Fear and Feeding

Meal time.  Just the mention of those two little words is enough to make the pulse quicken and anxiety levels rise.

And that’s just me.

Feeding has been a huge issue in our house since day one.  Literally.  While I was still in the hospital recovering from an emergency c-section, my son was being seen several times a day by lactation consultants who were trying to help him learn how to latch on and nurse correctly.  That never happened, so eventually we switched to bottle-feeding.  Bottle-feeding was a challenge, too.  It would take Jack over an hour to drink an 8-ounce bottle of formula, and he would then projectile vomit the entire contents of at least one bottle a day.  At the time, we considered ourselves lucky if it was only one bottle a day.

Everyone kept assuring me that solid foods would be easier.  It wasn’t.  Jack did not want solids, and it was a struggle to get him to take them.  When he would, he would gag and vomit, even on the smoothest stage one purees.  I had these grand illusions of making my own baby food, but alas it wasn’t meant to be.  I could never get the purees smooth enough for my baby.

By the time he was a year old, Jack was still eating only the smoothest stage one and two baby foods.  Any chunky food would cause him to vomit.  In vain, we tried food after food.  As he approached 18 months old, Jack still could not feed himself.  We spoke to his pediatrician, searching for a reason why feeding was so difficult for our boy, but we got no answers.  We were told that we were coddling him, that he was just being picky, and that we needed to stop feeding him.  After all, if he got hungry enough, he would eventually feed himself.

He never did.

After he was diagnosed with autism at 24 months, Jack entered feeding therapy.  In reality, I suspect that Jack should have started feeding therapy during his first year of life, as he had both sensory and oral-motor issues that resulted in his feeding problems.  The two stressful years of eating prior to that turning point resulted in a little boy who was terribly afraid of food, of eating, and it created an atmosphere of fear throughout our household at mealtimes.

Feeding therapy has helped my boy.  It was a slow process, but we got Jack to the point where he could take preferred foods without fear.  True, he has never really “enjoyed” eating as the rest of us do – we never see the expressions on his face that seem to say, “That’s good!” – but meals were no longer a battle.  Jack was gradually able to take increased textures.  He was eating a few new foods.  Best of all, he was no longer vomiting daily as he once was.  That, in and of itself, was a tremendous relief to this mama.

We entered a period of relative calm.  Sure, Jack had only 5 foods, but he ate those foods well and without a battle.  Approaching 3 years old, he was starting to take a more active role in meals by beginning to do some self-feeding.  He still needed a lot of assistance, but we were seeing the first glimpses of self-initiative in our boy.  However, Jack still had a long way to go, and recently it became time to change up things for our rigid-to-routine boy.  We were to start offering Jack what we were eating for our meals and nothing else.  He could make the choice to either eat what we ate or not eat at all.

You can surely guess what Jack chose.  So many of our kids will starve themselves rather than take a non-preferred food.  Jack’s therapists can get him to take non-preferred foods, and I’m not quite sure of their secret, because I watch feeding sessions occasionally and attempt to replicate it at home to the letter, but without their success.  The result?  A kid who has slowly shown signs of that same fear that we once experienced.

Here’s the thing – that was a very dark place for us.  The anxiety was thick in our house in those first couple of years.  Jack feared eating.  He feared the food.  We feared his meltdowns about eating.  We feared the vomiting.  We feared how he was slowly dropping in weight percentiles.  We feared that if he started to meltdown, he would surely vomit.  We actually kept a bucket by our dining room table – which was luckily located in a room with all hardwood flooring – just waiting for Jack to vomit.  Meals were eaten on eggshells in our house, and everyone had to tread lightly for fear of upsetting Jack.

We didn’t want to revisit those times.

We have followed the therapists recommendations.  We’ve had some limited successes – Jack will now eat jelly on his peanut butter sandwich! – and we’ve had some failures.  We still have to force the first bite of food into his mouth to get him to even try it, which I absolutely hate and refuse to do (my husband doesn’t have the same qualms about that as I do).  Meals still take upwards of an hour to finish.  It is a tedious cycle of giving Jack a bite, encouraging him to chew, rubbing his cheek to stimulate him to chew, giving him liquids to try to get him to swallow, and repeating the entire cycle until the food is gone.

I think that another problem we have is that Jack doesn’t sense hunger.  He never has acted hungry in his life.  As a baby, he never once woke up to eat – we had to wake him – nor did he ever cry to be fed.  In fact, he was eerily quiet as a baby.  I often think that feeding would be so much easier if Jack just felt a bit hungry.  Instead, we have to resort to continuing to feed him on a schedule, just to ensure that he gets the appropriate nutritional intake.

I think that the one thing I’ve learned about feeding therapy since we began it over 15 months ago is that it is a process – a long process.  You take baby steps.  You push boundaries.  You take a few steps forward and then, when you hit a roadblock, you take a few steps back.

The good thing is that the fear seems to not be as severe with this feeding push, both for Jack and for us.  It’s there, believe me, but not every meal results in a colossal meltdown.  We also have more tools in our belt – like sensory activities prior to eating and oral stimulation techniques to help “wake” his mouth before meals.  We’ve got a long way to go, but at least it seems like we will not revisit the dark days we once knew.

Related Posts Plugin for WordPress, Blogger...
Be Sociable, Share!

Tags: , ,
Be Sociable, Share!

About ReinventingMommy

Jeanie is a former engineer turned stay-at-home wife and mom to an amazing 3-year old little boy on the autism spectrum. After her only child was diagnosed at 24-months with autism and an alphabet soup of special needs, she began to write about life parenting a very young child with special needs with honesty and, as always, a touch of humor. When not posting here, you can find Jeanie at her blog, Reinventing Mommy (http://reinventingmommy.blogspot.com/).

    Comments

  • Heather


    Oh man, I have a picky/throw up eater too and I know exactly how rough it is. We are looking into eating therapy in the fall for him since he has a total of 5 things he will touch.

    I feel for you and I am glad it is getting better! That gives me hope!

    • ReinventingMommy


      It is a slow process, but you absolutely will see progress. This time last year, my son could only eat purees (and he was about 2.5). Now, at nearly 3.5, he’s eating more foods that he has to actually chew! We have a long way to go, but it absolutely does get better with time.

      I’m right there in the feeding trenches with you, mama!

  • Susan S.


    My heart goes out to you, and it’s singing with joy for your successes. We, too have food issues, but not the life threatening sort. At times my son will not be hungry for hours, and then his hunger will kick in so much that he could sit and eat 3 meals equivalent if we didn’t stop him. So, at the doctor’s office, I get the evil eye because my child is overweight. And the last time, the RN assumed that I knew nothing about nutrition and offered to send us to a nutritionist. He, obviously, knows nothing about kids with SPD.

    Hoping lots of continued success for Jack and for you!

    • ReinventingMommy


      I feel your frustration with the doctor’s office! It’s been my experience that our general pediatrician’s office doesn’t have the same insight into sensory issues and feeding (and what constitutes a feeding issue that warrants therapy!). We’ve gotten the “he won’t starve himself” advice many times. Only after 3 years of being a parent do I finally have the courage to take those snippets with a grain of salt and trust my own instincts. I tend to leave the business of feeding issues to my son’s developmental pediatrician these days.

      Thanks for reading! It’s always nice to hear that none of us are alone with these feeding battles!

  • Ellie


    This is so so close to my own family’s experience, except that our little boy never got any help and we just had to learn to cope as best we could. He’s 8 now and I’m only just realising there is help to be had.

    • ReinventingMommy


      It’s never too late, though! My son was 2 when I found out that he had a swallowing disorder and, therefore, should have been in feeding therapy since early in his life. It’s a slow process, but it’s never too late. Best wishes (and progress!) to you and your family with your own feeding challenges.

  • Martianne


    My son, now six an a half, was beyond “picky” but never down to just five foods like yours and also
    not prone to vomitting. So, I cannot say I have been where you are. I can say, howeverm that I relate…

    Food battles and meltdowns were common in our household for years. So, I finally took my son to an awesome fedding specialist who, like yours, worked magic (magic that was hard to replicate at home.)

    That specialist also helped to uncover a truth about my son — his eating issues were more behaviorial than sensory. Sure, there was (is!) a sensory piece and an oral-motor piece, but the mental/behavior portion was so much bigger. It’s always hard to untangle the web of what’s what, but, with her help, we have been doing so and now my son is officially just “picky”. (Her rule of thumb is that if a child eats at least ten foods, the child is picky. If not, the child needs regular appointments.) So, we have had some success and relief.

    I pray you do, too, with your continued process.

    • ReinventingMommy


      You are absolutely right that for many kids there can be a behavioral component as well. I know that many of my son’s feeding issues began as purely neurological/oral-motor/sensory, but as he’s aged, behavioral issues have crept in. They’re not the primary component, but boy when they do sneak into the equation they cause all kinds of headaches!

      So glad to hear of your success! It gives all of us mamas some hope that it will continue to get a little better.

  • Deenie


    My son is very picky. He only eats about 5 things, the most nutritious one being cheese doodles. He does get hungry though and gets very cranky when he’s hungry but he still won’t eat unless we give him 1 of his 5 things. We’ve tried to wait him out. He didn’t eat for 2 entire days and nights. We caved and gave him the cheese doodles he wanted. It’s very difficult. We tried to get him into a feeding clinic but insurance wouldn’t cover it so we had to skip out on that one. I’m so glad you’re seeing some improvement.

  • Jenny from the Block


    That is rough! My daughter still only eats a handful of food and it is frustrating. She doe snot get sick or take an hour, but the limited selection is tricky. And, if something happens once, like a little crunch that is not supposed to be there is on her bread or noddle, she gags and will not eat anymore, sometimes she will not eat that food for months or ever again. She gets overwhelmed by food, too. If you ask her what she would like to eat, it is usually I do not know, and if you push it, a meltdown. So then you guess and bring something, but if it is “wrong” she will not eat. Argh!

    Leave a Comment

    Your email is never shared.
    Required fields are marked *