Hope: Losing a Child

  1. 22

    For those who had lost a child in a hospital bed and still searching for their lost hope.

    Hope: Losing a Child

    Their stories were all congruent.

    In expectation, they have waited for their first born.

    They were once the typical parents who adorned their babies' small hands and feet or their velvety skin and round eyes--minutes after an arduous childbirth experience. With gentle whispers, they once assured their first born that the world is not a scary place to live even though they themselves arbitrarily believed that the world is indeed atrocious. That life, if ideal, is filled with shallow contentment but if realistic is nothing but everything.

    They celebrated each night they were wide awake by their firsts' hungry whimpers and wails or instances of his distinct chuckling on dancing lights. In the child's eyes, they felt that for once all their flaws and mistakes were bygones. But the world is indeed harsh for those who believed that life should only be rainbows, laughter and merriment and not about bills, provision and inconsistencies. Hers was the soreness and discomfort of providing for the milk if he was not able to make the ends meet.

    They compromised...they sacrificed-- after all they have waited for ten years and so.
    On the third month, they had not anticipated their child's limpness and poor sucking. They miscalculated their aspirations; he wanted to teach his son how to ride a cheap second-hand bicycle on his eight and she dreamt of becoming her son's tutor on fractions on his ten. But they only had thirty days- according to a doctor's intelligent articulation about their son's rare cardiac condition.

    As soon as the disclosure was given, they went through the grieving process. They denied that their child's skin was abnormally an ash grey. They were hoping for years instead of days. They kept their dreams alive but in evaery moment they saw their child's closed eyes--their dreams waivered and were shattered into silhouettes.

    They designated their short term plans to fit into their child's thirty days; he just wanted to be strong and man enough to stop all the tears from falling while she stopped blaming herself. In meager, they provided for all the things required from them. They were unselfish and unconditional-- they sacrificed their meal for their child's anti-pyretics and they made him secured by ignoring their own fatigue.

    Not once they had faltered; they waited for their son's recovery. Softly in his ear, they told him that together they will make fireworks last, sunsets will be paused in between the hues of orange and red, falling stars will populate every night sky and there will be no rain on happy days (if there is, it would be skipped until the rainbow part).

    People around them were counting the days. They did not want them to count. They only begged for answers from them and not numbers. They counted: "twenty nine...thirty" and provided no answers.

    In despair, they have grieved their first (probably their last).
    They stopped hoping...they stopped living.
    Last edit by Joe V on Jan 9, '15
    Do you like this Article? Click Like?

  2. Visit jvqantipolo profile page

    About jvqantipolo

    Joined: Jul '07; Posts: 13; Likes: 41

    Read My Articles


  3. by   Southern Magnolia
    I lost my daughter two years ago to anencephaly . . . she lived for 33 days. Despite knowing what the diagnosis meant you do hope . . . hope that somehow you can fit a lifetime of love in a few hours or days. Her passing was not in a hospital bed but on my chest as we slept at home. I have not lost hope though . . . I will see her again.
  4. by   jvqantipolo
    "Hope" has inspired me to write this article. Many times I had witnessed those who hoped and fought for their child until the last breath. My salutation goes out to every parent who had let go and live for their lost child. Even though I am not a parent (yet), I feel for all the loss.
  5. by   VivaLasViejas
    Quote from NomadMomma
    I lost my daughter two years ago to anencephaly . . . she lived for 33 days. Despite knowing what the diagnosis meant you do hope . . . hope that somehow you can fit a lifetime of love in a few hours or days. Her passing was not in a hospital bed but on my chest as we slept at home. I have not lost hope though . . . I will see her again.
    Mine was born 25 years ago, and she lived for just seven hours..........long enough to leave an emptiness in my heart that I pray will be filled one day when Jesus meets me at the door of Heaven, holding my daughter in His strong arms and saying, "Look who's here, Melissa, your mamma's home at last!"

    What a sad, poignant, beautifully told story. Thank you for sharing it with us.
  6. by   luv2canoe
    Almost 2000 views and 3 comments. Nothing will change your view on life more than caring for a dying child. It is an opportunity few of us will have.
  7. by   Mimi2RN
    We sent home a Trisomy 18 baby a few months ago, on hospice care and being partially gavage fed. Last week we heard that she is nippling all her feedings and had been discharged from hospice. Her parents have been given a reprieve. Nobody knows how long this little one will live.
  8. by   Doula2Nurse
    you sent home a BABY with Trisomy 18. Sorry, just a pet peeve of mine. Person FIRST condition second. It's not a Trisomy 18... she's a baby. When I had my son I was the "section in room 4" When my daughter had RSV, she was the RSV in 11. Makes me nuts.
  9. by   NurseDaddy2006
    MY wife and I went through ten years of infertility struggles. All sorts of failed treatments. We started to conceive, and then misscarry all of four pregnancies at 6 weeks. We flew to Chicago to see a doctor that had appeared on Oprah. We tried his methods, even though they were not covered by insurance. After spending our emotions, efforts, and money we did not have, we were ready to give up.

    We called a NY infertility clinic in January. Next available appointment was July. So much for our one last effort. We hung up, we gave up. We celebrated our 12th wedding anniversary in February. We found out in March that were were pregnant again. When we saw that heartbeat on the sono, we were beyond any emotions that could be written here. We had a picture perfect pregnancy. Two weeks before our boy was due, my wife celebrated with her coworkers, we went out to eat that last night preparing for a life that was to change, celebrating how we would finally become a family, finally become parents. The next morning my wife awoke and told me that she'd slept so well, and she did not feel any movement. We took our time getting to the hospital because this had happened before and we felt silly after a perfect sono. When the nurse put the sono pickup to my wife's belly and our son was gone, our world was crushed. Jacob Sebastian was born with his cord around his neck twice, around his torso, and his legs. He'd gotten tangled up and cut off from his supply. We lost our miracle boy.

    With many thoughts of packing it in and leaving a note behind, we found the courage to go on and to try again. Eight months would go by and we were not getting anywhere. We figured we'd had and lost the only child we'd ever get to hold. During a sono to see that everything was alright, my wife was told that she had an egg a couple of days away from being released. That was Tuesday. We made love Thursday. We left Saturday on a cruise. We were on a docked boat and my wife threw up. We got home and took a test. Bingo.

    We were absolute maniacs for the next 37 weeks until we induced. Born healthy and perfect, our son is now 7, and truly a miracle boy if there ever was one. He knows of his brother, and has his brother's first name as his middle name. We went through 4 more miscarriages since he was born, and now we're at the age that we just can't do it anymore.

    I became a nurse because I wanted to help people the way we were helped when we went through our crisis. Now I enjoy nursing in behavioral health, helping people through crisis. Unfortunately I left my last job thinking I could find another, and find that I can not. It's no fun being without the money, but it gives me time to be there for my son, and I'm glad today I got to go to his 1st grade science fair.

    Last edit by NurseDaddy2006 on May 15, '09
  10. by   Doula2Nurse
    NurseDaddy2006 .... God Bless You.
  11. by   PedsAtHeart
    Without hope we have nothing. Thanks for the story. Very touching.
    I had a patient who had severe spinal muscular atrophy. They were told he wouldnt make it past the age of 1. I met him when he was 15. He passed after his 18th birthday. Miracles are all around us.
  12. by   jvqantipolo
    nursedaddy-- that was very touching, going through the entire ordeal of frustrations, disappointments and momentary joy. But God allowed us to go through experiencing pain just so we could rejoice on how mysterious He is.

    Thanks for sharing
  13. by   OrthoFNP
    Nurse daddy,

    WOW! That story was very touching. God bless your family and your little miracle.
  14. by   chenoaspirit
    I too lost a son, who died at 2 days old. I didnt even get to take him home from the hospital. I had a placental abruption. I was finally transferred to a larger city hospital who later told me....5 minutes later and I would have died, 20 minutes sooner my son would have lived. I held my son as he died and it was the most heart-wrenching experience Ive ever had to live through. I nearly died myself from heartache. I had tried to pump breastmilk for him those 2 days and was unsuccessful. I wanted to give my son the best, but I failed. After I went home from the hospital, my milk was abundant and wasted. I remember waking up one morning thinking it had been a nightmare and found my belly empty and my breasts full. I had a hard time accepting that it was reality.
    I now have a daughter who is 9 years old and she is my life. I cannot have anymore children due to health problems and a hysterectomy but I thank God for my little girl.
    Later I had a patient, a baby who also suffered a placental abruption but survived. She was hospice and her parents had brought her to die. I was assigned to this patient. At first I refused because my heart couldnt stand it. But I did decide to take care of her because I felt that I was the best fit for the situation. I felt I could relate and empathize/sympathize with the family and their loss. It was like living it all over again, but it also gave me a strange peace.
    I pray for all who have suffered the loss of a child. They say that time heals and it does....some. But you never fully get over it.