Myrtle Beach Airport Opens Sensory-Friendly ‘Quiet Room’

Myrtle Beach Airport2Back in the beginning of 2016, the town of Surfside Beach, South Carolina, made news when it became the first “autism-friendly” travel destination in the U.S. That accomplishment was due, in very large part, to the work of the Champion Autism Network (CAN) in the Surfside Beach area.

Founded in 2012 by Becky Large, CAN is working to spread autism awareness through the community, as well as helping to implement judgment-free zones and overall acceptance.

Today, the Myrtle Beach International Airport, just north of Surfside Beach, officially cut the ribbon on its new sensory-friendly “Quiet Room.” The space is intended for people with autism and special needs who are in need of a place to decompress after their flight. The room is located just off of the baggage claim area, and features cushioned cubicles, pillows and chairs, for people to lie down or just sit and relax.

“This is a wonderful partnership and a victory for families of children with autism who are vacationing in our area,” said CAN’s Becky Large. “This room provides a safe and fun environment for children on the autism spectrum and a caregiver to relax and decompress after a flight while family members retrieve their baggage and rental car.”

In other words, families traveling on to a holiday in Surfside Beach can get their vacation off to a good start in a judgment-free zone, with potentially fewer meltdowns.

And that’s not all. Tyler Servant, the council vice chair of Horry County, which encompasses Myrtle and Surfside beaches, says that the goal is for the entire county to become autism-friendly: “Myrtle Beach area is a great destination for families and by offering these services it was our hope that Horry County would become a place where families that have children on the autism spectrum could come and visit and enjoy their vacation and their time with their families because that is what this area is all about.”

We can’t wait to see more beaches, towns, airports, and entire counties, doing the same.

His First Time at the Theatre

Child Theatre1My son Ethan has fallen in love with the Gruffalo series. It is safe to say that, at times, our house has been taken over by the Gruffalo and the big bad mouse. From reading the books to watching the DVDs, making our very own Gruffalo teddy bear and pom-pom figures, and even taking a walk through a real-life Gruffalo trail. You name it, we have done it.

When I saw that The Gruffalo’s Child was being shown at our local theatre, I was quick off the mark to make sure we had tickets. If ever a new experience arises that Ethan has never done before, I try to make sure that we put our names down for it.

Activites such as going to the cinema or to the theatre can be a no-go for families who have children with autism or other special needs. There is such a huge level of planning ahead required: running through what will happen, how you’ll get there, etc. Then, by the time you get to the place, your child might be too overwhelmed by the environment to actually stay and enjoy the movie or play.

The day finally arrived for us to go and see Ethan’s first theatre show; it is always interesting to see what Ethan’s reaction will be. We prepared him for two days, telling him what we were going to see, where the show would be held, and who we would see once we were there. It helps Ethan cope a bit better when he knows what will be happening ahead of time.

We got to the theatre and there were a lot of excited children captivated by the thought of what they were about to see. There were also pictures of The Gruffalo Child on sticks; we got Ethan a stick that he immediately fell in love with and held proudly.

Stepping into the theatre, I looked around for our seats, and then realised that the tickets I had ordered were for seats located one row from the front. One part of me was really pleased with the fact that we were up-close and personal with the characters, while the other part of me thought, “How will Ethan deal with the proximity of our chairs to the stage?”

By this point, I had Ethan in my arms–he was unsure about the lighting in the room, the number of people, and the level of noise being given off. When we’re home, depending on where Ethan is in the house, he usually has to have every light on before he can walk around confidently. The sound of people chatting and laughing is something that I can filter out for the most part, but for Ethan it can be unbearable for him as he struggles to process sounds.

After finding our seats, we tried to put Ethan in the middle seat to stop him from wandering off mid-play. However, he refused to leave my lap, clinging onto me for dear life. With his hands over his ears, he sat on my lap, repeating the words, “don’t hurt me, don’t hurt me,” over and over again. He felt safe and comforted in this position.

Sure, other people saw Ethan, his body language, and his size  (he’s very tall for his age), and likely wondered why he was acting this way. I didn’t care–my main thought was whether Ethan would be able to enjoy the story that he had come to love, or whether he would have a complete meltdown before it even began. I hugged him tightly, rubbing his hand to calm him, and told him about the book to familiarise him with what he was about to see. The lights dimmed; everyone fell silent.

Ethan spent the first five minutes with his hands over his face, and no amount of coersion was able to get him to take his hands away. I was just happy that he was still sitting. If it meant he had to watch the whole play through his fingers, so be it.

As the play went on, he slowly but surely let his hands down. He became engrossed in the characters, the storytelling, and the singing and dancing. He wasn’t so keen for me or his daddy to sing along with the story or get him involved. It was very much on his own terms or not at all.

As his mum, I was so happy that he was enjoying this new experience. He adapted so well to the environment, going from being completely overwhelmed to clapping along, laughing his little socks off, and generally interacting with the characters. It was such a heartwarming thing to experience with him: I couldn’t help but smile proudly, with a little happy tear in my eye,  to see him so happy and enjoying something that he relates to in such a huge way.

Ethan seems to adjust really well to new situations, so that will continue to drive me to put him outside of his comfort zone. It will be small baby steps–nothing too extreme–but things that I know he will enjoy and love. I guess skydiving is a few years away yet!!

 

{The original version of this post appeared first on Mummy Logs.}

Not Your Typical Therapy Pets

Pygmy Goats4Pygmy Goats
Thanks to his mom, Alicia, 16-year-old Jackson Seaton is the happy owner of not just one, but two pygmy goats. Though they don’t live with him at his home, Jackson and Alicia visit the goats—named Jasper and Zephyr—often, at a farm in Folsom, California. Alicia got the goats after hearing other success stories about children with autism using therapy goats, and hoped they’d help Jackson out, too.

She bought them from Kathy Griffith of Griffith’s Pygmies in Meadow Vista. Kathy has two daughters with learning disabilities, and she’s happy to have been able to help out several families with autism. “Being able to give back to these kids, where others may not take the time to do so” she explains, “just means the world to me.” In addition to training some of the pygmies to be therapy goats, Kathy also breeds and shows them. The goats can be smarter than dogs, and research has shown that they’re entirely capable of building emotional relationships with humans.

Pygmy Goats2

Jackson cares for the two goats, not just feeding them, but also talking to them and learning to love them. His mom watches as Jackson reads to a goat; its head cradled in his lap. She considers it a success just to get him out of the house, off electronics, and into the fresh air, but also says that he’s becoming more vocal because of his interaction with the goats. Even his speech teacher has noticed the improvement, as Jackson tells her stories about the goats.

Jackson’s mom says the goats make him feel just like everybody else. “I love them,” he stated.

Things To Do in the Summer With Children With Autism

Summer can be long and stressful for any family, but for those who have autistic children the changes in routine, lack of structure, isolation from friends, and sensory issues can make holidays seem even harder. As a parent of two children with autism–one who has significant learning difficulties and is non-verbal–I often struggle with ways to keep the children occupied all day, every day, for nearly two months. My stamina, enthusiasm, and excitement are already beginning to waiver after too many late nights, early mornings, and far too many meltdowns.

However, I sat down tonight and decided it is not too late for things to change. Summer CAN be a great time for my family, and for yours too.

Not all of these will work for your children and many may need tweaking to suit your own family dynamics, but why not try something different? Try to have fun with your children even if they have communication or social difficulties.

Get Outside!
Fresh air is so good for everyone. It gives us a better appetite (something my ASD daughter really struggles with!), makes you feel happier and more relaxed, and doesn’t cost a thing.

My son needs 1-1 support at all times, but even he enjoys a bit of crazy golf or swimming. Lots of children are able to cycle, or if not, perhaps they can use a scooter, a trike, or even a skateboard. However they feel comfortable, get out and about with them together on a bird hunt, a picnic, a walk in the woods, a treasure hunt, or just a trip to the local park.

Neither of my children can hula hoop but we enjoy spinning the hoop, wheeling it to each other, and jumping in and out of it. There are often football teams looking for new members and a quick Google search may even yield a team for children with special needs.

Neither of my children enjoy sports or climbing, but my son still loves the swing and the slide, and we try and walk to these whenever possible, even if we need reins. Drawing with pavement chalk, playing hopscotch, kicking a ball, and picking fruit are all popular with my two (although I have to say my son eats much more fruit than he takes home!)

Miriam2Garden Play!
If going outside your own property is difficult with your child, what about playing in the garden? A cheap paddling pool (how about adding a little food colouring or blowing bubbles into the water to add something different?) or a sand pit can keep some children entertained for hours. Garden picnics can turn the most mundane lunch into something much more exciting for a fussy eater.

Trampolines, slides, summer houses, and large sit-in vehicles may be expensive, but could potentially amuse a sensory-seeking child for many a day all summer. Here is my young daughter having the time of her life watering the grass with a hose recently after a few dry days. Simple and inexpensive!

Go Somewhere!
A quick visit to your local tourist information centre or on sites like Days Out with Kids might surprise you with the local attractions that are suitable for your child. Some may even offer discounts for carers or children with autism or other disabilities, so it’s always worth asking. Some museums are even free! I recently took my kids to an airplane museum where my son’s favourite thing was the hand dryers in the bathrooms! The fact was we still went and on whatever level, he had a nice time.

Swimming, ten-pin bowling, the lifts at the local shopping centre, trips on trains or buses, pottery painting, the cinema (many have autism viewings), and a local sensory room are favourites for my two. Even just a few hours out of the house can really break a day up. To prepare my children I use Google Images and Google Maps, as this always helps ease anxiety about the unknown.

Sensory Play at Home
Miriam3Some days, due to bad weather, tired children, or the everyday struggle to get them away from screens, going out just doesn’t happen. My son misses his school sensory room so much when he’s at home all summer, so I try and find sensory activities to help him regulate.

Playdoh (under strict supervision, as my son eats it!), water play, burying toys in rice or uncooked pasta, painting (even water painting can be fun!), junk modelling (my unique way of recycling when it is wet!) baking, fake snow, shaving foam, bubble pictures, puppets, and making homemade musical instruments can all help my children overcome sensory avoidance or give them the sensory stimuli they seek.

My daughter loves jelly baff (bath good) but my son hates it, so using a basin instead of the bath helps a lot. We have made masks before, which for my daughter with selective mutism was a great way to avoid talking if someone suddenly came to visit. I am sure most families have built a den from blankets too!

Games With Rules
My daughter loves rules and fairness, so boxed games of any sort are a firm favourite. There are lots of adaptions of the traditional snakes and ladders if your child is more motivated by Frozen or Superman, for example. Other favourites are Guess Who, pairs, Hungry Hippo, hide and seek, and many of the Orchard games for children. For older children, Scrabble or solitary games like sudoku or word searches can help them unwind when they need some alone time. The key is to get involved with them while finding the balance between having time together and time apart. Some children with autism will struggle to take turns or wait, but simple quick games like Snap can be ideal to work on these.

Construction Toys
Legos are often a firm favourite of children with autism. While some children will prefer to be left alone to build and play, it is always worth encouraging teamwork and co-operation. Legos may be an ideal activity to have a playdate around or for siblings to work together. My two are still at the wooden blocks, Duplo and Mega Blocks stage but their friends enjoy Meccano, K’nex, stickle bricks, magnets, gears, and even marble runs.

Miriam4 Imagination
One of the biggest myths about autism is that children with autism lack imagination. The type of imagination some children with autism struggle with is “social imagination,” which involves joining in games already established by other children that do not have set rules. Summer is an ideal time to allow your ASD child to take the lead with their own imagination. They could dress up, play with dolls (boys and girls!) reenact in a dollhouse, play cars, or trains or castles, be a superhero or a pirate or what about a fireman?

Many children find reacting programmes or stories the easiest way to play, so why not watch the episode with them and join in? It doesn’t even need to be expensive! How about using an old roll of wallpaper to draw your own train track or road layout? Or put a blue towel on the floor to be the seaside?

I know some of you will have read this with skepticism. I know the battle to get your child off an iPad or computer or even to get dressed. I know all too well the anxiety that can come with try something new for many with autism. Not everything will work and that is OK.

Find a local support group or ask around to see if any places do times that are quiet or even ASD specific. Plan ahead for changing facilities, access, price, and parking, and always pack a camera!

Summer does not need to be a stressful time. Even trying just one new thing a week can create memories and smiles that make everything worthwhile.

‘Wow! My Autistic Child Is Socializing!’

There’s no denying that the Pokémon Go craze has taken a few countries by storm. If you’re like me, you’re probably way past eye rolls at the mention of Poke gyms and Poke stops and more. But the incessant chattering about all things Pokémon Go has a huge silver lining—it’s helping to get many people (kids and adults) out of the house and socializing with strangers. Especially kids with autism. And that’s a wonderful thing.

Take a look at this heartwarming note from Brooklyn mom Lenore Koppelman about the impact that Pokémon Go has had on her son, Ralphie. Six-year-old Ralphie was diagnosed with autism and hyperlexia four years ago. He doesn’t interact with strangers and doesn’t tend to be very adventurous. He likes his routines and doesn’t typically like them disturbed. That is, until Pokémon Go.

Pokemon Go2

Since he started playing the game, his parents have noticed that Ralphie secludes himself a little less than he did before, and also talks more to the people he’s familiar with. Given the positive effects of Pokémon Go on her son, Lenore does recommend it to the parents of other children on the ASD spectrum, but cautions them to keep an eye out:

“It’s tempting for Ralph to wander off to find Pokemon, so I have to keep a close eye on him,” she said. “However, I don’t want to be so afraid of the dangers that I deprive him of the potential positive outcomes as well.”

Making a Connection: Photographing Children With Autism

Anna1As a professional lifestyle photographer, Jessica Orlowicz of Peach and Port Photography takes stunning photos of families using nature as the backdrop. She also lends her talent to a non-profit organization called “Spectrum Inspired,” taking both color and black & white photos of children on the autism spectrum in free, individual sessions, where she strives to capture the essence and personality of each child.

“It’s sometimes rare to catch eye contact, which makes those images a little more powerful to me. The unique thing about photographing children with autism is that it requires a little more patience, but sometimes having a camera between you two takes the pressure off of them to interact directly. They can be their wonderful selves, and you’re just there to document it.”

But it’s one of her own children who serves as the inspiration for her photography. Anna, one of Jessica’s daughters is autistic, with a “complicated personality,” as explained by Jessica. “Some days the only way we connect is through the lens.” Whether sharing a quiet moment after a meltdown, or capturing a tender interaction between Anna and her sisters, it’s beautifully apparent that Jessica knows how to use her camera to connect to the very essence of kids with autism.

This unplanned shot illustrates how much my toddler loves and cares for her big sister, who is autistic and doesn't always accept touch. She was tenderly petting her and asking if she was O.K. in between strokes. ~ Jessica

This unplanned shot illustrates how much my toddler loves and cares for her big sister, who is autistic and doesn’t always accept touch. She was tenderly petting her and asking if she was O.K. in between strokes. ~ Jessica

 

Sensory Friendly Kits Available to Diners at Mary’s Pizza Shack

Autism Kit2Mary’s Pizza Shack in Northern California has begun offering “sensory friendly” kits to customers. The kits, which were first announced in April, are part of a joint initiative with Anova, a local non-profit autism services organization. Anova reached out to other Sonoma-based restaurants, and Mary’s was the first chain to express interest.

Mike Clark, the manager of the Mary’s Pizza Shack in Sonoma Plaza, said, “We have a number of employees whose lives have been touched by autism or learning differences in one way or the other and so our staff was 100 percent enthusiastic about our partnership with Anova.” He wants to show sensory-sensitive people that, “they are welcome here.”

Anova co-founder Andrew Bailey noted, “Many families [choose] not to dine out or enjoy many activities because of the overwhelming challenges involved. We want to turn that around by equipping restaurants such as Mary’s Pizza Shack with tools that will help create a stress-free dining environment for those families in need.”

The tools are meant to keep sensory-sensitive individuals, no matter what their age, from feeling overwhelmed in a public place. They include a weighted lap pad, noise-reduction ear muffs, a chart with an emotional scale on it, assorted sensory toys, and one small item for the child to take home with them. They come packed in a plastic “toolbox” with instructions and the children and families are free to choose and use what they’d like. All of the items are thoroughly cleaned before being packed back into the kit for the next person. The kits are free and available to anybody upon request.

Each of Mary’s locations carry the kits, and each restaurant has a sticker on their window advertising their availability. The chain also plans to have tent cards on each table informing diners about the kits. Anova hopes that word about the sensory-friendly kits spreads through word-of-mouth, and with the help of the local radio station, and that other restaurants and businesses sign up to offer the kits. Anova’s end goal is to encourage inclusion in their community, and also enable families with special needs to go out to dine, shop, and participate in typical community activities.

Additionally, Anova has providing sensory training for all employees of every Mary’s Pizza Shack restaurant, and has developed an informational video for them. Mary’s Pizza Shacks are now the first sensory-friendly restaurants in Sonoma County.

A Meaningful Life, Animated

Life Animated2For many of us, Disney animated films are just entertainment. But for the Suskind family, these films are much, much more. After all, it was through these films that their son Owen learned to relate to the world around him and make sense of it after autism took him away. And it was through these films that his parents found a way back to him.

As happens with many children eventually diagnosed with autism, Owen was a “typical” developing kid until the age of 3. Then he became a shadow of his old self, no longer talking, playing, looking people in the eye—he was there physically, but had otherwise disappeared. He stayed that way for another 3 ½ years, until one day when they were all watching a Disney movie. Owen looked at Ron and Cornelia and said, out of the blue, that he didn’t “want to grow up, like Mowgli or Peter Pan.”

It was the first time Owen had communicated in years, and it was both a substantial thought and a substantial sentence. His parents finally realized that he hadn’t been gone all of those years; he’d simply been locked inside himself. And during that time, he’d watched and memorized and processed every single animated Disney movie they’d played for him. He’d formed his identity based on Disney characters and his understanding based on the films’ lessons.

Although doctors cautioned the Suskinds from getting their hopes up, they continued to use Disney animation and characters to reach and reconnect with their son. As Ron explained, “the goal was to do whatever worked.” Ron, a Pulitzer Prize-winning journalist and author, wrote a book about the journey to reach his son, “Life, Animated: A Story of Sidekicks, Heroes and Autism,” and recently realized his dream of having the book made into a movie.

That movie, “Life, Animated,” presents Owen’s story in the closest way possible to relate to what he went through—using animation. The result is something amazing and precious, heartwarming and heartbreaking. “Life, Animated” is a stunning tribute to the selfless love of two parents who were willing to do whatever it took to help their child live in our world, on his own terms.

As Cornelia says, “Who decides what a meaningful life is?”

U.S. Army to Open First Autism Therapy Center

Army Dad and KidAccording to many military parents, the U.S. Department of Defense isn’t the most progressive employer. Some parents of military dependents with autism—said to number 23,000—have been trying to find services for those dependents for years.

Others have found amazing services for their children, only to lose them when they’ve gotten reassigned to another base and country. Parents have even had their children waitlisted for multiple schools and centers, as they get on a list, get transferred, put their child’s name on another wait list, and get transferred again. In the meantime, their child is missing out on vital therapies and interventions.

In a move to help alleviate this problem, the Army has announced plans to open its first therapy center for children with autism. The JBLM Cares Center will be part of the Madigan Army Medical Center in Tacoma, Washington, and is expected to start providing care in early 2017. The Center will be overseen by Lt. Col Eric Flake, a doctor and the director of Madigan Army Medical Center’s developmental and behavioral pediatric program.

Lt. Col. Flake explained that the center will have programs to help parents whose child has just received an autism diagnosis, as well as “group after-school therapy opportunities.” Furthermore, he said, “During the work day this will also be a therapy center where kids will get direct speech therapy, will get direct occupational therapy.”

Gretchen Shea, a regional administrator for American Military Families Autism Support—an online group for parents—says that many families have mixed feelings about the announcement. But while it may be, in her words, a “drop in the bucket,” we’re big believers that small steps in the right direction are better than no steps at all. Sometimes small movement is all you need for something to gain momentum, and we hope the Department of Defense considers the need and opens more autism therapy centers where possible.

Summer Is Hard.

Summer Sunglasses

It’s that time of the year again… Summer! I have a love/hate relationship with summer. Don’t get me wrong, I enjoy the warm weather. In fact, I love the warm weather! I love being outdoors. Before I had my children, I loved to soak up the sun as much as I could. There’s nothing better than having a little tan, watching baseball, cooking out, picnics, going to the lake, taking vacations, enjoying the summer holidays, etc.

It’s amazing how quickly your life can change. Seven years ago I was enjoying all those summer activities. Now, six years after the birth of my first son who has severe autism, I no longer have any idea what it is like to enjoy the slightest ounce of summer fun.

My oldest son is an eloper and is attracted to water. Therefore, having him around any water in the summertime can be dangerous. With that said, we spend a lot of our time locked in our house so he doesn’t elope and get into a dangerous situation.

Taking him to a baseball game is totally out of the question. He has severe ADHD, severe autism, and sensory processing disorder. Those three things do not allow for a child to sit still or handle the smallest of crowds, let alone a baseball game or a short weekend getaway somewhere.

I haven’t been able to attend any summer holiday activities either. Taking my boys to a family gathering that entails a cookout, fireworks, or whatever your family might enjoy doing is totally out of our league. Between the high anxiety, rigidness of routine, and all the traits that autism brings into their lives, anything out of the ordinary, such as holiday fun activities, cannot be done. If I try to attend, I find myself back in our van and on our way home within 20 minutes of arriving.

Summer is very hard. It is just as hard as any other season of the year. Severe autism is the same today as it was yesterday and as it will be tomorrow. Sometimes it is easy to forget how trapped we are in an autism house. If you are like me, I am so used to our routine and strict schedule that I simply forget what life can be like in the “typical” world. But, as soon as the nice, warm weather arrives, I hear the neighbors outside enjoying their pools. I hear their friends gathering for cookouts and I am reminded of what life is like for my family.

However, I won’t let it get me down. Even though I would love to enjoy just one of the things that I used to love to do, it’s OK that I don’t. Do I get jealous at times? Sure I do! Does it make me feel lonely and isolated? Of course, but it is our life. Therefore, I will continue my love/hate relationship with summer and make sure we do the best that we can to enjoy it our way.

 

Would you like to contribute to AutismAwareness.com?

Please send an email to contribute@autismawareness.com or check out our submission guidelines here.