Helicopter Parenting: According to Wikipedia “is a colloquial, late 20th and early 21st-century term for a parent who pays extremely close attention to their child’s or children’s experiences and problems.” It is a parent who hovers “like a helicopter” over their child and intervenes too much when they see the child struggling vs. giving their child a chance to work things out on their own.
I am starting to feel like a helicopter parent when it comes to Leah. I am not like this with my other two daughters, one older and one younger than her. I give them quite a bit of room actually, to the point that some parents think I give them too much. Let’s just say, I was giving the opportunity to travel around Asia all expenses paid when my oldest was 2.5, and I didn’t even think twice about leaving her for 3 weeks with her grandparents.
Leah is different she has SPD, depression, and anxiety that causes really bad acid reflux. She also has some extreme behaviors that have had Dr.’s list other acronyms ODD, ASD, ADHD but no one wanting to commit to anything except SPD, depression and anxiety with the hopes she will get better as she gets older. Her father and I keep our fingers crossed that this will be true for her.
I hover over her and I really don’t want to. I feel I do it out of necessity to avoid the massive meltdowns and anxiety she experiences when I don’t hover. I feel like I am the only one that can tell when she is experiencing sensory overload. I have gotten so good at sensing it I can now intervene and do a sensory task before she erupts.
Her special needs teachers, her OT, her ABA therapist, and I, have been working very hard with her to try and get her to recognize when she is reaching her boiling point and giving her the tools and knowledge of what to do in those situations. She has made tremendous strides in being able to do this but she still has a long way to go.
Although my hovering seems to help her out and me being there lowers her anxiety, I am getting worn out in the process. When do I back off and just let her try to manage on her own?
Before she was born my husband and I were quite social, we had Leah’s older sister but we always managed to have a babysitter stay with her a few times a month so that we could go to a movie, see friends, or have a child free dinner. We entertained often and had friends and family to our house several times a month. Now we don’t! We are lucky if we do something child free every other month. Our friends have disappeared and the ones we still are in contact with, we are lucky if we see them every 6 months.
I know that my hovering is getting in the way of our social life because I can’t stand leaving them with a babysitter. Every time we get one it is never good. Leah always has a meltdown, they don’t know how to deal with her, and the next several days she is so thrown off that it takes a while to get things back on track. I have gotten to the point that I feel it just isn’t worth it, and that bothers me.
I have always thought that as a parent it is our job to help our kids grow up to be self-sufficient adults, to let them learn from their mistakes while giving them the tools to problem solve. By hovering so much I know that I am not doing this for her. When do I back off and let her work through her problems herself? By hovering am I prolonging this process? Is that a bad thing or a good thing taking into account her special needs? I just don’t know, but it is something I think about every once in a while.







Comments
Jenny
I always maintain that mothers are usually right about what they think there child needs. Keep on with what you think she needs for now and grow together. Its tough but worth it in the end.
sanndem1
What a great blog. I was a sped teacher before kiddos and I was always preaching about not being a helicopter parent..well fill me up with gas and start my engine because I am right there with you. I am exhausted as well. We still struggle with the babysitter and really never go out. I keep telling myself it will end soon and we will look back at this time and long in sleep hours!!
Mysensorybaby
Hey you know what my first thought here is this … There is no protocol for being a good parent! Our kids are all different they need different things, they learn at different paces. I’ve got four kids under 7 yet none are as ‘needy’ as my 5yr old sensory seeker. Do I hover? Yes. Why? Because nobody else recognises when Harry is in meltdown mode and I don’t want to spend hours fighting to bring him back to an even balance! Have things improved? Yes! Will they get better? You bet they will! Thanx for sharing this it’s a reminder to us all that it’s ok to not be feeling ok! Xxx’
Jenny
I’ve been called a helicopter mom at the park chasing Max around but I was just trying to keep the kid alive!
Joanna Bloom
This is such a great topic. Awareness in itself probably means we’re on the right track.
kate blue
I agree with MySensory baby…it all depends on the age of your child too and where you are. My son is 7 YO and if we are at home, then I back off. If we are at grocery store or the library, then I do hover since those places send him into a bit of sensory overload. Other times, I kinda gauge it and “semi hover” lol
Jordan
I’m the same way, but I know I have to be. I try and back off, but when I do it leads to a meltdown or even an injury (he also has physical delays in addition to SPD). So even though I’m a firm believer in letting a child learn on their own I am most definitely a helicopter mom. My belief is that there is no one-size-fits-all parenting style. Some kids need more. And I have faith that eventually all of this hovering will actually help him learn to recognize his own limitations and sensory needs. I will be his senses until he is able to use his own.
Elle
Sweetie, you’re not hovering, you’re just parenting.
Like others have said, you know what’s best for your girl and it obviously IS best because she is making progress. I agree, it is exhausting though! Have you tried asking any of her therapists and teachers if they have any recommended baby sitters? Maybe they’d heard of some good ones, or know some retired special ed teachers.
Kelli
Do you have a mothers helper? Someone who comes into your home and helps you out. If so good, I would encourage you to train that person to learn how to manage the meltdowns. Then you could use that person as the babysitter too, they would be trained and ready to handle the meltdowns and you can have that much needed date with your spouse. If not, get one.