Gracie's Gowns
Follow Gracie's Gowns on Facebook
  • Home
    • Our Story
    • Programs
    • Our Sponsors
    • Contact
    • In the News
  • Request a Gown
    • Sponsorship Opportunities
  • How to Help
    • Donate
    • Sewing Opportunities
    • Shop
    • Events >
      • Crawlin'4 Gracie's Gowns
  • Our Angels
  • Giving Back
    • Gown Donations
    • Hem/Onc Donations
    • Fabric Donations
    • Pampering Kits
  • Our Blog

Operation NICU Surprise - Tripler Army Medical Center (Hawaii)

5/20/2014

0 Comments

 
Picture
Earlier in the month we asked everyone on our Facebook page to nominate a NICU and/or Hematology/Oncology unit or clinic that was there favorite to receive a special surprise from Gracie's Gowns!

We are choosing two NICUs and two Hematology/Oncology units from those nominated to receive a special box from us. The first NICU was chosen - and it is going to Tripler Army Medical Center's NICU in Honolulu, Hawaii! Jennifer nominated the hospital after her son Colton (who is also a Gracie's Gowns recipient) was born and cared for by the NICU staff. She was awesome enough to include a story of his stay and just how wonderful the staff was - and some sweet photos to share as well!

Picture
Here is her precious Colton when he was born and cared for back in August of 2011. She includes the following about the hospital and staff at Tripler Army Medical Center's NICU.


"Our son was in the NICU for 12 days in August 2011. Our pregnancy with my son was very rough. Not many doctors believed he would make it or he wouldn't live long after brith. The NICU was just very amazing with him. They did everything they could to help him and it was so nice to finally have someone believe in him. They felt like family to us when we were there. And they just went above and beyond for my son. The NICU staff was just amazing! My son had an MRI when he was 1 1/2 months old and they let my son back into the NICU to be observed overnight bc they knew I was very uncomfortable with him going to the PICU with a bunch of sick kids. They were very understanding and cared very much for my son! And being a Military Hospital a lot of kids are in there with just one parent and no other family members to help them out during a stressful time in life and they could use a little a cute hospital gown!"

The photo above on the left is Colton in his gown from us back in September of last year (2013) and the photo on the right is him today at 2.5 years old! Look how much he has grown and how precious that smile is!! Way to go Colton - you've come so far and we have no doubt it was because of the fabulous start and care you have received since coming into this world! 
Picture
So what's the surprise we're sending to Tripler Army Medical Center's NICU?

Well, we are sending them thirty NICU smocks to be distributed to the babies they care for! We know it doesn't remotely even make a dent into the 1,100 babies they serve annually, but at least there will be thirty styling babies this year!

These will be sent out this week to Hawaii and we hope they are received with much love and bring many smiles to the families that receive on of the gowns!

Picture
Thank you Jennifer for nominating Triple Army Medical Center's NICU and sharing Colton's NICU story with us and allowing us to share it with all that may read our posting!

Thank you as well to Kim for sewing pretty much every single one of these thirty gowns going to the NICU (after we drew the name - we learned Kim's granddaughter was born at this hospital as well, but fortunately did not need to be admitted to the NICU). 

Stay tuned for our second NICU to be drawn once we have the items completed - but also for our Hematology and Oncology units/clinics to be chosen!

Lots of Gracie's Gowns cuteness to come!
0 Comments

A Little Break in Routine

4/15/2014

1 Comment

 
Picture
Okay - so old picture, but had to use something with the sewing machine. I love sewing these hospital gowns, I love sewing them for your little ones and seeing their smiling faces and knowing how it can literally change a hospital experience from bad to at least tolerable. 

Sometimes though, I have to break the routine of making gowns and work on other projects, just to keep from crying over how many precious little ones are in need of such an item. It breaks my heart in so many pieces at times, that I have to sit back and remember how much of a blessing each child is, how they have changed the lives of those around them...how they fight, just to make it through another day and while yes, the odds are usually stacked against them, they inspire others to do such amazing things - like Gracie's Gowns and so many other organizations!

Picture
One of the items that have been done and still being worked on were these squishy little monsters! We sold them over the course of a couple days in order to raise shipping funds for gowns.

I am happy to say they are almost all done and out in the mail (still have maybe 7 more in total to make I believe). Here is some of the ones that went out last week, as I didn't get pictures of the previous ones made to post. My apologies on that...they are too cute not to picture and post.

These guys come from leftover minky fabric that I have from making millions of blankets over the last few years I have been making for friends and family.

Picture
One of the other items that get worked on in those little breaks are some bags for Beads of Courage - I love making these little bags from leftover pieces from gowns!

They are easy enough to make and still give that feeling of inspiration and fulfillment I suppose in knowing the fabric we use won't go to waste and can brighten the days of so many other children too.

This year we have 17 bags made so far to donate to Beads of Courage and will probably have close to 50 by the time the donation is ready to be made. We are hoping to be able to donate them to our local hospital with a Beads of Courage program. 

Lastly, whenever I really want to venture out into my sewing fun - I go back to making little items from leftover pieces of fabric and working through my own personal fabric stash and creating other items that we will be taking with us for our craft show in October - last year we raised $900 for Gracie's Gowns with items made from leftover pieces and whatever fabric I had on hand - this year we're hoping to meet and exceed that amount...especially with the Christmas Box Program coming up at that time of the year as well. Right now we've loaded the items into an etsy store (which will be put in vacation the Thursday before the show) to try and sell some of the items throughout the year with all the money being put into our shipping expenses. So here is the etsy mini with links in case you want to browse it!
With all that fun being said and shown - no worries, gowns are still being made, still being sent out and Gracie's Gowns is rolling right along like we always do. Sometimes just a little slower than normal, because we are in the process of moving and my health has gotten a little "interesting" for lack of a better word, but we are still upholding and maintaining our mission to provide every child we can a special hospital gown of their own to wear while in treatments, surgeries and hospital stays!

Much Love and Many Blessings,
Jessica
1 Comment

Donation to the Little and Dependent

1/25/2014

0 Comments

 
Picture
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.

Picture
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.

Picture
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.

Picture
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.

Picture
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.
0 Comments

Fingers and Toes

8/1/2013

0 Comments

 
Picture
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
Picture
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. 
0 Comments

Working Together and Latching On

8/1/2013

0 Comments

 
This is a bit off from my normal blogs for Gracie's Gowns, but I wanted to share an exciting event that is taking place this weekend near us.

The event is called The Big Latch On - and with next week being World Breastfeeding Week, couldn't be a more appropriate time to host such an event. The event in our area is located in Culpeper, Virginia at Yowell Meadow Park.
Picture
As a mother to three children - the importance of breastfeeding is huge, especially when David and Madeline were born, not only did it become important for my own health and wellness, but also to help save our family money on formula costs. I was never able to nurse Aubrey, the NICU at the hospital we delivered at wasn't very helpful and really wasn't on board with breastfeeding, so when we brought her home and I tried to nurse, it just wasn't happening and became very frustrating for us both. It also turned out that she had a milk allergy. When I wasn't able to continue nursing David because he wasn't gaining any weight, I searched and searched for someone that would be able to donate milk, because I knew the benefits for his own health...unfortunately, I wasn't able to find anyone...and the same with Madeline when I had to wean her from nursing because of the surgery I was going to have on my neck.

It was depressing for me to stop nursing Madeline because she was so great - and healthy and the bonding time was amazing! I loved every second, but I was also working a job that wasn't near as supportive in allowing me time to pump between transports or even the right environment. I lucked out in comparison to my fellow co-workers that were also nursing mothers, but it was still rough.

Anyway - one day while surfing Facebook I came across Pink Cocoon and was just blown away. Cindy is an amazing woman and actually helped Culpeper Regional Hospital become the first Baby Friendly Hospital in the Commonwealth of Virginia. I was working at the hospital when the announcement was made they received the accreditation, it was amazing! Cindy has gone above and beyond in the region since then holding meetings, breastfeeding consultations, Douala services, childbirth classes and so much more...all while working in the birthing center at Culpeper Regional Hospital. And this weekend she is organizing The Big Latch On event.
Picture
So where does Gracie's Gowns fit into the picture? Well most know that I have sewn for several years now, and before the last 18 months of sewing our precious hospital gowns I sewed everything from quilts to burp cloths, nap mats to i-spy bags and several reusable items - reusable snack and sandwich bags, organic hot/cold packs, cloth diapers, un-paper towels and reusable nursing pads. This past weekend I was going through my containers of items I have sewn for sale at craft shows, and found a couple nursing covers and several sets of reusable nursing pads. I gathered the items and messaged Cindy on Facebook offering them to her for The Big Latch On this weekend to use a raffle items/goodie bags, whatever she'd like to use them for.

The other amazing part is Cindy also asked for a sample of our Newborn gowns for use at Culpeper Regional Hospital in the birthing center. We've already donated some 2-4 size gowns to the hospital for use in their Step-Down unit. They are reused by the hospital because they don't have that many children admitted, and when they do they don't stay very long. We will also be making them some 6-10 size gowns as well this year.

Here is the package we sent over to Cindy for The Big Latch On event this Saturday - anyone that is in or around the area is welcome to attend. Groups of breastfeeding women coming together at registered locations around the world to all latch on their child at a set time. All the breastfeeding women and children are latched on for one minute at the set time and are counted by the witnesses. The numbers are added up and we see if we can beat previous Big Latch On records or maybe even the world record! 
Picture
Good luck to all participating in The Big Latch On event this weekend and enjoy nursing your babies together! Hope those that win the items we donated like them!
0 Comments

Gracie's Gowns Meets: Callista

1/1/2013

1 Comment

 
Picture
Going to start out the new year, yes it really is 2013 already, by introducing you all to a few more of the kiddos that we have made gowns for. This morning I am going to tell you a little about Miss. Callista!


Callista an 11 month old little girl with Spina Bifida and Chiari Malformation. I remember when I first even knew about Spina Bifida it was from a picture on the refrigerator of the parents of a friend of the guy I was dating at the time (follow that...anyway) it was from the newspaper article of the very FIRST fetal surgery being done on a baby with Spina Bifida and the baby reached out and grabbed the doctor's finger. Anyone else remember that? Well now that is almost STANDARD practice for these precious little ones!


Here is what little Callista has undergone since the fetal surgery from her mommy:
Callista and I underwent fetal surgery to repair her spina bifida when she was 22 weeks gestation at Vanderbilt Children's Hospital.

At 2 days old, she a shunt placed for hydrocephalus.

At two months old she had a decompression surgery.

At four months old she had a g-tube placed.

At eight months old she had a double hernia repair and a vesicostomy.

She currently has physical and occupational therapy 1-2 times a week.

These precious sweet pea still has a long way to go with more surgeries potentially in her future, the need for leg braces so she can being to bear weight and learn to walk (my son had to wear leg braces because he was bow-legged...this was not a fun experience for him or us, but one that luckily we didn't have to continue for a considerably amount of time) and she may also need a wheelchair in the future. 


I've had the joy in celebrating some successes with Callista through her Facebook group and watching her grow and develop. Even though she is delayed compared to most children, she is meeting milestones in her own time and fashion and it is such a joy to see her and her family get so excited about what she is able to accomplish now!


Here is another bit from Callista's mommy about her journey so far:
The most frightening thing was the initial fetal surgery as we had to deal with the fact that we could lose her by trying to help her. She could have been born extremely early because of the surgery as well.

We also had a pretty frightening beginning. 12 days after we were allowed to bring her home, she started acting very funny. We took her to the ER and thank goodness we did. As soon as we got there, she stopped breathing and turned blue. They rescued her quickly but we ended up with another 2 month stay in the hospital where they did her decompression.

The most exciting part of our lives is just simply seeing her grow. Although she is far behind on her developmental milestones, every time she reaches one is a celebration. She is beginning to support her own head and has said her first word (Da-Da!).

Picture



And here is the precious little princess!!



To follow and support Callista visit the following pages:
https://www.facebook.com/groups/callistasjourney

http://www.callistasjourney.blogspot.com

To learn more about Spina Bifida you can visit the following website (there are TONS of resources and information out there, but this is one that I liked):
http://www.spinabifida.net/

1 Comment

Pink and Blue in October? 

10/11/2012

0 Comments

 
Picture
October is typically seen as Breast Cancer Awareness Month and don't get me wrong, that is definitely a worthy cause that needs to be funded greatly, but it is also a month that raises awareness for something a little closer to home...

October (particularly the 15th), is Pregnancy and Infant Loss Awareness Month as well. This was established in 1988 by President Ronald Reagan (which I love...and his wife too!). The former president was quoted to say this:
 
    "When a child loses a parent, they are called an orphan. When a spouse loses his or her partner, they are called a widow or widower. When parents lose their child, there isn't a word to describe them. This month recognizes the loss so many parents experience across the United States and around the world. It is also meant to inform and provide resources for parents who have lost children due to miscarriage, ectopic pregnancy, molar pregnancy, stillbirths, birth defects, SIDS and other causes."

How well said is that?? It is even more important when you look at the statistics and see that over 15% of pregnancies over the past several years ended in either miscarriages or stillbirths. My husband and I have lost two babies due to miscarriage, both early in pregnancy, but far enough along, they had a heartbeat, a personality, a soul...a purpose that was better served in Heaven than here on Earth.

Our first miscarriage was in 2007...new year's eve to be exact. And it was a miscarriage that we didn't know we were pregnant until we miscarried. Our oldest was only 5 months old, that last thing we were expecting was another baby. They determined based off hormone levels we were roughly 9wks. We saw Aubrey's heartbeat at 6wks...we heard her's at 10wks using the doppler...this was crushing for us. We named our baby Serenity Grace (now of course we did not know the gender, but it was a fitting name). 

Several years went by, two more complicated pregnancies, but two healthy babies became a part of our family and then last fall, the night of our 5th wedding anniversary, I told my husband we were pregnant again!! We were shocked, I had my tubes tied after my c-section with Madeline, but we were happy! It was truly the hand of God at work...and then about 5wks later, we loss our precious miracle baby. Once again roughly a 9-10wk gestation. We were shattered, especially me. How could I be give something so special...just to have it taken almost immediately away?! We named this baby John Ezekiel, and once again we didn't know the baby's gender, but the name just seemed to fit. 

Now with this, I do not want to down play any other awareness cause that is in October, but I know many of those who read this are impacted deeply by a pregnancy loss, or the loss of an infant. Either you are the mother, sister, aunt, grandmother, father, brother, grandfather, uncle, god-parent, best friend of someone with a loss, etc. It is a reminder that while it may have been years ago...the pain is still there. And sometimes, it is just nice to know that you still think about them and remember their loss.

So, on October 15th, light a candle for your angel babies. Even if you have not had a pregnancy loss, or lost an infant, light a candle in honor and remembrance of those who have. I know there are several precious little ones who have gone to dance in Heaven over the past few weeks and months that I have been working on Gracie's Gowns...my candle will be going in their honor and in remembrance of my own angel babies.

Say a prayer for these families, as they continue to cope with the loss of their child over the days, weeks, months and years to come. No matter how far along, or how old...the loss of a child creates a void that can never be filled in our hearts.

Picture
"Your eyes saw my unformed body;
all the days ordained for me were written in your book
before one of them came to be."
Psalms 139: 16


The Kidds
Gracie's Gowns
0 Comments

Eye of the Storm

10/10/2012

0 Comments

 
Picture
What a week and it is only Wednesday night!! And I can't say this is a week that I would ever want to relive. And I know that sounds silly to many of you, because you go through much more complex surgeries and treatments and the life of your child is literally in limbo depending on how the procedure/treatment does or doesn't work...but for me, this was probably one of the most terrifying experiences of my life to date.

We learned today though, that a lot of the issues we had in the PACU and post-op recovery, were related to David's autism and the fact that "in general" child with autism tend to breathe off the anesthesia quicker than children who do not have it, but also once they are "awake" it is sensory overload to the extreme because everything comes back to them all at the same time. But even more so, we learned for fact after having the physician review the anesthesiologist report, that David was not breathing on his own for a "period of time" when he should have been and that his heart stopped as well...so much for a routine surgery right?

I knew something wasn't right, I knew something happened to my baby...and now it was confirmed. And while they do not think at this time it will or have caused any damage, I realize just how fragile even the life of my own children can be. The picture at the top, is David holding onto my hand the best he could on his chest while watching a movie. It is a moment I will never forget...it was the most calming moment of the time in the hospital. 

This first part of October is always a test for me emotionally and mentally. It is something that nearly ruins my family every year...and this year was no different. I was ready to leave everything behind and go in whatever direction the wind took me. My mother died 22 years ago this past Monday, which was also the day of David's surgery...and I almost lost my son. First and foremost, I am a mother, my children ARE my job and as miserable as I can be sometimes, their needs will always come first. Without them, I would be even more lost than I already am.

While in the hospital with David and everything that he was going through and in turn I was going through, I didn't have time to do ANYTHING I thought I would be able to there. The theory was he would sleep a good bit, and he didn't. My poor kiddo didn't fall asleep until 9:30p Monday night, after being up since 4:30a (minus while he was in surgery)...and by then, I was exhausted! Even in how tired I was, I was able to stay level-headed for his sake, take care of his needs and comfort him in every way possible. He kept me calm in return.

And while there is a storm going on inside my life...the moments my children want to cuddle, love, hug and just be around mommy, are the calm, the center of who I am...and sometimes, the only reason I am still here. I don't remember having that type of bond with my own mother...to be honest, there isn't much that I do remember about her anymore. So, even more of a reason I will NOT deny my children the mother that they deserve to have in their life.

Below is one of my favorite pictures of my mother and I. Looking at myself in the picture compared to others...this would have been very close to the time she committed suicide. Either the summer before or the fall during (and assuming by the pants and all, the fall because it is cooler at the beach this time of year). 
Picture
I will close with this quote ~ it is one that I have loved since the first moment I read it, one that brings me to tears and yet fills me with honor at the same time. A quote I plan to pass down to my daughters and granddaughters and if I am lucky enough, my great-granddaughters. 


"A daughter needs a mom, because without her she will have less in her life than she deserves."




God Bless,
The Kidds
Gracie's Gowns
0 Comments

    Archives

    October 2020
    January 2020
    May 2019
    March 2019
    August 2018
    July 2018
    April 2017
    February 2017
    January 2017
    December 2016
    November 2016
    October 2016
    August 2016
    July 2016
    February 2016
    December 2015
    September 2015
    August 2015
    July 2015
    May 2015
    April 2015
    March 2015
    February 2015
    January 2015
    December 2014
    November 2014
    September 2014
    July 2014
    June 2014
    May 2014
    April 2014
    March 2014
    February 2014
    January 2014
    December 2013
    November 2013
    September 2013
    August 2013
    June 2013
    March 2013
    January 2013
    December 2012
    November 2012
    October 2012
    September 2012
    August 2012
    July 2012
    June 2012
    May 2012

    Categories

    All
    Angel Love Boxes
    Autism
    Awareness
    Bake Sale
    Bead
    Beads Of Courage
    Bee Brave
    Big Latch On
    Blanket
    Brain
    Brayden
    Breastfeeding
    Build A Bear
    Build-a-Bear
    Busy Buddy
    Butterfly
    Caringbridge
    Cathedral
    Chartres
    Chd
    Christmas Box Project
    Cope
    Cure
    Daysforgirlsinternational
    Donations
    Dreams
    Drug Dependent
    Drug-Dependent
    Event
    Fabric
    Facebook
    Faith
    Family
    Fear
    Feeding Tube
    Fingers
    France
    Fundraiser
    Goals
    God
    Gracie's Gowns
    Gracie's Gowns
    Handful Of Hope
    Harley
    Healing Helpers
    Healing Helpers
    Heart
    Hope
    Inspire
    Invisible
    Juvenile Dermatomyositis
    Kamsnaps
    Karingforkyler
    Lia Sophia
    Lilahroo's
    Loss
    Love Monster
    Madelyn's Hats
    Maggie's Sticker Box
    Mothers
    Mps
    Mucopolysaccharidosis
    Neonatal Abstinence Syndrome
    Neuroblastoma
    Neuropathy
    NICU Smock
    Nursing
    Nursing Cover
    Nursing Pad
    Pampered Chef
    Payitforward
    Pediatric Cancer
    Pink Cocoon
    Prayer
    Pregnancy
    Promise
    Quilt
    Raffle
    Record
    Remembrance
    Scentsy
    Selvage
    Sensory
    Siblings
    Socks4Surgery
    Special Needs
    Special Needs
    Sponsor
    St. Jude
    Sugarbooger
    Surgery
    The Gocf
    Timbuk2
    Toes
    TPN/Tube Feed
    Travel
    Treatment
    Tubies
    Weighted Blanket
    World
    Worry
    Yard Sale
    Yowell Meadow Park

    RSS Feed

Proudly powered by Weebly