Baby Zakk with his Mother

Our Journey with Zakk

On April 15th 2009 we went to hospital for a 20 week scan to ensure all was well with our baby. This took so long that we both knew something was wrong and when we were told there appeared to be a hernia we both thought it wasn’t very good but we had no idea how serious it really was. We were taken aside to wait for a Doctor who would come and explain what a congenital diaphragmatic hernia (CDH) was and what would happen now that it had been detected.

The doctor told us babies with this condition had a 40% chance of survival providing life saving surgery was carried out, normally within 48 hours of birth, and that we would be referred to the Royal Victoria Hospital(RVH) in Belfast to have the diagnosis confirmed and arrange special care and treatment for our baby after the birth. He also told us the hospital would want to carry out further tests to ensure nothing else was wrong, probably amniocentesis and we would have to wait a few weeks to be called for an appointment and possibly a few weeks after that for results.

We left devastated and in tears but we were hopeful nothing else could be wrong and that our baby would be one of the lucky ones who would survive the surgery if the diagnosis was confirmed. We had no idea then what really lay ahead.

From that point every waking minute was consumed by this awful news and there was nothing we could do except wait. I began that night to research the CDH and while it was much worse than we had initially thought it was something we knew could be treated and our baby could survive to live a long, happy and full life.

On 17th April a letter arrived with an appointment at RVH the following Thursday 23rd. This set me off worrying even more as it had come so quickly. I decided we needed to stay positive and that night we decided on 2 names for our baby, Zakk if it was a boy. We tried to keep busy and get on with things for the next week. Marcus went to work and I spent hours on the internet learning as much as I could about CDH.

On 23rd April we headed to the RVH for our appointment. The Doctor confirmed the CDH and was very keen to carry out amnio as she put it to rule out any other issues and ensure they had all the information possible to be well prepared and do the best they could for our baby. We agreed and it was done there and then. We were reassured as everything else looked OK although they thought the baby could have a clenched fist, but again we were reassured this was a minor thing and could be corrected. We also met a geneticist who asked us questions and discussed possibilities with us but again from our scans she too felt any other problems were unlikely.

We were booked back for a further appointment the next week and a heart scan a few weeks later, and we went home feeling anxious but hopeful that all would be well and hoping the results of the amnio would be back soon and would give us some peace of mind.

The next day I was again very anxious but resisted the temptation to research any possible genetic conditions as I felt I did not want to know and did not want to increase my worry unless I really had to know. I still naively thought the worst possible outcome would be Downs Syndrome but that I would cross that bridge if I had to and deal with it as best I could then, taking whatever child God sent me. I still had every hope my baby would live and be OK. Our daughter Cerys was just 20 months and had to go to my parents for the day so I could rest after the amnio as advised. That afternoon at 3.30 the phone rang and it was the geneticist. The call was a surprise as I had not expected to hear from her for a while. She explained the results were conclusive and our baby had Trisomy 18 (Edwards’s syndrome) and there was no hope as nothing could be done, our baby would die. She confirmed he was a little boy and he could be born alive if we were very lucky but would die soon afterwards as it was in every cell. There was a high risk that he would arrive early and be still born as many babies with T18 are.

I was so shocked I could not speak and could barely breathe. I hung up the phone and called Marcus who I could barely speak to either, I just told him to come home between sobs and gasps for breath. He left work and was home a while later. It was less than an hour but felt like several. We were so heart broken by this news, we will never forget the devastation.

Our hearts were broken and I had never been so sad before that day. I had the ominous feeling that this was just the beginning of our heart ache. From then on Zakk was in my every thought. I was consumed by grief and my baby boy was 4 months from being born. I did the only thing I could, and went back to the computer and began to research trisomy 18. I begged God to let Zakk live long enough to let us hold him just for a little while and to get him Christened, but I had lost all hope.

During our second visit to RVH we were told Zakk could not live and they confirmed no-one would do anything to repair his hernia because he had T18. It is the view of all the medical professionals I have met that T18 is not “compatible with life” as they put it and they will not intervene in any way to help a baby like ours. The Doctor advised me I could return to my local hospital to deliver the baby if I wanted as nothing would be done anyway and it would make no difference to the outcome where the baby was delivered.

We were devastated beyond belief, and every hospital visit after that just brought more bad news when we thought things could get no worse. The baby was very small, his heart had an atrioventricular septal defect with a ventricular imbalance (AVSD),no surgery would be done for this or the CDH as he was “not compatible with life”. I got so sick of hearing this from doctors I wanted to shout at them all “who are you to tell me my child doesn’t deserve to live”, and yet I was intimidated by their expertise and while I later questioned many things, initially I accepted what I was told and felt hopeless.

We were advised to consider a termination which I could not even think about as this was my baby and Zakk was already as much a part of the family as my other children. I could not let him go or play any part in ending his life earlier than God intended.

I cried day and night but I kept on looking at the internet and came across Prenatal Partners for life and a few other web sites were I saw children alive and doing well despite having T18 or other serious chromosome disorders. I contacted some of these web sites and found other parents who understood the dark place we found ourselves in as parents of a child with a very negative prenatal diagnosis. From this sprang hope that all was not lost and from this hope we both began to pick ourselves up as we realised Doctors don’t know everything, babies just like ours can and do survive, and sometimes even miracles can happen.

It was this hope we needed to help us through each day, greatly aided by the support and prayers of others. From then on my days were filled with lots of research, I thought if I could find the right Doctor he could help us save Zakk. I was upset that no-one I spoke too would agree to help keep Zakk alive and this for me was the hardest thing to accept. I knew my child’s life would never be like my other children. He would probably not communicate as they did or be as able bodied but I could not accept that he didn’t deserve to live, or that no-one was prepared to help us keep him alive when that was the only thing I wanted.

When I went back to my local hospital we were asked to attend a meeting where we were formally advised nothing would be done to assist our baby live, and what would happen when he died. We were told about the mortician and asked to think about what we wanted regarding taking our baby home and where we would bury him. We were told there was no rush in making these decisions until the time came, but we needed to bear them in mind… I think part of the hospitals motivation was to also try and re-assure us that we would not be put in the post natal ward with other babies, and they would do their best to give us privacy in our grief, but I was distraught by the whole thing. Our precious son was being written off by Doctors months before he was even born and no-one could understand the shock of hearing these things unless they too have been in the same situation. Instead of looking for a new pram we were now deciding where we wanted to bury our baby son and feeling under pressure to make such awful decisions in-case he arrived early as predicted.

Never before had it even occurred to me despite years of life experience that anyone ever carried their unborn child for months with such a heavy burden. I even knew family members who had lost babies and still it had not registered with me that anyone could know so far in advance and go through months of anxious waiting and hoping.

I have always struggled to accept no-one could help Zakk, but I could find no-one within my reach who said they would or thought there would be any point. Everyone I spoke to felt that with his combination of problems it would only cause him unnecessary suffering to artificially prolong his life by attaching him to machines, nor did anyone feel he would be able to survive surgery. I just feel that if I had unlimited resources or lived somewhere else maybe he would still be here with us now. Or maybe I just didn’t try hard enough to find a more sympathetic Doctor. Knowing I was treated within the policy guidelines of the National Health Service in the UK does not console me in any way. I continue to struggle with accepting these decisions even now, and can only pray that some day I will be at peace with them. Although I can’t help feeling these policies are wrong and a parent should have a right to choose to ask for more aggressive measures to be taken in an attempt to save their child if at all possible rather than be forced down a route of comfort care if it is not what they want.

We had a number of family birthdays between May and August and we lived through all these events in an almost auto pilot fashion. We went through the motions, celebrated the birthdays and tried our best to act as normally as we could, while all the time hoping and praying Zakk would by some miracle be born alive and be OK. I had trouble sleeping not helped by the usual pregnancy issues as I got bigger. Everywhere I went it seemed like the world was pregnant and I was the only one whose baby was going to die. I got really cross when I saw pregnant women smoking or worse, drinking alcohol and sometimes I wondered what I had done to upset God so much. I had been so careful to stay as healthy as I could and have a proper diet and this was what I got for all my careful care of my unborn child. I felt guilty for thinking previously Downs Syndrome would be so terrible and wished that Zakk had this instead as at least he could live. I bitterly regretted allowing the Doctor to carry out the amnio test as I felt they would still be planning for surgery and doing all they could to help Zakk had they not known for certain he had T18. Realistically I know that they would have soon figured it out after he was born, but I still feel we would have got more time

with him as they would have helped him even for a little while in the absence of this information.
The next few months were filled with hopeful anticipation as we approached the birth of this very special child, coupled with dreading the day as I knew Zakk was safer where he was. I didn’t want him to be born, knowing he would face such a great struggle to live and I would not be able to help him, nor could I find any Doctor willing to do anything except agree to give him a little oxygen if he was born alive and struggling to breathe.

Every day I carried Zakk was a blessing. Every move and kick was a great joy, much more than with any normal pregnancy as my little boy was reassuring me he was alive and well and getting stronger. I had been told I would not feel much as he would be weak and very small, so when I felt Zakk it was wonderful. Doctors don’t know everything. Zakk moved well and did not feel weak or small and with every movement my hope strengthened.

Many others helped us through this journey. One very bad day my sister sent me a text message containing a little prayer:

May God grant you the strength and faith to count your blessing, not your crosses, count your gains, not your losses, count your joys, not your woes, count your friends, not your foes, count your smiles, not your tears, count your courage, not your fears.

Gradually my mood changed as the time went on and Zakk continued to defy the odds and live. My hope grew with the help of people who were there for us when we needed support, my family and close friends and those in the Trisomy family who have also been down this road. Just knowing that Mary and others from Prenatal partners for life remembered us and many people we were unlikely to ever even meet in person kept us in their prayers brought great comfort and strength and helped us face each day with hope rather than hopelessness.

I read a lovely poem on the Prenatal partners for life web site, ”God sent to me an Angel”, and it has helped me through many dark days then and now.

To me my baby was perfect and special and I loved him. I prayed for minutes, I wished for hours and I hoped God would grant us the miracle of days. Every single movement Zakk made each day made up for all the worry and upset we went through. Every second I carried him really was precious and I only wish now I could turn back time and feel him move once more.

I went week about to the Doctor or Midwife to check he was alive and had a heart beat, but Zakk kept reassuring me he was OK. The appointments with the Midwife were OK as I only saw one of 2 midwives and they were both great, very encouraging and supportive, but I hated the Doctors appointments as I was waiting in a room full of other pregnant women and I so wanted to be just like them with their healthy babies.

Life is full of unexpected twists and turns. I had always feared having a child with a serious disability and wondered irrationally if this was my punishment. I knew the risk increased as I got older I just always thought I could never cope and now I found myself having just such a child and hoping and praying he would stay with me and not die. I just wanted Zakk to live and not be suffering or in pain. I didn’t mind what he could or couldn’t do, I just wanted him with me and I promised God I would look after and cherish him no matter what. It is a strange thing to wish if only your child could have had a less serious chromosome disorder such as Trisomy 21 as at least it would not be as the Doctors described T18 a “lethal Trisomy”.
Zakk did not come early, and the week before my due date I was persuaded that to give him the best possible chance and avoid putting him through the trauma of a natural birth I should have a caesarean section as his heart coupled with the CDH and T18 left the situation very dire. We were booked in for 11th August and suddenly Zakk’s birth was upon us. far too soon.

So many times before he was born I wondered what would happen. I hoped and prayed for a miracle, and I wondered how I would get through if my miracle didn’t come.

Zakk came into the world on 11th August at 12.10pm weighing 5 lb and looking just like the perfect and beautiful Angel he is. He was given a little oxygen as promised to help him breathe, and a midwife Christened him for us as we had wanted. After a few minutes a paediatrician came to speak to us and advised us the oxygen was not helping and he would only live another minute or two and we were asked if we were happy they stopped and gave him to us otherwise we would not get to hold him alive.

We didn’t want to waste his last few minutes and we wanted to hold him in our arms so he was handed to his Daddy at which point he opened his left eye to the Doctors surprise. When I took him in my arms a few minutes later I just talked to him and begged him to be strong and hold on for us as long as he could. I was so desperate he would live but I knew in my heart he was very weak and it was a great struggle for his little lungs to breath and his little heart to keep beating.

Despite everything and to the amazement of the paediatrician our brave and precious son lived on for 70 minutes and got to meet his big brother and sister and his Granny, Granda and Aunt. He fought as hard as he could to live, and passed away peacefully in his Daddy’s arms surrounded by those who loved him most in the world. My prayers had been answered.

I could not have asked God for any greater gift than being Zakk’s Mummy. It was the greatest honour and privilege of my life to carry him and hold him in my arms. I know I will have to live a lifetime on the precious but all too short time I had with him. I know somehow I will get through my grief and life will go on. I know too that there is a reason why we were blessed with such a special and inspirational child, and while his time with us was very short, he has forever changed our lives and the lives of those closest to us.

We spent the next two days with Zakk in hospital by our side, and then we took him home to meet the rest of our family and friends. He stayed with us until the 15th August, his original due date, when we had a very moving funeral service for him at home with a mass in his honour and later we laid his little body to rest.
Nothing could be so precious as the brief time we held Zakk in our arms while he fought for life, but every minute we spent with Zakk over those four days was also precious to us and we will always treasure this time. We got to say goodbye properly to our little boy and he has left behind everlasting memories.

I cannot begin to explain how devastated we are by his passing, but nor would we have missed this journey for the world. He is our inspiration and reason to go on. I know that we will eventually learn to live with this great loss, and until then we will remember how brave he was and how hard he fought to stay with us and these thoughts of him will help us through.

I will never be the person I used to be, Zakk has forever changed me for the better and I believe this change will continue to happen for as long as I live. This journey has renewed my faith in human nature as I have been overwhelmed by the support of all those who travelled this path with us, and he has renewed my faith in God as I know for certain Zakk’s spirit lives on and he is with us always Our precious Angel.

For this child I prayed and the Lord has given me what I asked of him, so now I give him to the Lord…
(Samuel 1:27-28)

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-The support, information and encouragement provided by the PPFL parents is not meant to take the place of medical advice by a medical professional. Any specific questions about care should be directed to a health care professional familiar with the situation.