Showing posts with label Mother's Day; love; hope; grief; family; friends; anniversaries. Show all posts
Showing posts with label Mother's Day; love; hope; grief; family; friends; anniversaries. Show all posts

Sunday, 22 November 2015

Six Years Is A Long Time by Dani

It has been six years since precious Jasper died.  In this blog, Dani shares with us her memories of what has occurred since Jasper died and her memories of the time surrounding his death.

Photo taken and copyrighted to Dani Hall
Every once in awhile, I remember how long it’s been. Days like today (18th November) – his 6th birthday, particularly mark the passing of time. Time really passes. It is not something we imagine. But the passing of time is both objective time and subjective time. But there is also personal time, which is measured in your relationship to memory.

When I stop to think about it – really think – so much has happened since his passing. We lost our house, went through fertility clinics to try and discover my infertility problems, we had a rainbow, we raised money for a camera kit for Heartfelt, I’ve lost 3 nephews – one to SIDS and two to prematurity, I’ve been blessed with 4 nieces, helped my mother-in-law find happiness with another partner and watched her get married, gotten a job as a sleep scientist, graduated university with a Bachelor of Justice and currently enrolled to complete a Master of Social Work, volunteered online with SANDS, enrolled my rainbow in prep, took a family road trip, watched Gangad pass, had two sisters get married, my rainbow had surgery and broke his leg, watched many friends get married and have babies and I’ve gotten 3 tattoos. And that’s just what I can think of, off the top of my head.

But then there’s the other side of time. Where it seems like it hasn’t passed at all. Where I think about his birth – rushing for an emergency caesarean and his admittance to the NICU. The strong yearning to see my baby – to hear him cry. The fond memory that we thought he was a girl right up until the moment he was born. The name we had picked out for him – Taryn – until he was born and we had to think of his name on the spot. The sheer relief that flooded through me when he was born, knowing he would be taken care of. The feeling of my heart plummeting when they told me to make the choice to continue care or remove him from life support. The knowledge that I had seen him only a few hours earlier and he was alive – kicking, responding to my touch – and knowing I’d never see that again. And in there hazily, the memory of my dad holding his oldest grandson, saying goodbye, telling him how proud he was of him. Getting wheeled back to my room after kissing him goodbye, knowing I’d never see him again. The sheer pain in my heart – hurting to move – hurting to breathe. The guilt for removing support. Preparing a cremation and funeral. Something no parent should have to do.

The overwhelming support and the text from my dad I will never forget “Dani, you should be very proud for creating a life and trying to give him the best chance possible – not many people can do that”. The foggy memories of loved ones visiting – and trying – really trying to connect but not being able to. The loss of friends.

The memories are right there, as though it all happened yesterday, but it’s been 6 years. 6 years ago we still thought he was a girl. 6 years ago we knew our baby would be born early we just didn't know when. 6 years ago I was still in ignorant bliss that our baby would survive. Little did we know in 24 hours our baby boy (surprise not a girl) would be born at 25+6 weeks and another 10 hours after that we would have to take him off life support and watch him go to heaven in my arms.

Time has taken away a lot of my innocence, given me a lot of grief, taken my son further and further away from me. But it has also given me many happy moments, blessed me with another son, made me who I am today.


“No matter how much time passes, no matter what takes place in the interim, there are some things we can never assign to oblivion, memories we can never rub away.” 
– Hakuri Murakami

Dani
If you require support after reading this blog please contact

Sands on 13 000 72637

Danielle Hall
Wife to Corey and Mumma to two boys: Jasper Rhys in heaven and Harrison Phillip Robert in her arms. Jasper passed away after PPROM at 23 weeks and birth at 26 weeks, surviving for 10 hours in the NICU unit. Currently completing a Master of Social Work with the goal to aid in the safety and protection of all children, because all children deserve to feel safe and loved.

Thursday, 19 November 2015

Couldn't Live Without Three.....by Tiffany

Tiff has written very honestly about the physical experience of the miscarriage which followed the death of her son from SIDS.  However, she herself says she is still too numb to be able to explore her emotions in a similar way. We hope that she will be able to do so in the future.



Three  days after Mother’s Day in 2014, I lost my 7 week old baby boy Wade to SIDS. Days and weeks went past and my husband and I were finding it hard to adjust to having two kids again and we were talking about having another:  not to replace our little man but to help us with our grief.

In September 2014 we found out we were pregnant again, but this time our fear was not losing our baby to SIDS -  never did we think of the unthinkable.
When I was 7 weeks pregnant I unfortunately went through trauma. I was checked and the baby and I were doing great.

At 12 weeks that all changed. I started bleeding very heavily. I went to the doctor and had an ultrasound done. They found I had a subchorionic hematoma (which is bleeding in the wall of the uterus) caused by the trauma. They told me it would either grow or shrink and it was a waiting game. My daughters witnessed everything during this pregnancy and I wished I could take it all away.

By 16 weeks my bleeding had died down to just spotting and we were so excited that everything was going well at this point.  But then it turned again.
By 17 weeks I ended up in hospital with gastro and even worse bleeding, to the point where I was literally standing in pools of blood.  I had frequent ultrasounds and the clot was growing. It was now at the point that there was more clot than baby. I was in and out of hospital all week when I suddenly went into labour at 18 weeks on the 10/01/15, only 9 days after my 21st birthday.

The birth was horrific, the worst birth I’d ever had. At 3cm dilated I was already pushing and my baby was holding on until my cervix shut on him. My husband was sitting by me through the whole thing and I told him to pick a name as we knew it was a boy. We named him Jax. They told us straight out that because I was 18 weeks,  no matter happened what he wouldn’t make it. He took his last breath in my husband’s arms. I was expecting a normal looking baby but to start with I was extremely overwhelmed and it made me realise it was bad news. I was hoping it was all a dream.

After the birth they told me I lost about half my blood volume and given that I’m anaemic it was more serious. They told me I needed a blood transfusion, and I turned out that I needed 3 bags. During my first bag I recall my monitors going off and a lot of people in my room when I finally came to they told me my blood pressure dropped dramatically. But I recall nothing as I passed out for a few moments.

That night I spent in the ICU. Constantly being monitored for blood loss and having my extra bags of blood. The next afternoon all I wanted was to go home with my husband and girls. The hospital was too much for me. They hospital refused to let me leave and I kicked up a storm. I couldn’t stand being there. I couldn’t stand the doctors saying I was good and I knew that I wasn’t and it was my heart that wasn’t good.
I feel all this happened just because I was so used to having 3 kids and the routine I was in I wanted to bring another baby into our world so badly. My eldest constantly asks for a new baby brother and to this day I still can’t give her that wish.
Tiff
If you require support after reading this blog please contact
Sands on 13 000 72637


Tiffany Aghan

Wife to Luke and mummy to Tamara and Summer, in her arms, and Wade, Jax and Tristan, in heaven. I have recently completed certificates in law and in psychology and in the process of completing certificate in medicine. I am having time off at the moment to spend more time with my girls. But I am hoping one day I will continue where I want to go.

Wednesday, 4 November 2015

Jeremy's Story - Alisha

Alisha shared the poem she wrote for Jeremy which was published on August 31st.  She now shares with us precious Jeremy's story.


'At my husband’s insistence we had a very small funeral with only immediate family.  It was the smallest coffin I’ve ever seen, but it was decorated with gorgeous flowers and the blue elephant that reminded me of him and it was just perfect.'


After three years of infertility and countless treatments, my husband and I were finally successful in conceiving thanks to a round of IVF.  I was so ecstatic to finally be pregnant; I never dreamt it wouldn’t result in my family dream coming true.  I had already bought everything I needed, decorated the perfect nursery, and had the big scary 20 week scan and everything was more or less how it should be.  There was a strange comment about low amnio fluid, so my obstetrician suggested we come and see him the following week, just to put my mind at ease.  Neither he nor us had any idea that the next time he saw us he would be telling us he couldn’t find a heartbeat and then organising for me to be induced the following day.

My husband wouldn’t really acknowledge that we had a child, to him this was just another setback in our journey to become parents, so we just needed to get the medical part out of the way and get on with our lives.  As a result he wasn’t really there for me at the hospital, preferring to sit in a chair on the other side of the room rather than hold my hand as I gave birth to our son.  He refused to look at him, and I’m not sure if it was the drugs, his attitude, the exhaustion, the shock, or his pressure to leave the hospital, but as a result I didn’t really hold my son.  I didn’t spend any real time with him, didn’t take photos or anything to remember him.  Instead I left him with the nurses and headed home so my husband could go to the gym, and at the time that seemed like acceptable behaviour.

I think after such a long journey to conceive my son and only being 21 weeks, it was as if I didn’t feel entitled to grieve - these things happen and you just need to focus on what comes next.  I had already been through so much grieving for the children I couldn’t conceive over the last three years; this was just another part of this journey.  I felt like a fraud saying my son was stillborn!  To me stillborn children only happened to the poor women who had to carry their babies full term and then they died.  Even though I had just gone through labour and delivered my son naturally it was so hard for me to think of myself as being in the same category as them – what they go through must be the most devastating thing in the world.

I am so grateful to the wonderful family and friends who came to visit me the next day and who messaged and sent so many beautiful flowers.  All of the support and how upset they all were helped me realise the severity of what I had actually just been through, and to help me see that I was a Mother and I had lost my child – it wasn’t just another medical procedure.  Once that sunk in I felt sick with guilt that I hadn’t spent more time with him, we hadn’t even named him.  My husband wasn’t interested in naming him and refused to let me use any of the names on our list.  I had always liked the name “Jeremy” and when I looked up the meaning it was “God will raise him and God will set him free”.  I’m not a religious person, but this just fitted perfectly.  After that moment I started to get selfish and do what I needed to do to honour my son and how much he meant to me. 

Work was amazingly supportive and gave me as much time off as I needed so I spent my first few days reading other’s stories - the first story I found was actually a DJ from a local radio station that I had listened to most mornings since I was young and it gave me so much comfort and hope to know I wasn’t alone.  This can be such an isolating time, especially when you don’t have partner support, and while I knew of people who had suffered miscarriages, I didn’t know of anyone who had ever had a stillborn - I got so much comfort from strangers generous enough to share their stories.  I then focused on planning the perfect funeral and found great healing in writing.  The wonderful funeral director had angel babies of her own and was heavily involved in SANDS and she gave me some amazing books that really helped.  She could also see that my husband was not in the same place as I was and managed us very well so she could offer me so much support and guidance.  Through her I organised for myself, my parents and my Mother in Law to be able to spend some time with Jeremy.  I know this meant a lot to all of them.  Jeremy was the first Grandchild for both sets of parents, and they really appreciated being able to see him, hold him and say goodbye.

At my husband’s insistence we had a very small funeral with only immediate family.  It was the smallest coffin I’ve ever seen, but it was decorated with gorgeous flowers and the blue elephant that reminded me of him and it was just perfect.  I read the a poem I had written for him, others spoke and I created the perfect soundtrack.  A good friend sent a bag of gorgeous baby blue helium balloons to my house that morning which we released after the ceremony.  At my insistence we followed the funeral with a large wake to celebrate Jeremy and what he meant to me. I was so touched that over 70 people came to the wake to celebrate Jeremy, his significance and how much he meant to all of us. 

At the time I passed off my husband’s behaviour as just his way of grieving, but the death of Jeremy was the last straw for him and he wasn’t prepared to go through any more to get our family.  As a result he left me a week later. 

On August 31 it will be 3 years since Jeremy was born sleeping.  I like to think his passing was the greatest gift a child could ever give a parent.  I can now see my marriage would not have survived regardless and Jeremy has given me a clean break and a second chance at happiness.  I still have good and bad days, and think of Jeremy at some point during most days - I just hope he is proud of the life I am living thanks to his sacrifice.


Alisha


If you require support after reading this blog please contact

Sands on 13 000 72637

Alisha Burns


Alisha is a 35 year old kiwi marketer living in Melbourne and mother of one angel, Jeremy, who was stillborn at 21 weeks in 2012.  Alisha loves exploring the world, impressing people with her ability to walk in 6 inch stilettos, anything Disney, experimenting in the kitchen, pretending she can sing at karaoke. One day she would love a French Bulldog to complete her menagerie if she isn't lucky enough to have children of her own.

Thursday, 15 October 2015

In Loving Memory of Thomas Bowden - Lyndy

In her first blog post, read about how Lyndy marked a special, but heartbreaking milestone – her precious son, Thomas’s 18th birthday.


This year marked a very special time in my life, I turned 50 and my precious son Thomas turned 18. I will tell you a little of my story. Thomas Bowden was born on the 20th August 1997. Unfortunately Thomas was diagnosed with HRHS, a condition where the right ventricle of the heart is underdeveloped and Transposition of the Great Arteries (TGA) at 26 weeks gestation.
The specialists all believed that Thomas would survive, but would require surgery. Thomas was born by C-section in our small hometown of Hobart Tasmania. He looked a picture of health, 9lb 15 oz of pure joy.
However, not long after he was born things started to go wrong. Thomas was placed on a ventilator and flown 600km away by air ambulance to the Royal Children's Hospital in Melbourne for treatment. On day 3, Thomas underwent a 10 hour surgery, the first of what was to be many surgeries. For 24 hours following Thomas heart surgery things went so well, he was placed on at least 20 different machines doing so many different things to keep him alive.
Day 4 brought with it a special celebration. When I arrived at Thomas's bed that morning there was a special card saying "HAPPY BIRTHDAY MUMMY LOVE THOMAS", what a beautiful gift. The day went along smoothly until around dinner time when suddenly machines started to beep everywhere. Doctors were called but in my mind I still believed everything would be okay. More machines beeped and alarms went off. Code Blue is called and people come from everywhere to try and save Thomas's life. I paced, I cried, in my mind I screamed, how could I stand here and watch this happen to my child, my baby. This will always be something I later regret, I left the room. I was placed in a small room for what seemed like an eternity but in reality probably was not. I remember the Doctor entering the room but still to this day I cannot remember him telling me Thomas had died.
For all I remember is that sound, the sound that came deep from within me, the sound of my heart breaking, the sound that only a parent who has a child die can truly understand.
When I returned from Melbourne a friend told me about Sands. I needed to be able to talk with people who understood my pain and what my journey would now be like without Thomas in my life. Over the past nearly 18 years Sands has been by my side, supporting me and acknowledging that grief is a lifetime journey. Sands gave me hope and understanding.
Over the years, I have thought about long and hard about what I could do to mark this very special but heartbreaking birthday. I could have organised a party, or had a special dinner but I needed to do something that had meaning, something that could make a difference, something that allowed others to celebrate Thomas’s life.
I came across a site called Everyday Hero. The title of the page resinated with me, for Thomas is my hero, I am the person I am today because of Thomas’s existence, however brief it was.
I decided that I would seek donations for Sands in memory of Thomas’s 18th Birthday. Setting up Everyday Hero was so easy, I needed that, I didn’t want anything complicated for me or for the people that were going to donate. I was not sure how it would go but set a target of $500, sent the link to all my friends and family and was truly overwhelmed with the generosity by my loved ones, and even people that I didn’t know. Together we raised $798 for Sands. To me this page meant so much, to be able to give back to Sands in memory of my beautiful son. There are no words to describe how this felt, but I will say I felt privileged that Thomas meant so much to so many people. 
A poem for Thomas:
In the quiet of the night I remember like it was yesterday..... and as the tears fall softly down my cheek I think of how you felt in my arms and how you smelt like the sweetest spring day..... the bond between parent and child is so powerful...I wish beyond wishes that things were different but as a wise person once said...." When you accept what has happened, you aren't acknowledging that it is okay but rather, that you know you must find a way to keep growing and living - even if you don't feel like it...Don't let grief be your constant companion...Realize that your grief is born out of unconditional love for your child and rejoice in that love which will never end... Embracing life again is not a sign that you have stopped missing your baby, but an example of a love that is eternal" 

 I love you and miss you Thomas Anthony Bowden 
20/08/97 ~ 24/08/97
Thank you for taking the time to read about my Thomas. If you would like to create a tribute page for your baby like I did, click on the link below and sign up. 

https://www.everydayhero.com.au/event/Inmemorysands


Lyndy        

If you require support after reading this blog please contact

Sands on 13 000 72637

Friday, 8 May 2015

Levi's Story.....

Adin shares her story about the birth and death of her precious son, Levi.

"Just recently I read an excerpt contributed by Deborah L. Davis PhD from 
the book "Never Forgotten".  She wrote "it may help you to remember
that you were in the impossible position of having to 
choose between terrible and horrible.” I have a profound connection 
with this statement, and it provides me with bittersweet comfort."


I was always afraid of becoming a mother because I was scared my baby might die.
There wasn't one thing that particularly scared me. I was scared of the “what if’s?” In my head I resolved to the fact that every prospective parent must worry at some point about these things. It comforted me to know that over one hundred billion people have ever been born, and of the seven billion on the planet right now, the average life expectancy was about 70 years of age. Millions, no, billions of people do this parenting thing every day. So surely I could?
So, I did.

And guess what? My baby died.

Actually, that’s a selfish thing to say.

Our baby died.

My husband lost his baby too.

Our first child, a son, Levi Duxbury Hewat was born on at 4.58pm on Saturday 8 November 2014 at 38 weeks exactly, and was 2.92kg and 49cm of perfection.
Levi died six days later.
Surprisingly, when I fell pregnant the fears I had weren’t really bothering me and we had 38 weeks of joy, excitement and anticipation. I was fortunate to be one of those enviable women with a ‘breezy’ pregnancy (thank you, Levi).  
I was due to finish work on 7 November. Levi had other plans. My membranes ruptured on Thursday 6 November.
We went to the hospital for a check-up that afternoon. It seemed my membranes hadn't ruptured completely, and all was looking OK, so I was given the option to join the queue for an induction or go home to await the natural onset of labour. We chose to wait and get one last good night’s sleep in (Ha! We didn't sleep a wink). We were advised to return to the hospital the following morning if nothing was happening. Apparently the vast majority of women will go into labour naturally, and are likely to give birth within 24 hours of a rupture. I’m one of the minority.

We returned to the hospital on the Friday morning. Again we had the option to join the queue for an induction that day or go home to await the natural onset of labour. This time we chose the induction.

The labour was long and difficult: medical staff struggled to insert the cannula; nine hours after contractions commenced I requested pain relief and it made me vomit (hard to do ‘nicely’ when you’re contracting); several hours later I opted for an epidural. The first attempt resulted in a dural tap, so the anesthetist gave it a second go. A short while after the epidural kicked in there was a prolonged fall in Levi’s heart rate and I was being prepped for an emergency caesarean. Levi’s heart rate recovered, and labour continued as before. Late into afternoon I was able to start pushing. Over an hour later the doctor was called to perform a vacuum assisted delivery. Around fifteen minutes later, our Levi was born.

After the birth, Levi was administered oxygen. Eventually, he was placed on my chest for a few minutes. He had big, dark eyes, my lips, and his Dad’s dimple. He is the cutest baby I have ever seen. Because Levi was administered oxygen, he was going to the special care nursery for observation and I was going into the theatre room to receive a blood patch following the dural puncture.

While Levi was in the SCN staff saw him have a seizure so he was moved to the Neonatal Critical Care Unit and was being monitored by an EEG machine. The second time I saw my son he was covered in wires. He was in an open crib so whilst we were unable to cuddle him we could gently cup his feet or hold his hand. He was to be given an MRI and a lumbar puncture to determine or rule out possible causes of the seizures. Throughout the next 48 hours, my husband and I along with our family members would sit with Levi and wait for updates on his condition. The seizures seemed to have subsided, initial blood tests came back clear, the EEG and the majority of the wires were removed. The lumbar puncture however wasn’t successful and he was still waiting for his MRI.

By the Monday evening, and throughout Tuesday, Levi’s condition was stable, or at least hadn't regressed. In fact on the Tuesday evening, the clinical nurse was going to arrange for us to have a cuddle. The nurse told us to go and have dinner and by the time we finished, she would get him ready for to nurse. In the time it took to have dinner Levi’s condition deteriorated. I can’t recall exactly what happened, but we weren't able to get our cuddle with him that night. They tried another lumbar puncture, but again it was unsuccessful.

The following day was tense, and they were hoping that the MRI would go ahead. The doctors felt that Levi was battling an infection and more seizures were visible. They suspected Levi had E.coli which more than likely meant he would also have meningitis. As such, they began treating him for E.coli and meningitis. That afternoon they took more blood cultures and put Levi back on the EEG machine for some testing before he was finally taken for his MRI.

It was later confirmed that Levi had E.coli and the strand of E.coli he had was resistant to the usual E.coli medication that is prescribed. He would still be treated for meningitis, however they were unable to confirm or rule this out due to the unsuccessful lumbar punctures. A neurologist also confirmed that the lesion on Levi’s brain was the result of a stroke, but they were unable to confirm if it occurred in utero (causing my membranes to rupture), during labour, or was exacerbated by his vacuum delivery.

I was hoping the first time I had to write out Levi’s name was on his birth registration. Instead I was  days into motherhood and filling out his details so he could receive blood, platelet transfusions, further brain testing, and various other interventions. As it would happen, we would sign and pay for his funeral before we would lodge his record of birth.

It was apparent that Levi’s infection was taking over his body. His blood wasn’t clotting properly and the platelet transfusions weren't working. The E.coli, which was septic, was compromising Levi’s organs, and as such he was put on further support. He was being administered a number of medications to combat the infection and seizures, and as a result his body was becoming swollen. The seizures became more apparent, but no one was sure if that was a result of the stroke, or the infection taking over his body, or both.
Just recently I read an excerpt contributed by Deborah L. Davis PhD from the book “Never Forgotten.” She wrote “it may help you to remember that you were in the impossible position of having to choose between terrible and horrible.” I have a profound connection with this statement, and it provides me with bittersweet comfort.

The doctors conceded that Levi was receiving the maximum dosage of medication that his body could handle. His seizures were occurring almost every minute and were distressing to witness, and we was becoming unresponsive to stimuli.

The afternoon of Friday 14 November 2014 my husband and I made the decision to withdraw Levi’s life support.

We had time to notify our immediate families, enabling those who were able, the opportunity to say goodbye (and hello in some cases). The hospital arranged a blessing and we were fortunate to have a volunteer from Heartfelt come and take some photographs.

When the machines were turned off I got to hold Levi for the second time, but my husband got to hold his son for the very first time. We held Levi; kissed Levi; talked to Levi; bathed and dressed Levi (we were terrible at it); and held him some more. We had the opportunity to say good bye and tell him how much we loved him. We are very thankful for that.

Levi had been born, lived, died, and farewelled all before his estimate due date arrived. It’s been almost six months since then. My husband and I have our daily memorial rituals that keep him alive in our hearts and our home. We’ve had help and love from family and friends, and sought help from organisations such as SANDS and SIDS and Kids. We just want to live a life that honours Levi and makes him proud of us.

In a couple of weeks I’ll be running in the 2015 Mother’s Day Classic. When I was pregnant the 8km fun run was my personal ‘benchmark’ event to aim for in my post-natal fitness quest. I was going to push Levi around the course. Exercise has been a big part of my therapy, and as it turns out, Levi’s going to be the one pushing me.  
By Adin  – Levi’s Mum
27 April 2015.

If you require support after reading this blog please contact
Sands on 13 000 72637

Adin Hewat

Adin loves camping, the beach, travelling, quizzes, puns, (bad) dancing, (really bad) karaoke, and shamelessly laughing at her own jokes.  She hates clutter, is scared of dogs, won’t eat fruits touching and struggles to swallow tablets.  Adin is a wife to Adrian and a Mum to Levi who passed away in November 2014 at six days’ of age. She currently lives in Brisbane but supports NSW in the State of Origin


Sunday, 3 May 2015

Choosing to Celebrate Love.

Jess shares with us her thoughts on approaching her first Mother's Day as a bereaved mother.

"As bereaved mothers we have to make too many decisions that no parent should ever have to make. So let’s make a decision for us, let’s celebrate Mother’s Day, because we are mothers too."



Through all the anniversary and festive dates of our 8 month journey, I have come to learn that the lead up is always the worst. But just like every other day, you crawl into bed as night falls and you take a deep breath, and you acknowledge that you have survived another day.

We lost our Isobel just weeks before Father’s Day last year. The upcoming event didn't even occur to us until the day we needed to refill my painkillers prescription. There in the pharmacy was a nice little display of Father’s Day gifts, a table of dad-like products staring back at us. At the time I chose to ignore it, not realising how painful those 5 minutes were for my husband, until we got home and he broke down. That was the day we wondered if we would ever celebrate a special day again.

Christmas was just as hard. We thought putting up a tree would help, and we were even lucky to receive beautiful ornament gifts for Isobel. But the days leading up to it were torture, and the day itself even worst. Friends posted pictures of their baby's first Christmas. Strangers wished us a "Merry Christmas" but we couldn't even say the words in return, we weren't 'merry', there was nothing 'merry' about Christmas to us. We put smiles on for our families on Christmas Day so they could at least enjoy it without feeling guilty, but we were heartbroken inside.

Now Mother’s Day approaches and the fear lurks in my mind - how will I survive it?

I know that I am not alone in this fear. Mother’s Day is a "trigger" for thousands of mothers out there, although one of many triggers I'm sure they feel every day; for me it's the colour yellow, her songs, hearing her name called out in the supermarket. The triggers never really stop, but the Mother’s Day trigger is a big one. For a bereaved mother, Mother’s Day is a blend of numbness, disbelief and sorrow. It feels like everything in the world is reminding you of your loss, every television ad, every display in the shop window, even the sight of every mother with their child knowing they will have the chance that you won’t have to celebrate together.

As bereaved mothers we have to make too many decisions that no parent should ever have to make. So let’s make a decision for us, let’s celebrate Mother’s Day, because we are mothers too.

I recently watched a beautiful video about motherhood by American blogger Missy Lanning. It talks about what motherhood means, and to Missy it means love. And I agree. Love is the most important part of being a mother because it is there from the very beginning and it never goes away. The moment we started trying for Isobel I felt the love for our unborn child, although it took a long 3 years; my love just grew stronger. As my belly grew I remember feeling strange because I loved our child so much but I couldn't define if my love was for a girl or a boy, it was just pure love. The moment she was born I felt instinctive love of wanting to protect her, and I always will.

This Mother’s Day I will tell the world that I am a mother. I love my daughter unconditionally, a love which grows stronger each day. I worry about her, hoping she is safe. I am proud of her, and I hope she is proud of me. I feel guilt that I am not doing enough for her, or giving her enough attention. I share every moment with her. I am her mother. She is my daughter. I choose to celebrate our love on Mother’s Day, and I hope all mothers will choose to celebrate their love with their child.


Jess

If you require support after reading this blog please contact
Sands on 13 000 72637


Jess Schulz

Living in quiet beachside Adelaide, Jess is a fundraising officer for Motor Neurone Disease SA, freelance graphic designer, and social blogger. Married for 5 years (together for 12), Jess and her husband experienced the saddened loss of their first child in 2014 at 40 weeks. Their daughter Isobel Lola, passed away 6 days after she was born. A perfect pregnancy ended with a cord prolapse during labour, and now Jess and her husband are walking the road of grief while trying to survive each day without their Isobel. Love, hope and support are the essence of their survival, and Jess has chosen to share their story on Sands to hopefully support other bereaved parents walking this road too.