Tube weaning resources and tips

I receive many emails from parents seeking tips on how to wean their child off of an NG tube or G tube. My heart goes out to each and every one of you. To make it easier for you to find the key weaning information on this site, I’m listing the references and resources here. I truly hope it’s helpful to you. Your child deserves to enjoy food, and you deserve to find some peace.

Research and guidelines for weaning

Online tube weaning support group

Tube weaning clinic in Graz, Austria

Occupational therapy

Feeding strategies that worked for Stella

Be fierce! And kind to yourself.

Research and guidelines for weaning

Prevention and treatment of tube dependency in infancy and early childhood, published in ICAN: Infant, Child, & Adolescent Nutrition, Vol. 1, No. 2, 73-82 (2009).

Standardized tube weaning in children with long-term feeding-tube dependency: Retrospective analysis of 221 patients, for publication in Infant Mental Health Journal.

I would like to call out one of many GREAT points in this research, which came from the renowned tube weaning clinic in Graz, Austria. Tubes should never be put in without a PLAN to take them out! Get your child’s medical plan to agree on a tube weaning approach. Demand it and don’t take no for an answer. Show them this research–most medical professionals have very little specific expertise on tube weaning. This research is precious and rare and we need to spread the word.

Online tube weaning support group

Please visit Tube Fed Children Deserve to Eat, it’s a social network that is aimed at “Connecting Parents of Children with Tube Feeding Issues.” Great information, invaluable camaraderie and wonderful support can be found there.

Tube weaning clinic in Graz, Austria

You may have heard of the Graz model of tube weaning. It’s based on the idea that hunger drives the motivation to eat and that the child must be in total control of their own intake and not pressured to eat. It makes A LOT of sense, doesn’t it? The Graz clinic has a 92% success rate with weaning babies and children of all ages–the ones who are not able to be weaned often have many serious health issues that make eating impossible, not just a feeding aversion.

The clinic’s URL is notube. at and since you’re reading this you’ll  likely need to check out the section in English. Don’t miss all the English navigation links at the lower left (within the English section) or you won’t see the wealth of information available. I almost didn’t see it myself!

This is big: They provide email coaching, which was helpful to me and Stella. They recently made improvements to this program, so it’s more organized and better than ever, so I highly recommend it. First, you’ll need to get in touch with them to see if email coaching is appropriate for your child. If you are interested in email coaching or going to Graz (which I hear is beautiful, by the way) for what is typically three weeks of treatment, email Marguerite Dunitz-Scheer. She is the world’s best expert on tube weaning, a GODSEND! One of the most valuable contributions she made to our weaning process was confidence. She knew Stella could do it–that it was up to me to let go, and trust my daughter.

Occupational Therapy

Stella’s occupational therapist, Robin Glass, was central to her recovery. We were blessed to find an absolute rock star in that field. She is a real expert on infant feeding issues and very wise and experienced. She told me from the start that Stella could do this and that she would leave the tube behind. We met with her weekly, and it was huge. Find your own Robin, and work with them to come up with a plan for weaning. Then get everyone else on board–pediatricians, GI, etc.

Feeding Strategies that Worked for Stella

Here, we’d like to share with you the specific feeding strategies that have worked for us. Please note that Stella was weaned from the tube when she was just four months old. Age plays a big role in how to appropriately approach weaning and feeding, of course!They may or may not work for your child and we are not doctors, but we know how stressful it is to deal with feeding difficulties and would be thrilled if these tips and tricks make life a little easier for just one other family.

Best of luck. And if you have any feeding tips to share, please let me know and I’ll add them to the list!

STRATEGIES USED DURING STELLA’S AVERSION

We used to do the following, when Stella’s feeding aversion was in full effect. I think each feeding was a form of therapy. The main thing we did, however, was to not force the bottle in any fashion. We let her tell us if she was hungry, we let her decide how much she wanted to take from the bottle, even if it was zero mls sometimes. Ending the battle is step #1. Otherwise, no feeding strategy is going to work.

Swaddling

Stella is a very squirmy, active baby. She never stops moving and has been like this from the beginning. It’s very fun, but can get in the way of eating. When her aversion reached its peak, she would push away the bottle or block her mouth with her flailing arms and hands.  So as we worked on overcoming her feeding aversion, we would very lightly and loosely swaddle her when we fed her. Please note that we did not force-feed her. We would bring the bottle to her lips and it was up to her to accept or reject it. Her arms could still move a bit, and sometimes her hands would poke out and I’d let her hold one of my fingers while I fed her. But she stayed much more calm this way, and focused on eating rather than grabbing at or playing with the bottle, my shirt, etc.  It was a big day when we were first able to feed her without swaddling her, but for a while, it was a huge key to successful feeding.

Standing, Squatting and Shushing

Back when Stella still had the aversion and as we worked with her to over come it, we’d stand up to feed her, holding her in a cradle position while keeping her body straight and at an angle so that her head was higher than the rest of her body. We were careful to not let her head tilt to far back, to prevent any gagging or choking, as she had some swallowing difficulties. When she needed some extra calming, we’d even do squats while feeding her. The up-and-down motion helped Stella mellow out. Sometimes, I’d also shush her in the rhythm of my squatting.

Yes, standing (with a 15-pounder in one arm) while squatting and shushing is a lot of work and I’d often get out of breath! But I knew it wouldn’t be like that forever, and it was worth it if it helped her eat comfortably on days when she needs a little extra support in order to get in the eating groove.

“Taste Enhancement”

The jury is still out on this, but I suppose it’s worth a shot if you suspect that your little one simply dislikes the nasty taste of formula–especially hypoallergenic formula. Stella’s Elecare smelled like feet and tasted like a ground-up multivitamin. One evening, back in our tube weaning time, I was desperate because we’d tried EVERYTHING and Stella wasn’t making as much progress as we’d hoped. We added a bit of baby food to the bottle, just enough to add a more appetizing flavor. I used organic Gerber bananas, because they are incredibly smooth and highly caloric (believe me, I compared all the brands to figure out which would be most suitable). Lo and behold, she started eating more.

It could’ve been coincidence. But breast milk is supposedly flavored by whatever mom eats. So even if flavor wasn’t one of the reasons she came around to liking the bottle, I like the idea of giving Stella a more interesting and tasty experience.

Removal of the Tube!

I wanted to note that Stella was really bothered by the NG tube. It affected her swallowing, exacerbated her reflux, and prevented her from ever feeling very hungry, since we were pumping food into her at night and whenever she didn’t take a full feeding during the day. We had to push to get support from her doctor to take it out. As soon as we did, her eating improved dramatically! It took about three weeks for her to start gaining weight again, as her intake ramped up, but she never lost weight.

I don’t know if it happens this way for every baby, but Stella’s recovery was SPECTACULAR. After she’d been given those three weeks without the tube, a switch in Stella’s brain was flipped. Something clicked, and she started to enjoy eating. It was like magic. Where once she would scream and cry at the sight of the bottle, she started to lunge at it and cry when it was taken away! In our case, faith and patience paid off. As Marguerite as the Graz tube weaning clinic explained, it takes time for the baby to adjust to feeling hunger and getting in touch with what that means and how to address it (by eating). For Stella, it took three weeks. I think many parents are tempted to put that tube right back in after a few days of their newly tube-free baby not eating “enough.” But if the child has energy and generally seems okay, and you have support from a doctor or some sort of medical professional who is aware of your weaning efforts, I say hang in there!

So to sum it up, at first, the tube was helpful in allowing us to get some calories into Stella’s belly without having to fight with her over every feeding. We could simply stop when she wanted to stop. Our occupational therapist put it brilliantly. She said we had to let Stella say “no,” and have her feel that she was really being heard, to enable her to later be comfortable enough to say “yes.” But after a while, the tube caused more problems than it solved. Therefore, I am very concerned about longterm use of NG tubes. Here is an article about preventing tube dependency and guidelines for weaning.

My feeling is that babies and children without major health issues, who may not eat much at a time but have shown that they have the physical ability to eat, and whose pain or source of aversion has been identified and addressed (i.e. reflux medication given), should be given a month to show that they can thrive without the tube! If this is your situation, make a case for it and get the support you need to wean your child off the tube. The tube weaning clinic in Graz, Austria has a very high success rate with weaning, and it’s all based on the idea that most children will eat if freed from tubes, allowed to feel hunger, and able to determine when and how much they want to eat. Once the core issue is treated, we have to trust our little ones to know what is best for them, which I know is hard to do after the trials and tribulations of a feeding aversion.

POST-WEANING STRATEGIES

In the time immediately following the resolution of Stella’s feeding aversion,  a few weeks after the tube’s removal, we didn’t have to go to great lengths to ensure a good feeding.  However, we still had to take a couple of extra steps to make sure swallowing was easier and she didn’t get too distracted.

Thickening

We started out with a ratio of one packet of Simply Thick (nectar consistency) per six ounces of formula and using a Dr. Brown’s number 2 nipple. This was too slow for Stella. She was bored and uninterested. So we changed the ratio to one packet of Simply Thick to eight ounces of formula and saw improvement. But we thought she still seemed a little bored (there were too many sucks per swallow), so we switched to a number three nipple. Even better, but we noticed some difficulty swallowing, so we adjusted the ratio once again to one packet of Simply Thick per seven ounces of formula, using the number three nipple. It took us a while to get there, but once we did, it made a huge difference!

This ratio lasted a while and got us through the tube weaning period successfully, but as Stella improved, we adjusted. It wasn’t long before we used a number 4 Dr. Brown’s nipple. Then, Stella evolved to the point where we were using one packet of Simply Thick with 12 ounces of formula (with the number 4 nipple). Then, we weaned her off of Simply Thick altogether (but went down to a number 3 nipple as unthickened with a number 4 was too fast for her, and  really too fast for most babies).

How did I know to adjust the amount of thickener? How could I tell that Stella had improved? It’s hard to explain, but mostly, I gauged her overall comfort level during feeding. For instance, early on, a bit of formula used to dribble out of her mouth during feedings. When that stopped, I knew her feeding and swallowing skills had improved. But in general, I knew I could gradually reduce thickening as she got more practice.

We encountered an issue with Simply Thick in that it can clog the nipple if it is not completely emulsified. We had simply been shaking it up in a large bottle, and clogging became a common problem. I called Simply Thick customer service and they recommended whisking. So, based on that, we mixed the formula powder, water and Simply Thick in Dr. Brown’s Formula Mixing Pitcher, then I used a small metal whisk to mix it up even more, and then I shook it in the bottle before feeding. It sound like a lot of work, but it’s not too bad, and we completely solved the clogging issue!

You probably already know this, and I allude to this above, but you can figure out if you’ve found the right combination of thickener and nipple flow by watching and listening. There should be two or three sucks before each swallow. Breathing should sound pretty smooth and steady. With Stella, any gasping and panting meant the milk was flowing to fast and she would quickly pull away from the bottle, sometimes gagging or choking a bit, or crying.

Quiet, Dimly Lit Setting

Stella still takes a bottle most comfortably and calmly in a quiet, dim room. Eating was her most immature skill, so it was very easily thrown off by distractions. Taking her to a quiet place helped her relax and remain focused on eating. I enjoyed feeding her in this setting as well. Very peaceful.

Sleep Sack?

For a while, after swaddling during eating was not necessary, we put Stella in a sleep sack when we fed her. I put a question mark next to this one because I’m not really sure how much of a difference it made. But I think it served as a good cue and calming influence. Stella is very active and likes to flail her legs, whichgot her more riled up and distracted her from feeding. With the sleep sack, she may’ve felt a bit more contained and secure.

Dr. Brown’s Bottles

We use Dr. Brown’s bottles and really like them. The excellent occupational therapists at Seatttle Children’s Hospital use them. In fact, they gave us our first couple of bottles during our hospital stay, and we’ve stuck with Dr. Brown’s ever since. Stella isn’t too gassy or gaggy, and she’s never had an ear infection, which may be partly attributable to the bottles. The bottles are BPA-free, of course. Their wide-neck bottles recently became available in BPA-free as well. I heard from a salesperson at Babies R Us that many moms believe that the wide-neck bottles reduce gagging and that they more closely mimic breastfeeding.

Formula Mixing Pitcher

Dr. Brown’s Formula Mixing Pitcher was very helpful in that we could easily whip up a large batch of thickened formula. The propeller, which spins when you pump the handle, ensures there are no lumps of unmixed formula or thickener. Just make sure you don’t let the propeller go above the surface of the formula as you are mixing, or it could create air bubbles. Honestly, I don’t know how we got by without this pitcher.

Side note: I recently read a study, on the Dr. Brown’s website, about nutrient loss in formula and breast milk–during feedings and whenever exposed to air. It happens pretty quickly. So it’s best to store it in bottles that are as full as can be, with as little air above the prepared formula as possible. I do think that this is somewhat alarmist news, and I don’t really give it much thought. But it’s good to be aware of.

Be fierce! And kind to yourself.

I can’t tell you how many times I cried and pleaded to doctors and therapists. I got hysterical. I pushed and pushed and pushed. I think you have to be really proactive to get the support you need, because health care is not stepping up to help tube fed children in most countries. It’s an outrage. Do not take no for an answer. If your child has the ability to eat but not the willingness, they can learn to enjoy food. Unfortunately, you have to be a warrior to make it happen. You can do it. Stella and I know you can.

Feeding aversions and tubes are pretty much a nightmare. I know I am not alone when I say I almost lost my mind. For months, I didn’t sleep much, didn’t eat much and didn’t take care of myself. I was falling apart. But I did hire a postpartum doula to give myself a break now and then. I did go get my hair cut. I did manage to get three hours of sleep at a time now and then–which is necessary for a full cycle of sleep. I know you won’t be okay until your child is okay, but do your best to take care of yourself, so you can be strong for your little one.

I wish you the very best. We got through it and so can you.

9 Comments

  • I’ve been scouring the net for the type of information you’re providing concerning tube weaning. My own little one is now 3 and half months old, having survived open heart surgery at 10 days old and cataract surgery just yesterday. Soon as she get some vision, I’m wanting to take on the tube weaning project and have been desperate for some backup. I’ll definately be arming myself with some of the data you’ve found. I know Grace can eat. She’s literally never been given a chance, but I have to believe she can do it. It’s just another hurdle and she’s my little track star.

    • Gina, how are things going? I’d love to hear how Grace is doing, but I know how little time you have to spare! Anyway, I hope she is eating and thriving.

  • Jennifer Miller

    I feel like I can relate to you in so many ways. Thanks for your candidness and willingness to help others who are in the same position that you were in with your baby.

    I am currently in the phase where I only get 3 hours of uninterrupted sleep. My baby is 3 months old and has been on the NG tube for one week and 4 days. She is slowly starting to take more milk from the tube than she will nurse so I am concerned about the future.

    All the info is so overwhelming. It will take me a while to get through it all since I have such limited personal time.

    But again, thanks!

    • Hi Jennifer,

      Just wanted to reply to your post with a couple of comments. Our daughter is also 3 months old, she has been on an NG tube since she was discharged from the hospital at 2 weeks old after stomach surgery. In the mean time, she has decreased from taking about half her food by mouth to taking only somewhere between nothing and about 4 ounces by mouth each day. We are now working with a speech therapist to try to improve things (won’t really be able to start weaning her until after her heart surgery next month though). I wish someone had told to us to stay more aggressive about trying to get her to take the bottle – not pushing her it on her if she clearly doesn’t want it, of course, but if she is just not too interested to try harder.

      Also, in the interest of getting more sleep, we decided pretty quickly that she was only going to be fed 7 times a day not eight, with a longer stretch at night (we just took the total quantity of food per day and divided it by 7 not eight). Now she goes about 5 hours at night between feeding, plus there is another hour available for times during the day when we get behind (we have three other kids, so it is really hard to stay on schedule). I go to bed around 10, my husband stay up & feeds her at midnight, and then I get up at 5 am to feed her again. You may want to check with your doctor, of course, and be sure she can tolerated the larger volume at each feeding, but this has worked well for us because one just cannot function for very long when one never gets to sleep more then 2 hours at a stretch!

      • Jennifer Miller

        Hi Linnets Mom,

        Has your little one had her surgery yet? How is she doing with her tube feeding?

        I also have 4 children. It has been very difficult to meet everyone’s needs with our youngest having such difficulities. I am sure you can relate.

        Hope you are doing well.

    • Jennifer, how are you doing? I would love to get an update–but I know how hard it can be to find time. I hope you’re now getting more rest and my best to you and your daughter!

      • Jennifer Miller

        Hi Amber,

        I have not been on this site in a while and searching for tube weaning info brought me back here. And it was such a nice surprise that you had asked about Abbey. Thanks!!

        Abbey has been on the NG tube since July 23 (almost 3 months). She did indeed become completey dependent on it as I was fearing might happen in my earlier comments. She does nurse a few minutes from time to time on occasion because I always offer the breast before each tube feeding. And she began “tasting” solids this week. She moves them around in her mouth and spits them out.

        Just as a little history… she was placed on the tube because she had developed an oral aversion and FTT due to severe reflux. Her surgeon placed her on the tube so she could gain weight and thrive in preparation for removal of a congenital lung mass. The lung mass supposedly has had nothing to do with the reflux or feeding problems. She had her surgery 3 weeks ago. She is currently thriving now taking in 34 ounces of breastmilk through the tube each day (4 oz gravity bolus feeds 4-5 times a day and 15 oz through the pump at night). She is starting to develop fat rolls and it looks great!! Once we started the pump at night (around the beginning of August) she started sleeping throught the night from 9:30 pm until I wake her up at 7:30 am. That part has been awseome!! So, I have a love/hate relationship with the tube.

        However, I am in the pit of depression because it is time to wean her and there are several issues a foot. One is that I am unsure if her reflux is truly under control yet. Second is that I don’t feel like I can trust many of the health care professionals in my life. I know when things are BS because I am an Occuaptional therapist myself. Thirdly, the only way that she will occasionally take anything by mouth is through nursing. Bottles make her gag and vomit. It could be a sensory issue but it probably has more to do with her strong preference towards only taking the breast as many breastfed babies develop. She swats and turns her head if I try to cup feed her.

        So, I spent this afternoon crying after an unproductive visit with her GI doc this afternoon. He says I should consider taking her off breastmilk and use formula (concentrated for more calories) and get her to eat baby food (like I am not trying ). And he wants to take her off her Prevacid in 2 months (even though I have told him her reflux is worse than ever and she vomits at least one entire feeding per day).

        I am seriously thinking about taking out the NG tube (because it makes her swallowing uncomfortable) and just nursing her for a few days and offering solids and just seeing what she does. I know that her surgeon would be very supportive of us doing that since it was his idea to do it that way. I on the other hand tend to over analyze everything and over think things till I make myself crazy. Each way we could go seems to have a web of what ifs- if that makes any sense. Like you said, tube parents do start to go crazy. She had open chest surgery and was in the PICU… and still the feeding issues are so much more overwhelming at times.

        I am also looking into the info on the Graz method also. Thank you so much for posting it.

  • Carole (Luke's mum)

    Hi, I’m skimming your webiste very quickly inbetween a hospital visit to my son. We are waiting are in the process of phased discharge home after he has spent 12 months (since birth) in hospital (SCBU/NICU/PICU and now a Children’s Unit). He spent his first night at home aged 365 days on home leave from hospital. Luke has been tube fed since birth (NG) and we are being pushed towards a PEG. he currently has 6 feeds a day through a pump; 10, 14, 18, 22, 02, 06.

    I found your webiste from recomendation on a UK website for premature babies- Bliss. I am looking forward to getting lots of tips as I am desperate for Luke to feed orally.

    this is our story about feeding nightmares.

    Luke has had his NG tube since his birth 12 months ago. he has either been ventilated or on CPAP and more recently a tracheostomy on Long Term Ventilation.

    He did have a dummy from about 4 weeks old and loved it. he would suck really hard and found it very comforting, but refused it after a very bad period requiring ventilation at 9 months, which also coincided with his teeth coming through. I wondered if his gums were too sensitive, but he won’t have it anymore and he now has 6 full sized teeth which he loves to bite with, rather than suck – ouch!

    We have had Speech And Language Therapy input from early on. Initially they said he needed to get his respiratory problems sorted out before any oral feeds because the risk of aspiration was too great and would compromise his breathing and infection. Once he had his trachy done and was a bit more stable they suggested baby rice via a spoon. It was his first oral feed and he was over 6 months old. Luke was belwildered by it all and didn’t know what to do. He became unwell again and was sedated and feeding got put to the back of the list. I should add that I was continuing to express throughout all this in the hope that Luke would be able to feed from me. I painfully came to the decision that I would stop expressing after Luke having my EBM for 6 months and he was started on formula.

    There was a period when he was about 7 months old and still interested in his dummy that we tried a bottle with a long teat Medela Special Needs Feeder. Luke could suck but didn’t quite get the hang of feeding and was vomiting. SALT said that he could be aspirating and advised against doing too many feeds. In the end he became quite ill again and was sedated and paralysed and lost interest in the dummy and sucking.

    So now we are 12 months on and the advice is to try purees and thickened milk. Luke won’t have a spoon in his mouth, although he will put his fingers/toys/chew his wires/bite our fingers. If you try to put your finger near his mouth with a bit of puree on he clamps his mouth shut, but will gladly pull your fingers to his mouth if he wants a chew, all on his terms?

    i’ve tried the distraction technique ie make him laugh and pop a bit in when he’s not looking but its not very successful for large amounts and he seems to have vision like a fly and wacks my hand out of the way! The bottle is out of the question now so I tried a beaker, but he won’t have the spout anywhere near his mouth, which confuses me as it’s plastic like a toy and he will chew on those. I tried thinkening his milk to double cream consitency and using it open to his lips which sometimes he likes to ‘hoover’ it in, but it is very hit and miss. Mostly miss, all over him and me!

    SALT want me to help desensitive his face and mouth area by giving him as many opportunites and tastes as possible. I’d like to try finger food but he can’t deal with ‘bits’ in his mouth and tends to inhale them, this happened when I gave him rusk to suck on and he managed to bite a small piece off and vomitted straight away. I feel confused as he sucks in his sleep when he is dreaming (quite cute) and loves to hold my face in his hands and suck kisses all over me. SALt though it was like rooting and said I smell of ‘mummy’ so it’s comforting. That actually makes me a little sad as we didn’t even get to have skin to boob contact to try to BF all the time I was expressing.

    the reason for this long post is that PEGs are going to be discussed at our next MDT and although it seems likely that Luke will continue to need his nutrition from a tube a PEG is an operation and would mean a transfer to our specialist childrens hospital and as we have only just reached the point where home discharged is being planned and I don’t want to finally get home and then have an appointment sent through. Also PEGs seem a bit more pernament and don’t want to seem like I’ve given up on Luke having oral feeds and we’ve tried everything possible. I don’t to replace one tube with another; I want to get rid of it! I feel sad that I went from hoping that he could breast feed to just wanting him to eat something.
    _________________
    Luke born at 31+5 emer c-sect HELLP syndrome, 14.09.08. CHD: repaired Coarctation (narrowing) of the aorta, complex respiratory problems; tracheobronchomalacia, vocal cord palsy, Left hemi-diaphragm, tracheostomy for long term ventilation. 1st night home 365 days

  • Just wanted to give you a huge thank you for making all of your tube-weaning experiences available for all of us who are desperately trying to survive a nightmare! You have given us hope that our little Amelia (and us) will be able to have some sort of a normal life. We started weaning yesterday and pray that we will soon be able to move on! Thank you, thank you, thank you! Stella is a beautiful girl. You are really bleassed.


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