Something Is Wrong with Your Baby: 5 Things I Wish I’d Known
Something is wrong with your baby. I remember, as though it happened yesterday and not in 1982, the day our doctor sat down beside my hospital bed and uttered those words. Something is wrong with your baby.
I reach through the decades at the young mother and wish I could go back in time and sit beside her. I wish I could tell her what we learned between then and now about raising the baby we both love. I wish I could calm her anxiety with these 5 nuggets of wisdom our baby taught us through the years.
- One day you will meet other parents of children with your baby’s rare diagnosis, EA/TEF, and it will be wonderful. Thanks to the internet, which will come into its own when our son is in his 20s, you will meet families who understand the challenges of caring for your baby. They will validate your hunches and applaud your advocacy on behalf of your son.
- You are the expert about how your baby’s condition is manifested in your child. Surgeons and pediatricians will know more about the condition your child has. But you know more about your child than the professionals do. Therefore, your expertise is equal to that of the professionals, and you deserve to be heard. When you find a doctor, a therapist, a nurse, or a caregiver who treats you as such, rejoice and make them part of your child’s care team. They are golden.
- You must be the keeper of your baby’s medical history. The details of your child’s early medical history will be seared in your memory. Your baby will not remember the details at all, though the experience will be stored in your child’s brain in a different way. You must document the early medical history so your child has it to refer to as an adult.
- Reach out and ask for help. People care about what you and your baby are going through. Most of them have not raised a child with special needs and have no idea of how to help. So when they say, “Let us know what we can do,” have some practical suggestions ready for them. Things like picking up your grocery order, bringing a meal, driving you to an appointment, bringing your mail or clean clothes to the hospital, or specific prayer requests. You’ll be surprised how quickly they’ll say yes.
- You’ll adjust to your new normal. Your life will never go back to the normal it was before your baby was born. But you will adapt to your new normal more quickly than you think. You will become stronger. You will mature. You will grieve, but you will also rejoice in the gift of each moment with your child. You will one day be able to encourage young parents in similar circumstances who need to know what you wished you had known when the doctor sat beside you and said, “Something is wrong with your baby.” You will discover the beauty of your new normal and be comforted by it.
Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the quarterly Different Dream newsletter and signing up for the daily RSS feed delivered to your email inbox. You can sign up for the first in the pop up box and the second at the bottom of this page.
By Jolene
Jolene Philo is a published author, speaker, wife, and mother of a son with special needs.
9 Comments
Submit a Comment
Subscribe for Updates from Jolene
Related Posts
Enjoying the Holidays with a Food Allergy
Jolene talks about her own family’s struggles and explains her strategies for enjoying the holidays with a food allergy.
God’s Plans for our Children are Like a Puzzle
God’s plans for our children are like a puzzle larger than any Sandy Ramsey-Trayvick has ever completed. In today’s post she describes how putting together jigsaw puzzles had shown her to trust in God’s plans for her kids. I began doing jigsaw puzzles again while we...
Middle-Grade Fiction about Kids with Special Needs
Guest blogger Lisa Pelissier introduces and explains her latest middle-grade fiction for kids with special needs.
Good for you and your son. Sometimes educating neighbors is a place to start. They are totally unprepared otherwise, just like we were when our kids were diagnosed. Educating others is a big part of an EA/TEF parent’s life.
That is a sad and true reality. It is also joyful, as a life, no matter how long or short is reason to celebrate and make connections.
Hi Becky, that is HARD. My parents were 750 miles away when our son was born, and my MIL was in Alaska. I know they struggled with the distances, too. Even if you can send them gift cards for gas and restaurants and lots of encouraging notes, you can make a big difference. Jolene
Thank you for this post. I have a special needs grandchild that is 1800 miles away from me. I want to help them out but it’s a long way from Oklahoma to Boston and he can’t travel from there.
Most important tip: Enjoy your child each day and be thankful for each day you have with them. One day they may be gone.
My son is 23 and just yesterday I was outside helping him get a chip unstuck. It was very scary but everything turned OK. The neighbor across the street was threatening to call an ambulance. This is my life. I’m good at it❤️
Diane, thanks for your kind words. You must have oodles of wisdom to pass along, also. Jolene
My son has autism and ADHD. I have kept everything in a binder since day one so I don’t lose or forget anything.
Thank you for sharing this. My son was born in 1982 as well. It was an experience I will never forget. We are the experts for sure when it comes to our child with special needs.