As part of new kid's book project, we will have a song and a video. We need videos of kid's explaining what Congenital Diaphragmatic Hernia is in their own terms. The best one will be created into the text of the new kid's book!
Simply video tape your child (cherub or sibling or cousin) explaining the best that they can (in kid's term) what CDH is. Then send us the video to events@cdhsupport.org
Video entry deadline is August 5th - we need to hurry these up so we can vote and get these books done for our CHERUBS HOPE totebags! :)
Wednesday, July 29, 2009
Tuesday, July 28, 2009
CHERUBS Adopt A Hospital CDH Program - CHOP adopted in honor of Braden Holt
Braden HoltCongenital Diaphragmatic Hernia Survivor
For more information on our Adopt A Hospital program, please visit http://www.cdhsupport.org/donate/hospitaladopt.php
Braden's Story:
Braden was due to arrive on March 19th, 2008. We were anxiously awaiting the arrival of our second child, our first boy. Our daughter Brooke, a week shy of her fourth birthday, couldn’t wait to be a big sister. After an uneventful pregnancy, Braden arrived six days early on Thursday, March 13th, 2008.
The moments after his birth seemed normal. He arrived alert with his eyes open ready to greet the world. My husband cut the cord and his nurse took him to be cleaned. We heard him cry. He was swaddled. It was then that that nurse told me she didn’t like his breathing. She let me visit with him for a minute and he was placed in my arms. Our visit lasted a few seconds as we realized he was not weighed. The nurse unwrapped him, placed him on the scale, told us he weighed seven pounds and six ounces, and took him away to the nursery.
At this time I was still in the birthing room with my husband and my mother. My labor nurse explained that Braden was probably having some transitional breathing problems. We weren’t worried about anything. Braden has made his entrance to the world, the fast and painful labor was behind me, and soon we would be bringing our beautiful daughter to meet her baby brother. My labor nurse kept coming in to say that she would send a doctor in to talk to us but that never happened. She had to deliver the devastating news herself. Braden needed surgery.
We could barely comprehend what we heard. We knew he was going to be transported to The Children’s Hospital of Philadelphia (CHOP). Although we were told, we had no idea what was wrong with our son other than that he needed surgery to correct something with his intestines. I was taken to a recovery room. My husband, mother, and I were able to get to the nursery to see Braden before they transported him by helicopter. We just cried as the nurses were helping him breathe. We tried to be strong, we told him to fight, and then we kissed him for the first time. After our short visit he was on his way.
There was not room on the helicopter for my husband. We returned to my room still in shock. We were still trying to understand what was wrong Braden. How could someone so perfect on the outside have something wrong on the inside? I was told I could be released whenever I wanted but my mother insisted I stay in the hospital for at least one night. It was determined that my husband would return home, break the news to our daughter and the rest of our family who thought Braden arrived healthy, and immediately drive to CHOP to be with our son. Luckily, Philadelphia is only an hour away from our home.
The next few hours were spent trying to understand what was going on with my son. I knew he had arrived safely at CHOP. I knew he was stable and most likely going to have surgery the next day. Many doctors came to visit me and my obstetrician said you are going to hear “CDH” a lot. That was the first time I actually heard Braden’s diagnosis as he explained that “CDH” stood for Congenital Diaphragmatic Hernia. I had never heard of it before. Everyone that came to see me kept saying things like, “My prayers are with you” or “I’ll be praying for your son.” I didn’t understand why everyone was praying; I thought they were just trying to be nice. After all, I was a mother in a maternity ward without a newborn. Why did my son need prayers? Nobody told me he had anything seriously wrong with him. He simply needed to have his intestines fixed.
There was no time to be emotional as my daughter arrived at noon for visiting hours. I didn’t want her to see my fear. She understood that her brother had a “boo-boo” that needed to be fixed but she really wanted him to be with me in the hospital. After all, every big sister book we read to her happened that way. One of the pediatricians from the practice I take my kids to came in to check on me. She also offered her prayers. By this time I was used to politely saying thank you. She then said something that shook me. She said, “It’s really hard to say how these babies will do.” I didn’t hear exactly what came next but it was something about lung function. Suddenly, I realized why everyone was praying. Braden’s condition was very serious.
I tried to remain positive, as the reports I was receiving from my husband on Braden’s condition were good. My husband was becoming the expert on CDH and was told all about ECMO and his diaphragm repair. We tried not to think about how long he would remain in the NICU. We just wanted our son to have his surgery and start on his recovery so we could bring him home. We refused to look up any information on CDH and put our trust in the doctors who were caring for Braden.
I was released from the hospital the next morning and my father drove me to CHOP in time for Braden’s surgery. It was so difficult to see him on the ventilator but his nurse, Laura, explained everything and made the situation a lot less scary. She had him all prepped for his surgery and would be with him throughout the procedure. My husband and I stayed with Braden as all the equipment for his repair was wheeled into the NICU. We couldn’t believe they were bringing the surgery to him in the NICU. He didn’t have to be moved at all! His surgery was a success and he did not require a gore-tex patch. Braden also never required ECMO support.
Braden stayed on the ventilator for a few days after his repair. We were able to hold him two days after his surgery. He was excavated the next day and was able to breathe on his own. He was able to eat by mouth and did not require an NG tube. He was slowly increased to full feeds. As a precaution he was placed on reflux medicines since many CDH babies experience reflux. His scar opened at one end; which required a seven-day treatment of antibiotics for an infection. Braden had a hearing test and an MRI before he was released. Mom and Dad were required by the hospital to take an infant CPR class and watch videos on Shaken Baby Syndrome. Braden experienced no major set backs during his CDH journey. He was definitely the rock star of the NICU!
Braden came home on March 25, 2008 after twelve days in the NICU. This is an incredibly short stay for a CDH baby. He came off all of his reflux medicines at two months of age. He is now seven months old and is doing remarkably well. He can light up the room with his smile and is the most delightful baby. He will always be our miracle and we are so blessed to have him as the newest addition to our family.
CHERUBS Adopt A Hospital CDH Program - Duke University Medical Center adopted in memory of Shane Torrence
Shane Torrence(1/28/93-9/11/99)
Left-Sided Congenital Diaphragmatic Hernia
The family of Shane Torrence has donated funds as part of our Adopt A Hospital program to send CDH materials to childrens' hospitals who treat babies born with Congenital Diaphragmatic Hernia. Shane's family has chosen to adopt Duke University Medical Center, where Shane spent the first 10 months of his life. Donated were; CDH information poster, "Stories of Cherubs" Vols I & II, Congenital Diaphragmatic Hernia Awareness Ribbon pins, Parent Reference Guides, Newsletters and brochures. This is enough CDH information for 100 families.Left-Sided Congenital Diaphragmatic Hernia
Shane's Story:
This is our family's story- Shane's story. I am a firm believer of the "telling it like it is" ideology, so this story is very personal, this is my life, my son’s journal.......
I was 18 when my son was conceived, in May of 1992. I was still a baby myself though you couldn't convince me of that at the time. My husband, Jeremy, and I were newlyweds. We were high school sweethearts and were married 2 months after graduation in the small church that his father pastored. My family had moved to our small town in Virginia when I was 14, after my father retired from the Navy. Jeremy arrived here a year earlier when his father was called to preach at the local Methodist church. Jeremy was working at a carpet mill and I was working at a grocery store. We were thrilled when the home pregnancy test that I took came out positive. I had miscarried right after we were married and again, 5 months earlier, on Christmas Eve, and we wanted this baby more than anything. I immediately quit my job; I was afraid standing on my feet all day would cause another miscarriage. Our families were less than thrilled about our pregnancy, though they never said so. But we were young and determined to make a family of our own. I quite smoking and started prenatal vitamins. I was so set on having a healthy baby that I didn't even stand near the microwave when it was on. Life looked promising and we were madly in love with each other and the baby growing inside me.
I went to my first prenatal visit to an Ob-Gyn clinic affiliated with the closest hospital, 30 miles away. Everything looked good, until 3 weeks later when I started to bleed. I was terrified. I was only 7 weeks along and I knew the chance of another miscarriage was possible. "I can't go through this again", I thought to myself as I cried while Jeremy phoned my doctor. The doctor told us that there was nothing they could do, nature would just have to run it's course and that I should come to my next appointment, the following week. The bleeding continued for 2 days. We hadn't told our families that I was pregnant the first 2 times we miscarried. We were planning to tell them after midnight mass (I was raised Catholic). This time, I knew if I miscarried it would be a public loss. The days of waiting until my scheduled doctor's appointment were hell. But hell had only began.
During that visit to the clinic, the doctor performed an ultrasound. The baby was alive! He was moving, he even seemed to wave! Words can't describe the relief I felt. It was after that doctor's visit that my nightmares began. They plagued me every night for the rest of my pregnancy. They were always the same; the baby was born, a boy, laid upon my chest, and then when the cord was cut he turned blue. The doctor's took him away and I was left screaming "Where is my baby? What's wrong with my baby?" over and over until I woke up on my tear-stained pillow. It wasn't long before they invaded my daydreams also.
On August 26, during my third appointment, I told my doctors that I thought something was wrong but they all said I was a nervous "first-timer". I was diagnosed with a urinary tract infection, given a prescription, and sent home. A week later, I was back at the doctors office complaining of stomach pains. I was given more antibiotics and sent home. On September 10th, the pains returned. I went back to the clinic and was sent home, again.
Now four months along, we started to sing to the baby and reading it stories. I was very thin and started to show early and could feel every movement that they baby was making. Nighttime soon became "baby time". We began our ritual of family prayer, which included asking God for this baby to be healthy. Now September, Jeremy's mill was shutting down. It was the only mill in our small town and finding a job proved impossible. With the recession and unemployment rates soaring, jobs were as valuable as diamonds. Soon, our prayers included asking God to help Jeremy find a new job and to help us get along. The financial pressures, Jeremy's problems dealing with all this new responsibility, and my hormones were causing our first fights.
The next months went by fast as we tried to prepare for the holidays. Jeremy found odd jobs to sustain us until a permanent one could be found. He was not eligible for unemployment benefits and we were overdue on every bill. I tried substitute teaching but it didn't work out. We had to apply for Medicaid.. It was a terrible blow to our pride. It was a secret we tried to keep from our family and friends. We were ashamed to be on welfare but we had no other choice. This was not our dream for our baby's future.
By October 22nd, I weighed 136 lbs, up 26 lbs from my pre-pregnancy rate. The baby started a case of hiccups that lasted on and off for the next 3 months. Jeremy found work with a friend that owned a construction business but it seemed to rain constantly and work was often canceled. Halloween, my nineteenth birthday, came. I made my 18-month-old nephew a clown costume out of one of his sleepers and longed for the day when I could make a costume for my own baby. This day proved to be a distraction from our financial problems. Our families tried to help us out by loaning us money and it tore at our hearts every time it was offered. Our family, friends, and church were such wonderful support. We will always be grateful. Jeremy went hunting when he couldn't work but his luck wasn't any good when it came to hunting venison. With food running out, and all of our money going to pay bills, we started to worry about what to fix for meals. Then one night a strange howl came out from the back yard; it was a lost hunting dog owned by a neighbor a couple of miles down the road. We called the number on the dog's I.D. tag and his owner came to retrieve him. He was grateful to get his dog back and brought us venison. It was an answer to our prayers. That man will never know how much that meant to us.
Thanksgiving came and went with family celebrations. Maybe it was the pregnancy or maybe it was all the turkey I ate, but I was up to 150 lbs; the extra 40 pounds seemed to be all in my stomach. That Christmas we made every present that we gave. Jeremy was still making rounds to all the factories in a 50 mile radius every week, searching for a steady job. I stayed busy cross-stitching gifts for my mom and sisters and helping Jeremy with gifts he made from wood. During the second week of December, I went for another ultrasound. All of my doctors visits had been uneventful but my nightmares continued and after weeks of begging for another ultrasound, the doctors gave in. My mother and Jeremy were there with me. There was only us, the doctor, and a nurse in that small room, no trained ultrasound technician. We were in that room for over an hour and the doctor told me that everything looked normal. I was not given a picture of the ultrasound, though it is common for expectant mothers these days to be given at least three pictures. At my next appointment I had to ask for a picture. It was quite an attractive view of my baby's backside! Memories of the previous Christmas haunted me but this year I longed to share with my baby the story of Jesus, the trip to midnight mass, and the legend of Santa Clause.
During the last month of my pregnancy, I worked on the nursery constantly. I painted Precious Moments angels for the wall, sewed curtains and blankets, and sterilized all the baby clothes and equipment I collected from showers, yard sales, and hand-me-downs from my nephew, Clint. I was up to 160 lbs with only a little extra weight in my face and breasts; the rest was in my stomach. I looked like a snake that had swallowed a watermelon. On January 18th I came down with what I and the doctors thought was the flu. I started to dehydrate and Braxton-Hicks contractions began. When my fever reached 102F, I went to the emergency room. I was hooked up to IVs and stayed overnight. The next day I was released and I started to bleed. I went into false labor, went to the hospital, and was sent home though I still continued to bleed. Two days later, I almost fainted at home. I had a hard time keeping my balance and even fell in the shower. I was scared to death, but finally, after 3 days, the bleeding stopped. The baby barely kicked and I worried constantly. With less than a month to my due date of February 7, 1993, my nightmares became more frequent and casted a dark shadow over the end of my pregnancy.
At 6:00 a.m., on January 28, 1993, my water broke. The bed was soaked and after assuring Jeremy that it definitely was my water breaking, we prepared to go to the hospital. Jeremy called the doctor while I took a bath. The contractions hadn't started yet and there was no way I was going to get on a delivery table until I shaved my legs first! We were at the hospital by 7:30 and I was leaking amniotic fluid constantly. The car seat was soaked, the hospital stretcher was soaked, and the delivery table was soaked. I had watched films on giving birth and I didn't remember all this fluid in the films! Our families arrived by 9:00 a.m. and filled the waiting room. We are both blessed to come from large, healthy families. Soon my contractions became noticeable. From 9:00 a.m. to 4:00 p.m., they remained bearable and I only dilated 1 cm. With every contraction, now 5 minutes apart, my nightmare invaded my mind. I only mentioned this nightmare to Jeremy once or twice and to my doctors; I didn't want to worry our families over something that seemed like a one-in-a-million chance. I was never more wrong. At 6:00 I started to beg for pain killers. I was given 2 shots of Demerol and at 6:30, I had an epidural. I was fully dilated and started to push. The baby's head seemed to be stuck in the birth canal. The doctor performed an episiotomy and at 6:55 p.m. my son made his entrance into the world with the help of forceps. With only the doctor, a nurse, an anesthesiologist, and Jeremy in the room, the baby was laid on my chest as the doctor cut the umbilical cord. Then my nightmare came true.
The baby turned blue as he tried to cry, with only little whimpers coming out of his tiny mouth. Jeremy had just left the room to announce to the world that he had a son. The nurse grabbed the baby and took him to the other side of the room, which was equipped with medical paraphernalia. The doctor delivered the placenta while I repeatedly asked; "Is he OK?". The baby was taken out of the room and over the hospital intercom blared "Code red, Newborn Nursery". I was in a state of shock, my nightmare was really coming true. For a while, I could only lay there, left alone on the delivery table, absorbing this fact. Jeremy came in and we both knew that the intercom operator was talking about our son. Jeremy went to tell the families but when he entered the waiting room, he broke down crying. I began screaming "Where's my baby? What's wrong with my baby?". My doctor came in to stitch up the episiotomy and the tearing that was caused by delivering the baby by forceps. He wouldn't answer my pleas, only did his job and kept quiet while listening to my screams and threats. I was starting to yell that I was going to get up off that delivery table and hunt my baby down when a pediatrician came into the room, an hour and a half after my son was born. In such a small hospital the staff was little and the pediatrician and respiratory therapist had to come from home. He was cold as he said, with no expression on his face, "By x-ray we can tell your son has many problems. He was born with multiple, severe birth defects that affect his lungs, heart, and reproductive system. He has a Congenital Diaphragmatic Hernia, which means there is a hole in his diaphragm and organs in his chest cavity preventing him from breathing. He will need surgery to correct all his problems. We have sent for a helicopter to transport him to a trauma center. Tell him good-bye because this will probably be the last time that you will see your son alive." Then he left me alone on that table. Jeremy came in and I told him what the doctor had said. He went to tell our families and his father, whom we all affectionately call "Pop", came in. It was the only time I had ever seen this big, strong man cry. He was a preacher, and being raised Catholic I wanted my baby baptized in case anything happened to him. Pop wasn't prepared to do this, materially or emotionally. He prayed with me as I cried.
Jeremy and a nurse helped me off of the table and into a wheelchair. They wheeled me down the hall to a small room that contained an incubator, IV poles, a respirator, monitors, and my son. I was only allowed to see him from the doorway, he looked so tiny at 6 lbs 9 oz. Tubes and wires covered him. He had black hair and looked as if someone had given him a crew cut, but that was how his hair came in. He looked perfect on the outside, but on the inside he was struggling to survive. The nurse said "We're putting you in a single room so you have privacy." I knew the real reason that they were wheeling me to the geriatric ward. Only one other baby had been born and I could have had a room on the maternity ward all to myself but the staff had decided it would have been better to separate me from the other mother so that she wouldn't have to hear my cries and screams if my son, Jeremy "Shane", didn't survive. I wanted to yell that this wasn't fair but I needed to stay focused on Shane.
My sister, Trisha, and her boyfriend at the time took Jeremy home so that he could grab some clothes and take off for the trauma center to be there when Shane arrived. The pediatrician came into my room, surrounded by our family, to tell me that the trauma center he had ordered the helicopter from had called to tell him that their helicopter was broken. He then called the next closest trauma center, in North Carolina, and ordered their helicopter. I asked if I could see Shane before they took him and he told me no. After my family bombarded him with questions, he left. I called my neighbors, who were the dearest landlords we will ever have, to ask them to stop Jeremy and send him back to the hospital. They already knew; small town word of mouth had already started and Shane was only 3 hours old.
The helicopter crew arrived at the same time Jeremy did. I asked them a million questions as I filled out the consent forms. "What are his chances?" "Have you ever seen a baby with his problems?" "Is the weather safe for flying?" They comforted me, assured me, and gave me a chance to tell my son how much I loved him as they wheeled him into my room in his incubator. He was awake! He looked at me with those intense blue eyes that most newborns have. It was as if he was asking me for help. He looked directly at me, out of a room full of people. He knew that I was his mother. I felt my heart breaking. I will never forget that look or how wonderful the helicopter crew was, especially one of the flight nurses, Ed. He was an angel sent to us in our darkest hour to give us the hope that the hospital hadn't. Around midnight, my son was taken away as I listened to the helicopter blades break the silence of that cold night.
That night I couldn't sleep. Jeremy's brother, James, drove him to the trauma center. My mom stayed at the hospital with me. The rest of our families went home to prepare for the long days ahead. I called the hospital P.I.C.U. where Shane was taken to check on him and to give the staff permission to perform procedures. I was young, ignorant, and on pain killers, yet I was in charge of making decisions that would save or end my son's life. I thank God my mom was with me. I started the ritual of pumping my breast milk every 3 hours. I barely had any strength left to operate the manual pump, my arm muscles were weak from pulling up and pushing during labor, but I was determined to do this; to give my son the best nutrition and to do something for him that the medical staff couldn't.
My father came the next morning and picked up my mother and me to go to the trauma center. I left the hospital 18 hours after giving birth, despite protests from my doctors. As I was being wheeled out of the hospital, the other new mom who had delivered that night came to wish me the best and offer her prayers. I don't remember her at all, but I apparently nodded and thanked her; at least that is what I am told happened. After a 2 hour drive, we made our way up to the P.I.C.U.. I could barely walk and sitting was almost impossible. Labor was nothing compared to the bruising and sutures I had from the episiotomy and forceps. But the pain in my heart was worse than any physical pain.
The first time I walked into the P.I.C.U. I was overwhelmed. No one told me what to expect. It was constructed of 2 large rooms with beds lined up against the walls. Sick children were everywhere. Children awake and playing video games, children in comas, children on life support. Among these children was Shane. He looked even smaller than the night before. He had IVs in every limb and the ventilator took every breath for him. He was sedated and paralyzed from the medications. Yet despite all the medical equipment, he was the most beautiful baby I'd ever seen (of course I'm a little prejudiced, like all mothers). The ventilator was giving him 420 breaths a minute to keep his lungs from collapsing and a heart and lung bypass (E.C.M.O.) machine stood beside him as a precaution in the event that his heart and lungs quit. The surgeon came and introduced himself as Dr. Caffy* and scheduled surgery for that Monday, 2 days later. I had no idea of what he was explaining to me, I just agreed to everything and put my son's life into his and God's hands.
We were lucky enough to get a room at the local Ronald McDonald House. That night we settled in and Jeremy told me that his brother, James, had found out that Jeremy's application for a job at the local lumber yard had been accepted. After four months, Jeremy had a job. It solved some of our money problems but they didn't seem to matter quite so much any more. Our church and other churches who had never met us began to take up collections to help us get by. My faith in humanity was beginning to grow. I prayed harder than I've ever prayed in my life that night. I prayed for God to watch over Shane and most importantly I gave Shane to God, to do his will, whatever that might be.
That Monday, the day of Shane's surgery, while our parents waited in the operating room waiting area, Jeremy took me to the emergency room. I was in so much pain and I hadn't had an internal exam since Shane was born, not even by my doctors before I left the hospital. I was given painkillers and told that I was just bruised. Jeremy ran back and forth from the E.R. to the O.R.. Shane was in surgery for 6 hours. Finally, the surgeon came in. The surgery went well and Shane was given a 50% chance of survival. We were told that if all went well, he could be home in 2 weeks.
The next few weeks left Shane holding his own but not improving as much as we had hoped for. I pumped breast milk regularly, and when I didn't have the strength, Jeremy helped me. When Shane was 2 weeks old, Jeremy went back to Virginia to start his new job and I stayed at the Ronald McDonald House at night and the hospital during the day. My days consisted of eating, sleeping, pumping, and keeping vigil at Shane's bedside. We brought toys and clothes from home for him; including a stuffed Precious Moment’s angel pillow.
When Shane was 3 weeks old, I held him for the first time. A brave nurse, and dear friend, juggled tubes and wires to place Shane in my arms. I held him for over 5 hours. I would have held him forever if I could have, but my breasts were becoming engorged. I wish someone would have warned me about that. Jeremy held Shane for the first time a week later. All of the members of the nursing staff were more than just the people who took care of Shane, they were friends and for a long time, family. Rachel, Shane's primary nurse, immediately "adopted" him. She referred to him as "her baby" and she made sure he got the best care, even if it meant standing up to the doctors to get it. Shane came down with his first infection at a few weeks old. It was one blood infection after another, and in between, he came down with pneumonia. It seemed he would only get over an infection when another one would start. He was sedated and paralyzed by medication for most of his first 3 months. In total, Shane had over 20 infections (blood, urinary tract, and kidney) and pneumonia 5 times.
It was during this time that I learned 2 of my 3 sisters were pregnant, Christie and Trisha (I also have a baby sister, Debra). I felt betrayed. How could they get pregnant knowing what I was going through? How will I be able to fight off the jealousy when they have healthy babies? They were single moms and I was married, and had done everything to try to insure a healthy pregnancy and baby. It would take me months to forgive them, though I knew I had no justified reason to be angry with them.
When you live this type of life, you become very close with the families of the children you meet. They are the only ones who truly know what you are going through. I prayed for many other children, and the list became longer with each passing day. P.I.C.U.s are like war zones. Children battle for their lives. Parents battle for their children. The medical staff battle disease, armed with medication and knowledge. A lot of these battles are lost. The first child I watched die was a 6-year-old little boy with multiple problems. He died the second day Shane was in the P.I.C.U.. He was in the bed beside Shane's. I tried to ignore it; I couldn't handle it. I had never been this close to death before. A little girl was put in that same bed space hours later. She was born on the same day as Shane, with the same problem as Shane had. Her mother was single and the same age as Jeremy and I. This baby girl fought for 2 weeks. The little girl died. I wanted to comfort her mother but it hit too close to home, I just walked out, went to bathroom and cried. I knew Shane could be next. I will always regret not going up to that mother and holding her as she grieved. We have known dozens of children who have died since then and they have each taken a piece of my heart with them.
I met another mom of a child with this birth defect who had a little boy, a month older than Shane, that died at age 2 months. She gave me more strength in her strength than she could ever know. Rhonda was there for me even after Preston died. When another mom lost her little girl from complications after a heart surgery, Rhonda was there, a month after Preston died, to give her comfort and to help guide her through the funeral arrangements. I will never forget the selfless generosity that she gave everyone, even while still grieving for Preston. How can we send a man to the moon but not prevent all this pain and needless death on Earth to innocent, little babies?
At 4 months old, Shane underwent surgery again, a procedure that was not supposed to be needed. By this time, I had spent many hours at the hospital's medical library and was becoming pretty knowledgeable about Shane's condition; to the annoyance of his doctors. I looked at every x-ray and the results of every test. Through my studying, I learned of a procedure that involved repairing the defect with use of muscle from the abdominal wall. I begged Dr. Caffey and his partner, Dr. Olden*, to try this instead of using the Gortex (nylon) patch they intended to use. The Gortex couldn't fight infection and wouldn't grow with Shane, which meant it would have to be replaced as Shane grew. They insisted they had never heard of this and even when I gave them articles taken from medical journals, they refused.
The tension between us was growing thicker everyday. They were surgeons from one of the top 10 hospitals in the country, how dare I even think to question them? I wasn't worried about their egos, only my son's health. Shane was now so unstable that there was no way he could be transported to another hospital, so I reluctantly gave in.
I was having health problems of my own. I developed a large knot between my right breast and my arm. Pumping that breast was excruciatingly painful and while pumping one evening at the House, in our room, I pumped blood. Then I began to have cold chills. Jeremy got more blankets and even laid on top of me, but I couldn't get warm. I was sweating so bad the sheets were drenched. When Jeremy took my temperature, I had a fever of 105F. He took me to the emergency room, where the doctors diagnosed me with severe mastitis (an infection of a milk duct in the breast). My temperature reached 106F before they could hook up IV fluids. My case was so severe, they were calling in medical students to come look at me; I started to feel like a guinea pig. I was dehydrated and they wanted to admit me, but as stubborn as I was, and as sick as Shane was, there was no way I was going to be separated from my son when he needed me so badly. They filled me up with fluids, gave me antibiotics, and released me. I lost my breast milk and I never got to nurse Shane. I felt like I had lost a bond with him that I could never regain.
Weeks later, and still on oxygen and a ventilator, Shane got his trach. By now, the surgeons and I were butting heads constantly. Shane continued to come down with infections and I continued to act like a tigress protecting her cub. I questioned the surgeons' decisions and they questioned mine. They were not used to dealing with a patient's mother for such an extended amount of time. It was during this time that Lance*, a little boy a week younger than Shane, came back to have his 2nd heart surgery. His parents, Jenny* and Ronnie*, had stayed at the House with us during Lance's first surgery visit. After Lance's second surgery, he came down with a staph infection at the same time as Shane. They were side by side in the Unit. Jenny and I spent a lot of hours together and we became good friends. Lance died a few weeks after his surgery. Writing this now brings tears to my eyes. I never thought I could hurt so much for another person as I did for Jenny. I never want to go to another baby's funeral as long as I live. Rhonda was at Lance's funeral; she was now pregnant with her third child. Shane recovered from his infection and by now, I felt as if we were waiting in line to be the next to lose our child.
Soon after, Shane came down with pneumonia. The oxygen level his blood had went so low that it caused brain damage. He was now blind, deaf, and what some people would call a "vegetable". Jeremy and I wouldn't give up until Shane did, and he wouldn't either. We argued with the surgeons, who now wanted a D.N.R. (Do Not Resuscitate) order. We refused and had to go up in front of the ethics committee. The meeting was full of accusations, from both sides, and I spoke through choked tears. When it was over, the doctors did not get their D.N.R. order and care for Shane was continued. Rachel was beside us the whole way.
The next few months went by slowly. Shane was seen by neurologists who said that he would never get any better, but we didn't listen. We knew God had a special plan for Shane. Shane started to interact with people and show discomfort at about 7-months-old. His trach site was starting to erode and Dr. Caffy changed the brand of trach. His trach site grew worse. I went to the medical library and researched to find different brands. When I learned that trachs could be made to order and specified to fit the trach site so that the erosion would be minimal, I asked the surgeon to change the trach brand. He told me that there were only two types of trachs in the world and that we had tried them both. I knew he was lying to me. I suppose I had become an annoyance, but Shane's site was so bad that it threatened to open the main artery in his throat. When I presented Dr. Olden with illustrations from medical journals, along with manufacturers phone numbers and addresses, the surgeons avoided me for weeks. I had to leave notes for them on Shane's bed because they would only make rounds before visiting hours and all my questions were answered by other doctors. I wasn't on a quest to be right, I simply wanted to stop the pain that that type of trach must have been causing Shane. After about a month, the surgeons got tired of arguing and changed the trach brand. Shane's trach site immediately got better and healed, though he will always have a noticeable scar there.The nurses and respiratory staff were wonderful, I went out to eat with a few of them, and Jeremy and I went out with them and double dated a few times. They were, and are, friends in every sense of the word. They took the time to try to cheer us up or distract us from Shane's problems. They bought Shane clothes and toys and spent hours playing with him, even tough he couldn't respond very well, if at all. They went beyond the call of duty, and we will always be grateful. The flight nurse, Ed, that bought Shane to the trauma center, checked in on him often, bought him a stuffed animal and a flight pin, and even gave us a tour of the helicopter. Rachel became one of Shane's three godmothers, along with my sister, Christie, and my sister-in-law, Teresa.
At eight-months-old, Shane was still on the vent but stable. We started to make plans to take him home. The Ronald McDonald House closed down for renovations and I was taken in by other families for 2 months. They let me into their homes, took me back and forth to the hospital, and treated me like family, even though they had sick children of their own. I contacted home health agencies in Virginia, but the surgeons refused to let Shane go back to our home because we were too far from a trauma center. Instead, they wanted Shane to go the nearest chronic care facility, 3 hours from our home. We refused and learned CPR and how to work the medical equipment. We had to go in front of the ethic's committee again. After another heated discussion, the doctors agreed to release Shane if we moved closer to the hospital. They never thought we would leave our families and move to North Carolina. I started to look for a house near the hospital and set up home health care. One of our friends gave Jeremy a job.
After looking at rentals for weeks, we found we could not afford to move. I called a few local churches to see if any of their parishioners had places to rent. A local church pastor announced our situation to his congregation and a church member, Jackie, made it her mission to help us find a home. She organized a barbecue, which was announced on a local television station, and raised enough money for us to put a down payment on a mobile home with payments that we could afford. Jackie was a Godsend.
The doctors still did not want to release Shane, even after everything was set up. They said that he wouldn't live to make it to the parking lot. We were determined to get him home anyway and on November 29, 1993, after 10 months, we took Shane home. We later learned that the surgeons had a money pool going over how long Shane would survive once he left the hospital. Dr. Olden bet 2 weeks, Dr. Caffy bet 24 hours. We are happy to say that they both lost.
With home health nurses and equipment, we started on another leg of our long journey. Shane quickly settled into his nursery, with his painted cherubs looking over him from the walls. I tried my best to keep Shane's room looking like a nursery and not a hospital room, despite his ventilator, oxygen tanks, feeding pump, and monitors. We had nurses 16 hours a day and I watched him for 8 hours.
Our second day home, during my shift, our electricity went out. Shane's vent battery kicked in; it had an hour internal battery. I took him off his oxygen concentrator and hooked up a tank. I frantically called the power company, who told me a car had run into a generator and the power would be out for at least another 2 hours. Shane was on their emergency power list, but there was nothing else they could do. I called our medical equipment company and they talked me through hooking the vent up to a boat battery, and then the director came out to sit with me until the power came back on.
Shane's first Christmas was the best Christmas we'll ever have, even though we couldn't go home to our families or to our new niece, Kirstin, and nephew, Frankie, healthy babies, born to my sisters. I love them like they were my own. Those jealous feelings went away and were replaced by relief that they wouldn't have to go through what Shane did. When we put up the Christmas tree, Shane started to look at the lights. He could see! Our very own Christmas miracle, after we were told he would never regain his sight! Local churches donated money, toys, and even gifts for me and Jeremy. The local police station donated a $200.00 gift certificate to a nearby grocery store. My parents traded us their '88 Aerostar mini-van for our tiny '91 Escort so that we could transport Shane and all of his equipment to his doctor appointments. An anonymous, and I'm certain, wonderful person donated a double stroller so that we could carry Shane, his ventilator, his oxygen tanks, suction machine, diaper bag, feeding pump, and other medical equipment. Shane has shown us the truly wonderful side of humanity. So many strangers helped us out in our time of need. We have had many ups and downs since Shane's been home. He wasn't gaining weight from the formula he was sent home on, so his nutritionist decided to try to switch his formula to a higher calorie formula that was milk-based. Shane had a severe allergic reaction to the formula and went into anaphylactic shock. We almost lost him. We now know he is allergic to all milk products, eggs, chicken, and red food dye. We have to keep an Epinephrine dose with us at all times. Even if a drop of anything containing milk touches his skin, he can go into shock.
We turned Shane's first birthday into a major event; we didn't know if he would ever have another. I spent 3 days painting Precious Moments clowns on his cake and decorating our kitchen. We couldn't have open flames around Shane, so I make one out of construction paper to put on his candle. Our tiny home was filled with family and friends. Shane was oblivious to all the activity, but he did manage to accidentally put his hands in the cake. We actually got a picture that the parents of "normal" one-year-olds get to take of first birthdays! Life seemed good again. Shane slowly progressed. He still couldn't eat by mouth, he was fed by a feeding tube that was inserted down his nose into his stomach. He remained on the vent and oxygen and we all got used to having nurses in our home. Rachel and a few other nurses from the hospital joined our home nursing company to come work with Shane. Nurses came and went, a few stayed on permanently. They all became members of the family.
When Shane was 15-months-old, a new nurse, Ana*, after undergoing training, was working a night shift. At 6 am, she lightly tapped on our bedroom door and asked me to come to Shane's room. As I got halfway there, I heard Ana screaming. I ran into Shane's room and looked at my baby. He was blue, his eyes were open, but they were rolled into the back of his head. I screamed for Jeremy. He came in, saw Shane, and ran to call 911. Ana was screaming and shaking Shane. He was still on the ventilator, she hadn't even started CPR. I had to push Ana out of the way, and thankfully, everything I learned about CPR came back to me. I took Shane off of the vent, hooked up the ambu bag to his trach, yelled to Ana to turn up his oxygen, and checked Shane's pulse. His heart had stopped. I started CPR and finally Ana regained controlled and helped. Jeremy came into the room and told us an ambulance was on the way. He started to check the ventilator, which had been alarming since I first came into the room. Ana had empty the humidification trap to release the collected vapor and forgotten to close it. The ventilator must have been alarming for at least ten minutes. The first thing we learned in our training was that if the ventilator alarms and you don't know why, you take the patient off of the ventilator and manually respirate them until you fix the problem. Ana had left Shane on the vent. Imagine trying to breath through a very small straw that had no oxygen. That's how Shane felt. I fired her on the spot. After 10 minutes of CPR, Shane started to come back. By the time the ambulance got there, he was fine. Of course we took him to the hospital anyway, and he was released the same day. Ana was never disciplined by the company or the state nursing board. We will never forget what it looks like to see our baby dead, and we are more cautious about the nurses we let take care of Shane, in fact, we are probably neurotic about new nurses.
The stress of everything was taking it's toll on our marriage. Jeremy and I began to fight constantly and that April we agreed to separate. Jeremy moved around and I went through severe depression. A male nurse that had been taking care of Shane for 5 months decided he should take it upon himself to try to cheer me up. He almost raped me but I was able to fight him off, though I don't know how. He was married (we had met his wife) and we trusted him and had treated him like family. I had to call the police and even though I decided not to press charges (I wasn't emotionally stable enough for a trial), he lost his nursing license. My depression deepened. Jeremy and I started family counseling and I was put on anti-depressants.
We switched Shane's surgical care to another hospital. At a routine check-up, an x-ray showed that his sutures were giving way and that he would need another surgery. By now Shane was off oxygen, and only on the vent at night. He was interacting with us, starting to roll, and his smile lit up a room. In August of 1994, Shane underwent his 3rd major surgery. Everything went as planned and two weeks later he was home.
That October, Jeremy moved back home. I was still battling depression and we were still fighting, but we wanted to give it another shot for Shane's sake. Shane was doing great and I got to make him a Halloween costume. He and his 3 cousins were firemen and Dalmatians and his stroller was converted into a fire engine. Thanksgiving came and we got to go to Jeremy's family's house to celebrate. At Christmas, we went back to Virginia and I got to do all the things that I had wished for during the Christmas I was pregnant. Jeremy even played Santa Clause. Shane now played with his toys, rolled around in the wrapping paper, and could go from room to room without equipment and tubes. It's amazing what parents of healthy babies take for granted. The first time I could actually walk Shane around was like magic. It was like Shane and I were dancing in our own little world and he was almost "normal". We received another miracle that Christmas when I accidentally left my anti-depressant and birth control pills at home. After 6 months, I realized that the birth control pills were making me depressed.
Shane turned 2-years-old in January of 1995. His cake this year was a hypo-allergenic, applesauce cake. His cherubs have been removed from his walls and replaced with more "boyish" pictures of Looney Tunes characters. Shane came off his vent in May. On the 4th of July, he went into respiratory distress and we went to the emergency room. He had emergency surgery, his 4th, and went home 2 and half weeks later, off oxygen. This past October, he needed yet another surgery. He went through surgery number 5 and came home after 5 days. We make frequent trips back and forth to the hospital for viruses and for appointments to all the many specialists involved in Shane's care. We don't know when and if Shane will need another surgery. He never does anything by the book. Yet another Christmas came and I hoped against hope that we could possibly receive another miracle. I prayed nightly that God would heal Shane and prevent him from suffering through more surgeries. In early December, we went for a routine check-up with Shane's surgeon and an x-ray was taken. I have learned how to read these x-rays and was scared when I saw a mass. It wasn't a tumor. The doctor's say it is scar tissue, but Jeremy and I say it is the touch of God because whatever it is, it's holding his organs straight and as long as that happens, he won't need another surgery. He gave us yet another miracle and I believe that Shane will not need future surgeries. Of course I am terrified that we have used up all of our miracles; most people never receive even one. They say you stay on this earth until you finish your work and I worry that Shane has already finished his. He is so young but he has touched so many lives and forever changed ours.
As I write this, Shane will be 3 in 2 weeks. He now wears hearing aids and glasses. I heard him cry for the first time this past summer when we started to use a Pacimuer Valve, a small valve fit over his trach that allows him to make noises by teaching him to exhale through his mouth and nose. He started to crawl after his forth surgery and is "cruising" now. God willing, he will walk soon. The feeding tube in his nose was removed and replaced with a more permanent one placed directly in his stomach through his abdomen. He is starting to eat and drink by mouth and maybe someday, when he can eat as well as he needs to, the tube in his stomach will be removed. He can't talk yet, but he is very expressive with his facial expressions. His trach will be out this spring. He runs the house and gets into everything. He's a stubborn as a mule, but I suppose that's what has kept him here. It's impossible to discipline him and where most children learn not to climb or get into things after they fall once or twice, Shane is so used to pain, that when he falls or we pat him on the butt to keep away from things that could hurt him, he laughs hysterically. Jeremy now has a new job with better benefits and is learning a trade, thanks to Jackie. I have started college and started a support group for the families of children like Shane. Jeremy and I are madly in love again and are considering having another child. Shane is doing well and will be at least 4-years-old before we have another one, and the time seems right. Of course we are terrified at the thought of having another sick baby, but the doctors and research have told us that the chance of that is rare. Like the parents of all babies, sick or healthy, we long to do "normal" things; come home a few days after giving birth, breast feeding, and having baby-sitters instead of nurses. We will never again be oblivious to what might happen, but we need to, and want to, have a good birth experience. Besides, Shane is getting a little too spoiled and another baby would do us all good. No matter what happens, Shane will always be a little more special, that's a feeling all mothers of disabled children have. I love him more than life itself and I would trade places with him in a millisecond. He the sorrow and joy in my life, as all children are to their parents, only multiply that by 100 when you have a disabled child. Every step forward and every step back is more noticed and more dramatic. It's hard, but I wouldn't trade it for anything. He has made me a stronger person.
I still get into arguments with doctors and nurses, but I know how to choose my battles. I have alienated quite a few of medical professionals, but I know Shane and his medical history best because I deal with it everyday of our lives. The latest battle was with a nurse who wanted to put Shane in a hospital room with 2 preemies when he was admitted with a virus. After asking to be put in a private room and told "no", I had to go into my "mom from hell" mode to get us moved and within 5 minutes we had a private room. There was no way I was going to subject to those two tiny babies to Shane's virus when they already had their own health problems to fight. Unfortunately, many of us moms with sick kids have had to learn about the "mom from hell" mode. Jeremy has supported me all the way. We no longer go to the hospital where Shane spent his first 10 months. Because of Shane, and our experiences of having a child with this birth defect, I started a support group. It is the only support group of it's kind in the world. This defect strikes 1 in every 2500 babies. The cause is not yet known. It is not a prejudiced birth defect. It affects babies of healthy families, of parents of any age, of any color, of any religion, and any financial status; no matter how good the prenatal care. Most are found during routine ultrasounds. It can strike alone or with other birth or genetic defects. Fifty percent of babies born with this do not survive. Most survivors of this defect do not have any complications (other than feeding problems) or more than one repair.
I now know, after researching that the "flu" I had during my pregnancy, along with stomach pains, what I then thought was "more amniotic fluid that I had seen in birthing videos", and all the weight gain just in my stomach was undiagnosed polyhydramnios, excess amniotic fluid. Polyhydramnios is an indicator of fetal abnormalities. If my doctors had diagnosed me correctly maybe they would have diagnosed Shane's problems by ultrasound and we could have been prepared and had him at a trauma center better equipped to care for him.
I swore to myself that if I could help it, I would try to prepare other parents of children with this birth defect. These parents need to be better informed so they can make educated decisions for their child's health care. They need to know they are not alone. Most people have never heard of this birth defect, and if they are lucky, they never will. I started this support to help these parents the way Rhonda helped me. I wrote a newsletter in my kitchen, took it to a printer (who donated the service), and mailed it to a couple hundred parents and doctors. In 12 months, we now have families plus hospitals, universities, and research centers across the country and in Canada, Europe and Australia in our membership. The response has been overwhelming; this support group has been needed for forever.
Rhonda and Jenny have each had healthy baby girls since the deaths of their sons. We no longer keep in touch, it's a little uncomfortable for all of us; they have healthy babies but still grieve for their lost children and I still have Shane. They will always be in my heart, and I think they would agree, that our friendships were part of the worst times in our lives, but they are also a part of what helped all of us survive. I will never forget them. I hope the best for Rhonda and Jenny and their new babies, and I know one day I will have a healthy baby, too. I feel it in my heart as sure as I knew Shane was sick. But for right now, we'll be content will our own living, little angel.
updated 11/10/97
I wrote that story almost 2 years ago, but it seems like a million years. Reading it, I realize I was still in my "martyr stage"; a stage all of us parents of disabled children go through. Now, I'm back to "normal people stage" and Shane is almost 5. He is walking (actually running around the house and leaving a trail of toys behind him), eating a few ounces by mouth at a time, is completely off the ventilator and oxygen, and had his trach removed a year ago. He wears glasses and hearing aids and is going to a preschool for the deaf. He begs constantly to watch the SAME episode of Sesame Street over and over again; I guess that’s typical pre-school behavior. We only have "respite" nursing care at home now- no more strangers practically living with us. His nurse goes to pre-school with him twice a week, to take care of his feeding and medications while he is there. We no longer go to doctor appointments every other week; now we go every other month. He still winds up in the hospital a few times a year for viruses and pneumonia, but luckily they have been short visits. No more physical therapy (Shane has reached all his PT goals); only occupational and speech therapy now, with visits from a sight therapist to keep an eye on his vision. He has a Mic-Key feeding button now, which is actually helping to anchor his stomach into place. He throws tantrums, pouts, and flirts, like most "normal" kids his age, he truly can melt me with just a smile. Looking at him now, it’s hard to believe all we went through. Jeremy and I doing well. We are now living the "American Dream", ok, the warped version, but it’s a dream! Haha. We bought a house, have settled down in North Carolina, Jeremy has had a wonderful job for a few years now, and I have Shane and the support group to keep me busy and on my toes. I still battle depession on and off (a result of Post Traumatic Stress, which most of us parents of sick kids get) but life can be good! We have thought about trying for another baby; actually we lost another one (#2) through miscarriage this past summer. Shane still carries around that stuffed Precious Moments’ cherub doll (ok, so it’s "baby" #5, the first 4 fell apart from all the trips to the washing machine, but he doesn’t know that). Rhonda and I have made contact and she is now a member of the group; both of her children are healthy and happy, but Preston will always be a part of all of us.
update 7/5/98Shane is doing really well- still carrying around "Baby", watching Sesame Street non-stop, eating much better by mouth, has learned 10 sign-language signs, and starts home-school this fall (after going rounds with the local school board who refused to put him in the county's only deaf class and wanted him in the L.D. class instead- where no one knew sign language, even though the deaf class is only 1 year ahead of him and has only 3 students). He plays with cat, loves going outside and riding in the car, and loves to be read to. He makes the silliest faces and has a wonderful sense of humor- you just can't help but smile when he does. I feel like the luckiest woman in the world to be chosen to be this wonderful little boy's mom.
1998 has been hard on us- a house fire (in which Jeremy was seriously injured), e-coli (food poisoning from seafood), a tornado that hit our house, yet another miscarriage, I lost my best friend, my parents are divorcing after 25 years, I had a hard time coping with the birth of my new niece who was born near the due date of the baby I lost last year, a lovely little "web war" over graphics, and Jeremy and I separated for a while again. With all that's happened, my depression really hit hard for a while as I tried to cope with everything. It still hits once in a while, but it's much better. Jeremy and I back together, this time for good. We separate when the depression hits me- and it's always my choice to separate, when I can't think straight. But Jeremy always sticks by me, and gives me space when I need it and a shoulder when I need that too. It only took me 7 years to realize this! J So now we're back on track. I have a new job, the support group now covers 47 states and 8 countries and is keeping me busy- so you can say I work 2 full-time jobs. We're trying for another baby again and we finally feel like life is going well and we're almost "normal". J I knew we would have it rough after Jeremy broke that mirror 3 months after we were married! Lol. 2 months to go and the 7 years of bad luck is over!
Update 4/25/99
Shane is now 6 years old and doing better than ever. He hasn't been hospitalized for over a year and started home-school last fall. He still watches Sesame Street far too much, "baby doll" (#10. Shhhhh- the others fell apart.) is still with us, and he loves to look at books. He now recognizes 20 signs and consistently does 10, and the biggest news- he's talking!!!! He says "Daddy" (figures! Lol) and "eat". He follows Jeremy around like a puppy and his favorite thing to do is hop in his dad's truck and ride again (he doesn't care where he goes, as long as he's riding. Haha). He helps to dress himself and starting to learn to pick up after himself a little. School and 2 new cats have helped him overcome his textile aversions. He loves the cats and they're great with him and really gentle. He caught a virus last fall and somehow (the doctors can't figure it out), his hearing and sight have improved!!!! Not bad for a kid they said would never see or hear. J His eyeglass and hearing aid prescriptions have changed for the better and he is responding to normal speaking voices without the hearing aids. We are sure this is what led him to finally be able to talk. Next month, he is scheduled for a tonsillectomy, because the virus caused inflammation of his tonsils and adenoids and the swelling hasn't gone down after 6 months. We're hoping that after the surgery he'll be able to talk more and start to eat. Jeremy and I are doing really well, better than ever and have gotten really close after the last year's traumas, with the fire, hurricane, 2 tornadoes, another miscarriage, personal problems, and all the infertility procedures. For the first time, our major problems don't include Shane's medical problems, just "semi-normal" problems- it's wonderful! After working for a horrible company for a few months, I started my own web site design company in February and we are doing better than my wildest dreams already. We have employees, an office, clients, and a good reputation. I love my work, and with the company, the support group, home-schooling, remodeling, and raising a family, life is hectic- but I wouldn't change a thing. We are so blessed to have been given so many miracles, to be given each other and Shane. Life can turn around in a split second and though it may never be the same, it doesn't mean it can't be good.
Updated 9/99
Shane was born on January 28, 1993 with Left-Sided CDH, ASD, Hypospadius, Left Pulmonary Sequestration, Microcephaly, High Palate, and Undescended Testes, yet he was the most perfect child in the world to us (our slightly biased opinion). He spent his first 10 months in the P.I.C.U., overcoming pneumonia 4 times, over 30 blood, kidney, and urinary tract infections, brain damage, blindness, deafness, and 2 CDH repairs. Fighting the doctors, we brought him home, trached and vent and oxygen dependent. He regained his sight a month later and 2 years later the trach, oxygen, and vent were gone. By the time he was 3 years old, he was walking, had developed his own means of communication, and had survived more hospitalizations for pneumonia, viruses, and even coding at home once from a ventilator malfunction. At 4 and a half he started going to a deaf preschool and when the time came for kindergarten, we made the decision to homeschool him because our local school system was not adequate to meet all his needs. By the time he was 6 years old, he had regained his hearing (the audiologist never could figure out how- we call it a miracle), was terrorizing the cat, destroying the house with toys, using Sign Language, and worshipped Sesame Street (we soon learned every word, of every song, of every episode…).
In July he started coughing so we took him to his pediatrician, who was very afraid of Shane's medical history but we live in the sticks and don't have many options for local doctors. After demanding an x-ray we saw the x-ray film- the entire left side of his chest was whited out as if someone had taken paint to the x-ray. We left the pediatrician's office and went straight to Shane's surgeon. We all thought it was pneumonia and he was admitted to the hospital and put on antibiotics. When it didn't clear up and he got worse, we guessed he had reherniated (the x-rays were so bad you couldn't see any organs at all on that side) so he went into surgery. He had reherniated- for the 6th time. Shane never had much diaphragm to work with and the empty space between his lung and his diaphragm never filled, so it created a vacuum and basically it "sucked" the Gore-tex up. Apparently he had been reherniated for a while and the Gore-tex was wrapped up like a ball and had torn a tiny hole in his stomach and in his lung, allowing formula and stomach bile to enter his lung. This is called a gastroplueral fistula and is so rare that there are only a handful of cases in the last 30 years. We only found a few research articles on it and Shane's surgeon had never seen anything like it before. She repaired the hernia and sutured up the holes and we thought we'd be going home in a few days, but the pneumonia got worse. The hole in his stomach was so high up and in such an awkward place that the suture didn't hold. Shane was also so malnutritioned because of a lack of calories with the formula he was on (he never did decide that eating by mouth wasn't a bad thing) that his body couldn't heal properly. We decided to pump him with extra calories through his intestines and keep his stomach drained so that his lungs would clear and he would heal. Through it all he was a happy little trooper. He played in the hospital, rode around in a wagon, the nurses were tripping over toys (matchbox cars make a very cool sound when they hit tiled floors), and we had to have a room with a VCR so he could watch Sesame Street. We spent almost 2 months in the hospital and when we came home he still was fed through his intestines, his stomach was still being drained, he was on antibiotics, and he had to sit up all the time, even while sleeping. We came home the beginning of September, deciding that if the holes didn't close by the first of November he would have had enough nutrition to have surgery again. On September 9th we went for our weekly visit to see Shane's surgeon. He was coughing a little, but we thought that was a good thing because he was clearing his lungs finally. Everything looked good and we drove the hour trip back home. All the way home, the kid who always looked out the car window and smiled at all the transfer trucks wouldn't take his eyes off me. He stared at me for an entire hour and for an entire hour I worried and wondered about why he was doing that. The next day he wanted me to sit beside him and play with him all day long. It was the first day in months that I didn't work (even while in the hospital) and just sat and played with him and held him. He was never a real clingy child and I wondered then if we should take him back to the hospital, but I didn't know what to tell the doctors, "He's clingy". I stayed up with him all night that night and finally went to bed when Jeremy got home from work at 11am that Saturday morning.
September 11th- Jeremy woke me up at about 4pm. His parents were visiting and Shane was "acting funny" so I got out of bed. When I went into the living room, Shane was sitting in the floor, surrounded by toys, Sesame Street blaring on the television, holding his best friend, "baby" (a stuffed Precious Moments pillow) and his Mimi (Grandma) was doing chest p.t. on him. He was coughing and the ends of his fingers were a little blue. I started to give him an albuterol treatment and sent Jeremy to the store to get a bulb syringe to see if we could clear his throat for him because he kept pointing to his mouth. I finished the treatment and started doing chest pt with Shane sitting in my lap. He was getting a little bluer so I called 911 and told them to send an ambulance just in case. One minute he was sitting there, seemingly ok except for the cough, and then he just passed out. I laid him down and tried starting beating his chest and shaking him to wake him up. Jeremy walked in just as he passed out. He was turning blue and I couldn't see his chest moving. I tried to get a pulse but I couldn't. I called 911 again, screaming "Where is the ambulance, he's coded. I called 5 minutes ago and we only live 2 blocks from the hospital!!!!!", all the while trying to do CPR. I handed the phone to Jeremy's mom so I could do mouth-to-mouth and when I went to blow in I could hear gurgling. I could barely get air in. Jeremy's mom was on the phone and running around the house getting me the oxygen tank, ambu bag and anything else I screamed for (God bless that woman for being there and being calm and being such a huge help). While I was doing CPR, his chest tube blew. I was flashing back to the day he was born throughout it all- I could hear words coming out of my mouth, I was doing CPR mechanically without thinking about it, and yet an entirely different conversation and experience was going on in my head. It was like I was watching and not participating and all I could think was "Please God, no, please God, no….".
The ambulance finally got there. It was probably only 10 minutes from the first 911 call but it seemed like forever. I TOLD them I was riding along, they didn't want me in the ambulance. They had an ET-tube in Shane and were trying to get an IV line in. We got to the hospital and the staff wouldn't allow me in the crash room. I stood outside the door screaming that I was his mother and that they didn't know his history and I was no typical mom and they had better kill me before they were keeping me out of that room. One of the doctors finally relented when I started rolling off Shane's medical history and medical terms that he probably couldn't believe were coming out of this strange woman's mouth who obviously didn't look like a medical professional, having not even had time to brush my hair and wearing a stained sweat suit (stained from Shane). When I finally got in there I talked a nurse into finding Jeremy (who had followed us to the hospital) and bringing him in and talked the doctor into calling Shane's surgeon (thank God for Dr. Taylor explaining to him who we were and what we knew, the doctor's attitude toward us did a 180 after that phone conversation). Jeremy and I just stood there, holding each other, and watching the monitors. They couldn't shock Shane because he still had systolic pressure. It took an hour to get a good line in him (and surgery to get it). There were a dozen people in there working on him and every 10 minutes or so the doctor came over to us and told us that they weren't getting any response, even after pumping him with Epinephrine. I only left the room for a few minutes to call my family.
In what seemed like only seconds, 2 hours had passed and then I had this calm come over me. I always told other parents that they would "know when it was time to let go". Now we knew it was time. After 2 hours and pnuemothoracies (air in his chest cavity from all the bagging), his diaphragm probably totally gone, and his brain irreversibly damaged, Shane was gone. Shane was gone before we even left the house. The doctor came over to us again and we told him we knew it was over. I asked them to keep working on him long enough so that we could say a prayer and Jeremy and I could hold him when they stopped. All the doctors and nurses held hands with Jeremy, his parents, and me and even the doctor said a prayer. We held him when they stopped bagging him. I was so numb and I didn't want to let him go and at the same time I just wanted to run away. We left so they could clean him up and they brought a rocking chair down from the maternity ward. I called Judi and told her what happened and in a few hours she was on her way to NC to be with us and she was calling some of the members. My family got there and we took turns holding him, even my little nieces and nephews wanted to hold him. They were confused but not scared and I'm glad they got to say good-bye. We had to take Shane to the deserted x-ray waiting room to hold him because they needed to empty the crash room. We held him for hours and took pictures and cried and cried. We told him it was ok to go to heaven about 10 times before it felt like he left. He didn't want to leave us and it broke my heart to tell him to go. I just couldn't comprehend that I would never get to hold him again. I never wanted to hand him back to the hospital.
Judi and more of our family arrived at our house that night and the next day Tara Hall, one of our members and a dear friend, drove down from Ohio to be with us. I e-mailed the Listserv that night and the next morning we called more family and friends and had to tell Shane's home health nurse, Delores, who had been with him for 5 years and next to Jeremy and I, the closest person to him. Thankfully her husband answered the phone, because I just couldn't bear to tell her. Everyone at the house was trying to help us make arrangements and make more phone calls. I kept myself busy by making the funeral programs- I couldn't sit and think about what happened because I knew if I started crying I couldn't make sure everything was done the way we wanted. It was the last thing we would be able to do for Shane, I wanted to remember it and not be in the tearful fog I'd fall into if I let myself cry. Now I know that postponing grief was a horrible decision, but it was the only decision I could make at the time that would allow me to survive those first few days and weeks.
We decided to bury Shane in Virginia, at my parents' house in an small orchard. We had moved to NC to bring him home from the hospital, now we wanted him in Virginia where he should have come home. The funeral director did a great job and found a white casket with cherubs on it and even took handprints and footprints for us. Shane was laid to rest in a Sesame Street outfit, his sneakers, wearing his favorite baseball cap and his glasses and holding his baby and surrounded by his favorite toys. We had a viewing the night before the funeral and we asked everyone not to whisper, but to talk loud enough for Shane to hear them from heaven. The funeral service was beautiful and the programs were Sesame Street themed and the church was literally overflowing with CHERUBS' members, Shane's nurses, family, and friends. People we hadn't seen in 10 or more years came to say goodbye to a little boy they never even got to meet during his short 6 and a half years on Earth. One of Shane's Godmothers, Rachel, who was his primary nurse during those first 10 months, wore a bright fuchsia and yellow dress to the funeral- she knew Shane would have loved that dress. I wish I had thought of telling everyone to dress in bright colors. During the service Judi read a letter and a beautiful poem written by Jennifer Wasik, another member and dear friend. My sister and her husband read letters to Shane that Jeremy and I had written, Shane's uncle, James, sang "The Dance" (a song we had sung to Shane since the day he was born) and Shane's uncle, David, read a very touching eulogy. At the graveside we released 6 Elmo balloons for every year he spent here and 100 blue, red, and yellow balloons for every year he should have spent here. It was raining that day but it stopped just as the funeral started and the clouds actually parted over the cemetery. We had a Sesame Street cake at the wake (the wake was after the burial). It was not a typical funeral, but he was not a typical kid. We wanted to celebrate his life.
After everyone had left after the wake I was outside in my parent's yard and pollen from a tree I had never noticed before and never remembered having pollen starting falling and blowing around like snow. The pollen was just the shape and size of little feathers from the wings of cherubs. It blew around me like a scene from a Christmas movie and I was very peaceful at that moment. Maybe it wasn't pollen. Maybe it was Shane letting us know he had reached heaven and was now with the other cherubs.
His headstone has pictures of Elmo, Big Bird, a truck (he loved his dad's truck), and one of the logos I had drawn for CHERUBS web site- a cherub wearing suspenders and glasses (one I had created to look like Shane). How do you fit an entire, even though short, life on a stone? We wrote a few words about Shane on it, his name, the dates, and also carved on the stone is "Psalms 18:10"- He flew upon the wings of cherubs, yeah he did fly like the wind.
We had a memorial service in NC the following week and more members of CHERUBS came, including Susie and Jim from SC and our dear, dear friend, Rhonda, who was with us in the very beginning when our sons were hospital roommates so many years ago. One of our members, Beth, had even come to visit Shane when he was in the hospital. I don't believe there could ever be a better group of people like we have in CHERUBS.
We miss him so much. I can't believe this isn't just a bad dream. I hear him and see him all the time through memories. Sometimes I expect to see him walk through the door, dragging toys into the living room and smiling at me. Shane was such a happy kid. He was always smiling and laughing and even though he was stubborn he had the best temperament and sense of humor. Looking back on that day in the car, I believe he knew it was his time to go and he wanted to make sure he remembered what we looked like. I used to joke that he was psychic because we always understood him, even before he had a means of communication. Now we believe he was just a very spiritual kid with the soul of an old man. His eyes were much too old to belong to a 6-year-old.
We take each day at a time and are thankful for all the time we had with him. We know that even though we didn't have him as long as parents of healthy kids have them, we had him longer than a lot of other parents have their children, and even though his life was hard it was a good, happy life and we wouldn't change a single second of it or have traded for him any healthy child. I sleep with the "baby doll" he had when he died (we buried him with one of the other 12 that he owned- they kept multiplying over the years). Holding that doll makes me feel closer to Shane. Shane will forever be our hero and in our hearts. The picture you saw at the benning of this story is of me and Shane telling Jeremy "Happy Father's Day" (there was a sign, but I had to crop it out). It was one of the last ones we have of Shane and it is the last one of him before he got sick. During his last week we had planned on taking him to get professional pictures taken, but we kept procrastinating. We regret that so much now.
Other than losing Shane and letting him go, writing an e-mail to tell the on-line members what happened was one of the hardest things I have ever done, next to writing this story. I know that Shane's story will scare so many of you, but please know that Shane was atypical his entire life. I don't know what to tell new families that call who ask "Was your child a survivor?". Now we know both sides- life as parents of a survivor and life as parents without their child. I hope that something good will come out of this and it will make me a better President for CHERUBS. Like I've said for years "You can't compare one CDH child to another"- that holds very true in this instance. We'd already had 2 families quit because what happened scared them so much, but what happened to Shane was a 1 in a million complication. I don't want anything else horrible to come from Shane's death, his death was horrible enough. I especially don't want families leaving the support of CHERUBS. If any of you have questions or worries about your own child because of reading Shane's story, please get in touch with me and I will be glad to talk to you about it.
Updated 2006:
It’s been 7 years since I lost my cherub. It’s hard to believe he’d be a teenager now if he had survived. Life without him hasn’t been the same at all. Jeremy and I divorced in 2003 after 12 years together and 2 seperated. We just handled grief very differently and we couldn’t manage to be strong enough to stay together through it. My entire life was Jeremy and Shane and I had to rebuild from nothing. During all this I lost 3 more family members, including my youngest sister. Debra was 22 years old when she died of cancer. She’s now taking care of my son in Heaven as I watch after her children on Earth. I pray someday that I am blessed with a family again but I am so thankful that I had such a wonderful little family if even just for a little while. I wouldn’t trade those years for anything. Shane taught me much more than I could have ever taught him.I’m 33 years old now… hard to believe I was such a baby myself during most of this. I think I’ve finally grown up. I now run my own company creating web sites for businesses, but CHERUBS is still my true passion. There were a few slow years where I tried to rebuild my life and now I am back in full force and hopefully CHERUBS will be even stronger.
Update 2008:
CHERUBS is back full force. We are so busy doing so many things that it's exhausting most days. We have a new web site, over 2200 members, a conference planned, several awareness events planned, fundraisers, new logos, new volunteers and a research site underway. I love my work with this wonderful organization.
CHERUBS is now 13 years old... twice as old as Shane was when he died. There are still bad days when I miss him so much I can barely breathe. I dream about him often and it helps so much to spend time with him and to feel like I've held him, if only in my dreams for a little while.Life has gone on, though there were days I didn't think it would. There were days I didn't think it should. But I am happy again, when I didn't think it was possible. It's happiness without the innocence that I had before I lost my son, before I lost my sister, my grandfather/father figure, other family members, my husband through divorce, my home through divorce.... add in a broken engagement and losing another little boy that I helped to raise for 2 years through that break-up, plus attacks and slander and lies from someone determined on destroying CHERUBS out of petty jealousy and all the hell that that entailed, and the man I was dating last year was killed on patrol as a Durham policeman... it's been a lot to deal with and overcome on top of all that CDH threw at us and losing Shane. I haven't always given CHERUBS as much time as I've wanted to the past few years because I've been busy going through hell and back. But hell is over and I survived and I am happy. It's a new kind of happiness. But it's still happiness. I still run my web design company and I am in an incredible relationship with the most amazing man who couldn't be more supportive of CHERUBS and my son's memory if he was Shane's biological dad. He has twin sons that I adore and I feel so blessed to have all 3 of them in my life. I look at the boys skateboarding, both 12 yrs old, and I can't help but wonder what it would be like to see a 15-yr-old Shane skateboarding with them. I will always wonder, but I accept that wondering now. I know that right now, I am where God wants me to be, doing the work that He wants me to while He is taking care of my son. There is so much peace in that.
CHERUBS... wow, how we've grown and what we've been through! The amazing friends I've made through CHERUBS have given me so much. Driving 100's of miles when Shane died just to be with me. Holding me up through grief. Listening to me cry when my life was a mess and I didn't know how I'd make it through. Rallying around me during drama and showing what a support group is really about. And look at us... some of us friends for over a decade now, making new friends every day. Working together with the whole CDH community to bring support, awareness and research to Congenital Diaphragmatic Hernia. I look back 15 years ago at that scared 19 year old kid and all the things that have happened in the past 15 years for all of us.... I am blessed. With the time I had with my son. With CHERUBS. With the work that I do. With the friends I have made. With my wonderful family. With the love of my life as my best friend. Life has been hard at times, but through it all, I have been blessed.
Written by Shane’s mom, Dawn M. Torrence (North Carolina)
1995, Updated 1999, 2006, 2008
Monday, July 27, 2009
CHERUBS 2009 International Member Congenital Diaphragmatic Hernia Conference
Our 2009 International Member Conference for families affected by CDH was a wonderful success!
We had 17 families and 8 organizations represented from 4 countries. It was truly an international CDH conference. One person called it a "CDH Summit" but we hate to use the word "summit" as that is a meeting of peace of countries / organizations who can't get along - and we most definitely all get along! :) It was a "CDH Conference" - for and about Congenital Diaphragmatic Hernia. It included CDH Research, Awareness and Support.
It began on Wednesday with our Pizza Party and Introductions. We presented Danielle Kessner of CHERUBS Australia with a cherub statue. In 2000, CHERUBS members presented Dawn with a crystal statue. Now that CHERUBS Australia and CHERUBS UK have their own non-profit status and president, it is fitting that all 3 have the statue. Brenda Lane of CHERUBS UK received hers on Thursday as they missed the Pizza Party. Also at the Pizza Party, the new CDH song "I'll Never Let You Go" by The Jammies was unveiled. We will post that video in a few days.
Our hotel was just beautiful and Chris Arango of the San Antonio Holiday Inn Select was wonderful. There were a few issues but he fixed them ASAP. We were very impressed with them!
On Thursday, we were blessed with incredible guest speakers!!! Daryl Scott MD and David Pearson from Baylor's CDH Research Team were wonderful! Their presentation was very informative and the parents were able to ask lots of questions. We all learned quite a bit about genetics and CDH!
Then Dr. Kevin Lally presented from the CDH Study Group and we learned about the history of CDH, the future of CDH and all the research that the group is doing. And Pam Lally was so sweet to provide us with the latest (unpublished) survey tabulations. The parents were able to ask more questions about ECMO, CDH repair and survival rates. It was extremely informative.
On Friday, Drs. Meaghan Russell and Mauro Longoni from Boston Children's spoke on their CDH Research Study. We learned even more about CDH and genetics and how they use mice to create diaphragmatic hernias. The parents got to ask more genetic questions. They bought us copies of CDH News, their newsletter, as well and it featured a photo of last year's conference! :)
On Saturday and also on Friday we had round-table discussions and parents had the opportunity to talk to each other about their stories and various topics dealing with CDH. We all learned a lot from each other and we laughed, cried and shared so much. The doctors sat in on the discussions and learned from parents just as we learned from them. It was such a blessing to have the opportunity to do this.
And on Saturday, the kids learned a little song about CDH and performed it for us. Video to come soon!
Our conference ended each day at noon so that families could sightsee and socialize with other CDH families. Families went to the Alamo, Sea World, the River Walk, rodeos, shopping and more. Often, you would find families convening at the hotel swimming pool. The doctors fit right in and 2 of our Board Members had dinner with Meaghan and Mauro and had the opportunity to ask them lots of questions face-to-face. Videos will be posted soon!
This conference was also a milestone for CHERUBS - it was the first time the Presidents of all 3 CHERUBS have met in person. Dawn Williamson of CHERUBS (USA), Danielle Kessner of CHERUBS Australia and Brenda Lane of CHERUBS UK came together for the first time this year. We also welcomed Kim Richards of The Olivia Raine Foundation and Michelle Brown of Little Lambs. Not to mention doctors from 3 more CDH studies - Kevin and Pam Lally of the CDH Study Group, Meaghan Russell and Mauro Longoni of Mass General / Boston Children's CDH Study and Daryl Scott and David Pearson from Baylor College's CDH Study. All 8 organizations are members of ACDHO, The Alliance of Congenital Diaphragmatic Hernia Organizations - a group of CDH organizations and research centers dedicated to working together to help support, protect and advance the CDH community. 8 CDH organizations all together at once to help each other and CDH families!!!!
Talking to the other members of ACDHO and to the families we got such great advice on how else we can help the CDH community. It was wonderful to talk to the other organization leaders and get their opinions on so much and learn about services that they offer, rules they give their volunteers, how they deal with certain situations, etc. Listening to the families during the round-table discussions and listening to the questions that they asked the doctors, we learned what topics they really want to know more about and want to see us post more about. We learned so much that we will all bring forward to the CDH community!
We want to say thank you to our guest speakers and to Karen Myers, a member who went above and beyond to make this conference possible. We'd also like to thank Barbara Wagner, who showed what a CHERUBS volunteer is all about with all she's done to help us. And to our sponsors and volunteers:
Conference Volunteers
A very, very special thank you goes to the following individuals:
Alec Myers – in memory of Kaleigh Myers
Barbara Wagner – in honor of Logan Wagner
Chad Knudsen
Charles Hess – in honor of Adam Hess
Chris Arango
Chris Meats - in honor of Ian Meats
Craig Williamson – in memory of Shane Torrence
Dave Holt - in honor of Braden Holt
Dave Lipsit
Dawn Williamson – in memory of Shane Torrence
Fernanda Arce – in honor of Juan Pablo Arce
Jean Williamson – in memory of Shane Torrence
Jennifer Brown – in honor of Adrian Brown
Kara Hess – in honor of Adam Hess
Karla Holt – in honor of Braden Holt
Karen Myers - in memory of Kaleigh Myers
Kevin Lally, MD
Kimberly Richards – in memory of Olivia Raine Richards
Kimberly Switzer – in memory of Asher Switzer-McCoy
Lynne Brogdon – in honor of Baer Brogdon
Pam Lally, MD
Penny Campsey – in honor of Cole Campsey
Primerica
Tara Hall - in honor of Brandon Hall
The Jammies
We would like the following for their generous donations:
Chuck and Kara Hess, in honor of Adam Hess
Jennifer Brown, in honor of Adrian Rivera
Karen Myers, in memory of Kaleigh Myers
Kevin and Barbara Wagner, in honor of Logan Wagner
Kimberly Richards, in memory of Olivia Raine Richards
Our conference concluded on Saturday, much to everyone's sadness. There were a few tears saying good-bye. We hope to all see each other again next year in San Francisco at our 2010 CDH Conference - along with lots of new families.
It truly was a wonderful week. Hopefully everyone left with more information on CDH, new friends and knowing that we are a big CDH family working together to help them and all those affected by Congenital Diaphragmatic Hernia.
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