Our friends with an autistic DS catered to his tantrums and gave him chicken nuggets for every meal. He was 350 pounds by the time he finished high school and now they must institutionalize him because physically, they can't handle him. Anecdotes aren't universally applicable. Once that parent bought the Costco hotdog, they didn't need to go back and provide that again and again, because the job of parents is to do the hard thing when it is in the best interest of the child, even when they are throwing tantrums about food. |
I think this is negligence. I would only be okay with this if they were working with an occupational therapist on feeding.
DH and I have struggled with our kids and our solution is that they eat the vegetable but don't have to eat the entre. There is no other food that gets offered. Vegetables were the hill we were going to die on. We consider nutrition akin to sitting in car seats and brushing your teeth (two other hills we were going to die on). |
You clearly have NO CLUE what some people go through. GTFO with your “I have all the answers” BS. Ps - you’re not nearly amazing as you think you are Signed, Parent of two really good eaters who has no skin in this game but can’t stand people like you |
My kid will happily eat all the vegetables on his plate but vomit at all forms of meat. If it's not a tantrum, but they literally vomit on the table, maybe people get the picture that it's not just about the parents? |
Thank you Signed, Parent of an autistic 6yo who weighs 35 pounds and has been to multiple nutritionists, Children's National, etc. ps to those who think these kids and their "tantrums" are being "catered" to. YOU.DO.NOT.HAVE.A.CLUE. The terror of your child literally not eating is real and, btw, the nutritionists, etc all say the same thing-get them to eat anything and go from there. This process takes YEARS and it is so isolating to feel that kind of pressure. OP is likely not privy to any details regarding the niece's situation because the parent's can FEEL the sneering judgement emanating from her. |
I have a child with restricted eating. I think the kind way to interpret op’s post is that she is concerned about her niece and whether her sibling has sufficient information. I’m sympathetic to that—I had a sibling with a child that could not speak at 3, and he legitimately did not realize how far behind his child was, and that they should be receiving therapy for it. It’s very likely that OP’s niece is autistic or has an anxiety disorder or OCD. They should be working with medical professionals. That’s a really hard conversation to have in a productive and tactful way. I would start with something like “so how’s everything going with Larla?” And maybe progress from there to “how long has she been on the hotdog kick?” One of my kids had an issue that no one flagged for me — I do wish someone had educated me that this condition even existed so I could have sought treatment for it when she was young. There’s a way to express concern and help potentially educate but it has to be done from a place of kindness, not condemnation. |
Honestly I’m so repulsed by your incorrect use of “literally” that I almost couldn’t read the rest.
But sometimes we have to get over our judgment or behavior traits we ourselves find distasteful because they are, alas, none of our business. In your case, if you want an enduring relationship with your sibling and niece, you need to butt out. In my case I can tell you it would benefit you enormously as an individual and a member of society to read a book. |
I wish I knew you in real life/ protein is our biggest struggle to and my kid will also gag/vomit from meats. But eats tons of fruit and some vegetables. Would love to hear more about how you are helping your son. We have done feeding therapy but it doesn’t seem to help as much with the gagging (have had more success in expanding other food groups). |
It's possible that the girl has one of those conditions. It's equally possible that the parents are seeking treatment but aren't sharing that with their judgmental relative because it's none of her business and she's made it clear how she feels about them. Someone might be able to ask those questions with kindness, but it's not OP. |
The comparison was perfectly apt. You’re just dim. (not PP) |
This post is very kind, & very on point. There is a way to inquire - and then if you learn that that they are dealing with ARFID or working with a professional or whatever, give them some grace. |
When it’s someone else’s child and not OP’s? Yes, it is a helpful comment. |
Oh, you think this is about “tantrums.” That’s why you’re confused. Got it. |
I am a parent of a child with ARFID (previously posted once before) and I am not open to discussing my child’s medical condition with the majority of people. Unlike another of my child’s medical condition, people are consistently rude, dismissive and often tell me to disregard professional advice, as well as telling both me and my child that this happened to us because of my poor parenting and/or because my child is stubborn, often a combination of both. As a result my child started asking at 5 that I talk with her before disclosing her issues. So unless you are a very trusted family member who has demonstrated empathy in other situations I would not have this conversation with you. Please keep in mind this; if you decide to say your piece you are very likely doing for yourself. |
You know it’s common for children, especially autistic children, who don’t speak until later to start talking in full sentences when they are 5. There is nothing wrong with that. Don’t assume you as an outsider know what is best for a child. |