Part 2

Forgive me in delaying Sloane’s story. I’ve realized so much of this is still so raw along with the fear and anxiety because of what we walked through with her and continue to walk through. Let me be VERY clear we are the lucky ones because there are many others that aren’t here to write a story as beautiful as ours. I tell the story because it’s painful, raw, full of fear, full of emotions, and in truth it’s real life. As I’ve gotten older I’ve realized everyone has a story worth hearing, but many of us don’t bother in finding out. Instead we are so wrapped up in our own lives we don’t even notice the person next to us who is struggling with addiction, who’s child is sick, or their spouse lost a job that they desperately needed. Instead we focus on our own problems never seeking out how to help a friend in need. I’ve also learned that sometime lending an ear, hand, or shoulder, makes our very own pain or struggle seem so much less painful. Why is that, maybe because we allow the focus not to be on us for once. Through Sloane’s story I’m pulling back the VERY layers that left me crippled in fear for years. Without facing them, walking through it, or understanding that purpose comes through our pain I wouldn’t be writing these words. So without further ado and I do hope I am much better this month in continuing our medically complex journey but if life gets in the way and I find myself enjoying the moments I’m going to do that to. Enjoy the moments because life is fleeting and when I’m hopefully old and grey I can look back and remember all the smiles, despite the anxiety, remember the laughter that filled my house despite the worry of the next scan, and say I pushed past all of that and I enjoyed the everyday moments that make up a lifetime of memories.

Waking up the day after our initial scan was a blur. I remember thinking everything that happened the pervious day was a terrible nightmare. A nightmare that I realized I couldn’t escape. Looking back it was like living in someone else’s reality. As much as I wanted to stay in bed and process what happened, life keeps moving. Graham needed to get to school, we both had work because we had bills to pay, and we had NO idea what was next so we needed to work while we could. I was working from home a little bit by that point and knew going into an office wasn’t going to work in fear of having an emotional breakdown while on a conference call. I also couldn’t be alone in my house with my thoughts, so I went to my parents. They lived 10 minutes away at the time and I knew I needed to be with someone.

So I packed Graham up for school, my work bag, and headed over to my parents to work. I seriously worked like nothing was happening, in between calls/meetings I would sob to my parents trying to understand what was happening. I think we were all in shock. We left the doctors office without knowing much. Of course we started googling and we honestly didn’t know what we wanted her diagnose to be. At first I was hopeful it was just a mis-diagnosis but as I started to replay the words and search on the internet what it could possible be - we were still at a loss. We knew we were waiting to hear from the MFM doctor when my MRI would be in hopes that it would tell us more. We also went in to to see my doctor and started to talk through what this could be.

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There were sooo many conversations that led up to us leaving Charlotte but the jist of it was - no doctor in Charlotte knew what they were dealing with. After looking at the scans, my doctors said we would try and do a c-section and meet with a brain surgeon here. He made one comment that stuck with us and probably helped direct our path. In the midst of our googling, we found children hospitals all over, Philly, Cincinnati, Boston, and Duke. He said don’t bother with the small ones if you’re going to leave - you either “GO BIG OR GO HOME”. That was it. As much as we wanted to stay in Charlotte to be close to our home, we left it up to God to decide our path and this is what’s crazy. He confirmed everything that we were thinking in one phone call. In between the googling, trying to decide what to do next, scheduling a c-section in Charlotte, meeting with a brain surgeon here in hopes they knew what they were doing. We started to read about Exit Procedures, we mentioned it to my doctor and he never heard of it. There were 3-4 hospitals that did this and it was known to save the unborn’s baby’s lives. I won’t go into the details but here’s a link about the procedure. https://www.chop.edu/treatments/ex-utero-intrapartum-treatment-exit-procedure

In between all the talks with my doctor, our parents, and now waiting on the MRI results we decided that if we needed to go elsewhere we would. As terrible as it would be to leave Graham we felt we needed to give Sloane every opportunity to survive. That was the first part. I had my MRI on a Monday and on Tuesday morning at 8 am the MFM doctor called me with an update. I can’t remember if she confirmed the mass on Sloane’s head was a teratoma but she said I’m sending your scans to the Children’s Hospital of Philadelphia to see if they can help because no one in Charlotte has dealt successfully with what we are seeing. I hung up the phone and figured ok, let’s see what happens. I’m not joking, at 8:17 am (17 minutes later) the Fetal Center for Medicine from Philadelphia called my cell phone and said “We just received your scans and you need to get on a plane to Philly today, we can help”. First I was in shock I received a call so fast, second I wasn’t in the mindset to leave so I pushed back and asked for a later appointment saying we have a two year old who needs to be taken care of and the women on the other end was insistent……She said you are in risk of going into labor and if you go into labor your child won’t survive. I hung up the phone, called Jay and told him we had to go, called my mom and told her what happened and while we were on the phone she booked us two flights to Philly that afternoon. We coordinated everything we could in the shortest amount of time and headed to the airport around 3 pm. All we knew was that we had 8 hours of appointments the next day. In between the crying, packing a bag for three days, calling my boss, saying goodbye to Graham and the worry I think I was going through the motions. I just kept praying for whatever was on her head to be gone by the time we showed up. That whatever it was it would be ok. I literally ran to the doctors to get a note that I could fly and he asked me, why were we leaving since it was such a drastic change from trying to make it work in Charlotte. I said at this point when CHOP gave us hope, we had no choice but to hear them out. We owed it to Sloane, to our future family, and to our sanity to at least go somewhere that could tell us something more than, “we will try”. I had no idea when I boarded that plane I wouldn’t return to Charlotte for almost three months.

Helicopter parenting at it's finest

Y’all, let me first apologize in advance if we have a play date anywhere where my children could potentially get hurt because I’m a self admitted helicopter parent. Maybe it was giving CPR to Sloane three years ago or maybe it’s just who I am, but I audibly gasp when Sloane bikes, swings, runs, dodges branches, or pretty much does anything that could hurt her. I say this with laughter but let me paint you a picture and then you can decide if my behavior is totally normal or if I'm a little crazy. 

SO excited for Disney World!!! 

Last October we took the kids to Disney World with Jay's parents. Of course we had our fast passes booked for Space Mountain because that’s what you’re supposed to do when you go to Disney World.  Jay, Jay's dad, Graham, and myself headed to the ride while Jay's mom took Sloane to the smaller roller coasters.   We made it through the line fairly quickly and Graham and myself ended up in the first car together, separated by the seats, arms distance apart.  The car takes off and, for those that don't know Space Mountain, it's a roller coaster in pitch black and you have no idea what turn is next.  Clearly, I didn't remember this ride from my childhood and in this moment, I'm thinking, Dear Heaven save us now!!! So I do the only thing that any mom would do, I LITERALLY reach over the shoulder rests and hold Graham down by the shoulders as tight as I possible can, SCREAMING it's ok buddy it's ok, I have you!!  First, did I really think I could hold his body in the car if the straps or bar were loose?  Second, he was measured for the ride and there have been millions of children his size that have been perfectly fine.  In my madness, I'm scaring the bejesus out of him even more. As the ride pulls up to the station the poor child gets off shaking and in tears from the absolute horror that just happened.  Walking out I don't know who left the ride more scarred, me due to the vision of his small body flying through the air or him because his mom was screaming at the top of her lungs clutching him trying to control a ROLLER COASTER.  Meanwhile my husband was more perplexed at what happened then ever before.  While walking to meet the rest of our family and replaying what in the world just transpired, I started to wonder what happened to the girl who used to LOVE roller coasters.  Life happened, fear took over, and it was slowly destroying everything in my wake.  My fear of the "what if's" traumatized my five year old at Disney world!!  If that isn’t a come to Jesus moment I don’t know what is.

After this spectacle, I tried to process how I was parenting my children and I started to realize I wasn't empowering them to be brave, instead I was making them scared because I was scared.  I wasn't allowing them to fail when I was protecting their every move in hopes of preventing pain.  I wasn't allowing them to learn through failure, through brokenness, through sadness, through character building moments,  that those are the moments that end up defining us.  It's hard to write these words knowing that for the first few years of Sloane's life we were surviving and not thriving.  Of course we had no choice, but what I don't want is to create timid children afraid to tackle hard things in life.  Fearful of failure, fearful of having their hearts broken, and fearful of life because of my own anxieties and fears of the unknown and that's when I decided to make a choice, a daily choice to not let fear rule my life. 

Through processing all of this and intentional efforts, and I say intentional because is NOT normal for me not to want to protect my kids.  It doesn't feel right when I let them fall and scrape their knees because I'm their mom and my job is to keep them safe.  However, it it's also my job to help them get back up again when they fall.  If I don't empower them to do so, who will? So, while I still gasp, I let them fall, I let them fail, and I let Sloane stand up to other kids and proudly state why she has to wear an eye patch for 8 hours a day or why her eyes look funny when all I want to do is jump in and protect her.   As I continue to push forward in these unnatural feelings, guess what I'm starting to witness, they are gaining confidence in who they are and it makes my heart soar greater than any fear could.  

It’s so hard as parents not to protect them because we can. We have every right to do so, but we also have the responsibility to send our kids back out into the world empowered to overcome the challenges they will inevitably face.  So ask yourself, how are you empowering your children, are you letting them fall down, and letting them learn how to pick themselves back up again.  We HAVE to work at this DAILY in our house.  We TALK , we communicate about mistakes, and pushing through and I'm honest with Graham that life is hard.  Maybe too honest at times but he's also seen hard times from the age of 2.  As much as we wanted to protect him, we couldn't.  His sister lived in a hospital for almost 5 months, and when she came home we were living with my parents and Sloane had nurses and her nanny and two broken parents trying to figure out how to survive this new normal.  It wasn't easy.  I still look back and can't believe that was my life, BUT without that road, we wouldn't be where we are today.  My goal is to share a little bit of our story over the next couple of weeks/months.  Let's be honest Sloane's story is CRAZY and LONG and it will be chapters upon chapters but it's a page turner and it's taught me more valuable lessons in these four years than I would have ever learned anywhere else.  

One final thought because I can't end my helicopter parenting rant without the best part.  On our last day at Disney Graham decided he wanted to ride Space Mountain to overcome his fear.  So the three of us headed over to the 2 hour wait and got in line to support him.  I was also feeling guilty and secretly was hoping to redeem myself.  While we were standing in line I decided to check our fast passes just to see if there was anything for Space Mountain.  I still smile to myself when it plays out in my head.  TWO FAST PASSES opened up for the exact time we were waiting in line.   Jay jumped at the chance to take him and the two of them hopped over the railing and off they went.  As I watched them both walk away I knew this was God's way of showing me to let him go, he was going to be fine AND my fear couldn't rule over my child's ability to want to overcome a fear that I misplaced the day before.  10 minutes later Graham walked out with the biggest smile on his face knowing he overcame the biggest roller coaster of his life without one tear or one crazy mom holding him back.  Sometimes all it takes is intentionality of letting go even when all we want to do is hold on tight.     

On the resource tabs I have some AMAZING kid books that we read to our kids about failure, rising above challenges, and learning from your mistakes.  Graham and Sloane both love them and we do too.  xoxo

 

Beauty out of Ashes

He makes beauty out of ashes – have you ever sat around to think about what that actually means?  I have, and I know first hand out of our own pain and struggles; there is joy that might not have been found without walking THROUGH it.   I’ve contemplated this space, blog, or whatever you want to call it for a VERY long time. Back in January one of  my best friends told me I should start a blog and run a ½ marathon.  She told me I needed to set goals for myself.  I distinctly remember laughing and saying I hate running and I have nothing to say.  For some reason I’m now doing both.  At points while typing I've asked myself why, but then realized why not.  It may be hard and scary but you know what's worse.  REGRET.  So here I am attempting to be vulnerable and real about raising a medically complex child and walking this unknown path all while still trying to manage being a good wife, present mom, daughter, sister, friend, employee etc.. and let me be honest it’s HARD and lonely at times. 

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More often than not, I have wished there was a road map for our journey, wishing, hoping, and praying for answers.  Four year ago when our lives were turned upside down I remember Googling some of Sloane’s conditions and there wasn’t much to read and the doctors couldn't tell us anything definitive about her future.  Instead we live in 6-month increments, with appointments and therapies in-between MRIs believing everything is stable.  What I’ve started to realize in the midst of these waiting periods, maybe it’s better this way.  I don’t want a diagnosis defining our future of what she can and can’t do.  I want to push her forward to be the best she can be.  I remember telling the doctors that she can do everything everyone else does until she shows us differently.  Guess what, so far she does everything.  We were told she wouldn’t hear out of her right ear.   When I whisper in her ear that is sutured shut and tell her she’s a superhero, she repeats back to me what I've said.  When the doctors told us she wouldn’t be an athlete because of the tumor on her cerebellum, she is starting her first soccer season this fall.   It's incredible to see a child overcome the supposed limits of a diagnosis.  So I say all of that to say this - I hope this will be a space of hope and lots of laugher and learning together how to navigate the everyday challenges or raising medically complex kids but doing it gracefully and with JOY.