Tuesday, November 10, 2015

Happy Lungaversary to Me!!

A year ago today as I was signing a consent to be put on life support, the phone rang and it changed my future. "My" lungs were available! 
I was rushed through the preop process, they found the lungs to be perfectly suited for me and I was wheeled into surgery. 
However, as surgery began, my body finally gave up. They had to do CPR for 10 minutes. They finally did get my heart to play nice and decided to go ahead and put me on bypass and start the surgery and hope for the best, not knowing what kind of brain damage might have occurred from the CPR. 
About 20 hours later I woke up. Heavily sedated, but awake enough to see my parents and Steve standing over me with big worried eyes. I was still intubated but I could see the relief in everyone's eyes through their tears and mine, when they told my I was all finished. They told me that my lungs were perfect and asked if I was feeling ok. I'm pretty sure I shrugged my shoulders and rolled my eyes at that question, (hee hee) that's when they knew I was going to be ok.  
From the moment I took my first "new" breath, I felt better than I had in years. Of course my body was sore, but those lungs immediately felt like they were right where they were supposed to be. 
My recovery overall has been amazing. Zero rejection from day one, praise God! I still say I'm recovering because I think it's a long physical AND emotional process. My body changed so much in the last year. From being nearly bedridden for 6 weeks preop, and then immediately on a treadmill 10 days after surgery, my body was certainly thrown for a loop. It's been a long road to get any sort of muscle tone back. Taking a handful of pills every morning and night is no fun either, but if that's all I can complain about,  I'd say I'm doin just fine! Being able to actively participate in my family and friends' lives again has been nothing less than amazing. I'm pretty much back to "normal" (haha relatively speaking) and able to play with the kids, take care of my family, run up and down stairs (sounds mundane to you, but it was something I couldn't dream of doing for the last 2 years!) 
I'm very proud to say I have  finished three 5ks. I'm pretty sure i'll never set any blazing records, but I'm hoping to someday actually have a decent time.  For now I'm over the moon with the progress I've made. 
Everyday I'm just so thankful for God's faithfulness to me for delivering me through a trial that just 5 years ago we never could have even imagined would happen. It will always bring tears to my eyes to look back and see how miracle upon miracle happened in my transplant process and I just can't call that luck. God's grace and mercy certainly did shine on me.
I'm so grateful for the awesome family and friends that we have. It's an amazing thing to see a community of people- from my friends, to the church, the kids' school, the fire department, and even complete strangers pulling together not only for me but for Steve and the kids, too. From calls, texts, visits, prayers, food, facebook messages, donations and gifts-even though I was hundreds of miles from home I never felt alone. Steve definitely got to deal with the "worse" part of "for better or for worse" and I can't even imagine going through that without him. His strength and encouragement when I was ready to give up was what got me through many of those preop days. 
He and Jolie really kept the kids life as "normal" as possible and I'm so thankful for both of them and the sacrifices they made to be with me or the kids at all times. 
Lastly, I'm eternally grateful to my donor and family who made the decision to donate organs in what was probably one the most horrible moments of their life. I absolutely do think about my donor on a daily basis. People often ask if my lungs feels different or if breathing feels different. It's not at all. It's like a Cinderella story actually (ha-minus the princess part)  A perfect fit! The only difference is in my head- I very consciously do think of my donor every day, every time I take a walk, do something fun, celebrate my kids' birthdays, look at the ocean, swim in the pool... EVERYTHING makes me think of him. (for the record I don't know if its a him, but I've always had a feeling) Days that I don't feel like working out, days that I wanna sleep til noon - those are the days that I make myself get up and move. They can't. But I can. And I will! 
Making the decision to donate your (child, spouse, mother, etc)  organs when you're facing the imminent loss of a loved one is so brave and selfless and I'm so thankful for them. So while I celebrate this day- a whole new year that I'm living and breathing, remember someone is remembering this day, too and probably grieving. Please say a prayer for that family, too. For without them I'd not be here either. 

So anyway, I will continue to be thankful for every breath and every moment. So take a big deep breath with me and celebrate every day. Life is so amazing and breathing is beautiful! 





Sent from my iPhone

Thursday, January 1, 2015

Happy New Year!

It has certainly been a while since I last posted. I am happy to say it's because I am home! I have been busy unpacking and getting ready for Christmas and just enjoying my family. It's been a long time since I first left home and I can't describe how good it is to be home again.

I guess I have a lot of catching up to do. Most of you know the details but I'll give you a quick rundown of life since the transplant.I was discharged from the Cleveland Clinic on November 19th. 9DAYS after I had my surgery.  My post op course was pretty easy.  One slight speed bump is that I had a pretty traumatic intubation which damaged a vocal cord.  So I had Botox injected into my paralyzed cord. (I tried to get him to do my eyes and forehead too...but no dice) My voice still isn't 100% the same, but it's not really a problem. The pain has really never been too intense.  In fact, I still think it was harder to move around after my C-sections. It has lingered a bit longer then the c-section pain, but I guess until my sternum is totally healed I'll feel it every time I cough, sneeze, hiccup, etc.  My incision is about 6' long right down the center of my chest.  I wouldn't think twice about posting a picture but I forget not everyone is a nurse or fireman and that ugly scar is probably not family friendly reading. haha

After my discharge from the hospital I moved into an apartment in Westlake. My Dr wanted me to stay in the Cleveland area for about 4 weeks. I had a home health nurse and physical therapist come by a few times to check in and had appointments about once a week at the clinic. Steve spent most of this time at home during the week managing the kids and working, and my family and friends graciously took time away from their own families and took time off of work to come and stay with me because I wasn't allowed to be alone. So Jolie, Amie, Carrie, Deborah, my parents, Billy and Teri carting our kids up to us...I know that THANK YOU will never be enough, but I hope you all know how your sacrifice to help me and my family was so appreciated and I don't know what we would have done without you. It an amazing feeling to know that I have such an amazing support system in place without ever even having to ask, they just kinda dropped everything on a few days notice and showed up. It was amazing and I'll be forever grateful. It definitely changed my perspective on the true meaning of loving your friends. God obviously put these people in my life for a reason and I'm very thankful for that.

I had a few (routine) bronchoscopies- one at 3 weeks and one at 5 weeks.  This is an outpatient procedure where they put me to sleep and stick a camera down into my lungs to check the anastamosis sites (where the new lungs are sewn to my own bronchi) and also take a few biopsies. Both showed no rejection or infection so after about 5 weeks I was released from Cleveland's snowy grip and I got to come home. My goal was to be home for Christmas, and I made it home on December 19th.

Literally on our way back into town we were greeted by the Fire Department where Steve is the Chief in the front of the firehouse with all the trucks pulled out with the lights on and a few trucks and personnel from the neighboring departments too. The TV news and the newspaper were both there too. I wish I would have known this.  I may have at lest attempted to put on some makeup or comb my hair, but I guess my sweats and baseball hat is the "real me" anyway.  haha
The Fire department and our local community, the kids' school, teachers, and our church have also been an amazing source of support for us. Letters, donations, phone calls, yard work, all were done with no questions asked...sometimes by total strangers. Donations from FD's across the country who all just wanted to "help a brother and his family".  I'm humbled and blessed to be a part of such a tight knit community of people just wanting to lend a hand-no questions asked, and no thank you needed. SO to those of you who got overlooked in my attempts to keep up with my thank you's- THANK YOU!!! We sincerely appreciate your support of our family.

Since I have been home I'm slowly adjusting to life with really nice new lungs that are working perfectly! I have more energy than I have had in years. I am now 7 weeks out from the transplant and other than some soreness and still getting tired pretty easily, I'm feeling great-even able to walk on the treadmill 1.5-2 miles a day.   We enjoyed Christmas with the family. The Christmas stomach bug of 2014 took a few of us out for a few days...some of us were lucky enough to have it twice...but other than that, it has been wonderful to be home. The kids are adjusting to the "iron fist'" being back in town (haha) and we are all slowly settling back in where we left off. My problem is I THINK I have more strength and endurance than I really do and I end up exhausting myself around the house or running little errands by 2:00 in the afternoon. I have to remind myself that recovery is a marathon not a sprint.

I'm slowly becoming more sociable, but with flu season in full swing and worse than ever, I'm still pretty picky about where I go and who I see.  It's not going to be back to "normal" activities  (school functions, church, parties, etc) for a while. I take medicine that keeps my immune system from attacking the new lungs because it thinks they are foreign objects that don't belong here. This, in turn makes me extra susceptible to any and all germs that come my way. So I tell myself I have all the time in the world to catch up with all of my friends and favorite restaurants. I'll get to them eventually, but right now I have to be super vigilant about protecting myself.  I  am constantly using hand sanitizer and I'm even getting used to the looks of disgust when I walk into Walgreens with a mask on. I want to yell at the staring mothers who steer their kids away from the germy lady with the mask on "I'M NOT CONTAGIOUS! YOU ARE!!! haha  (but thanks anyway from steering your snot-bag kid in another direction!) ha

So that's about where we are. I'll go back to Cleveland next week for a couple of appointments. Hopefully everything is still A-OK and we keep on keepin' on.

Thanks again for your continued support. Your thoughts, prayers, donations, calls, texts...they all mean the world to us.  Any time I'm having a bad day, or I'm depressed about sitting here in this house all day, I can open the mail or facebook or twitter and have new messages of encouragement waiting to be read, or a package from a stranger. That's all it takes to get my head back on the right way and realize I have so much to be thankful for. I have been given such an amazing gift. A second chance, and I hope to make the best of it. I can't wait to start paying it forward.

So here's to 2015. Be thankful, and make every breath count.  I know I will! Love you all!

~Mollie
 

Saturday, December 20, 2014

Mollie HOME!!!

Just wanted to let everyone know Mollie is HOME!!! The local paper and tv news did a story about her one more about her and the journey (see link below) and the other about the importance of being a organ donor.

What an amazing journey it has been, I have started to write something, I am not sure if it will be a class, speech, book, blog or something just for me but the whole process has been extremely humbling and making me realize how precious life is, how quickly it can change and how important the little people in your life are that you often take for granted.

With that said I hope everyone has a GREAT holiday season, Merry Christmas, Happy New Year and know the I appreciate everything you do for my family, the fire service, the schools, our communities and our church’s, but again especially what you have done for me and my family and we love you!


Thursday, November 27, 2014

What we are thankful for this year By Steve Pegram

Twenty-five years ago, before most people across our country knew who he was, my good friend, mentor, brother and adopted father Billy Goldfeder invited me to his home in Virginia for Thanksgiving. The first year it was me, Billy’s wife their three little kids and a crazy friend from Florida. At dinner Billy asked each of us what we were thankful for? In recent years that Thanksgiving dinner of 7 has transitioned into a table of more than 40 people. As the “kids” became adults, they have their own kids and many new friends and families have joined in the annual tradition. Billy still asks each person to briefly say what they are thankful for and let me tell you over the past 25 years there have been a lot a laughs and a lot of tears at that thanksgiving table. The tradition continues today, but for the first time in 25 years I wont be there.

Thanksgiving has always been my favorite holiday of the year, I think for two reasons:

1. It is the least commercialized (no cards, no gifts and until a few years ago no shopping). 
2. It is truly a time to spend with our families and friends and reflect on what we are thankful for.     

Normally for me to miss this thanksgiving tradition would NOT HAPPEN! under any circumstance, but this year I am missing this tradition and it is so I can spend it with my family (Mollie, Jack and Riley) as we celebrate the greatest thanksgiving ever!

As most of you know my wife Mollie got sick, very suddenly three years ago. Her disease, pulmonary fibrosis progressed over the past three years quickly. Mollie’s doctors stated a lung transplant would be the only thing that could save her life. Mollie was “listed” for double lung transplant at the Cleveland Clinic in May of this year and we started to wait. First we cancelled our summer vacation and other plans because we thought surely the call to go to Cleveland would come soon, but that didn't happen. Summer came and went with no call and Mollie continued to get sicker. When the kids went back to school in the fall both Mollie and I were very discouraged, we had hoped to get the transplant call while the kids were off and everything would be so much easier, but that was not the way things were going to work.

By September Mollie was failing her lung test’s and the doctors at CC started to warn us that hospitalization pre-transplant might be needed. By October Mollie and I knew she was starving for air and the only way to get her the oxygen she needed would be in the hospital. On October 17th (The third Friday of October) I drove Mollie to the Cleveland Clinic where she was admitted to the lung/heart transplant unit. Ironically Mollie’s first hospital visit of this disease was on the third Friday in October 2011, exactly three years to the day.

At CC they increased her oxygen to almost 30 liters, for those of you who are not EMS people thats twice the flow we can deliver by mask in an ambulance to a patient and sounds and feels like someone is shooting an air compressor hose at your face. In the hospital Mollie was finally getting enough oxygen, but her lungs continued to deteriorate at a rapid pace. During this time I drove back and forth between home near Cincinnati and Cleveland multiple times as did Mollie’s parents, sister and other friends and family. We took care of the kids at home and tried to make their life as normal as possible while also carrying for Mollie. We tried to make life in a hospital bed as comfortable as possible. On the weekend of November 8 - 9 I was in Cleveland just for a weekend visit, but I felt like I needed to stay a few more days.

On Monday November 10th the doctors told Mollie that her breathing was getting too hard, she wasn't oxygenating her blood enough and damage to her other vital organs had started and would progress which would be very very bad. The doctors recommended we put Mollie on ECMO (Lung ByPass) which is a surgical procedure that would also require a trache to be inserted in her throat. Mollie was very upset, as a nurse for more than 15 years she knew that this was the end stage/last resort treatment for a patient awaiting a lung transplant. It would mean Mollie would leave the comfort of a private hospital room and be moved to the ICU till transplant and potentially be placed on a ventilator. The doctors assured us that ECMO would keep Mollie alive longer and healthier to await transplant. 

Around 1 PM Monday I updated Mollie’s blog http://waitingformysecondwind.blogspot.com as well as our Facbook and Twitter sites asking for prayers for Mollie, as well as the doctors and the procedure she was facing. Our pastor driving home from an appointment prayed in his car, many of our friends texted us, posted, re-posted, tweeted etc prayers across the country for Mollie and this difficult next step in this process. Mollie was scared, I was scared, but we put our trust in each other and especially our faith and trust in God that things would be OK. 

Around 2 PM the surgeon who would do Mollie’s ECMO surgery came to meet with us and answer any questions before she would sign the consent for surgery. Literally as Mollie was signing the paperwork her phone started to ring, the caller calmly said “Mollie we think we have your new lungs”!

Imagine the joy, excitement, fear, love, and every other feeling/emotion you have ever had; when you got married, when you got engaged, when you saw your first born child for the first time and then triple those emotions and thats how I felt all at once. Mollie and I hadn't really talked about it but thru the unspoken words that only spouses can communicate threw both Mollie and I knew the end of her life here on earth was close and now she would get that second chance we had almost given up on. 

We received at that moment a true answer to prayer, our prayers, our friends prayers, our families prayers all at once lifted Mollie up and gave her the second chance, the second wind we had been waiting for. 

We quickly packed weeks worth of decorations pictures, clothes, flowers etc so Mollie could be moved to pre-op. When you are a transplant recipient there is not much you know about the donor, where its is coming from? who? how old? what happen and after a little while and it all settles in you realize in this moment of your greatest joy for a “second wind” some other family somewhere else had to say goodbye to a loved one in order for Mollie’s life to be saved. I said many prayers that night; for Mollie, for the doctors, but especially for the donor’s family for if they hadn’t made the decision to donate organs Mollie’s life wouldn't have been saved that night. 

Family and friends scrambled to pick up kids and others headed to Cleveland. Mollie’s Mom and Dad arrived and were able to visit with her for a few minutes, one of our pastors Elder Justin Huffman also arrived and said a prayer with Mollie and I bedside in the ICU. My best friend since I was 12 Ed Kline jumped on an airplane in Philadelphia and arrived in Cleveland just after midnight to sit with me during the 10-hour surgery.

Mollie went into surgery just before 2AM on 11-11-14, Veterans Day. We didn't get any updates for almost 6 hours, to say it was the longest night of my life would be an understatement. I walked, prayed, eat, tried to nap, walked, paced, eat, tried to nap for an eternity. Just before 8 AM we received a call that the surgery was progressing well, everything looked good. A small relief, but still we wanted to see the surgeon and hear it from him. Around 10 AM Dr Tong walked out to meet with us the surgery was over, the lungs looked “perfect” and overall the surgery went well. Just before they started the surgery there were some complications that I wont go into, but lets just say Mollie took a peek at heaven for a few minutes and decided to stay with us here on earth! What a blessing! The doctors only concern was would Mollie wake up? 

We got to see Mollie a few hours later, still asleep, intubated in the ICU. As I leaned over and whispered in her ear that the surgery was over, she had new lungs and the doctor said they were perfect. Tears rolled out of the corner of her eyes. We had discussed pre-operation if she would be able to hear me when she was asleep? Mollie told me “just talk to me” so I did and  apparently she could hear me and that brought comfort to me knowing that she knew she was going to be OK.

The next few hours was monitoring her in the ICU, she would wake up and look at me, nod yes and no to some questions before she would fall asleep again. The ventilator was removed and Mollie was breathing on her own with her new lungs within 12 hours of surgery. By Wednesday morning the breathing tube had been removed and Mollie’s “second wind” was working on its own. It was amazing to look over and see the oxygen saturation which had been so low for so long reading 98%. Thank You God.

Mollie spent a few days in the ICU, a few more days back on the heart/lung floor before being discharged from the hospital10 days post transplant. We are now living in an apartment in Cleveland. Transplant patients have to stay near the hospital for several weeks for checks up and meetings with the doctors. The biggest thing they are watching for is rejection, our body has a very sophisticated immune system and it will detect and attack the donor lungs as not belonging. To combat this the doctors placed Mollie on a host of medications to trick her body into not rejecting her lungs and allowing them to heal.

Early on in this process the transplant coordinators told us that we need to prepare financially for the post transplant medical expenses. They told us how important it was to raise money. Neither Mollie or I felt comfortable with asking people for donations, quickly a group of our friends led by Steve Oughterson, Billy Goldfeder and the Goshen IAFF Local assisted by many others did it for us. While Mollie was still at home they had a dinner with a silent auction in her honor. The group was able to raise several thousand dollars for Mollie’s post transplant care and medications. They started a tax deductible donation website at helphopelive.com for Mollie and hundreds of friends, family and even strangers donated to Mollie’s campaign. 

It all paid off in a big way. While still in the hospital they provide the patient and their care giver (me) several classes on signs and symptoms of rejection, PT and pharmaceuticals. They then run all the meds that have been prescribed for you thru your insurance company and then tell you the cost for the first 30-day supply. Mollie’s medication for the first 30-days was $3,600 after insurance. What a blessing to know that we had the money to pay for her medication thanks to the giving of so many of you! The doctors told us the first few months would be the worse, but as some medications are weened off the cost would go down to closer to $1,000 a month. So far we have the first few months of medication paid for; so thank you for all of you who have donated to Mollie’s fund.

That pretty much brings us today, Thanksgiving. So what am I thankful for? 

I am thankful for:

First and foremost Mollie, my wife, my friend, my babies momma and the gift of her second wind.
My kids, they have been super through all this and seem so easy to just live out of a backpack for months.
Jolie Autry, Mollie’s twin sister who probably in a weird twin sort of way was closer to how Mollie felt than anyone, Jolie watched our kids, loved them like her own, stayed with Mollie when I had to work, coordinated fund raisers, updated friends and family and was an absolute rock throughout this whole process. 

The rest of our family, especially Mitch (Jolie’s husband), Nick and Judy Sargent her mom and dad who also pulled multiple shifts at home with the kids, babysitting so I could go to a budget meeting, dog sitting etc. I have often said even before this event that one of the biggest bonuses of marring Mollie was gaining her parents, they are my best friends and I call them Mom and Dad like they are/were my own.

My Mom and Dad, They dropped everything and came to visit for several weeks and helped around the house, cleaned things I just didn't have time to, cooked dinners and provide some other support that only they could. They must be coming back because they left cloths in the closet and a suitcase, and thats OK with us.

The doctors, nurses, PCA’s and entire staff of the Cleveland Clinic. What an amazing place. We will be forever in debated to them for saving Mollie’s life and thru the process made some great friends, but also met many other families who have or a re going thru the same journey what a great place, its like the disney world and FDIC of the medical field all wrapped together.
The donor and their family, you are unknown to us but we are so thankful they choose to be a organ donor.

Steve and Deborah Oughterson, long time friends Steve and I both worked together at LSFD and we use to be neighbors. Steve has stepped up to do anything big or small, totally handled coordinating fund raising activities etc and even cut my grass and raked my leaves etc while I was in Cleveland. For those of you who are firefighters Steve puts the “brother” in the word “Brotherhood” and he always does it quietly and without any fanfare, thanks Steve O

Ed Kline, Ed has been my best friend since the early 1980’s, we became firefighters together, we were best man in each other wedding’s and talk regularly by phone. Mollie refers to Ed as my other wife, and honesty how many of you have a friend who with less than an hour notice drops everything he was doing and fly’s to Cleveland to hang out while Mollie was having surgery. Thats the kind of guy Ed is he would give the shirt off his back even though it would be a few sizes to big and not even ask why I needed it. thanks Ed.

Billy G, Teri and their family, just like Billy updates the fire service he updated many of you and served as the unofficial secretary of this little journey. He made sure everyone was in the loop and also consulted with experts all across the country to make sure Mollie’s care was the best and right choice. Thanks Billy, don't forget who was the original thanksgiving guest and save us our seats for next year.

Goshen Fire and EMS, especially Captain Robert Rose who has been serving as acting Chief off and on for the past few weeks. When I checked in with them I would get the same answer “Chief we got it” and they did. I am so proud to be their Chief and all the accomplishments we have made together over the last five years, but especially the love and support they have shown me and my family more recently. 

My boss Ray Snyder and the Goshen Township Trustees Lisa, Claire and Lois as well as our Fiscal Officer Cheryl who coordinated fund raisers, offered food and babysitting and when I tried to come to work told me to go home and take care of my family, thank you!

My kids school Milford Christian Academy, they raised money, sent cards, offered to baby sit, tutor, dog sit, cut grass and do anything we needed. Most of all they prayed for Mollie, me and the kids fervently and we felt their prayers working in our lives and especially in Mollie’s. I LOVE our school family.

My IMAT chief’s, those are the fire chiefs who boarder Goshen and respond on serious calls, they all have stepped up both in responding to calls in my absence but each of them routinely checked in and offered support. Thank You Chef’s Huber, Rose and Kelly!
The Board of Directors and Membership of ISFSI and Pennwell/Fire Engineering these fire service groups stepped up and took care of huge projects during my time away and also reached out all across the country to rally support for me and my family. The hundreds of prayers, post, emails, tweets, donations and phone calls were greatly appreciated and almost always came at the most low and opportunist time.
Our Church, another one of the greatest gifts I got by marring Mollie (besides our kids, her family, her parents, her crazy friends) was our church! Mollie is the 3rd generation attending Cincinnati Primitive Baptist Church. Pastor Lassere Bradley has been there for more than 50 years and baptized Mollies grandparents (Both sets), parents, brother, sister, Mollie, me and now Jack. He also married Nick and Judy as well as all the kids. To say we are a little close to our pastor and our church family would be a huge understatement. My faith in our lord and savior Jesus Christ, my salvation thru gods grace is all because Mollie took me to church with her, after wandering the earth unfaithful for so many years I found exactly what I was looking for in a church and a family at CPBC.
On Sunday 11-16 Brother Bradley spoke about Mollie as he used Philippians 4:13

“I can do all things through Christ which strengtheneth me.”

So as I celebrate my favorite holiday, Thanksgiving with my beautiful bride and our awesome kids I want to remind each of you that God is great, God answers prayers and we all can benefit from being a little less selfish, a little less worldly and a little more giving in our life in a lot of different ways. 

Your prayers saved Mollie’s life and that is what I am most thankful for this year! 

What are you thankful for?

Love 


Stephen

Monday, November 24, 2014

So excited to report that I had my 2 week(!!) post transplant appointment today. Everything looks great. My Doctor was THRILLED (her words!!) with my progress so far. My new Lungs are clear, vitals are great, and (based on blood work only) my body isn't "angry" as they say at the new lungs yet. No inflammatory response yet- that's awesome, and my body (liver and kidneys especially) seems to be handling the anti rejection meds well (except for a few expected side effects). I'll have a bronchoscopy next week to have some biopsies done and that will give a very clear picture of how they look on the inside, but this is the best possible news We could have asked for today.
Finally got some rest now that I have been out of the hospital for a few days. Steve and the kids are here for the week to spend thanksgiving together. I have been doing my excursuses and walking the halls here and am amazed at how well my new lungs work. Its almost hard to get use to breathing normal again after struggling for so long.

So continuously thankful to God for His daily miracles and mercies (and yes they are daily!) and I could never thank you all enough for the thoughts, prayers and support. 

Saturday, November 15, 2014

Steve here, thought I would give the whole week-long synopsis:

Sunday, Mollie was doing very poorly, not able to catch her breath, pulse was racing and her oxygen saturation was dropping dangerously low. Doctors recommended putting her on ECMO, which essentially is a lung bypass machine. This procedure would require surgery, and they would insert a tube about the size of a garden hose in her neck which would take the blood directly from her heart, filter and oxygenate it with a machine that bypasses the lungs and then pumps it back into the heart for distribution to the rest of her body. Once in place,  her lungs wouldn't work any more, ever, but it would keep her alive a few more weeks in hopes that a match would be found. As you can imagine, this was probably our lowest point in this three year journey, and we spent the night Sunday worrying and praying for wisdom, knowing that without this radical step or a new set of lungs, Mollie's life could be cut short very soon.

All along, Mollie has been listed very high on the donor list. The delay had been her size. At 5'2", she is considered small for transplant and most donors are adult males who are typically 5'10 -6'2", therefore their lungs won't fit. 

Monday, the doctors returned and told us if we were ready, they could perform the surgery to place her on ECMO that afternoon.  I posted an update on Mollie's blog and Facebook, asking for prayers on her behalf and several of our friends and family shared that request and "tweet's" were sent out all across the country, through friends and several firefighter networks as well. An hour after posting the prayer request for Mollie and the ECMO surgery, the doctor returned to get her written consent for surgery. As Mollie was signing the forms, her cell phone rang, and the voice on the other side of the phone very clearly said, "Mollie, we have lungs for you!"!

Prayers were answered just when Mollie needed them the most and the path of her life instantly changed. Instead of prepping for ECMO, we prepped for transplant! Doctors, nurses and techs from all over the hospital ran into our room to congratulate us on the good news. Mollie's nurses openly cried with her at the bedside, and tears full of fear moments before were replaced by tears of joy!

We quickly packed up her room where she had lived for three+ weeks, called the family, and she was moved to the ICU to be prepped for surgery. They do not tell you anything about your new lungs, where/who they came from is confidential. The only information we were told was that the surgery would be early in the morning on Tuesday. There was still several go/no-go hurdles we had to cross. The donor is tested for lots of diseases and other contra-indictors, just to make sure the organs are suitable for donation, and if everything looks good its a go. Next, a surgical team is sent by ambulance, helicopter or jet to harvest the lungs from the donor, and if they don't look good the surgical team can deny the lungs; they looked great, so we were still a go for transplant. Then the lungs arrive in Cleveland and the surgical team here inspects the lungs before surgery.  They determined that the lungs looked really good and we were given the green light for surgery around 1AM Tuesday. 

By this time, Mollie's parents and one of our pastors, Eder Justin Huffman, had arrived and we all sat with her and prayed with her as her anxiety was thru the roof. Mollie was having a very hard time breathing and the doctors were trying to calm her and keep her stable. Around 01:45 they took her back for surgery and we headed to the family waiting room to wait for news.

8 long hours later, her surgeon, Dr. Tong came out to let us know the surgery was over. Dr. Tong told us the lungs looked perfect, and the surgery overall had gone well. 

Mollie was in the ICU Tuesday - Friday. The first few hours she was sedated and intubated, but if you talked to her tears would roll out of her eyes and she would move her eyebrows. She had the tube removed from her throat and was breathing on her own with her new lungs within 12 hours of her surgery. Thursday she was sitting up, no longer sedated, talking, etc. Other than not getting any sleep, she was doing great. She did have a paralyzed vocal chord, which complicates swallowing and talking. Friday, they injected some gel into her left vocal chord, which appears to have fixed the problem. They tell us it is common with people who were intubated for an extended period of time.

Friday afternoon, after they did a swallow study to make sure she could eat properly, and after the vocal chord procedure she was discharged from the ICU, back to the 8th floor where she resided pre-transplant. She is back in a nice private room with more peace and quiet. She will start physical therapy bedside tomorrow and as long as there are no complications she should be released from the hospital by Thanksgiving. 

She is required to live in Cleveland for about 6 weeks. We have rented a furnished apartment for us to live in as she will have frequent visits to the Cleveland Clinic for check ups and tests. As long as there are no complications each week she will have fewer and fewer appointments, until they finally will let her go home. She will be on a host of medications for the rest of her life, these medicines are expensive ($1,000+ a month) after insurance, but will hopefully prevent her body from rejecting the lungs, which is always the major risk of any transplant. To help with the life long medical expenses Mollie has a taxer fundraising account set up at https://m.helphopelive.org/campaign/5178
The whole process has been amazing, from the care we have received, to the miracle gift of new lungs. More than anything, we have seen the HUGE benefit and power of prayer! We rejoice in God's grace and mercy on us and the miracle of the new life Mollie has been given. We also continue to pray for the donor's family, as they are unknown to us.  But their loss is our our gain, and we are so thankful they chose to be a donor family.

Thanks for your care, love, prayers and support.

Steve

Monday, November 10, 2014

Hey friends. Just thought I'd give you a short update. Still waiting for those lungs. Unfortunately, they are starting to think that I may need to be moved to the ICU to continue my wait. I'm holding my own and I'm stable for now, but the fear is if I take a bad turn it could go downhill fast. So I'm hoping I'll prove them wrong and I'll keep maintaining here, but it's a very real likelihood that I'll end up there in the next few days.
 
Please pray for me. It's obviously very scary and also discouraging to still be waiting for lungs. But I certainly know and trust that God's in control. The lady who cleans my room said "honey he didn't bring you all this way just to drop you off!" I know that's right and I ask that you guys all keep praying for me and my family