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I am not much of a jewelry person, so when I do wear something it is usually pretty special to me.
This particular necklace can also hold a small amount of personal remains of a loved one.
I have seen these before and honestly wasn’t sure how I felt about it. But now that I have one I am very glad I own it. It is my preferred piece of jewelry–It is stylish, well made, and nobody can tell what it holds inside. Basically, it simply looks like a very pretty piece of jewelry. Nobody knows it holds a small part of my son’s remains unless I tell them…and I don’t offer that information.
The opening on the top of the necklace is closed with a little screw. This shut tight since I was careful to not overfill. Originally I did not use the adhesive product that was sent with the necklace. It seemed to me the screw was secure so I did not think it needed the extra adhesive. However, after wearing the necklace almost daily for a few weeks I found myself checking the necklace regularly, making sure the pendant was still in place! I decided to buy some strong adhesive and securing the screw permanently. Once I secured the screw with some adhesive I feel more peaceful, knowing the pendant cannot accidentally come loose.
The chain itself is something I need to have fixed. The clasp is very difficult to attach to the other end as the opening is quite small. I have contacted the company and was assured this can be fixed/replaced. I just haven’t done it yet due to the craziness of life lately.
This is so good.
It is about understanding the valley we or others are going through–it validates our sorrow and pain. Look at the man in the booth—I know I can relate to that look and can “feel” that pain he is carrying.
This is also educational for those who may not understand how to respond to the pain we are feeling–how some responses are helpful and others are not.
THE MOURNING BOOTH–The Skit Guys
I remember sitting in the hospital the day after Dekar was born. I stared out the window while eating my breakfast.
I wondered why Dekar had to die when so many babies were not wanted. Why Dekar, when so many were not loved and cared for by their mothers. As soon as the question entered my mind, a gentle voice said, “That is why YOU were chosen to be Dekar’s mother. Because despite his diagnosis, I knew you would still give him a chance at life.” Then I thought of what could have happened with Dekar, specifically, if he had been one of those other women’s child—-and it stabbed me in the heart but then I was flooded with peace. Even though I felt the loss deeply, that gentle voice answered the question of “Why my baby?” Because Dekar was meant specifically for me.
Dekar was not just any baby–he was MY baby. God gave him to me, knowing I would be the best mother I could for him. No matter the outcome he would still be my son. Would I have really wanted him to be somebody else’s–knowing that they would abuse, abort, or not care for him? No.
I would never make light of the questions people ask: “Why me, why my baby….why, when I wanted a baby so bad?” If it were up to me NO babies would die or be hurt in any way. But I’m not in control of any of that. My recent miscarriage made no sense to me, and still doesn’t. The first thing I did was throw up my questions to God: What was He thinking? How could He allow this to happen? Why? I lost Dekar, why did you allow me to lose another one?
Even though I am not carrying that baby any longer and will never hold that baby in my arms, it doesn’t change that fact that I am still that baby’s mother. I still held a life inside of me that was precious. I still mothered that baby the best I knew how, just as I did with Dekar.
I can be sad about the outcome, but I can also thank God He gave me a baby to love–a baby meant for me, and nobody else.
From April 27th, 2009
Today Dekar would have been 10 months old. On my FaceBook account I simply typed out “Ice Cream”. I knew what it meant, and it didn’t matter if anybody else did.
This time “Dekar Day” is hitting me a bit harder because I am also dealing with the loss of another baby.
On April 8 I went into my first prenatal appt., very excited about the first ultrasound that I would be having with my new pregnancy. The due date would have been in mid-November. As soon as Dr. Jeakle started the ultrasound, I knew something was not right. He was humming—when my husband hums, I know that something is up—and the volume on the machine was not turned up so that I could hear the heartbeat. I knew it was taking too long for him to find what he was looking for. Long story short, my doctor saw the little baby just fine, but the heartbeat was not detected. I was numb. It was not what I expected at all. Add to the frustration is the fact that the little baby measured perfectly—according to my date I would have been just over eight weeks along, and that’s how big the baby measured. The baby’s heart may have stopped beating seconds before the ultrasound.
I left that appt. not understanding anything any more. I just looked up at God and threw Him some question marks.
I had hoped to let the miscarriage happen naturally, but found the waiting to be harder than I anticipated. It reminded me of the time I was waiting on Dekar to be born. Even though I knew Dekar may not be born live, I had that tinge of hope to hang onto. With this—-there was nothing. I was just waiting for the inevitable. Two weeks later, after no signs of miscarrying, I requested another u/s and went home with the confirmed bad news–but still desiring to miscarry naturally.
I couldn’t take it. Once I got home everything hit me hard again. I called the doctor’s office and left the message that I am emotionally spent and didn’t know what I wanted. The doctor called me back and was again very compassionate–he didn’t push me into anything and he let me make my own decisions through the whole process. We scheduled a d&c, which was performed on Friday, April 24th. I was not happy about it, but I felt it was better for me and my family to get it done.
Today I received a call from the hospital to see how I was feeling after the surgery on Friday. My pain is keeping me up at night, so I did a follow-up directly with Amy, Dr. Jeakle’s nurse. Pain meds would be ordered, and after talking “business” I asked if she had a Girl Scout, since I wanted to buy some cookies and didn’t know any who were taking orders. Found out that ordering was over, but Dr. Jeakle’s wife orders extra. Good. At least I can get some Thin Mints and Samoas.
While in town to pick up the pain meds and ice cream treats for Dekar Day, I got a call on my cell–it was Amy, telling me the cookies were in. That was quick, and such perfect timing! I asked how much they would be, and she said, “Nothing. I think you could use some G.S. cookies so we threw a bag together for you.”
Indeed, she and some others at the office (I am not sure who) put together a bag for me—four boxes of Girl Scout cookies, other candy treats, and a candle. It was a random act of kindness that meant more to me than they will ever understand. They went beyond their “work” mode and treated me with a measure of warmth and friendship that I won’t forget. It was just. so. nice.
After I got home I plopped in front of the computer with a box of cookies…..(and those who know me know I am not sappy)—-I got a lump in my throat when I saw a bunch of my friends let me know that they had eaten ice cream, or planned on it, in memory of Dekar. Through facebook and email, I was told they remembered…..
Tonight as I eat my ice-cream with my husband, I expect it to have a whole different feel to it. I will not only be mourning the loss of Dekar but also mourning the loss of a baby I never met, but desperately wanted to. Maybe they are eating ice-cream together in heaven?…..
Before I go to bed I’ll look at my children and thank God for the gifts that He has given me. And I will be sending up a special thank you to Him for putting people in my life who will show a random act of kindness and for all of the others that remind me they care—especially at a time when I needed it the most.
When I was pregnant I was active on a pregnancy board with other ladies due the same time as me. I visit the board occassionally and keep up with some of them who have blogs.
I see the pictures of their babies and how cute they are. It doesn’t bother me to see the pictures, because I am truly happy that they have healthy little babies to hold and love. I’m happy they got to take their babies home. But at times it hits me that the pictures of Dekar that I have are the ONLY ones I will EVER have. He will forever be that little infant…..it’s like part of my life is fragmented off because as my other children grow older, Dekar will always remain an infant. It’s just weird.
Dekar would eight months, and I love that age. They really start taking on more of their own attitude and personality. They smile a lot. They are a bit easier to care for because they can sit well on their own and entertain themselves.
A few days ago I was sitting on the couch with my son, Mel (4 yo). I told him that we’d get to have ice cream soon for Dekar Day, and that Dekar would have been eight months old.
“If Dekar were alive he would be driving you a little crazy, Mel, because he’d be getting into all of your toys.”
“Yeah,” said Mel, “But he could play with them!”
“Yes, he could. And I bet he’d try to chew on you— and drool, too!” Mel’s eyes brightened up and he giggled after he thought about that for a while.
“But he could play with my toys, and that would be nice!”
Yes, it would. But, Dekar isn’t here to play with toys, chew on his brother, or drool on his clothes. I do notice that Mel’s eyes brighten up when we talk about Dekar. Although I am not sure any of my kids understand the importance of Dekar Day, I do hope that it becomes so ingrained in them that even when they are off to college, get married, and have kids of their own, they will pause on the 27th of each month and eat some ice-cream in honor of their brother who is forever an infant.

Rachel holding Dekar with Mel looking on.
I never heard this song before today. It fits in so perfectly with the memorial ornament I purchased.
WITH HOPE–STEVEN CURTIS CHAPMAN
This is not at all how
We thought it was supposed to be
We had so many plans for you
We had so many dreams
And now you’ve gone away
And left us with the memories of your smile
And nothing we can say
And nothing we can do
Can take away the pain
The pain of losing you, but …
We can cry with hope
We can say goodbye with hope
‘Cause we know our goodbye is not the end, oh no
And we can grieve with hope
‘Cause we believe with hope
(There’s a place by God’s grace)
There’s a place where we’ll see your face again
We’ll see your face again
And never have I known
Anything so hard to understand
And never have I questioned more
The wisdom of God’s plan
But through the cloud of tears
I see the Father’s smile and say “Well done”
And I imagine you
Where you wanted most to be
Seeing all your dreams come true
‘Cause now you’re home
And now you’re free, and …
We can cry with hope
We can say goodbye with hope
‘Cause we know our goodbye is not the end, oh no
And we can grieve with hope
‘Cause we believe with hope
(There’s a place by God’s grace)
There’s a place where we’ll see your face again
We’ll see your face again
We have this hope as an anchor
‘Cause we believe that everything
God promised us is true, so …
So we can cry with hope
And say goodbye with hope
We wait with hope
And we ache with hope
We hold on with hope
We let go with hope
It’s hard to know what to write for an obituary when a whole life is encompassed in just over eight hours. The funeral director didn’t handle many baby/children’s funerals (thank goodness) and he didn’t have a template to work with that was suitable for an infant death.
I did some research on the internet, thinking it would be quite easy to find a guideline for an infant/child obituary. I was saddened that there was little to no help. We didn’t plan to have a service, since we felt that we had our own private time right at the hospital. We decided to have him cremated because we don’t have roots in this town and didn’t want to end up leaving him should we ever move. But I still wanted to honor Dekar and the life he gave us, even though it was short. I wrote up an obituary that said everything I felt was appropriate. The funeral director fixed it a bit, and then it was sent off to the newspaper, both online and print. I didn’t realize there was a price associated with submitting an obituary to the newspaper. We decided to just post it in the local paper, who also posted it online. This made it convenient to share with the many family members and friends who are out of town.
Below is Dekar’s obituary. For our situation it covered the basics. Some parents add a special note to their baby or a poem. Some share a picture. Some may want to include the reason for death. (I am not sure why I didn’t include that—if I could do it over, I would add that he had Trisomy 18 and hypoplastic left heart syndrome.)
Dekar was the son of Cortney and Marge Schmidt of Atwood (Ellsworth). He is survived by eight siblings, Hali, Aaron, Solomon, Eli, Rachel, Jadon, Melchizedek, and Isaiah, all at home.
Dekar gave us a lifetime of love during his short time on earth.
The Now I Lay Me Down To Sleep Foundation provided a volunteer photographer to record his short life with us. In lieu of flowers we would be pleased to have you support their mission to help other grieving parents through their remembrance photography at: The Now I Lay Me Down to Sleep Foundation, 7800 S Elati St. #111, Littleton, CO 80120, or: http://nowilaymedowntosleep.org/pageDisplay.php?page=42. Winchester Funeral Home in Charlevoix is handling the arrangements.
If you are in a situation that you are using the above as a guideline, I am very sorry and my heart goes out to you. I pray that this will serve to take away a little bit of added burden associated with your loss.
Since there is a need, I am working on a separate page of sample obituaries which other parents have graciously offered to share. I am updating it as often as a new obituary or memorial is offered.
Shortly after coming home from the hospital I told the family that the 27th of every month will be “Ice Cream for Dekar” day. This is a way that we can keep Dekar’s memory alive, and it’s a fun thing to do. I would get hassled by my family that I would go out for ice cream so much while pregnant—but I loved feeling Dekar kick and ice cream seemed to do it for him! I don’t know if it was the sugar or the coolness, but he reacted. Since we had gotten his diagnosis of Trisomy 18 and hypoplastic left heart, those kicks became even more precious to me. I looked forward to each outing and the movements that would soon follow.
So, July 27th we all went out for our first “Dekar Day”. My oldest son said, while licking ice cream, “I’m sure glad that Dekar didn’t like meatloaf. I mean, what would be the fun of having meatloaf every month.” 🙂
Eating the ice cream brings back fond memories for me. It also conveys to the kids who may not otherwise remember Dekar that their little brother is worth remembering and celebrating.
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February 27, 2009
Today Dekar would have been eight months old.
Sigh.
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I have rootbeer and ice-cream ready to go for tomorrow. (March 26, 2009)
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On Dekar’s first birthday we all had ice cream cones covered with sprinkles. What was so funny to me was hearing from several friends that on Dekar’s birthday they ALSO had ice cream with sprinkles! I’ll never look at ice-cream with sprinkles the same!
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