Mothering › Forums › Parenting › Special Needs Parenting › so tired of hearing "I'm sorry"
New Posts  All Forums:Forum Nav:

so tired of hearing "I'm sorry"

post #1 of 18
Thread Starter 
Are any of you as frustrated with this as I am? Someone asks whats wrong with my daughter (which I can understand-it's rude but people are curious) and when I explain that she's deaf and has some disabilities EVERYTIME I hear "I'm sorry" or "That's too bad". It's so frustrating! My little girl is perfect and I wouldn't want her any other way, this is the way God wanted her. Maybe she's not normal but it's definitely not something I'm "sorry" about. Why don't people understand? We went grocery shopping the other day and my daughter was wearing her helmet and the lady that was checking us out asked "Whats wrong with her head?" I couldn't beleive it! People are so rude I can't stand it!
Sorry---just had to vent!
post #2 of 18
I'm so sorry people are so rude. I just saw this in new posts, so I don't have a child with special needs, but I think this is just awful. If anyone asks what's wrong with her, I would look at them like they had two heads and say, "Absolutely nothing." And just walk away. A little shame could go a long way.
post #3 of 18
Quote:
Originally Posted by hdirks View Post
"Whats wrong with her head?"


"Nothing. What's wrong with yours?" *hold their gaze with a serious expression until they finally look away, ashamed*

I've been lucky enough not to get many rude comments. Most comments are well meaning and people at least TRY to have tact. A lot of people are curious but do try to phrase their questions in a way not to offend. I don't think I've had anyone ask "what's wrong with her?" They usually say something like "So what is her diagnosis?"

It's not wrong to say something very blunt back to people to let them know their comment was rude or hurtful. If they say "I'm sorry" say "I'm not! She's a wonderful little girl and I'm so thankful I have her!" At the very least, they'll realize their pity is misplaced. Hopefully though, they'll realize that disabilities are not the end of the world and you can have a great life despite challenges and obstacles....and that starts with having loving friends and family who accept you for who you are.
post #4 of 18
While I disagree with the "god wanted her that way," I totally get the rest. VeeGee is just who she is, and I think she ROCKS. I ALWAYS (if I've the time) say that I'm not sorry, or that she's not particularly "lucky to have us," etc. People, mostly, don't mean to be hurtful, and when I gently point it out that what they've said might not be all that kosher, they're pretty good about stepping back. The more that we do this, the easier it is for people to understand the "special needs lifestyle."

But, I'm sorry that it's crummy for you -- it's just crummy sometimes, I know.
post #5 of 18
I turn the moments you described into teaching moments. That way the person asking/commenting can hear what the disability, etc., really is and how it works, etc. I've never had anyone be rude or snarky about it either. They were truly interested.
post #6 of 18
I try to say something like "I'm sorry, too, sorry that he struggles, sorry that he has to deal with so much more than the average child. But he's happy, he's thriving, and he's a member of our family. So we're not sad or depressed, we're a happy family." What I don't want is fake sympathy, or pity, you know? I do appreciate those who recognize how hard this is, though. I appreciate offers for help, etc.

He's not "normal", he's not "perfect", and I WOULD change him if I could (I would take away his struggles in a heartbeat, absolutely). But I DO accept him as he is. I DO love him. I DO cherish him as my child. And I see his potential, and because of his potential, I'm not going to hide him away or pretend his disabilities don't exist.

At soccer the other night, another mom saw me signing to him and asked "does he use sign?" (stupid question, but I know how hard it is to broach a topic, especially if you're uncomfortable with it) so I answered "yes, he's Deaf." She said "oh, um, wow, that must be so hard." And I just looked at her. Here we were at soccer practice, he was out there with the other kids, having fun, playing, being a kid! How did she assume that it was hard?

So yeah, I hear you. I don't buy into the "it was meant to be" or "this must be God's plan" or "God gave him to you because you're so strong"...I don't like those thoughts, I think they are intended to be placating or an attempt at explaining the awfulness that is a child who is suffering. BUT...I dont' want or need pity. I just want my child to be accepted.
post #7 of 18
Quote:
Originally Posted by hdirks View Post
Are any of you as frustrated with this as I am? Someone asks whats wrong with my daughter (which I can understand-it's rude but people are curious) and when I explain that she's deaf and has some disabilities EVERYTIME I hear "I'm sorry" or "That's too bad". It's so frustrating! My little girl is perfect and I wouldn't want her any other way, this is the way God wanted her. Maybe she's not normal but it's definitely not something I'm "sorry" about. Why don't people understand? We went grocery shopping the other day and my daughter was wearing her helmet and the lady that was checking us out asked "Whats wrong with her head?" I couldn't beleive it! People are so rude I can't stand it!
Sorry---just had to vent!
Have you considered adding that to your "statment"

When people ask what is "differnt about" our son I say something like "God chose to bless us with some challanges with regard to T. We love him, he is perfect for us and i know there is a plan for him and these challanges." I try to be very upbeat -- even who feeling wron to the nubs in public with him and his little brother -- and SMILE .... very few people same much after that.
post #8 of 18
My children's special needs are not very obvious to others. (Well, Isaac's over the top temper tantrums are obvious, but not really special needs per se--more related to some adoption trauma). But anyway, 2 of my boys are adopted transracially, so their adoptive status is more obvious to others. You would not believe the questions people can ask sometimes! Anyway, a great piece of advice I received was to answer for your children's ears. So answer in a way that builds them up, rather than ignore, or get hostile to, the nosy person. That way, your child doesn't grow up feeling their is something about adoption, or in this case their SN, to be ashamed of or hidden. Also, at least with adoption, I have often found that the nosy or awkward or non PC statement is often a poorly worded attempt to make a connection with me and my children. So I am always polite, and mirror correct terminology and phrasing back at them and use positive language, and usually they say something like "my sister's little boy is from Korea", and we go on to have a nice little chat. I have met some really neat people this way. And my kids think it is cool that so and so's family is like ours.
post #9 of 18
My son's challenges aren't physical, he has a severe speech delay and now has ADHD and some residual SPD. When he was little and his speech and SPD were much worse, I'd get the "Sorry" comment. Sometimes I'd just stare and say, "Why?" Most people do not have an answer to that because what are they sorry for? Sorry for noticing? Sorry that my three year talks like he's one and half years old. Sorry because he's covering his ears? If I was really crabby, I'd say, "I'm not sorry."

The comments I can't stand is the "He's so lucky to have," or "I could never have a kid with special needs." No, we're lucky to have him. Being his mother has made me realize I'm a far better mother, advocate, and parent then I ever thought I could be. My husband and I are made of stronger stuff then we knew.

As for the "I could never have a kid with special needs." Seriously, what would they do? Send the kid back?
post #10 of 18
Quote:
Originally Posted by 2boyzmama View Post
What I don't want is fake sympathy, or pity, you know? I do appreciate those who recognize how hard this is, though. I appreciate offers for help, etc.

He's not "normal", he's not "perfect", and I WOULD change him if I could (I would take away his struggles in a heartbeat, absolutely). But I DO accept him as he is. I DO love him. I DO cherish him as my child.

She said "oh, um, wow, that must be so hard." And I just looked at her. Here we were at soccer practice, he was out there with the other kids, having fun, playing, being a kid! How did she assume that it was hard?

BUT...I dont' want or need pity. I just want my child to be accepted.
I saw under new posts also. I'd like to know what comments would be appropriate if any. Saying nothing feels like ignoring which seems rude. But comments that are made (hopefully) without malice are still often taken as rude. I agree that it is a teaching moment, and I would try (even though it must get old) to respond without anger if the person had good intentions.

The quote above first says recognizing how hard it is is appreciated. But a couple paragraphs down when a woman says just that, it is wrong. I assume a lot is said with tone and expression, but I am curious as to how one could respond without being offensive.

I completely understand wanting acceptance and not pity. How could I show that if we ran into each other at a soccer game or in an elevator?

And since the world is set up for kids with normal hearing, being deaf WOULD be hard. I know that it is still fun, rewarding, etc - but at times hard, no?
post #11 of 18
Quote:
Originally Posted by Kirsten View Post
And since the world is set up for kids with normal hearing, being deaf WOULD be hard. I know that it is still fun, rewarding, etc - but at times hard, no?
Having a SN kid IS hard and it's also hard on the kid, but what's upsetting about it is people automatically jump to the negative side of it. I personally just love it when people gush over DD. Why focus on her disabilities when her smile lights up the room? Like I said in my above post, we haven't dealt with a whole lot of negativity so maybe I can't relate too well. We HAVE dealt with a lot of positive, so maybe in a way I'm more able to tell people what I DO want. I want people to see DD as a beautiful, cheerful little girl who is very smart despite her brain damage and acts like any other 2 year old much of the time. She has favorites, like barney and elmo. She begs for tastes of our pop and candy. She starts grunting at me when my attention is on something else or I'm talking on the phone, getting increasingly louder the more impatient she gets. She thinks it's funny when her big brother gets in trouble. She can point to her colors on a good day despite her CP and CVI.

She's a little girl, not just one big disability. If you ask about a child's diagnosis and the parents feel comfortable talking to you about it, listen to what they have to say, but then don't linger and pity them or the child. Ask about the CHILD, not their medical problems. What do they like to do? Do they have favorite toys and TV shows? Do they like their home nurses? There's so much more to these little kids than just their conditions.

So it could go something like this:

You-"Do you mind if I ask what his diagnosis is?
Them-"Of course not, he has XYZ and needs this or that treatment"
You-"Wow, what a strong little guy! Look at that smile! He must be very happy despite his challenges! Does he like elmo? My kids liked elmo at that age."

It's just so much more refreshing than "Wow that sucks, I'm so sorry "

Sorry if that was too much of an explanation...I tend to ramble. LOL
post #12 of 18
Quote:
Originally Posted by Kirsten View Post
I saw under new posts also. I'd like to know what comments would be appropriate if any. Saying nothing feels like ignoring which seems rude. But comments that are made (hopefully) without malice are still often taken as rude. I agree that it is a teaching moment, and I would try (even though it must get old) to respond without anger if the person had good intentions.

The quote above first says recognizing how hard it is is appreciated. But a couple paragraphs down when a woman says just that, it is wrong. I assume a lot is said with tone and expression, but I am curious as to how one could respond without being offensive.

I completely understand wanting acceptance and not pity. How could I show that if we ran into each other at a soccer game or in an elevator?

And since the world is set up for kids with normal hearing, being deaf WOULD be hard. I know that it is still fun, rewarding, etc - but at times hard, no?
Thank you for asking!! Really

I guess I didn't word that well. In this case, there was no indication at all that his life was hard. She saw him for 30 minutes at soccer, being a normal kid, you know? His hearing loss and speech delay frankly are the absolute least of our worries, although I recognize that the other mom probably had no clue about his lengthy list of other medical issues or the future in front of him due to his syndrome. I also realize that she was probably just at a loss for words, it IS awkward.

Let's see...in this example...

Other mom: "I saw you signing with him, where did you learn it?" [this is a great way 'in' because my answer could be that we do baby signs just because, or in our case I'll answer that we have an in-home instructor to teach the whole family, which we do.]

Then she could say something like "When did you find out about his hearing loss? I've always been interested in sign language...what beautiful eyes he has, by the way!" Or "I think he did a good job kicking the ball, can you show me the sign for good job?" Or, like the example above, "I see his Elmo shirt, my son LOVES Elmo! What's the sign for Elmo?"

So now we've built a bit of a rapport. Once someone has shown some interest in getting to know my child, then if they comment about how hard the overall special needs journey is, I take it a lot better, you know? But to automatically jump to the negative, it does get old. And it brings me down sometimes. If someone instead says "he looks like he's doing so well, I'm sure it's not easy..." that's different.

What's ironic is that I sometimes have trouble approaching other special needs parents in public! You'd think I'd have this down by now, but I don't. I usually look for some sort of commonality..."I know a little girl in the special needs chat room I'm a member of that has an adaptive stroller just like that, I like the little sparkles on the rim!" And I always make sure to talk to the child, so I"ll tell the little girl "did you help pick out your chair? I like the stickers you put on your tray." Then once you've focussed on the child just like you would a "normal" child, you can say "can I ask why she uses a chair?" Almost certainly the mom will be glad you asked and will explain it. Then, instead of saying how hard overall life is, or instead of saying how sad it is, say something like "I bet you're a pro at fighting with insurance companies!"

I don't know if I'm making any sense...
post #13 of 18
For my situation, it's not "I'm sorry" that bothers me (I personally am sorry that my daughter has CF, too!), it's the hushed, sympathetic followup question "and is she your only child?". Like, are you stuck with just a broken one? She is my only, and probably will stay my only, and it sets my teeth on edge that so many people feel like I should 'try again', like, I rolled a bad die and lost, I should try again, maybe I'll win with the next kid. I *did* win, with *this* kid, she's fabulous!
post #14 of 18
Quote:
Originally Posted by SiobhanAoife View Post
For my situation, it's not "I'm sorry" that bothers me (I personally am sorry that my daughter has CF, too!), it's the hushed, sympathetic followup question "and is she your only child?". Like, are you stuck with just a broken one? She is my only, and probably will stay my only, and it sets my teeth on edge that so many people feel like I should 'try again', like, I rolled a bad die and lost, I should try again, maybe I'll win with the next kid. I *did* win, with *this* kid, she's fabulous!
Yikes! But those same people are probably thinking everyone should have 2 just in case one dies in a freak car accident or something.
post #15 of 18
I dunno. As irritating as it can be (esp. the sympathy that's really pity), I understand that people don't get it. Us parents of SN kids are part of a club that few people would ever choose to join. People are painfully ignorant, but I was at one time, too, and I cringe when I think of the unwittingly insensitive things I might have said in the past.

There are some true jerks out there, but I think most people just don't know how to act or what to say and are at least trying to say the right thing.
post #16 of 18
Quote:
Originally Posted by UptownZoo View Post
I dunno. As irritating as it can be (esp. the sympathy that's really pity), I understand that people don't get it. Us parents of SN kids are part of a club that few people would ever choose to join. People are painfully ignorant, but I was at one time, too, and I cringe when I think of the unwittingly insensitive things I might have said in the past.

There are some true jerks out there, but I think most people just don't know how to act or what to say and are at least trying to say the right thing.
This is what I get a lot of. People don't really know how to approach the subject very well and I prefer for them to ask that to just stare wondering what the deal is. It is fairly obvious that our son is different as he does have 2 implants on his head, I hate the backward glances that everyone does.
post #17 of 18
I just jumped in here from the new posts. I do not consider myself a mother of a SN child, although my DS does have some mild sensory issues that people often don't understand. They usually just think he's extra clingy or shy when he is afraid to play on the playground equipment or something.

I thought I would offer up the way I handle meeting a SN child for the first time, and maybe get some ideas of how I could handle it better. I usually just ignore the obvious SN (if it is obvious) and say something like, "Oh I just love her dress!" or "You have a balloon! I love balloons!" Often I'm curious about what that child's diagnosis is (as someone who is graduating form nursing school in 2 months and has a passion for children) but taking the chance of hurting someone isn't worth satisfying my curiosity. If it's a situation where we can spend a good amount of time getting to know each other, I have found that usually the mother will end up offering up the information, at which time I can go ahead and ask some questions.

I don't want to seem fake by ignoring the obvious (again, when it is obvious) but I really try hard to show that I am treating this little person just like I would any other little person. Having 2 close friends with sons who have autism, I have stumbled over my words and learned hard lessons along the way, but my friends have been very kind in helping me understand how they feel about having SN children, and how I can show them the most love and respect. I appreciate those lessons, as I never want to hurt anyone, especially when it comes to their children.
post #18 of 18
Someone asked me once if I'd know how DS would be if we would have had DD as well. People are so cruel.

I have a large family and aside from my parents and one sibling, no one knows what is going on with DS. (working on a SPD dx, severe speech delay, and possibly on the spectrum). One SIL caught wind of some the issues with DS and has said several times that she's sorry I'm going through stuff with him, and she has no idea what it'd feel like to have a kid like him.

DS is 30 months and we've adopted a phrase from VeggieTales (a huge hit with him).
"God made you special, and he loves me just the way you are". We teach him that God doesn't make mistakes and has an amazing plan for him.
While he doesn't say much, and we're not 100% sure what he's comprehending, I want to believe that he understands that we don't see him as different, or SN, we see him as him, special and unique. Yes times can be rough, but there are such positives. If he wasn't so sensory seeking, my active little boy wouldn't want to cuddle and be held. We wouldn't celebrate the little milestones so much. Yes there are challenges, but they far outway the bad times. I don't want anyone to be sorry for me or for him, but instead for what they are missing out on by not knowing such a wonderful little boy.
New Posts  All Forums:Forum Nav:
  Return Home
  Back to Forum: Special Needs Parenting
Mothering › Forums › Parenting › Special Needs Parenting › so tired of hearing "I'm sorry"