Inexpensive Ways to Help a Family Diagnosed With Autism

We’ve all heard the news: one in 91 children are now being diagnosed with autism in the United States alone. This is staggering. Today, almost everyone knows someone with autism. And yet, with all the talk about cures, causes and concerns, there is rarely any information on how we can support a family with this diagnosis. All too often, because folks don’t know what to do, they do nothing! Even to the extent of avoiding the family out of fear, or just out of not knowing what to do or say. In this post, I hope to show how simple acts of kindness can make a world of difference for families who have children with autism.

I will highlight seven easy, free (or inexpensive) ways that you can do to help: 

1.) Let’s start with the easiest: On the way to your weekly or daily trip to the grocery store, ask if there is anything you can pick up for their family.

Pick up some eggs, or a carton of milk and drop it by. If they insist on paying you back, accept. Then, the next time you ask them if there is anything they need, more than likely, they will feel okay to say, “yes, please.”

Why? Because often taking a child with autism to a grocery store can be overwhelming. I can remember when taking my son, Neal, anywhere was difficult. More often than not, when we drove in the car, Neal would have a temper tantrum in his car seat. He would kick the seat in front of him, wailing for me to stop. I would pull over, stop the car and help him calm down.

Taking him grocery shopping had it’s own challenges. On bad days, Neal would have a tantrum while I was shopping. The moment it started, I had to pull him out of the cart, then leave the cart — groceries and all — in the middle of an aisle while a kind and bewildered store employee helped me carry a kicking, screaming Neal to the car. I would tell Neal directly, okay, I guess you’re not ready to go to the grocery store, yet. And we would wait a few days before returning. In those days, many of our meals had to be take-out.

Today, when I speak at conferences and someone asks how they can help a family whose child has autism, the first thing I say, “Ask what you can pick up at the grocery store for them.”

2.) Learn the facts about autism, but don’t give advice.

Parents who have a child recently diagnosed with autism are often overwhelmed with “to dos.” Today there is lots of information to help unravel the intricacies of therapies, schools and protocols. There are special needs advocates, websites, books, journals — you name it, it’s out there. What families need more than additional information or advice is someone to listen to them — they need a friend. A friend who understands what they are going through and doesn’t judge, condemn or give advice.

I am blessed with wonderful friends. Two of my closest friends Rebecca and Nick, and Vida and Leven, lived walking distance from Neal and me. We got together as much as possible. In the beginning, we had dinners together, strolled our kids to the park, debated whether it’s better to use disposable diapers or to be more earth-friendly and stick to cloth. They were there for me when I got Neal’s diagnosis and supported me in every way they could. They listened to my challenges, but only gave advice when asked.

It’s okay to offer a magazine article, a blog post, etc., but only give advice if you are asked!

3.) Take the sibling of the child who has special needs out for a special treat.
When there is a child who has severe needs, the typically developing sibling may often feel left out, or become a “little adult” — over-responsible, learning at a young age to put their own needs aside. This can cause resentment or denial of their own feelings. Parents juggling their own schedules and therapies for the child with autism may not have the time or space to give what they would like to the sibling. This is where friends and family can be a tremendous support in a very easy way.

Ask if the sibling wants to join your kids for a movie, an ice cream, an outing. Or if you don’t have kids, find out what interests the sibling, and take them to a ball game, a dance concert or just a walk around the block.

And speaking of walks — this is really number three and a half — but if the family with autism has a dog, offer to take their dog for a walk. That’s one more thing they don’t have to think about. Siblings of a brother or sister with autism have a different life than their typically developing peers. Holly Robinson Peete and her daughter Ryan wrote a beautiful children’s book, “My Brother Charlie,” that reveals a sister’s experience with her twin autistic brother. Often, as the siblings mature, they see how their brother/sister has enriched their own lives. You can be the person who makes a difference in their young life.

4. ) Give the parents or single parent a night out.

Okay, this is a bit more challenging. You must be willing to leave your comfort zone to be available to be with a child who processes the world differently. Learn about autism. Learn about joining a child’s world. In my book, “Now I See the Moon,” I discuss ways to join a child with autism. I have found children, teens and adults with autism to be the most interesting and extraordinary people I have ever had the privilege to know, and yet I never would have known them had I not had been gifted with my own nonverbal autistic son. Spending time with a child who has autism can change the way you experience the world!

Start with just a half hour at a time. Or if you have the financial means, offer to pay for childcare once a month — or even once a year! With the divorce rate of parents with children who have autism at 80 percent (almost twice the national average) you can be the one who helps save a marriage. Or the one that helps a single mom or dad meet Mr. or Mrs. “Right!”

5.) Okay, you’re not good with kids. But you’re organized, and like to help others be the same. Offer to help with housework or organize their office.

Come over, wash their dishes, take out the trash — any small act can be so helpful. Or again, if you have the financial means, pay for someone to help clean their house. Parents with children who have special needs have to compromise on something and sometimes that’s household chores. I remember realizing that to be an A+ parent, friend and daughter to my aging parents, I had to resolve to being a B- housekeeper.

6.) Bring over a cooked meal.

I remember the evening when a neighbor brought me over an amazing cooked brisket. I had just moved back into my town house. I had boxes everywhere. Neal was having a difficult time adjusting, and the thought of cooking a meal felt overwhelming. It was a simple task for my neighbor (she just made an extra one the day she was cooking hers) but eight years later I can still taste and smell that brisket and remember her thoughtfulness!

If you are real ambitious, start a food bank with your neighbors, or synagogue or church group. Even having someone bring a cooked meal over once a month can make all the difference for a stressed recently diagnosed family with autism.

7.) Ask your high school child to volunteer their time weekly to play with the child who has autism.

Many schools now offer community service hours for teens who volunteer in the community: programs like Friendship Circle, Best Buddies and Circle of Friends. Friendship Circle pairs kids with special needs to go into the home and play with the child two hours a week. At The Miracle Project and Vista Del Mar, we have created the Inspired Teens group, a group of middle school and high school teens who raise awareness, funds and volunteer in our theater programs. These teens also become friends with our teens. They all say how their lives have been enriched by becoming friends with autistic teens.

Above all, the easiest and yet the most challenging thing that you can do with a family who has autism, is open your heart and mind with unconditional love and support. Take away judging a child as having “bad behavior” or a parent as being “overly permissive.” And instead if you see a parent having a rough day with their child, ask “how can I help?” Or, as Lori Guthrie’s neighbor said one day after witnessing a melt down, “Don’t worry about it. I didn’t notice a thing.”

Yes, we know how busy you are. But you may be amazed at how taking some time to help others can help you gain perspective and see your own life’s challenges reduced to bupkis. More than anything, however, your life will be enriched by being of service and from entering the miraculous world of autism.

Please send me your stories of how you have either been helped or help out a family with autism.

Elaine Hall “Coach E”
Founder of The Miracle Project.
Author: “Now I See the Moon: a mother, a son, a miracle”
www.nowiseethemoon.com

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Elaine Hall
Acting/Movement Coach. Speaker/ Media Personality - The Miracle Project, in Autism: The Musical. Author Now I See the Moon CoAuthor Seven Keys to Unlock Autism
Elaine Hall

Elaine Hall

Acting/Movement Coach. Speaker/ Media Personality - The Miracle Project, in Autism: The Musical. Author Now I See the Moon CoAuthor Seven Keys to Unlock Autism

0 thoughts on “Inexpensive Ways to Help a Family Diagnosed With Autism

  • August 24, 2010 at 2:12 pm
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    if you’re teaching a young grade, you don’t have to be a genius.  she just can’t learn physics, but i’ve seen anohter special person whiz it.  some people are meant to fail things.  she’s got a great memory and is good with crosswords and stuff.

  • August 24, 2010 at 2:09 pm
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    @MOM2_4@xanga – I’m not a big life person.  I was special needs.  I was above average.  I’m not going to blame anything for destroying my life, but i’m going to say that that didn’t help.  Most special needs are like trapped younger, which is bad.  i’m okay with letting slow people aroung, but not retards.  I have a grandma who was a teacherwith an intellectual disability. Back in the day, they weren’t as judgemental or using.  i also have a friend whose parents refused to put in special ed, and she’s special, and she flunks things a lot or d, but she still functions well in life.  I started out semi-gifted, and I can barely get up in the morning.  i don’t care, and I get used.  what they do is hold you back and destroy you in every way possible.  if there weren’t special people, problems wouldn’t there that are.  a lot of us there were neglected, abused or poor.  I was all three when i entered.

  • August 24, 2010 at 7:28 am
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    @Colorsofthenight@xanga – Very sorry you feel this way.  Getting to know a special needs child is a great opportunity.  They ARE wonderful people and they will bless you by getting to know them.   However, if you really believe they shouldn’t be allowed to live, then please stay away from them and keep your thoughts to yourself, because they and their parents don’t need the hate. 

  • August 24, 2010 at 7:22 am
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    This list would be wonderful for helping any family with a special needs child, not just Autism. 

  • August 21, 2010 at 12:02 pm
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    I’ve been tested, and I’m not autistic.  I’m psychotic.  Everyone in my family is crazy–or one half is (secrets–shh, no, tell, show and tell), and we’ve survived in society for a hundred years in all sorts of various trades. It wasn’t a shocker.  And, prior to their citement of anything, I was functioning in the classroom. 

    ADA makes me so mad!  If I could be angry.  It’s a long story of the decline of my being. 

    I’ve decided it isn’t personal, but it’s an indirect mission I have. 

    Flow, flow, flowingly go to flow on and on in flow. 

  • August 21, 2010 at 11:55 am
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    Slavery to disabled?  I think not.  I think, I don’t suggest as I can’t as I don’t have authority to do anything and neither do you and as such am merely sharing thoughts, that we should setup special communities for the disabled.  Those should be the people in the hood, not trapped in odd social problems but age.  We should kill off the ones that can’t function at all, or we should place them all in the same area to live to die.  Perhaps that is better, no new additions for failures. 

    Honestly, 

    I hate special kids, and I was one of them.  I’m average, despite whatever they pinned me with that doesn’t even count as a disability these days and they took it away, and I had to serve those little fuckers and wait on the rich children who were special, essentially their average-ass children could use ADA to soar to places that they didn’t belong. 

    My education has been random. I was behind everyone and tossed around, so my performance was always strange. To be truthful, I don’t even think I can learn in a classroom setting, though I do learn and use. I have to do it myself because that’s how I’m wired now. 

    Of course, it’s embedded itself as a severe ego strike, especially since it’s used to this day, so I have to go back to school, wastefully so because I can’t get anywhere due to psychotic problems, to prove that I can to the wind that doesn’t care but cares enough to make me bitter. 

  • August 21, 2010 at 10:08 am
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    this is brilliant, the first time i have ever seen someone offer practical and very good advice, now if only i actually knew anyone who cared enough to do any of these things , in the meantime i do hope this helps someone or moves someone enough to go help, thank you very much for posting this whilst i may not benefit from it i sincerely hope someone does. wishing you much good luck

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