May 2 2016

365 days since I last saw your little faces.

Life is so wonderful and more than I could ever imagined possible a year ago. It looks almost perfect from the outside looking in, but the truth is, it's never going to be fully complete just like I'll never fully heal. All these emotions and memories only become tolerable, never easier. 

I was sent three perfect miracles that have brought a level of healing some people will never have. How such an amazing blessing landed in my lap is only explained by a miracle. 

Sometimes I just like to pretend you three were sent back to me... And you really aren't gone.

Thank you for my perfect miracles. I know you guarded them&

I look for each of you in their faces. 

I will share (for the benefit of others that are or will brave the journey again...)

This pregnancy I put myself on auto pilot just wanted to get past the weeks and to the day I would meet them... Some days, most days, I believed I would lose them also. Constantly waiting for the "other shoe to drop" why wouldn't it... When something so horrific has happened once, you'll never feel exempt from disaster again. You'll never say never... 

You actually believe it's just part of your normal. I was actually convinced if nothing happened to them... It would be me. I was not going to be able to enjoy them... They weren't "real" yet, and maybe they never would be to me.

I was petrified during the entire csection... Waiting for my stats to drop, blood loss, I was the crazy patient that in the days leading up I was asking about iron infusions and blood transfusions to make sure I could have control of something... I would do anything to make sure it all went ok.

Time ticked by so slow it seemed like forever while I was in the middle of it, but now it's over, they are here. Safe. So I am. It happened So much faster than I thought possible. It's bitter sweet. I don't regret being fearful or closing myself up- that's what you do when you've lost a child, children and you've been put back at the start of a scary similar race...

BUT

 If there's one thing I've learned is time stops for no one. It keeps going and that's a good thing because it keeps you going too. For now my mind is still trying to catch up to my body.. 
I'm desperately trying to comprehend the fact they are indeed mine, all mine.
They are here with me...

To my children, What an amazing gift you've given me and what priceless lessons you've all taught me. You've given me something to stand for and live for. I will not stop talking, because my children are worth talking about and what I suffered through, my diagnosis, was and IS preventable. 

I WILL speak out for my children, and for others. 

Our Family Tradition.

May 2015

May 2, 2016

To know me Is to know them. 

Who I am right now, today, is because of them. I have more compassion, empathy and sensitivity than I've ever carried. They are a blessing not a sad story. 

"34 weeks"

My babies are 2 weeks old!

or "34 weeks"

Oh my!

My "goal" was 34 weeks, but what a wonderful surprise

 to get to meet them earlier than expected.

How blessed we are that they are so healthy and learning what they need to come home with us! 

Over the past week they have lost alittle weight, but then gained it back plus more. Asher and Aspen are wearing big boy and girl clothes! No more just diapers. Cross our tiny boy wore his first outfit today! He just needs a bit more fat to help him maintain his body temp and will be catching up soon!

Last week Aspen and Asher's oxygen was removed, Cross did not require any since birth, no more IVs, they are now feeder-growers! They are tolerating their feeds and taking their vitamins:). 

The doctor ordered a brain sono just as a precaution, major problems are rare at 32 weeks, but I'm thankful for the extra Checking. Everything was normal. 

They are starting to learn how to eat orally, they are making great progress and eating more everytime we try. Aspen is food motivated! Most of the time she takes her whole feed in the bottle, if she keeps this up she will be coming home first!

They love to be held and we love to hold them... 

They make the sweetest noises like little baby dinosaurs. 

The last few days have been pretty exciting (for me). 

Saturday

We had a photographer from "The tiny footprints project" come take photos of them. It's a wonderful organization that provides this free service to NICU families. We will look back on these memories and smile. We are so blessed. There is currently only photography for the DFW area, so if you are a photographer please consider donating alittle of your time- what a beautiful service you'd be providing. 

Today 

I got to snuggle them all skin to skin -together- for the first time. Cross thought he was an only child and was enjoying his freedom... He was a worm and fussy, then he got some lunch in his tummy and settled down alittle. It was pretty magical.

 I still can't believe they are mine... 

Here are some pictures our nurse took while the photographer was there so I could have a few now, I'm so impatient! 

And some pictures from today... Our skin to skin time. 

Thanks to everyone for being apart of our journey. We have no clue how we got so lucky. 

This is what a MIRACLE looks like...

Aspen, Cross, Asher 

If you think my hands are full, you should see my heart. 

Soon enough they will be too big to hold together. 

God IS Good.

SHOWER!

We were lucky enough be given two beautiful showers by amazing friends and family who love us and the babies SO much. We constantly feel supported and encouraged by those around us and that is the BEST gift.


My first Shower was given at 25 weeks and I was feeling pretty good, measuring in at around 32(ish) weeks... Most recently at 29 weeks I attended my 2nd! Boy, does 4 weeks make a difference when your carrying triplets! We played a game at the first shower where they measured "my circumference"... we repeated this game recently I've grown 3-4 inches around! I'm feeling it, but I am too blessed to be stressed.

These days I'm measuring around 38(ish) weeks!We are doing great, healthy and if we continue this trend we hope to make it 4-6 more weeks!

We want the healthiest premies we can manage so the longer we keep cooking the less time they will be on feed tubes, in isolation, hooked up to monitors etc.

DRINK OFF! Apple Juice out of Bottle, Jordan was a CHAMP.

I was really worried I would be on bed rest, hospital or at home by this time, but I am amazed by the TAC how secure it's made me feel. It's a God send, and without I know we would not be here!

We have an article coming out in Shattered Magazine this summer-

Please stay tuned I can't wait to share it with all of you. It's all about our journey over the past year.

We are of course overwhelmed by the amount of gifts and support!

Thanks a million we can never tell you enough.

TAC Surgery day.

There's nothing quite like the "empty sonogram" after a loss.

It's surprisingly painful and emotional. A lot of first...

Good news... everything looks good and procedure is about to start! 

I arrive at the hospital, get checked and they take me to my room to wait. The sterile, gloomy environment is too much and the tears start... another first... I'll admit I use to enjoy hospital stays, it's like a hotel, but better you lay in a bed and people take care of you!

Not after experiencing death. In this way. 

I wipe the tears away and I am brave.

As I am being wheeled into the OR to place my TAC I can't help but think about Jax, Stella and Beck. If only I could have saved them. If there was anyone who would do anything to go back in time, it's me. After losing them I threw myself into the whys- I came up with a million reasons and several were my own fault... I found peace finally. It was my body.

I don't  I Stopped blaming myself. I'm angry yes, could more have been done, maybe...  

Would they have still be born early... Probably.
I realize I can't control everything.

Two of my MOST favorite quotes. 

I'm no longer so focused on the fact my body failed me, and the "I wish I would've knowns" and all those other issues. I've made a decision to do all that I can do for anything that may happen in the future, It's not like I'm just left standing here with nothing; I'm armed with the knowledge and the resources and the fact that I can do this!

My complication potenically has a solution, and for that I am so thankful for. I am so thankful I went searching on the internet. I am so glad for the breakdown I had when I found out a TAC may have saved them... It helped me say YES I am doing this! Even thought it's too late to save them... It's another page turned in my story of healing.

The pain of losing Jax, Stella and back has pushed me to choose the most invasive procedure, but with the highest success rate. 

This procedure is life changing.

I can not trust my body so I have done all that I can do to help it. 

The dreams of having my triplets did not come true, 

but my dream of having a family and siblings for then will come true. 

Sometimes you have to be your own hero. 

You have to know what is good for you and go for it. 

No matter what anyone is telling you or what the medical books say... Go for it. 

I'm sore, uncomfortable and I've added a few more scars to my canvas,
 but this pain is nothing compare the hurt of loss. 

I don't care about anything that I have to endure as long as that means

 that I have a healthy family and that makes me feel like a mom.

I'm finally feeling almost back to normal and I have hope for the future and
 I'm bringing them with me.

Angels among us

This is just a little thank you, because I'll never be able to adequately show the amount of appreciation and gratitude I have for the many people who have reached out. (and continue)
Without you I'm not sure if I would be here.

"Some of my best friends I have never met in person. I know them only through Facebook, But that's ok- Friendship is not about touching the hand of another but rather it is touching their heart and should."

I am lucky enough to be surround by people of all ages, all walks of life that have sat with me, cried with me and talked with.  Have invited me to lunch, who've cooked & brought it to us.

Thank you. To the angels that sent cards and flowers, and to those who just kept us in their prayers.

Thank you. To those who are facing their own loss and found the strength to reach out... Thank you.

I joke I am getting so spoiled by this love... I may not recover.

The gifts given in their memory are my most favorite possessions
Every single one of them I will keep forever. 

Recently, The most incredible woman sent me a personalized gift (there were actually several bundled together).

The amount of time spent making this is absolutely unbelievable. I'm just, I'm speechless, I'm at a loss of words for what she has done for me, for what everyone has done. The most beautiful part- this lovely lady is not a friend that I talk to every day, we don't text, we don't call each other or hang out on the weekends, our paths crossed in high school and we have managed to stay in touch; Mostly by Facebook. But she is a woman who knows... she is one of the most creative and cutest women I have the pleasure of knowing. That is what makes this even more special to me.

She also has 2 young boys of her own that she took time away from to focus on me and mine, and created something just so personalized, and thought out. I was speechless. For weeks she would send me pictures teasing me daily of this beautiful project she was working on.

When I finally received it and held it in my hands I just didn't know what to do first. Tears flowed as I opened the box to everything Jax, Stella, and Beck- More happy tears than sad ones this time! I was overwhelmed. The pictures she has been sending over the past few weeks were a shadow compared to the final product. She did not let me down, she gave me hope, happiness, validation all at once.

I could spent hours reading and focusing the beautiful embellishments and verses. I love that she used some of my favorite quotes and added ones she knew would be appreciated.
In it I received a journaling bible that she has so beautifully started, a note pad for recording and remembering passages, inspiring notes, a handmade mug... it's a box full of art.

I don't need to speak her name because like she said,

"Let them bless you without giving recognition, because Jesus will give them recognition in Heaven and fill their crown with jewels!"

I show you these photos so you can share in the hope and healing I've gained from this. 

All of this giving has shown me that even the smallest gesture can have a HUGE impact... 

at a time when it's needed most.

I CAN NOT SAY IT ENOUGH

"Sometimes there are stormy moments in your life when your friends do more than just walk with you; they become angels that carry you and protect you with their wings."

Medically Necessary, not experimental!

Some people probably think I'm crazy, or worse, 

for being this open.

but I KNOW I am being helpful.
I will not apologize or be ashamed.

I would not be where I am right now without the help, research and knowledge of other woman who have been exactly where I am now. Their testimonies, their loses and their happiness after the darkest time in their life; reading their experiences gave me hope. When you've lost everything,

Hope is the ONLY thing you have to hold on to.

I announce the news of my surgery being covered by my insurance!
All my hospital visits, procedures, and their birth have led me to meet my deductibles and out-of-pockets for the year. (strange to be happy about that...)

They have approved this procedure as medically necessary, not experimental! 

Thank you LORD. 
We would have paid it without hesitation, regardless, but what a blessing to have one less burden on our plate.

Let me say that God broke me down and is slowly building me back up. That is what it felt like when I found out what a Trans-abdominal Cerclage was. The tears, the anger, devastation overwhelmed me. Why couldn't I know then what I know now... 

WHY CAN'T I HAVE A SECOND CHANCE.

I'm taking this as my second chance. 

It's all very bitter-sweet, I say this as tears well up in my eyes.

It's tears of happiness and sadness.

Thank you for the prayers and encouragements. 

If I haven't thanked you personally 

-PLEASE-

know that your actions are seen and heard and felt.

You are all an important part of my story.

MY SURGERY IS SET FOR WED, AUG 26TH.

Be your own hero...

Should be my new motto.

If words like cervix, transvaginal, uterus bother you- turn back now!

Who knew this journey would have so many medical terms and obstacles along the way...

This post is to educate and explain your options if you are a woman who may be in the same situation. 

Incompetent Cerivx, IC, weak cervix  etc... this is something that does not get enough exposure but nearly 1 in 100 pregnancies are lost each year due to some sort of IC. It's not commonly tested for, and I only know if this because I had a dear friend who lost a baby girl 3 years ago and if it happened to her, why couldn’t it happen to me? This was always in the forefront of my mind and that is what caused me to really monitor my body and say something when I did.

"Incompetent cervix is not routinely checked for during pregnancy and therefore is not usually diagnosed until after a second or third trimester miscarriage has occurred. Women can be evaluated before pregnancy, or in early pregnancy by ultrasound, if they have any of the factors that are potential causes of incompetent cervix. Diagnosis can be made by your physician though a pelvic exam or by an ultrasound. The ultrasound would be used to measure the cervical opening or the length of the cervix."

Because of there is lack of proactivity, woman have to suffer loss after loss before a solution is put in place.

THIS IS A PROBLEM.

Some Doctors encourage you to "just wait and see"

How many women would be ok with, "Lets wait and see if your body will hold your baby, or if it will go into labor too early to save your child"

If you're reading this chances are you have heard our story. 

According to the many conversations I've had with Drs I had preterm labor secondary to Incompetent cervix with Jax, Stella and Beck that ultimately sent me into preterm labor. My body was unable to hold the growing bodies of my babies, I started to dilate and thankfully I followed my instincts had my Dr check everything at 16 weeks. 

I saw the worry on his face and he sent me straight to the hospital where he preform an emergency cerclage(TVC) with only 1.5mm of cervix remaining to work with. (That's not a lot. At.all.)
By the time we realized all that was happening it was really too late... but we did all that we could do at that time. 

I can't begin to tell you how long those 2 hours felt, the fear, panic. 

I was sewn closed. 

He said I was my own hero that day. 

I stayed in the hospital a few days while they pumped me full of antibiotics and 

monitored how it was holding.

2 weeks later I funneled down to the stitch Jax's head was down, 

 "knocking at heavens doors". 

(I'm allowed some dark humor) 

This is worst case scenario at only 19 weeks. 

This is why multiples are so rare and so high risk.
Through everything I've researched and women I've talked to ...You can almost guarantee your going to have cervical complications carrying multiples. Preterm delivery is extremely common, your body thinks your further along than you are... but I had a few things working against me. 

All of this worth every second I had with them. They lit a fire in me and I'm determined to do everything I can to change the outcome for their siblings.

     I'd like to ask for prayers.

Prayers for a clear mind while we make a decision that can alter our family's future forever.

 we face a difficult, but life changing decision. 

We can use the TVC (transvaginal cerclage) -again- (technically)I don't think it failed me, but  I truly dd not have it long enough to find out and with a TVC you are on bed rest. However with a TAC (transadominal cerclage) they are placed much higher and it's *almost* impossible to funnel past the band or rupture membranes. This virtually guarantees I will make it full term, although anything can happen. 

I feel like I have no control over anything, but this is something I can do.

It's like a broken record in my head 'Could I have done more'...but now armed with knowledge, I can do more. They did not die in vain and I will do everything I can for them even though they are gone.

I need guidance on which to go with,

I've survived I'm surviving the loss of my first 3 babies- I can not do it again whether 1 2 or 3 again. 

Here is why the decision is more complicated than it seems- the TAC (transadominal) is a surgery. They cut you open like a csection, go around abdominal muscles and place the band at the highest point of your cervix. Once it is placed it's permanent. &You must have a c-section delivery. 

All terrifying for many reason.

But the possibility of losing another child is unbearable.

Did I mention there's only about 10 surgeons in the US that preform this procedure... leading surgeons are- #1 Dr.Haney in Chicago, #2 Dr. Davis in Tennessee. Neither are close to me. I could follow the trend- travel to Chicago and have the best surgeon place, but I located 2 highly recommended Drs in DFW. I meet with one tomorrow and the other Monday Aug. 17th.
I spoke directly with Dr. Haney and he is confident the TAC is the way to go, yes there are risk, there are always risk, but I am weighing my options.

 This decision is life changing and ultimately child saving. 

TVC is less invasion and successful around 80% of the time. They are removable and you can deliver naturally. This is what I had placed, and it held, but I funneled which is a concern- as the baby grows it presses on that stitch and it can possibly rip causing damage, or you may funnel past the stitch a that will cause premature rupture of membranes and preterm birth.

I hope if you are reading this you realize you have options. 

Trust your doctors, but ultimately you have to be willing to save yourself. 

Fight for what you want and search until you've found someone that will support you.

I have no idea what I plan to do at this point. I'm praying for clarity and comfort. I've had a lot of anxiety over this decision ever since I found out I have choices. When you read the facts- it's a pretty clear choice, TAC.

When Jax Stella and Beck were born so much blood was lost no one thought I would survive... facing a c-section scares me, and possible complications from the TAC and recovery, and so on. 

Our journey isn't easy, but it will be worth it.
Jax Stella and Beck's lives were not in vain they will save all their future siblings.
I only wish I could ave saved them. I promise I will not let them down. 

I plan on sharing this journey as well...
My procedure my recovery... and I hope beautiful things come from this.

All because of Jax Stella and Beck. They lit a fire in me no one can put out. 

3 Months

"Everybody has a chapter they don't read aloud. If you get to read that chapter in someone else's story, know that access to it is an honor. 

Sometimes the quiet parts carry the most treasure"

I never thought I would be so transparent. Believe it or not I'm actually quite a private person with anything personal, yes I'll always speak my opinions and beliefs but with personal matters I either hold it to myself or disclose to close friends and family. 

I'm happy Proud to share this Journey, it's really just about them. Not about me. I'm along for this ride. It's about me speaking their names, celebrating them, creating things for them, loving them.
I will never stop speaking their names. 

3 months ago,

I swaddled them up and said goodbye to their cold bodies, placed them in their baby casket. We snapped a few more photos, the only photos we would have of them. Forever frozen in time never to grow, never to walk. Beautiful little bodies photographed. Our most treasured possessions. 

We closed the lid and took them home. They didn't ride in a car seat, they rode in their baby casket in the back of our suburban we bought for them. This huge SUV is empty without them, 3 empty seats where their car seats should be. 

We brought them inside and sat the casket on our bed. I should have laid with them.
I wish I would have curled up next to their casket and just held it and them. 

I feel so close to them today. 

I want to reach out and pick them up again and I remember they are in the ground, across the yard, buried under a tree. 

It sickens me.
I don't want to believe it's been 3 months.

This month has been especially hard on me. As their due date approaches I find myself in a ball of emotions.

Confused...

Everything leads up to this one day.

For most people it will be here and gone, just another day. For me it will be finite.


Next month will be the most difficult, I am sure of this.

Once again I ask myself is it easier?

          No, it hasn't gotten easier, I still transcend from denial to anger and if I'm lucky I find a little hope. Every month, every day, I find something new to work through. There are many facets to grief and this type of grief is the stuff nightmare are made of. It's proven to be a difficult balance between mourning my 3 babies, and staying hopeful for future siblings. I expect it to be difficult to realize when we are pregnant again, that it's not Jax Stella or Beck- it's a new baby, a different baby(babies). One that I will get to know in a completely different way, I am scared. 

This is the only kind of mother I know how to be. 

I'm a puzzle with 3 missing pieces.

 The text, the calls, the support, the encouragement, the gifts, the care and just speaking their names... Thank you. 

This is not something to battle in silence and I am so blessed I don't have to! 

Thank you for riding this journey with me and allowing Jax, Stella, and Beck to enter your heart.

Life after Loss...

x3

With each day comes a new challenges. 

A new dilemma I have to figure out how to navigate. 

Like the time between then and now. The time makes them feel further away. & I find way to reel them back in. 

I have to learn ways I can remember them and have them as a part of my life without being on the verge of tears everyday. 

I'm learning to be their mom, relating to moms, even though I only knew them 19 weeks.

This is challenging. 

Having hope for the future and happiness for the present,

Is by far the most delicate and difficult balance. 

The most challenge obstacle is dealing with people who don't understand, or don't care. I like to think everyone cares... How can they not. Truth is to the outside world 3 babies died at 19 weeks, and yes it is sad. But they did not know them, they had no bond, But to me my future died with them. 

The littlest loves of my life are buried under a tree.



I am 26, I've lost my first and only children, I have to live without them for the rest of my life, a constant missing piece. 

Learning how to navigate the never ending announcements of pregnancy and new births.
I take a kick to the gut every.single.time.
It brings me to my knees and have to rebuild myself.

To me my world has stopped. It has died. My passion, my drive, my dreams have died with them. I struggle to find a purpose.  My life has stopped... while everyone else around me keeps moving forward.

 One day I'm sure I'll have it all back but for today I am empty, I am sad, anxious, I'm a shell. 
Old me is gone, new me is trying to figure out who I am.

 IF you haven't walked this you will NEVER come close to the heaviness we carry.