Skip to main content

How To Act Around a Feeding Tube

Sometimes when I'm hooking up Evie's g-tube in the food court in the mall, I look around to see if anyone is watching.  I still brace myself when someone shows interest in what we're doing.  I have no idea what they will say or conclude, but I do my best to explain why she has a feeding tube in a practical way.

The Feeding Tube Association just released a brochure that tells our friends and family how to be helpful to us.  I love their list of what is helpful and what is not so much, that I had to post it.  Here is the full brochure:

Evie's mommy's commentary in italics below (my original g-tube entry is here):

What is Helpful.
  1. Listening. Parents who are just starting on this process have a lot on their mind.
    They have concerns and they may not know all the answers yet.
    When Evie just got her g-tube, we were having trouble figuring things out post-NICU stay, and answering questions about the g-tube so early on was very hard for us.  But as we talked about it later with friends, it helped us to better formulate (in our sleep-deprived state) what questions we needed to ask the pediatrician.  
  2. Helping by doing other chores. Cooking, straightening up, taking care of our other children.
     Cooking and cleaning were so helpful to us in the early days. We are indebted to both of our moms for coming to stay with us in snowy New England and cooking and cleaning for us. 
  3. Understanding that parents are the experts. This can be hard if you have
    raised your own children. Unless you are involved with conversations with
    doctors, specialists, nurses and are with the child day and night, you may not
    fully understand the situation.    I am still navigating this.  I am the one who takes Evie to her feeding and GI specialists and I think day and night about her feeding. In my spare time, I am looking up ideas for food on Pinterest or reading the comments of other tubie families on a Facebook group.  Advice is nice, but when it comes from someone who doesn't know about g-tubes and feeding difficulties, it doesn't have the same effect. 
  4. Asking questions is fine. Just be mindful of our feelings. This is our child.
     I am totally ok with questions. It shows people are interested.  But sometimes the answer is so long, that it takes me a moment to figure out what to say.  Some good questions to ask are:  How are you feeling about her feeding these days, or How is she doing with trying new foods.  
  5. Talk directly to an older child. He or she may be able to answer questions.
  6. Understanding that tube feeding isn’t unpleasant. It is just another way to
    get in calories and hydration.  The first time I explained Evie's feeding tube to a young child, I just matter of factly said that Evie didn't eat enough using her mouth, so we had to use the tube to get food to her stomach. The child accepted this and went off on her way. It was that simple.
  7. Learning more. Try to understand the child’s medical conditions.

What isn’t Helpful.

  1. Saying you “hate” the feeding tube. Also, don’t say you wish that the child
    would just eat normally. We also wish that there wasn’t a need for a feeding
    tube, but we are very aware that tube feeding is making it possible for our
    children to get the nutrition and hydration they need to live, grow and thrive. If
    a child couldn’t breathe well enough, you wouldn’t hate the oxygen tank.
     This is an important one for me. More than anyone, I want her off the feeding tube, but right now it is a blessing to us, and I appreciate everyone treating it as such. It is what makes her look so strong and healthy right now. It is what enabled her to be strong enough to have heart surgery. It is what got us out of the NICU, because otherwise we might still be there today! 
  2. Feeling bad for us or our child. Empathy and acknowledging challenges is
    fine, but don’t feel bad for our child if he or she is unable to eat certain foods.
     Evie's birthday is coming up, and she will get a smash cake just like anyone else.  She won't eat the cake, but I sure hope she will eat some of the frosting!
  3. Help us find ways to make gatherings about more than food.
    This isn't as big a deal for us right now. We want Evie to notice that people are eating, and that they enjoy it.  
  4. Telling us that it is just a matter of finding foods that our child will eat. If it
    was that simple, the feeding tube wouldn’t exist. There are underlying medical
    issues that often can’t be seen.

     No one has said this to us, but I can see how this would be really frustrating for another parent of a tubie.
  5. Comparing apples and oranges. Something may have helped your friend’s
    cousin’s child with reflux, but that doesn’t mean it will help a child with a
    different medical history and conditions.
       When someone gives me advice, I listen and then sort out what might be helpful and what is not as applicable to Evie.  I need time to process and feel comfortable about trying new things with her. 
  6. Telling us not to feed our child in public because it will make this person or
    that person uncomfortable.
    Children shouldn’t have to be fed in a corner or a
    bathroom, or not fed at all because of social concerns.
     Thank God no one has said this to us! I think I would either cry or want to punch them. This tops my list of most unhelpful things to say.
  7. Giving a child food without the permission of the parent some children
    have dietary restrictions or are unable to eat food safely by mouth. This one is so important to me. With Evie's history of aspiration and her low oral muscle tone, I am pretty sensitive about what she can and can't eat. Just the density and weight of the food we give her can make her gag. She still has thickened fluids because it is hard for her to coordinate her swallowing quickly enough for liquids like water. 
If you've read this far, thank you!  If you've asked me any of these questions, please don't feel bad. I hope this helps you know how to help us in the future.

Here are some more FAQ's specific to Evie:

Q: What is she eating these days?
A: Evie is enjoying a luxurious taste of different foods. She eats expensive Siggi's kefir yogurt and Mommy just used a Baby Bullet for the first time to make her Asian pear puree and sweet potato puree.  She is still unable to eat lumpy foods without gagging, and because we don't want to create oral aversion, we are slowly introducing lumpier foods.  She eats a lot of Plum Organics pouches, and loves berry flavored things just like her mommy.
Q: How much does she drink?
A: Not much. Maybe two sips of formula if we are lucky. We've mixed in yummy things, changed formulas, tried different temperatures, and she just doesn't want to drink. Thankfully, she lets us spoon feed her, but that doesn't give much volume, so we end up giving the rest by g-tube.
Q: When will she get off the g-tube?  
A: It's going to be a long journey. For some kids, it takes years, and for others it takes months.  We are currently switching to a supplemental formula to see if Evie will get hungrier with less volume, but need to make sure she still gets enough calories and hydration.  This question stresses me out and makes me feel like I'm not doing enough to get her off the g-tube sometimes.   But we can't rush Evie--she has to feel like eating is fun and that she wants to eat.  This means stopping her oral feeding even if she's only eaten 2 good bites, and then trying again after a break, but not forcing her.  Right now we are up to about 5 good bites a meal.

Thanks for your prayers and good wishes for Evie!  To be continued...
Tubie button cover in the holiday spirit!


  1. Awesome post! Thank you for sharing so much about Evie! A few weeks ago I went back to the beginning of your blog and read the whole thing because I wanted to know all about Evie but didn't want to bug you with a million questions when you have lots on your plate. I think she is the cutest most squishable baby and love seeing her every Sunday!!! (And you too of course)

    1. Thanks for caring enough to read the whole thing, Lindsay! :)


Post a Comment

Popular posts from this blog

Repost with a giveaway! From Straitjacket to Starfish: A Shark Tank win

Update:   Hi all, I am doing my first giveaway! If you read my blog post the other day on the miraculous Zipadee Zip, then you know how this thing has changed our lives as parents.  The makers of Zipadee Zip liked my review so much, that they offered to help me do a giveaway. All you have to do is 1) "Like" their Zipadee Zip Facebook page and 2) leave a comment about why you could use a free Zipadee Zip on this post! The contest begins Wednesday, May 27 at 12:00 AM and ends on Sunday, May 31 at 12:00 AM.  Good luck! a Rafflecopter giveaway  ------------------------------------------------------------ Original post: There was a point in time when I was just proud I could swaddle teeny tiny Evie with a hospital blanket. Then she came home and started busting out of the blankets, and woke herself up all the time. Her arms flailed and her legs kicked while she was sleeping, which of course woke her up. But then she got bigger and craftier, and I needed to fin

Jumping and Friendship Crafts with Evie

This Youtube video was at first made to showcase Evie's first real jump on a trampoline. Then it became a video with a message about making new friends, because I was just so impressed with how Qole gave Evie the space she needed to feel comfortable enough to say yes to getting on the trampoline.   And then as we were making a paper craft about friendship, and we were pulling out different pieces of color, I was struck with how it became a teaching moment for my daughter that people of all colors can hold hands and can look out for each other. May it be so. The world needs it now more than ever. 

Going public: Down Syndrome Awareness Day and what it means to us.

Starting this blog was a big deal for me. It's hard to throw out there in conversation that my baby girl has Down Syndrome, because that extra chromosome makes people view her differently. But because it is Down Syndrome Awareness Day on 3/21, I'm going public. Do you know why it's on the 21st?  Because of the 21st chromosome having an extra copy! So far, Evie has just been our beautiful baby girl who is learning to smile and reach for things. But as she grows older, I want our extended circle of friends to know, so that they can treat her as a typical little girl who may be a little delayed in her development, but will want to be included just like other kids.  I want the other kids to play with her and to learn that little girls with disabilities like to have fun too. Our story about our diagnosis is here .   Now that we've met Evie and know what we're dealing with, it's not SO scary as it was before.  Still overwhelming sometimes , but I wouldn'