Sunday, September 30, 2018

Scars



  I was 10 years old when I had chicken pox. I vividly remember my mom telling me, "Don't scratch your chicken pox or they will leave a scar." In the moment, I didn't care about scars...I just wanted to the itching to go away. And to this day, I still have a scar from one of my chicken pox!

 Scars are inevitable in life- whether physical, spiritual, or emotional. Some scars are due to our own choices, some are due to the repercussions of choices of others, and others still are due to others choices for our own good. Each scar we have tells a story. Sometimes those scars tell stories of courage and valor, some tell stories of miracles, some tell stories we'd rather not retell, and some are scars that no one even knows we have.

 Abby has a lot of scars. From the G-tube site that gives her nutrition, to the port site that holds a special IV that allows her to have quick access for life saving fluids, to now an almost 10 inch scar that proves miracles happen. Abby also has a lot of emotional scars- being placed for adoption in early infancy due to the fact that the country her birthparents came from could not provide for her medical needs, the countless hospital stays that took the place of her newborn and early toddler years, and the many, many, scary, painful procedures she has been through in order for her to continue to thrive. But, I can guarantee you that she doesn't notice these scars. Yes, these scars are going to surface in the years to come and Dave and I pray now that we can share her story with her well as she grows and matures. Right now, Abby doesn't see the scars. She sees life. She sees couches to climb and messes to make. For once in her life, I believe she is seeing and noticing things in her little life that she never noticed before. She is conquering her eating and walking challenges. She is defying odds and pushing on...all because of scars. Scars that don't define her but drive her to become all that she can be.

 How often do we allow the scars of life to define us? Those teenage years of bad choices. The past relationships that ended over and over again. The physical scars of abuse, self-harm, and self-neglect. These scars don't have to define you. They aren't who you are. These scars are proof that you are human and in need of saving...in need of a Savior who loves you and wants to heal those broken places in your life. Don't let the scars of the past define who you are today; instead, let them drive you to the One who can make all things new. And then, like Abby, those scars become your story to tell. Your story that tells the world your scars were healed because of the scars of Jesus who died for you so that you could be made whole and complete in Him.
 


Thursday, September 20, 2018

Born for This


 There is song I am loving right now called, "Born for This" by Mandissa. It is about a girl from the Bible named, Esther. An unlikely person with an unimaginable task trusting in an all-knowing God. Esther didn't come from royal blood, but became queen. Esther was faced with the task of stopping her husband, the king, from destroying her people...the Jews. But this would take telling him who she was- a Jew...this would mean coming before him unannounced and requesting something that no one had ever requested before...this would mean telling him that it was his best friend, his right hand man that had been the one to make the decree to kill the Jews therefore leading to his demise. There was a lot at stake for Esther, but she trusted in a God who was so much bigger than her circumstances and because of her loyalty to her people and her faith in God, the Jews were saved.

You should really read the Bible...there are awesome, true stories of faith throughout the whole thing!

 I think so often of this task, this assignment that has been placed before myself and my husband. It has been a long, hard journey and one that is not over yet. And yet, I would do it over and over again for our precious, Abigail, who is doing so well right now!


 We are still on weekly appointments with the liver team and frequent blood draws down at CHOP. Our latest appointment this past Tuesday brought such great news though. As I had mentioned previously, Abby's kidney numbers were slightly higher than normal and we were trying to figure out why her potassium was still so high. Last Friday, the numbers hadn't changed much and so we started two medications- one to help decrease her potassium numbers and a second anti-rejection med to protect her liver so that the first anti-rejection med could run at a lower dose.
 Abby is now on 12 different medications, but because of these meds, her labs on Tuesday showed a significant decrease in her potassium levels and a slight improvement in her kidney numbers!! This kid never ceases to amaze me! The plan for now is to keep our medication regimen the same and go back next week for another appointment and more lab work.



 The other exciting piece of all of this is the fact that we are going to begin trialing a more complete protein based formula for Abby. Because of the MMA, Abby's protein intake has been restricted to about 2 eggs worth of protein for an entire day. And it's just not meat protein- any protein!! Her body sees protein as an enemy to wage war on hence, causing so many issues to her little body. But, now that we have this new liver that has the enzyme capability to breakdown protein, we have seen her MMA levels drop from 1M to 100,000!! A 90% IMPROVEMENT!! When you stop and think about how the body works and the miracle of organ transplant, you can't help but think that something more than a big bang created our amazing, intricate human bodies!



 I love this quote that I have heard several times- "God doesn't call the qualified; He qualifies the called." Maybe you think that you won't ever make a difference. Maybe you think that because of your upbringing, God could never use you. Maybe you think that because you don't have a lot of money, you don't have the resources to help others. Stop. All that God is looking for is a heart...a life...a mind that is willing to say, "God, I don't have it all. But all that I have is yours. Use me in whatever capacity You see fit and allow me to make a difference for you wherever you call me to!"

 This line from the song mentioned above is one of my favorites- "Long before your heart could run the risk, you were born for this." Long before I knew what MMA was, God knew I would be momma to this incredible blessing. Long before I knew I would be a nurse, God knew I would raise a child with severe medical needs. Long before I met my husband, God knew we would need to live in PA near one of the best children's hospitals in the country. Long before my heart could stop and think about the risks associated with saying "yes" to adopting a special needs baby girl, I knew that I was born for this.

"'For my thoughts are not your thoughts, neither are your ways my ways,' declares the Lord. 'As the heavens are higher than the earth, so are my ways higher than your ways and my thoughts than your thoughts.'" Isaiah 55:8-9

---All photographs by Meg Brock Photography

Friday, September 7, 2018

Joy in the Journey


As a nurse, I have seen a lot...like A LOT!! Some stories are miracles and some stories are ones that I care not to remember. But, in each of them, I have been thankful to be a part of that family's journey. At 4:30am when the OR nurse told us we could head up to the PICU to see Abby, my stomach went to knots. I had been that nurse bringing a family back to a loved one right after surgery and watched the looks of fear, of relief, of sadness, of confusion, and of just plain exhaustion. Now I was that mom. 
 When we walked into Abby's room, I caught myself just staring. The tubes, the wires, the machines, the 10+ nurse and doctors, and my baby girl just laying there. The anesthesia was still very much present in her body and because of all the IV lines, drains, tubes, and wires she couldn't be covered up as everyone needed to be able to assess her. Thankfully, she didn't need the breathing tube after surgery and was breathing comfortably on her own. Dave and I stood off to the side as the team worked seamlessly to get all of her medications up and running and make sure she was okay.
Then, I held her hand. I whispered in her ear, "Mommy is right here. Your daddy and I are so proud of you. You are so strong. You are so brave. You've got this, baby girl. Mommy loves you." And the tears flowed. Today, I was her mommy...not her nurse, not her caretaker, not the one worried about all her pumps and the million doctor's orders...today, I was mommy. They say that sometimes knowing too much is a bad thing and I would agree. Being a medical professional and having a daughter with medical needs can be overwhelming- ignorance is bliss, right?! But, I am also so thankful for the knowledge I have in order to give our daughter the best care possible. 

As the days went on, tubes and IV lines began to be removed. Abby was still dealing with pain and being super itchy. She was also on high doses of steroids and was having issues maintaining her blood sugars. We left the PICU on Wednesday afternoon, 3 days after surgery, but by Thursday night, she was back in the PICU for increased sugars. We stayed in the PICU until Sunday afternoon, and again, transferred back to the regular floor. Through all of this, Dave and I took turns staying with her. The nights brought no sleep and the days were filled with endless doctors, orders, pricks and pokes, and lab draws. But by God's grace, we endured. She endured.


The plan was for us to be discharged on Tuesday, August 28th, 10 days after a major surgery. Abby was doing pretty well and we felt confident we could go. Then, her liver enzymes came back from her blood draw that Monday morning. They were elevated. This was indicative of possible rejection and so, Tuesday the team wanted to do a liver biopsy and more lab work in order to rule that out. Rejection can be common after transplant and the team follows closely to catch any signs of it early. The treatment is usually an increase in medications or a change in medications with continued blood work for monitoring. So, Tuesday morning, we headed off to her liver biopsy. And by 5pm that night, we had the results. NO REJECTION!! Her liver looked good, was functioning well, and was just trying to heal. We were blown away and so thankful. 


Wednesday morning, 8/29/18, Abigail was able to go home. 11 days after a liver transplant we were bringing our baby girl home. We were shocked. Abby did amazingly well and the only person we could attribute that to was God. He has an amazing plan for this little one and watching Him work in her life every day is a complete miracle and gift. Dave and I are so humbled that God chose us to be this little MMA fighter's mommy and daddy!












Monday, September 3, 2018

The Call


It was 3:30 in the afternoon on Saturday, August 18th- 8/18/18. I was working and Dave was home with the kids. I was busy caring for my NICU babies and he was busy caring for our babies. We knew "the call" would come, but after almost 3 months of waiting for that call, we became kind of immune to the fact that soon "the call" was coming. 

I had just finished up with my little NICU baby when I took a break to look at my phone. I had a text that said, "Call now. Emergency." My heart dropped and I immediately called Dave. The first thing I thought was, "Uh oh. Something happened to one of the kids." When Dave picked up he said, "They have a liver for Abby!" It took a second for that to register. "The call" had come. 

From 3:30pm on, it was a crazy, emotional rollercoaster. I called my charge nurse and told her I needed coverage as soon as possible while Dave frantically packed things for myself, Abby and himself and found childcare for Andrew. Thankfully, I work at CHOP and that was exactly where Dave and Abby were headed. In a matter of minutes, our whole world was turned upside down.


By 5:30pm, we were all together up in Abby's room where we were getting her prepped for surgery. The liver team met us in the room and told us the liver looked good on paper but they needed to go put eyes on it themselves before they said it was a go. So, we prepped Abby for the OR and waited. The team had to travel about 2 hours away and told us not to expect any news until about 8:30pm. And, there was always the chance that this liver would not work and we would be going back home. We prayed and waited. And during the wait, our friend and photographer, Meg Brock, was able to come and take photos to document our liver transplant journey. The following photos are thanks to her incredible work.




At 7:30pm, we went to pre-op and continued our wait. The nurses were so kind and so excited with us. Abby was not sure what was going on but was content to watch Daniel Tiger. Dave and I cried, prayed, chatted and prayed some more. Choosing to place your child in surgery knowing that the next few weeks ahead were going to be so painful  but the resulting rest of her life was going to be amazing was so hard to do. Abby never ceases to amaze us and we knew she would do the same in this situation.

At 9:30pm, we got the call. The liver was a GO! This was Abby's liver.




We were ecstatic and yet, the wave of emotions knowing that in our joy another family was suffering a heart wrenching loss was quite the emotional journey to navigate. 

From that moment on, things moved quickly. At 10:20pm, we said our "See You Laters" and watched as they wheeled our precious baby girl back to surgery. We knew the risks. We knew the possibilities. But, we were trusting an All-Knowing God and Great Physician for the outcome. We knew beyond a shadow of a doubt that that night, God was in the OR room with Abby and her nurses and doctors.




Sending your child to surgery has got to be one of the hardest things you do as a parent. This was our 4th time watching her be wheeled into surgery... and it never gets easier. Dave and I bunked in the OR waiting room for the night. We were the only ones in there. We ate some snacks. We watched some TV. We texted friends and family. And, since we had both been up since 4:30am, we tried to close our eyes. At 3:30am on Sunday, the surgeon walked into the room. "Surgery went beautifully," she said. "Abby tolerated everything great. We were able to connect the liver up perfectly to all of Abby's veins, arteries and bile duct. We were also able to take the breathing tube out after surgery. There really isn't much to tell you. Surgery was pretty much textbook." The wave of relief was overwhelming. Then it occurred to me. "Wait, the whole liver?" I asked. "Yes, Abby received a whole liver." the surgeon said. The ramifications of that single word "whole" sent Dave and I into another realm of emotions. That night as we rejoiced in LIFE being given to our daughter, another family was mourning the loss of their child... a child in similar size to our Abby. Because of the selfless choice of another mother and father in a devastating situation, our daughter was given the gift of life. 
 
 As we waited another 45 minutes for Abigail to be transferred to the PICU, I couldn't help but think about all the times in Abby's life where we have seen the sacrifice of selfless love bring about an amazing opportunity for Abigail. Her birthparents, 2 1/2 years ago, selflessly choosing to place her for adoption knowing that her life depended on it. Dave and I choosing as her adoptive parents to selflessly raise her as our own regardless of the medical outcomes in her life. And now, another mother and father selflessly choosing to donate life from their own devastation so that other children, like our Abigail, could receive a new organ and continue to have LIFE.