What to say to the parents of special needs children

I was born and raised in a country with a warm climate, and as fate would have it, the beautiful woman who became my wife didn’t. To speed this along, I found myself moving pretty much to the other side of the planet to a new country, with a new climate and a new language to learn. Nurses Announcements Archive Article

The only job I could get before I could converse in this new language was to go and work with violent, self destructive autistics. It was the best job in the world- I was lucky enough to work for one of the most charming and spiritual people I have ever, and possibly will ever, meet. Of course there were bad times (when over a period of a few months he bit his tongue off) as well as good times (when he some how managed to communicate his appreciation for the help and assistance we gave him over and above his sever autistic limitations) and it was during these good periods of his life that I began to have these dreams.

I remember that I dreamt the same dream seven or eight times. I could never remember the specifics, but the theme was always unmistakable. I was working with the guy as some sort of training as I was going to have an autistic child of my own.

During this time of the re-occurring dreams my wife fell pregnant with our first born son, who I refer to as Hurricane One with the masses. Normal birth followed by a normal upbringing until we took him for his two year health check up. I asked the nurse about his speech- or lack of it- and was told that the delay was quite normal due to the fact that I spoke one language to him and his mother another. It wasn't until we were back in my home country, seeing a doctor within the health system there, that the penny dropped. Two months later he had his diagnosis- he was autistic.

Not long after Hurricane One became an elder brother to, naturally enough, Hurricane Two. Another routine birth and upbringing. After experiencing the same lack of speech development we took him to the specialist, and not long before his second birthday he also received his autism diagnosis. Two Hurricanes, two autistics. Why is that?

The question why is that is very different to the question why me. Academia says that autism is a hereditary condition, which has some merit as my wife has an acutely autistic brother. Online forums suggest that autism is a result of immunization, which also has some merit as Hurricane One's autistic behaviours increased markedly after his year two shots. But was this an evidence-in-fact or was it just a co-incidence? I don't now. Nor do I really care. Maybe the spiritual explanation is the best- that the souls of both my sons performed unimaginable acts of service in their pre-life experiences together, and that in order for them to remain brothers in this life they were given bodies requiring special needs...

I am very fortunate that I have never been angry enough to ask the why me question. That's because such a question is futile. The unfortunate thing is that I have met many other parents of specials needs children who, even after five years, still torment themselves with this question. Is this some sort of punishment? No, you didn't. Did I smoke too much weed and drop one too many acid trips in university? Well, you probably did but that's not why you now have special needs children. So what did I do wrong?

In my experiences it is the spiritual answer that has had the most lasting effects. Maybe it's not a case of what you did wrong but what right was done to you. Maybe you were the principle recipient of the unimaginable good works that you special needs child performed for you in your previous lives. Maybe you chose to be their parent in this life as a return act of selfless gratitude. Or maybe I am wrong, but in my experience it has the most powerful effect in explaining why we have special needs children to parents overwhelmed by their situation.. And unless you are a neuroscientist, it is definitely the easiest.

So how can this apply to nurses, or health care workers who through their occupations are sometimes in contact with special needs children? As one of those parents, you provide us a great disservice if you show us pity. Of course it is easiest to say what we want to hear- that you are very sorry for our situations- but in the long term it is more of a hindrance than a help. What we want to hear is different to what we need to hear.

The best thing to say if you ever find yourself in a situation where a parent is coming to terms with the fact that they have a special needs child is to say something like this: 'Wow, you must be a very strong person on the inside...' When they look at you with that puzzled look on their faces, continue with something like, 'special needs children aren't given to just anyone...'

Variations of these two sentences have the power to change the very attitudes of parents with special needs children, especially if they are told this soon after diagnosis. It creates strength where pity and guilt once stood, and provides a totally new and positive direction for parents to focus on, right when they need it the most.

Hi, I love your reply. Thanks, honestly I get a chuckle over the seven years remark. I only have five years to go, good to have something to look foreward to, ha ha. There are of course good days and bad days. And the floundering at sea but eventually finding a log then eventually heading to shore is good also. Just hard on days when the ache is so acute, I must remember eventually (only 5 years to go) it will go away.

Specializes in mental health, aged care/disability care.

As the mother of a 10yr old with Down syndrome and a 17yr old with spina bifida, I'm afraid I agree with RXTech.

I hate it when someone says to me something like only special people get special children. Get over it! They're my children, of course I'm going to look after them. And some days it's darn hard!

It may work with some parents saying things like that but for some of us, we're just going to bite your heads off.

Hi to all, this has been very theraputic for me, not the intent of this web site!!!! Everyone has some good ideas and suggestions. I read somewhere that when people say the "wrong" thing in these types of situations just think to yourself "they meant to say the right thing."

My second son was born with Down syndrome in 2005. I also, do not appreciate when some people come up to me and say "that God only gives special children to special parents" give me a break...this kind of talk makes me furious. ..so what are they saying that they are not special, therefore, they shall be void of any hardship life may present because they just could not handle it. What a bunch of "garbage" these people act like they are privileged to have healthy children. I agree with Grandpa brownbook life as I knew it has changed for me and my family forever and for this I'm sad and depressed. I'm sad for my husband, my other son and for my parents and my husband's parents. Don't get me wrong we love our child very much and will provide the best care for him, but that doesn't mean that I can't feel that I got the short end of the stick. It takes so much out of me when I'm out and about with him as the stares and back talk cut into my heart each time.

amulet 2010 hi, thanks, inspite of my "they meant to say the right thing," I feel badly when it is implied that I am a bad grandmother and must not love my grandson when I say I am really depressed about his condition!!! I honestly think if he were my own son I would deal with it better. My constant ache is for my first born daughter, his mother. I want so fiercely to protect her from being hurt. Mothers have strong feelings for their children that never go away. I think the accusations that my feelings are ?wong? come from the heart of mothers who love and ache for their children so much. They want the best for their child as I want for mine.

All children are special, and sometimes the most crippling disabilities and challenges are not visible to the casual observer. This is true for people of all ages.

:redpinkhe

rph3664

sorry i don't mean to be rude, but what is your point. nobody said anything about "not being special". we are all faulty humans in a global sense of the word and all special miracles on this earth. having a child with a disability whether visible or not is not in the norm...so people struggle with dealing with this new reality. i as a mother of a special needs child love my child. but this is not what i had wished for my child. i love both my children fiercely and this is why i'm so heartbroken that one is going to have major challenges in life.

i don't belong to any special needs support groups because i'm very verbose about my feelings. having a child with special needs "sucks" for me. there are some parents out there who wish to have more children with ds or any other disability and i applaud them, but it's not my wish...so they drown out those that have different feelings than themselves regarding this role. i just wish support groups show more diversity in feelings. it would keep more parents coming to forums and group settings. in closing, i love my child i don't love his ds.

amulet 2010, I keep e-mailing you then get interrupted and don't get to send. I think I can imagine your frustration with support groups. At the same time I can't imagine why they don't understand your saying, "This SUCKS" Why would anyone think you don't love your child with DS just because you say that????? I have gotten similar feedback in my few attempts at Internet support groups. "What is wrong with you don't you know your grandchild needs love???" I really don't get that????? I should just say, "yeah, I hate him!" ????? Of course I love him???!!!!! I don't know why it is hard to understand that I love him and hate his disability and what it has done and will do to his parents?????

Specializes in Psych - Mental Health.
... As the mother of a profoundly mentally handicapped and autistic young man it makes me very uncomfortable when people say things like "Oh, you're such a strong, noble person to raise such a child." I want to say, "What did you think I was gonna do, put him in a dumpster?" I believe most parents rise to the occasion when they have a child with disabilities. I am very well aware of the fact that I am doing the job of three people, I don't need a gold star for doing it. Parents don't need to be patronized, they need some assistance. Instead of patting them on the head with a word or two about "how wonderful you are", how about someone pitch in and offer to come babysit for an hour so I can have 60 minutes to concentrate on paying the bills? How about you offer to take my two normal children to church this week, or the movies, or the park? How about you give me 4hrs off so i can go to my daughter's senior dance show?

...

How about you talk about my boy like he MATTERS. That's the thing that I crave as a parent, not vapid platitudes.

Very well said. I am Mom to twelve y.o. survivng triplets. One is typical, one has spastic quad CP and our third little guy passed away at 21 months (he had CP, spina bifida, cortical blindness, bronchodysplasia, a crappy immune system and was the sweetest, cuddliest little guy ever :heartbeat).

Believe me we have heard it all: they are gifts from God, we are (pick one: special, blessed, brave, strong, unbelievable) parents, to be pitied, etc... People have asked what is wrong with them, how did they get this way, offered to pray for them, etc... :uhoh3: But what I hate is when people ignore my son - like he isn't even there. He is fully verbal but refuses to talk to anyone who doesn't talk to him (smart boy!) The absolute worst thing though is parents pulling their children away from him as if he were contagious or something. People can be horrible. :devil:

Not just strangers either: we lost many family members who "couldn't handle it" after the boys were born. Now I am happy not to have to deal with those toxic folks but at the time it hurt...

Personally, what helped was a counsellor telling me that I needed to let go of the notion that I have any real control over what happens in life - it has saved me countless hours of worry over things I can't control. The Serenity Prayer works for me as does living one day at a time - good advice for anyone, not just for AA! Also, I appreciated honesty: this was not what we signed on for as parents, it sucks a lot of the time and it is not fair. BUT it did get better after a while and like most people we found the strength to deal with what we were dealt in life. AND we get the privelege of having very wonderful children in our lives (and in our hearts) and now I wouldn't trade it for anything! :o

Specializes in Peds.

I have a disabled daughter..will be 21 this year.....I think some people can handle having a child that's disabled pretty well......I've heard every saying in the book...and some have been pretty funny, pretty dumb, and even downright unreal......yes I love my daughter and believe me......it hasn't been easy......lots I don't remember or care to either.......

But you just do what you have to and get through it...........that's all I can say.........

People say really dumb things, not meaning to alot ......lately one I've heard is..."Thank God mom's a nurse" ........Ummmm I was a mom and had my daughter long before I was a nurse.......lol

All ya can do is just go with the flow.....and throw in some humor.......I really love to say off the wall stuff to people to just see their expression...

I've said stuff like..."ya, we keep her in our shed and when she's really good we bring her inside", ...what else.....oh, when we take the van with the wheelchair access....."when she's been really good (or bad)"( depending on the moment) we tie her behind the van and pull her home.........lol.....

I love to see peoples reactions

My big pet peeve ...well a couple "I'm sorry" ..I now say "why? you didn't do it" or they say "you'll definetly have a place in heaven for what you've done with her".......oh really? Gee, thanks!.......lol.... Why must people always feel compelled to toss in religion????? I never got that one ever........ it's whatever gets you through I guess.....lol

I understand that special needs parents are instructed to never, ever say things like "Well, goody goody gumdrops for you! Your kid (insert accomplishment here)? Mine will never do that, so just shut your big fat yap!" but if this had happened to me, I would personally be tempted to do so every opportunity I could get.

:eek:

Specializes in Psych - Mental Health.
I understand that special needs parents are instructed to never, ever say things like "Well, goody goody gumdrops for you! Your kid (insert accomplishment here)? Mine will never do that, so just shut your big fat yap!" but if this had happened to me, I would personally be tempted to do so every opportunity I could get.

LOL. I only did this once. My triplets were about 18 months old and of course only one was walking/ crawling/ moving independantly (the other 2 had CP). We were at a multiple birth association party and the other mothers of toddlers were going on & on complaining about their kids being so busy and how exhausted they were as parents, etc. My husband had just spent the week juggling the kids to & from 12 different medical or therapy appointments (he had to quit his job to stay home with the kids when i went back to work full-time). Two of our kids were still not sleeping through the night yet as well so we were lucky to get 6 hours of sleep between us. I kind of lost it and remarked that they should be thankful they had to run after their children 'cause it was a lot less tiring than doing physio on your kids and renovating for wheelchair accessability...