Still Standing

In October of 2013, we took Alexandra on what we call her “Ivy League” tour, having a liver transplant evaluation at Yale in Connecticut and receiving a second cardiothoracic opinion on her by Harvard, or Boston Children’s. We then in April of 2014 did a combined heart/liver transplant evaluation at Boston Children’s, and in October of 2014 did a combined evaluation at Stanford Lucille Packard – all three ended in denials. This is the story of why we are still standing.

I remember the look on Dr. Miloh’s face implicitly. His lips were drawn, pursed almost. He looked like someone had stabbed him in the heart right in front of us. “She needs a liver transplant, the only way to help her is to get her a new liver.” My heart sank. I always thought maybe she’d need a heart one day, but never did I think another organ. I also didn’t think that any of this would have taken us on the journey we have been on. Never in my wildest dreams (or nightmares) could I have imagined the lengths we have gone to in search of an answer. In search of someone, anyone who would help her.
  

I seem to have all these memories of doctors faces over the years. Like frozen moments in time. The face I like to call her local cardiologists “oh s**t face”; Dr. Miloh’s face every time her ammonia was over 100; the look on Dr. Hellenbrand’s face (the chief of cardiology at Yale) when he told me there was no way she could have a stand-alone liver transplant; the look on her Boston cardiologists face when he had to tell us her heart wasn’t in the same shape we were being told it was at home. I will live with these doctors' faces etched in my memory forever.

I remember the last denial for transplant clearly. Dr. Kaufmann called me and discussed why Alexandra would not be a candidate for transplant. I didn’t say much other than “Okay, I understand.” What can you say? “She’s only got 1 SVC; her body is just not compatible with a four chambered heart.” What else could I say?

Three no’s from the most prestigious centers who see the most complex kids in the country, and the world. No one will touch her.

I felt raw. Alone. I had a breakdown. I alienated people who I felt were some of my closest friends because I couldn’t figure out why. I couldn’t figure out where to go or what to do. I fell apart.

Three no’s. I essentially spent the rest of 2014 and the first part of 2015 in a rage. I was so angry. The world, the entire world was against me and my child. I was lost in a storm of tears, and heartbroken from the fact that there would be no saving my first born gal.

But let me tell you where we are today – we are good. We are great. We are learning to live in the reality of this life. We are truly living.  No one will give her a transplant, and that’s okay. She told me herself that if I forced the transplant on her she would die. I think our kiddos know so much more then we think they do.

I’m going to bury my daughter. I say it all the time. People look at me like I’m crazy. I think it’s the least crazy thing I have ever said. I laugh wholeheartedly, and I wear everything out for the world to see. Yes, someday I will stand above her grave and my arms will be empty from the loss. But that day is not today.

What we have now is true freedom. I live in reality. I bet you’re thinking I’ve given up hope, but I am far from it. I have so much hope. Because I put the power and control into places that they needed to be in. I learned to be vulnerable, and not to be afraid of the pain or the craziness inside. We’ve been given a life. A life full of pain and heartbreak. Filled with open heart surgeries, and drugs, and therapies, and tons of crap to fill up every single day with no minute to spare. But it’s glorious. It’s messy. I’m messy – she is messy, and beautiful.

It’s a life. And even with three no’s to transplant, a left lung that’s just doing nothing but recycling unoxygenated blood, and worsening scoliosis – we live.  We live because it’s what we have to do. Yes, it took me to have a breakdown, to feel like I was coming apart at the seams (and sometimes I still feel that way), to question every move I’ve made since the day she was born – but I realized that this was our life. It isn’t going to be pretty, not everyone is going to want to be my friend, and sometimes I’m going to look horrendous – but it will be glorious.

Live gloriously. Live vulnerably. Just live. And if that fear of standing over your child’s grave hits you from time to time, remember today. Remember what’s right in front of you.

Remember and live gloriously. 

Danielle Edges (Mom to heterotaxy hero, Alexandra)

We Chose CHD!

Instead of Congenital Heart Disease (CHD) choosing us, I guess you can say that we chose CHD!  A common question I got asked by doctors who met Lily Grace for the first time was, "Did you know how complex her heart was when you adopted her?"  Imagine their shock when I tell them that we chose Lily specifically based upon how gloom and doom her medical prognosis was.  The very thing that caused other adoptive families to run away in fear had our family racing to bring our sweet girl home.

Lily was born in China with Hypoplastic Left Heart Syndrome (HLHS).  Simply put, Lily was born with only half of a heart.  She also has Heterotaxy, which means that all of her organs are on the wrong side of her body.  Lily’s heart is further complicated by being upside down, backward, and in the right hand side of her chest.  She had two open-heart surgeries in China, and then the surgeons deemed her “terminal” and inoperable.  At that point her orphanage had her adoption paperwork completed.  We came to find out on Gotcha Day, the day we met Lily for the very first time, that her orphanage truly believed a family would never ‘chose’ her. 

Children with HLHS typically have a series of three palliative open-heart surgeries.  It wasn’t until Lily was home from China, and she had her third open heart surgery that we understood why the Chinese surgeons deemed her inoperable.  The very first surgery that Lily ever had was to insert a shunt into her heart to increase pulmonary blood flow.  A textbook BT Shunt is placed on the right hand side of the heart, near the Superior Vena Cava.  Lily’s Superior Vena Cava is located on the left hand side of her heart due to Heterotaxy.  Unfortunately, the surgeon placed Lily’s BT Shunt on the right hand side of her heart, far away from her Superior Vena Cava.  This mistake began a series of critical issues for Lily Grace.  Shortly after her third open heart surgery, called the Fontan Procedure, Lily’s right pulmonary artery (RPA) became completely discontinuous from her heart.  In 2013 Lily’s surgeon attempted to reattach her RPA to her heart with a donor adult femoral vein, but unfortunately that surgery failed.  Lily is currently living with only one functioning lung. 

The US cardiologist who reviewed Lily's medical file while she was still in China was worried that he may have given us false hope about Lily's congenital heart defect.  The truth of the matter is that before we even knew if Lily was operable we submitted a letter of intent, asking China if we could please make her our daughter.  Lily needed heart surgery that China would not (could not) do.  But, what Lily really needed more than surgery was the love of a family.  Prior to bringing Lily home from China Jacques and I always said that we wanted desperately to show Lily the love of a family for as long as God allows her little heart to beat.  And here we are 3 ½ years “home” and Lily does KNOW the love of a family, and she knows about Jesus and how much He loves her too!!!! 

A small percentage of children who have had the Fontan Procedure end up with a life threatening condition called Protein Losing Enteropathy (PLE).  PLE caused horrible fluid retention in Lily’s lungs and abdomen.  Lily was essentially drowning to death in her own secretions.  Try as they might, Lily’s cardiac team was unable to control her PLE symptoms with medication.  We were told that the only cure for PLE is a heart transplant.  Lily was evaluated for a heart transplant, which is when we received the devastating news that due to her complex anatomy and the fact that she only had one lung attached to her heart, Lily was denied transplant listing by three transplant centers.  Shortly after we had conversations with the hospital’s hospice team about bringing Lily home to die, her heart failure cardiologist walked into the room and asked me if she could please present Lily one more time to their transplant committee.  Twenty-four hours later Lily was listed as a 1A, top priority, for a new heart.  On June 14^th, 2014 Lily Grace received the most precious gift that could ever be given - her Hero’s heart.  Lily’s donor was a non-lung donor due to the trauma he suffered in the motor vehicle accident.  What this meant for Lily was that she also received her donor’s left pulmonary artery.  Her surgical team was able to put Lily’s new heart in its correct anatomical position in her body even though all of Lily’s connections are upside down and backwards from her heterotaxy.  Lily’s new heart is only attached to her single left lung since her right lung had previously become discontinuous from her heart due to a blood clot, and the risk of Lily being on bypass longer was not an option.   Lily Grace is said to be the most complicated pediatric heart transplant to ever be done in the USA.  A huge miracle indeed!  

After a very difficult recovery, and 508 days on supplemental oxygen, Lily Grace is absolutely thriving!  She is filled with life, extreme love, and bountiful HOPE.  It has been an honor to be Lily’s mommy.  I have learned through this adoption that even more than Lily needing a family, I needed Lily.  She has taught me more about life and love in the 3 ½ years that I have known her than I learned in the prior 34 years combined.  Loving Lily is an excruciating love.  Selfishly, Jacques and I want more than anything for Lily to grow old and outlive us.  But whether she does that or not, if I am still alive to see her take her last breath, I will know without a shadow of a doubt that adopting Lily was exactly what God meant when he told us to go and be LOVE. 

Love is risky.

But let me tell you that it is SO worth it.  

A million times over.  

Love is worth the risk.

31 Years Ago...

Cameron Edward Price 3/21/85 - 6/25/85
31 years now. Seems time has flown by. Cameron was born with Dextrocardia and RAI. He had multiple heart defects and holes between the tissue dividing both sides of his heart. It caused problems with the blood returning from the lungs to the heart. He was to undergo 3 major surgeries where the surgeons would reconfigure his heart and circulatory system. He made it through the first one, but got an infection that he just couldn't get rid of and had a hard time fighting off.
31 years ago, not much was known about heterotaxy and NO support groups even existed. Trust me when I say, I was TOTALLY alone in this fight for my son and unbearable grief. I blamed myself, my husband and I even blamed God. I screamed, yelled, begged, pleaded, but NOTHING prepares you for the grief that comes upon you.

Over the years I have explained what heterotaxy is and how it has affected my entire life, but people who have never had a really sick child, yet alone a child that died, have no idea what it's like. I've learned to live with the heartache, but I have a tiny piece of my heart named Cameron that will never heal. I'll always wonder "what could have been," but at least I got to have "what was" for a short, brief time. And for that, I'll be eternally grateful.

Juliann Price ~ Mom to Heterotaxy Hero, Cameron

Cameron has 4 siblings: Daymun (29), RiAnn (27), Jade (26), and Jena (25)
Juliann is also grandmother to Aidyn (3 1/2) & Travis (3)

Travis ~ A Journey of the Heart (June 5, 2014 - April 8, 2015)

Travis was born on 07/04/2013, pink and vibrant, weighing 8 lbs. and 11 oz. at birth. And he was born with Heterotaxy, a rare congenital defect.

We learned about Travis’s heart condition at 25th week of the pregnancy and thought that was the only issue. Heterodoxy as a new diagnosis only came after 1 day he was born. We had intense meetings and discussions with our medical team and consultant before and after he was born and did extensive research regarding choosing the best medical and surgical team to care for him.

Boston Children’s was our final choice. 10/02/2013 we took Travis to meet the surgeon and the team for the 1st time. The initial echo looked promising. The size of his left ventricle is good enough for a Bi-Ventricular repair which is considered the best solution for babies who are born with a single ventricle. Although he had pulmonary stenosis and pulmonary hypertension, these two conditions together have formed a nice balance that lasted him a good 11 month before we were called for the surgery. Travis grew well in the first year with no medical intervention, the only thing that’s slightly noticeable setting him apart from other babies was his purple tint lips under a gradually declining blood sat, 83 at his 11th month, 93 to begin with at birth.

The 1st surgery, then the only surgery that he would need in our mind, was scheduled on 06/05/2014. Travis was all ready. I kissed his perfect little chest for the last and waved good bye while he was busy playing the new hospital toys in his premeditated drowsy state. 7.5 hours later, we shook hand with our surgeon. “All went well”. And we exhaled. Post-surgical recovery was longer than we expected. Soon we learned that the mitral valve regurgitation was the reason of the slow recovery and it had to be repaired. Reluctantly and sorrowfully, we opened our arms to welcome the surgery #2 to take place, envisioning this marking the successful ending of Travis’s surgical journey. It was over and again” all went well”. The prolonged recovery began again. At one point his recovery took an upward turn and we were happily relieved he was finally transferred on his one year birthday to the recovery floor.  Then 07/08 came, the darkest day of my life, we were pulled to the small meeting room to talk to the team, whom informed us, unfortunately the repair didn’t last, the regurgitation remained and persisted.

But they didn’t keep us there for more to be done. They let us go home with the hope that over some period of time, Travis can grow and hopefully the regurge will tame. We set our foot to home on 08/04, exactly two months after the first surgery. Travis did enjoy his home stay after being away for so much. He did grow and we did take many pictures with him smiling under the bright sun. Then he was hit by a cold 2 weeks he came home, then the decline began.

From later August to later October, Travis’s life was thinning out in a gradually but distinctive way. He started feeling more fatigued over time, eating half of what he used to, then 1/3, 1/4, then finally 1/10. Having no interest in activities and crying through his many days and nights with his very weak voice then. And the vomiting episodes became a potential of his daily routine, from once a week, to 3 times a week, he began to throw up every other day if not daily starting the end of October. We did engage in all doctors and psychologists, physical therapists in the picture and the overall conclusion was that he just needed more time to recover, based on his mystically great looking echo reports.

We called Boston Children’s and scheduled the painful trip of truth searching.  11/23/2014, 5 months after his first surgery, we came back. Friday morning was his cath, Travis went into cardiac arrest during the anesthetic process before the test began. And the answer was granted, finally. We were relieved, with pain. The 3rd surgery, an emergent one was scheduled right away, again to repair the much worn out mitral valve, as the final hope it would last this time. 11/24/2014 Monday, an already intubated Travis was sent to the operating room. We felt nervous more than ever before, knowing how very fragile he was, with absolutely no reserves through the month’s long decline. And he came out, same puffy, same cold, same pale and same breath. The days then was all about the monitor screens, every number change, every med change, and every plan change. No luck this time, still. His blood pressure and LA pressure remained high under all measures.  7 days later, the 4th surgery of mitral valve replacement took him back again on the surgical table. Now the new game was to watch if he AV node will come back after being injury during this surgery. 12/11/2014, 10 days after the 4th surgery, a permanent pacemaker was put in his belly, marking the 5th surgery during his mostly bedridden second year of life, from 11th month to the 18th month.  The storm did die down after all. He did seem getting better in his spirit and physical being through the rest of his recovery journey, there was really nice weight gain and plenty of happy faces and playful moods, all the way until the day we came back to Chicago, on the day upon departure we were rest assured that” Travis is nowhere near the need of a transplant” by our team.

01/25/2015. After another exact 2 months stay in Boston. We were happily returning home after the last day pictures taken with the whole Smith clang. Travis started throwing up in the taxi on the way to the airport. And he continued on during the entire flight until he ran out every single spare shirt and coat. We called Lurie as soon as we land and went straight to be admitted, the dust settled at 11:30 p.m. that night, our hearts sank into the endless dark night.

Travis didn’t get better as we and the local team had hoped. He kept throwing up multiple times at a day. Those were the toughest and wickedest days and nights with so much struggle of wanting water and milk and constantly being denied and rejected. A week later, he went into another cardiac shock while the nurses trying to replace his old IV. As much as the 3 pokes and 1 hour of hysterical crying did it, his tiny body of extreme weakness didn’t help whatsoever at all. The intensivist doc noticed me that the chance for him to be through this with a breathing tube put in is only half the chance. I refrained the selfie I was trying to take with my son whose life was again on a thin line in his forever land of hospital bed, gasping in every air he could use, holding the faith that I would take a good picture with his happy face, before I was asked to leave the room. Then the miracle boy survived through the heart wrenching night.

The team informed us that there was no way he could recover on his own unless with a new heart. With much debate in the eternal thought process, Travis, “the sickest child in Illinois”, was put on the wait list as a status 1A patient on 01/31/2015. Then our mind still shifted towards Boston, the last and the forever panacea, for the very last confirmation. With the med flight arrangements through overcoming the impossibilities, with the Boston CICU bed generously awaits, with our Boston surgeon’s one and always vision for his native heart, Travis declined the offer of leaving Lurie, with big drops of tears falling from his tightly closed eyes, as if he was saying” please let me be, no more and more”. 02/03/2015. Travis’s put back on the list. No more and more. And The Wait Began.

Midnight. 02/19/2015. We got the call with immense gratefulness.  Still and still, we talked about the decision with our consultant/family friend for another 2 good hours out of the deepest mind of dilemma. Yes came firmly after that.

Early morning.  02/20/2015. We said good bye to Travis, again. I listened to his to me still very fine heart beats and took picture of him with the surgeon whose eyes looked confident and compassionate.  8 hours later, we welcomed our new boy back, with a new heart beating in his brave chest.

Travis’s heart story didn’t end here. And it may never end. There were other unthinkable swirls of rejection issues that came with drastically invasive treatments, which did work wonders, before he was finally discharged on 04/08/2015.

We are deeply GRATEFUL with gratitude towards our little donor hero and his family, our most excellent local team and surgeon, our amazing medical consultant, our ever caring nurses and the floor staff, and our whole Boston team, our wonderful family and friends who supported us all along, and last but not least, our heartwarming fellow heart moms and their little ones who modeled and still are modeling for us, every single day, now then and ever, with their unbelievable courage and strength, All Beyond Words.

Today’s Travis is a thriving 2.5 years old, chasing his sister everywhere for the fun of life, loving the moments nonstop. He receives 5 therapies each week and has been making progress in his development steadily.

Thank you for reading Travis’s heart journey. We appreciate very much your sharing this special path of his with us.

God Bless. 

Once a Heart Mom...

When our daughter passed away, almost a year ago, I was suddenly thrust into a state of limbo.  The world of high intensity that I had come to know so well, was no longer mine to share with the heterotaxy community that I had come to call family.  And although her life was cut short and her time in the hospital was brief, I felt as though my very identity had been snatched away.  How was it possible that the monotonous sound of monitors and pumps (that were once deafening) had now become soothing and welcoming?

The transition from taxi mom to heart mom was a difficult one. There was so much heaviness at that time. Some of that stemmed from fear, some from confusion, some from my selfish desire for “normalcy” and much of it from a clear understanding that those around me simply didn’t get it.  But who could blame them?  We were talking heterotaxy here!  It’s not like there was an instruction manual or a field guide of what to expect.  Before I knew it though, the cardiac ICU became our home.  After two heart procedures and 4 weeks in the hospital, Rachel was finally moved to a step-down unit and I was coming out of the fog.  However, it was then that she, quite unexpectedly, passed.

Two weeks later, I returned to work.  It was one of the most difficult actions to carry through, but looking back, I’m so thankful that I did.  The predictability and routine was mind-numbing to say the least, but it allowed for me to keep busy.  What I wasn’t prepared for was how lost I would feel now in the world that was once my normal, everyday routine.  My CICU life and my office life didn’t collide, they actually repelled each other much like magnets do when two of the same poles come together…I was stuck in the void in the middle.

I had been living a dual life…one that revolved around heterotaxy at night and on Facebook and the other that consisted of the daily grind of paperwork and office tasks.  It wasn’t until Heterotaxy Awareness Day that my two lives came together.  I began posting information on my personal page about heterotaxy and the importance of raising awareness… and before I knew it, my worlds began to merge.  Of course my family, friends and coworkers had always been there, but it wasn’t until that day, that I realized what a support system I had from both worlds.  That day, I found a new purpose in this world…one of advocating for those that struggle daily with the unknown while at the same time raising awareness in a world that has never even heard of heterotaxy.  I lived the life of a heart mom for a reason, and while my time in the CICU was brief (by heterotaxy standards), I will hold tight to this truth… once a heart mom, always a heart mom.

Home

There’s a street I drive down almost every day to get back home from pretty much anywhere. It’s not a pretty one. Rundown houses and boarded-up taverns sit across from massive parking lots and big-box stores. It’s all concrete and gas stations and tiny storefronts, and the traffic is always terrible. I can remember so vividly the first time we drove the length of it. We were blindly following the GPS, heading to look at a house that we hoped to rent, a place to call our own after living in my parents’ basement for the better part of a year when what was supposed to be a short maternity leave turned into a nightmare of diagnosis and birth and my baby’s chest cracked open twice before he celebrated his first Christmas.

The whole world looked grey that day. We were facing the looming prospect of Ethan’s second surgery, walking the tightrope we call ‘interstage,’ that fragile time after the first operation when it feels like just looking at them wrong might be enough to make it all come crashing down. We had left our former life (as volunteers on board a charity hospital ship off the coast of West Africa for the better part of six years) with no idea that we’d never go back. I walked down the gangway into the hot, Congolese night, carrying only what I could pack into two suitcases, fully expecting to be unpacking again in my tiny cabin a few months later. But then, without the faintest whisper of warning, words like ‘heterotaxy’ and ‘complex, critical congenital heart defects’ wrenched everything that I’d ever held dear out of my shaking hands, and for some reason, on that gloomy day in November, the reality of it all was almost enough to suffocate me.

I didn’t want to live on land. I didn’t want to leave the vibrant community on board the ship, the community I was planning to surround myself with as I raised my children. I certainly didn’t want to be unceremoniously and irrevocably thrown headlong into this very different community, the one made up of mamas and papas fighting for their children’s lives against the shadowy spectre of heterotaxy.

I wanted to go home.

Home. To the ship and the wards and the familiarity of the ever-changing view outside my portholes. To the place where I cared for broken babies at work and went back to my cabin afterwards, certain that I could never find the kind of strength I saw in their mothers. I wanted to go back to the time before everything changed, but the vast, yawning canyon between now and then was deeper than death, and it felt like my heart was breaking all over again every time I thought about how much was wrong with my son’s. There was no way back.

I drove down that street this morning. We had just made a surprise visit to the thrift store, and the kids were happily looking through new-to-them books when Adele came on the radio. Shrieks of pure joy erupted from the back seat, and when I glanced in the mirror, both of them were holding imaginary microphones and lip-synching as though their very lives depended on it. We passed the tiny post office where the woman behind the desk knows my children by name and always has scraps of paper for Zoe to colour on while we take care of our business. We stopped at the light in front of the hole-in-the-wall restaurant that sells what I’m pretty sure is the best fried chicken in a fifty mile radius. My favourite tree, the huge one next to the tavern, reached its bare branches over my car, and I could picture the way it had looked through all the seasons, from the impossibly bright green of a nascent spring to the vibrant, red leaves that fell on us like a prayer through the fall. Zoe chanted the names of the side streets as we passed each one, calling out triumphantly as we passed the house with the purple door that we were almost home.

Home.

It looks nothing like what I expected, but as we’ve slowly filled these empty rooms with the things we’ve collected and covered the bare walls with still frames and memories, my feet are finding their way on this solid ground. I look back over the days and weeks and months between then and now, and I’m someone I barely recognize. We’ve been given the indescribably precious gift of time, and it has changed everything.

Time, when you’re spending it in the company of a medically fragile child, is a strange thing. There are stopping places along the road where it all but stands still, and you’re left staggering under the impossible weight of lost innocence for what feels like forever. There are sudden flashes of pure joy where everything is right with the world, but then you blink and it’s over and you’re left wondering whether you imagined it all in the first place. And there no way to know, just by looking at the clock, which one is coming next, so you put out your hands and you take what you’re given, and you hope with every fiber of your being that you’ll be strong enough to hold all of it.

And this is the beauty of this life, a life without guarantees. Every second of it is precious because none of them were promised. Every hour is made of gold, the awful and the awesome alike, and I think the reason I can’t see myself when I try to look back to before the day when everything changed is because I’m blinded by the truth of everything that’s come after it.

And the truth is that I’ve found my home. It’s the memories of the years spent on the ship, and it’s the pool of sunshine on my living room floor where my broken-hearted boy and his big sister sit together and play. It’s the hallways of the hospital where they cut him open and pieced him back together again, and it’s the playground where we jump in mud puddles. It’s here and there and everywhere in between, because when you’re not promised tomorrow, home is just where you are today.

Welcome home.

(Ali Chandra - Mom to Heterotaxy Hero, Ethan)

Reflections

As 2015 comes to a close, it brings reflection. Reflection on the year that has just flown by within the blink of an eye, and yet so slowly at the same time. It is a very odd combination and one you truly understand when your child has Heterotaxy.

One year. What does that truly mean? For most, it is filled with family fun and a carefree attitude. For us, it was deciding to move across the country and subsequently having to find a new care team for our daughter, Violet. It was finally taking the plunge to remove her feeding tube after having it for nearly three years. It was giving hope to newly diagnosed families and making connections. And it was, unfortunately, watching friends lose their children due to Heterotaxy-related complications. A year can have so many different twists and turns that it can be hard to plan for the future, even just the next year. Living in the moment is something that many of my fellow Heterotaxy parents abide by because we are afraid to make plans for a child that may not be there.

But I won’t do that this year. I can’t do it this year. I am deciding that it would be healthier for me to finally start looking forward to the future. We will plan first for Violet to go to school in March once I graduate school and am working. We will plan for a vacation in the summer, perhaps to Disneyland or back home. We will put her into preschool in the fall. We will buy presents all year long for Christmas. But what I won’t plan for is what “may happen” in regards to her health. We deserve to have a year where our first thoughts are not on a diagnosis, but rather how well she is doing and rejoice in that. 

All of the changes we faced this past year has made us a stronger family and we look forward to 2016 being just as prodigious. We wish all of our Heterotaxy families a happy, prosperous, and healthy year!

Danielle Leppo ~ Mom to Heterotaxy Hero, Violet