my go-to lady with all my questions...and if she doesn't know, she talks directly to the department necessary and we make a group plan.
  • Children sense your emotions, so when you are upset they act a fool, when you are sad they want to comfort you and when you are happy they give you more reasons to smile...remember to love on them through all of these emotions, so they know despite the craziness of it all, they are loved.
  • Last of all NEVER, EVER GIVE UP. If you are told "this is the best things are going to be, we will see you in 6 months" take those 6 months as a challenge to show them your child has the potential you know they have. 
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Now that have just been the most random list of things ever...but I hope it helps.

If you can have snow and a rainbow at the same time, there is always hope for a better tomorrow.

The Kidds

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