From the depths of sorrow, to finding peace and hope, our members have so much they want to share about this unexpected journey we are on...
There will never be the right words to convey the depth of my sorrow for the loss of your sweet baby. No one should have to experience the loss of a child, regardless of age or gestation. Please know that while you may feel alone, you are not. You may not know it, but there is a supportive community of other mothers of loss who will be there to guide you. They will reassure you of two things: it’s not your fault and some day you will be able to carry this loss more easily.
It's not your fault. There is still so much we do not know about the human body, which is maddening. Please know that you did everything right with the information you had available at the time. You were a fighter and if your love and strength were the sole factors in a different outcome, then it would have happened. Your sweet baby knows how much you love them and wanted them. You did everything you could, even if it may have meant putting yourself at risk. Please find peace in the time you carried your sweet baby and the way you got to say good-bye. Embrace the memories of the first ultrasound and the first kicks. Know that they felt your love when you’d talk, or sing, or read to them.
Take heart and be strong. I know how easy it is to fall into darkness and despair, but it’s important to look towards the light, even when it feels like you’re drowning. Reach out to your family and friends. Understand that they may not know the right thing to say or do. Forgive them for this. Tell them what you need. Let them comfort you. You deserve their comfort. Please don’t punish yourself for this. Your child would not want you to live your life in despair.
Your child matters and will always matter. Say their name. Look at their picture. Hold their blanket and think of them. Keep their memory alive however you feel necessary: plant a garden, make donations in their name, give them a stocking at Christmas, or include them in your family however feels right to you.
This will always hurt, and you’ll always miss them and wonder “what if?” but please don’t let this define you. You are more than the sum of your losses and struggles in life. Honor your child by living how you think they would want you to live. Care for yourself as you would want to care for them.
[On] October 1, 1991 — our son, Stefan James Teigland Narum, died. He lived for 12 days.
To say Stefan lived 12 days is not quite right. He was with his mother for nine months, and his relationship with her was both loving and intimate. And everything was fine for those nine months…until the moment it wasn’t. And then the world as we knew it fell apart.
There’s not enough time or pages to contain the thoughts of those twelve days Betsy and I had with our second child, and the journey of grief following. Five years later I would complete a masters thesis on perinatal bereavement for my marriage and family therapy degree. Looking back, I suppose I was trying to help others, but maybe with all that writing and talking I was really just trying to get my head around what happened to our son and to us his parents. Grief includes seeking to understand, but we don’t move forward because we finally receive some answers, but because we’re finally able to live with the questions.
The death of a child is every parent’s greatest fear. I recently turned 60, and I would’ve gladly stopped at 31 and given my remaining years to Stefan. I wasn’t offered that option, as many bereaved parents know…as you may well know if you’ve had a similar experience. We grieved Stefan while we also cared for Ingrid. For parents whose first child dies, they wonder what it means to be a parent when their hello also means goodbye. For us, our little 2-1/2 year-old daughter gave us solace and hope. But we were sad for her, too.
What is unique about perinatal death is that we parents don’t have a story to tell, we have no joyful pictures to share. With Stefan are no happy memories, and his only home was an isolette in the NICU at UM Hospital in Minneapolis. When a baby dies it’s the loss of what could have been, what might have been and, yes, what we feel should have been. Nevertheless, those 12 days were the most honest and real days I have ever lived. Life, and what’s most dear, was never clearer. And those 12 days are 12 more than some parents get. We were grateful for every moment we had with Stefan, for the time his grandparents and aunts and uncles had to meet him.
Grieving parents say there’s a hole in their heart with their child’s name on it. This is a sacred space, a holy emptiness, not to be filled in this lifetime. To all you parents who have experienced the death of a child, I am profoundly sorry. I do not know what you went through, because that experience and relationship is uniquely yours.
Though Stefan’s life was not filled with joyful moments, it was filled with love. We are grateful to have met him, held him, and in the goodbye let him know there’s a love that will bring us together again. May that promise and the hope sustain us all.
—Peter Narum, Stefan’s dad
(and also Ingrid’s & Soren’s dad!)
This piece has been edited from its original format with the author’s permission. Written initially as a devotional, we would be happy to share the unedited version with you. Please email email@example.com.
In July 2018, our son James was born. After being in the NICU with him for 16 hours a day for a week, we found out he was born with a severe brain injury.
With that he was moved to a children’s hospital a few days later for a g-tube surgery and more testing. We eventually found out that James may never walk, talk or be able to fully eat on his own. The doctors didn’t know for sure what his outlook would be. While they tried to give us an idea of what his and our future would look like, they never talked about his longevity.
Having a special needs child changes who you are. Your life revolves around their specialized doctor appointments, their therapy, their equipment. Your other children sacrifice too. They get taken on appointments, they don’t get as much attention and they’re expected to help out more. They grow up faster than they should. Your special needs child becomes who you and your family are. It’s your identity.
In October 2018 James died of SIDS at 12 weeks old and it completely devastated me, my husband and our daughter. My imperfectly perfect family; my dream of what our family would look like was crushed to pieces. I was lost, felt alone even though we have amazing family and friends and just didn’t feel like myself anymore. I didn’t recognize myself.
One of the hardest decisions we had to make after James died was, do we adopt again or not? I wanted to. I was willing to go through more heartbreak, but my husband wasn’t. It took months and a lot of conversation, but we decided that this is our family now. Our daughter here, our son in heaven. This decision wrecked me almost as much as losing my son. I continued to feel like I was losing my identity.
I never thought I would suffer from depression, let alone, anxiety, and PTSD. I was in denial about my mental health. I finally had to accept it, allow myself to feel my emotions, and humble myself enough to ask for help. There was no way I could get out of the darkness alone. It took time, patience through the setbacks and a lot of grace. It was worth it.
I feel more aligned with my purpose now than I ever thought possible. I did find myself again; my new self. You might think you will never feel like yourself again. You're right, you won’t feel like your old self again, but you can learn to embrace your new self. You can love yourself again, feel healthy again, and find out who you really are. You are here for a reason. You are worth it.
Michelle, James’ mom
As another school year approaches, every parent has the safety of sending their children back to school during a pandemic on their mind and may be feeling a little more stress than usual. Many people do not realize that each and every new school year has stressors for the bereaved parent. All the back to school pictures are complicated by the pictures that aren’t there…the babies that never got to go back- to-school shopping or hold the little sign with their dream occupation and anticipated graduation date. This is further complicated for me in that the first day/week of school is usually my dead son’s birthday…September 3rd.
As I anticipate (and dread) this new school year, I hear the reported statistics about COVID-19 in children and going back to school and I want to let loose a scream of frustration. When you are the statistic, the statistics mean nothing. I have had two miscarriages and buried my two-and-a-half month old who spent his entire short life in the hospital. He was supposed to have less than a 25 percent chance of even spending time in the NICU. He was born with a 1 in 40,000 chromosomal abnormality....and would have lived except he had a mutation on his genetic mutation, which in the end, was not survivable. I, myself, have lupus, and possibly psoriatic arthritis. I have had to have my heart cardio-verted at age 41 due to A-Fib and I've recovered from Takotsubo syndrome and Rocky Mountain Spotted Fever. When you are the statistic over and over and over again...well.... don't quote statistics to me. I'm not willing to risk it.
As I decide how my six-year old rainbow should learn this year, I cannot help but have my decision swayed by the traumas I have endured. Many may judge me for this, but, as a bereaved parent, I have learned that I am living the best possible life I can after having it shattered and putting it back together again. This is my new existence and I am doing the best that I can each and every day. My decisions as a bereaved parent are not the same as the decisions made by the stranger I was prior to loss. That woman is gone and, sometimes, I miss her, too. In the meantime, my Sam would have been 9 years old this year and I should have a fourth grader. He would be the graduating class of 2029. He will never reach that milestone or have a first day of school, but I will always imagine him standing next to his sister for the photo.
Amy Falkner, Sam’s mom
Share your story!
We are taking submissions for articles to share in our monthly e-newsletter. We believe it is healing for parents to share their experiences and valuable for the both community to relate and professionals to gather a better understanding.
Each of these stories was featured in an e-newsletter and distributed to parents and professionals in our community. We hope that parents reading these stories will feel less alone and that the caregivers and professionals that we trust can learn from our experiences.
For Information & Support:
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In person support suspended March 14, 2020. Zoom Support Group
3rd Thursday of every month, 7:30pm
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Bereaved Parents of Madison, Inc
PO BOX 46511
Madison, WI 53744
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Bereaved Parents of Madison Inc is a 501(c)(3)