

P.S.

Children must learn the difference between "I want" and "I will." They must learn to distract their thoughts when tempted to do what they may want but know is not right, and think of something else, or do something else, interesting enough to occupy their mind. After a short diversion, their mind will be refreshed and able to will with renewed strength. Principle 17 translated into modern English by Leslie Laurio
Warm parenting is a no-brainer for me. I had already determined how to help Pamela self-regulate by comparing borrowing with fractions to what she already knows. All I needed to do was to watch for moments of confusion and guide her thinking with an insightful question or statement.
Then, I pointed out to her how we can do the same thing with fractions. "What do you think we could do with the 4? . . . What fraction do you need? . . . What does the whole number 1 equal? . . . What can you do with the fractions I circled? . . . Do you see how we can rewrite the problem?"
Here is her first attempt. She did pause a couple of times and reference me when uncertain. She was quite excited to see that what puzzled her yesterday became clear as day today.



I analyzed entries from her journal to understand better how her memory works. Even though she does not truly remember her earliest years, she recorded an average of 9 sentences per year for her first four years of life. That average jumped to 19 sentences per year for her fifth through seventh years, 29 sentences for her eighth through twelfth year, and 43 for her thirteenth through fifteenth year. Pamela kept a journal for a writing class, which seared the idea of tracking memories into her mind. Since then, she has written an average of 201 sentences per year without consulting any journal or other material. She is still writing 2007 up in two separate places, her journal in a box and a journal received from her Aunt Pam for Christmas. The year with the highest number of entries is the year she kept a journal: 293 sentences for one year. However, if she continues to record two or three sentences per day for 2007 in her puppy dog journal, she will eclipse that record!"So my poor Agnes has had a very sad day?"One technique in RDI is to spotlight the emotions attached with the event, which the mother in this vignette does. She spotlights the sadness of her daughter Agnes as well as the entire family, evaluating how her sullen moods affect the entire family--a revelation to Agnes. She points out the source of the sadness, too. Whenever the sullen moods, they reminded her of the past to help her evaluate how the entire family feels. In time, all the parent needed to do was sadly look at Agnes to melt a sulky face into gentleness.
"Yes, mother," with a sob.
"And do you know we have all had a very sad day––father, mother, your little brother, Nurse––every one of us has felt as if a black curtain had been hung up to shut out the sunshine?"
The child was sympathetic, and shivered at the sight of the black curtain and the warm sunshine shut out.
"And do you know who has put us all out in the dark and the cold? Our little girl drew the curtain, because she would not speak to any of us, or be kind to any of us, or love any of us all the day long; so we could not get into the sunshine, and have been shivering and sad in the cold."
"Mother, mother!" with gasping sobs; "not you and father?"
"Ah! I thought my little girl would be sorry. Now let us try to find out how it all happened. Is it possible that Agnes noticed that her brother's pear was larger than her own?"
"Oh, mother, how could I?" The poor little face was hidden in her mother's breast, and the outbreak of sobs that followed was very painful. I feared it might mean actual illness for the sensitive child. I think it was the right thing to do; but I had barely courage enough to leave the results in more loving hands.
"Never mind; don't cry any more, darling, and we will ask 'Our Father' to forgive and forget all about it. Mother knows that her dear little Agnes will try not to love herself best any more. And then the black curtain will never fall, and we shall never again be a whole long day standing sadly out in the cold. Good-night from mother, and another good-night from father."
The treatment seems to answer. On the slightest return of the old sullen symptoms we show our little girl what they mean. The grief that follows is so painful that I'm afraid we could not go on with it for the sake of the child's health; but, happily, we very rarely see a sulky face now; and when we do we turn and look upon our child, and the look melts her into gentleness and penitence.
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The truth was that when Mother said those certain words all the good feelings came back. Grandma's whole house and yard and her whole Maple Hill were in those words, just the way Mother had described them ever since Marly could remember. Grandma was in them, too, with the way Mother said her voice was, like a bird's voice if it pretended to be cross but really wasn't. Mother was in them, too, but in a special way. Not the way she was now, but the way she had been when she was Marly's age. Every summer she had come to visit her Grandma at Maple Hill, right here in Pennsylvania's corner.
How so many things could be in a few words was something else Marly didn't know. But it was the same way the whole feel of school can be in the sound of a bill ringing. Or the way the whole feeling of spring can be in one robin on a fence post.
Narrating is an art, like poetry-making or painting, because it is there, in every child's mind, waiting to be discovered, and is not the result of any process of disciplinary education. A creative fiat calls it forth. 'Let him narrate'; and the child narrates, fluently, copiously, in ordered sequence, with fit and graphic details, with a just choice of words, without verbosity or tautology, so soon as he can speak with ease. This amazing gift with which normal children are born is allowed to lie fallow in their education (page 231).Autism and the Building Blocks of Narration
Today, I implemented my plans (listed at the end of this post) with interesting results. I made a point to be extra responsive to every interaction Pamela initiated. With verbal stims about Life Alert ("I've fallen and I can't get up") commercials which she finds funny, I would look at her sadly and talk about that poor woman, trying to redirect the stim along different lines of conversation every time. When she ignored my request to move her legs (she was sitting on the dog kennel with her feet resting on the washing machine), I crawled under her legs and pretended she was a bridge. Then, I stood up and waved, "Good bye, bridge!" Anything unusual catches her attention and treating her like a bridge was novel.
Pamela was not pleased about building her panda puzzle with me, but I had decided to do the puzzle first and then shop. I have already scaffolded this puzzle because of its difficulty. The first day, we focused only on the edges. The second day, we sorted the puzzles into three different colors (white, black, and green). The third day, she struggled with green on black pieces, so today I collected the white and black transitions on the fur.
While she put together her pieces, I worked on mine (pure black that you can only match by shape). Every time she fit two together, I smiled, waited for her to shift attention to my face, and made different remarks, "Hey! You put two together!" At one point, she put three together and shared her excitement with me. I responded enthusiastically again, this time with a high five. She found two to put together and referenced me to see if she was on track, "Help me with this!" I looked at it and told her, "I agree. It fits!" Then, she grabbed a third piece that she knew fit and put it together while I watched. I waited for her to shift attention and said, "Wow! White pieces are easier than black ones!"
My sister and her fiance (who is German) are planning to move to the United States and marry. They are master wine makers and great cooks like my Mom. Last week, they made some Hungarian goulash and noodles, which were delicious and intriguing. When she described how she made the noodles, I realized it might be a great RDI activity because the technique is unusual and could be framed for many different objectives. The big trick for me was to create a gluten-free, casein-free version so Pamela could actually eat it!
I did not measure the quantity, but I think the recipe yields 2 1/2 to 3 cups of nockerl. WOW! I found it delicious and ate some for lunch and dinner!
Pamela put tomato sauce on hers and ate it up! I stored the rest in a plastic bag and, when I served myself some for dinner later that day, the noodles still tasted yummy. They did not mush up on me like some GF/CF noodles do when stored.[Jesus] "comes to us, not to shield us from the harshness of the world but to give us the courage and strength to bear it; not to snatch us away by some miracle from the conflict of life, but to give us peace—His peace—in our hearts, by which we may be calmly steadfast while the conflict rages, and be able to bring to the torn world the healing that is peace."The reality is that Pamela has autism. That means I have to find ways to accommodate her special needs while celebrating Christmas. That means I have to expect some conflict and storms. That means I may not have a picture-perfect celebration out of some Norman Rockwell painting. But, I can have that inner peace and calm steadfastness if I turn to God with my burdens.
Pamela is on a special diet, and making exceptions for any holiday spells disaster! We have worked hard to find tasty versions of typical holiday recipes. In fact, people often eat Pamela's version without realizing it is "special" food. For many parents, the issue is not us, but clueless relatives. Those who approach our kids with a "just one cookie won't hurt" mentality unintentionally launch them into holiday meltdowns. I was fortunate because early on in the diet game all of Pamela's relatives on both sides of the family witnessed with their own eyes what the wrong food does to Pamela. They all help me figure out (1) what recipes and treats are safe for Pamela, (2) what foods I will need to bring as a replacement, and (3) what recipes they are willing to make Pamela friendly. Pamela has a better chance of relaxing and enjoying the celebration if she stays free of problem foods.
Pamela is much more resilient to sensory overload than she was ten years ago. We do not require her to wear special holiday attire, which can be itchy and uncomfortable for the tactile defensive--she has not worn a dress in years! In noisy settings, we allow her to protect her ears by covering them or leaving the room. She has learned to monitor her need for quiet and seek it on her own BEFORE she explodes. We accept that she might have to come and go, just to stay calm. When she was younger, I watched for signs that the ticking sensory-bomb was about to blow. I would whisk her out of the room and spin her until her body melted. We are very fortunate that Pamela's family on both sides accept our explanations of her sensory needs. They are not offended or upset when she quietly leaves a room to find an escape hatch. They know that her face rubbing, gentle rocking, or victory laps are her own expressions of joy. They also know that tantrums are a sign of extreme frustration, not of spoiled rotten behavior, which can be avoided if people follow our lead in helping Pamela cope with the holidays.
Christmas for some autistic people is like being held captive in one of those King-Kong complex, seizur-ific, multiple Clauses, snowman-in-laws, MORE IS NOT LESS tacky Christmas yards. In early childhood, you might help keep them calm by having a simpler Christmas: a small tree on a table rather than the six-foot monstrosity, a few highly desired presents, only your most cherished decorations, one or two special family events, etc. When we moved to Connecticut and first started homeschooling, Pamela was 6.5 years old. We developed a routine of shopping, going to the park, nature walks, and checking out library books. Even library storytime was a big flop! We attended only a handful of homeschooling events throughout the year. We did not live near family and could celebrate Christmas in the quiet, slow way Pamela needed. Between simplifying her life and going on a special diet, Pamela was able to attend a few holiday events, meltdown free. From year to year, we slowly added back activities into her life and even moved near family. We began to build a routine into our Christmas like I had as a child: singing carols on the four Sundays of advent, counting down on the advent calendar starting on December 1, etc. We kept our celebrations small and family-focused. In her teen years, Pamela could handle more and we added musical performances and church events to the mix.
Not all gifts produce joy and finding the right gifts often presents a challenge, especially for non-verbal children. While at Wal-Mart, I came out and asked Pamela directly about what she wanted for Christmas. A few days later she added one more thing to her list, but I could not understand what she wanted. So, she wrote down towel robe on a piece of paper. Some autistic children have difficulty making decisions or verbalizing their choices, in which case it pays to observe their behavior in the toy aisle and during television commercials. Usually, our relatives will ask what Pamela wants for Christmas and I try to give them suggestions based upon her wishes or strong interests. This year, all of the aunts headed to Wal-Mart together to give each other ideas about what the nieces and nephews wanted. We saw many smiling faces at our Christmas celebration.
Pamela spent about five minutes examining her red towel robe but hardly glanced at the matching red slippers. Occasionally, her reactions are like A Christmas Story's Ralphie and Randy tossing clothes over their shoulders (twenty seconds into this trailer). When Pamela has that blank, zoned-out look, I try to smooth over hurt feelings by letting people know she is going into sensory shutdown. Another option is to photograph or film your child playing with the gift later, and letting the relative see how treasured the gift really is. If it is a pink bunny suit moment, well, the giver either has thick-skin or is not used to getting compliments.
Like Maria in The Sound of Music, we let favorite things cheer up Pamela. Before we go on a trip or to someone's house, she packs her purple back-pack with her Game Boy Advance, Mario and Luigi Superstar Saga, paper, pencils, journals, Disney Charade cards, etc. When she was younger, I packed it for her, but now she has that responsibility. When that fails, reciting a couple of verbal stims together or talk about a strong interest helps her to regulate and reconnect. Lately, Baby Alive, the fifth member of our family, goes with us everywhere.
With family that I see regularly, I try to work in discussions about Pamela's autism and needs and win them to our side. For example, last Sunday, I was hanging out my mother, and we got to talking about RDI. I told her I was so happy with how Pamela interacted and related to people at Christmas Eve. Mom wanted to know what she could do, and I told her the two big tips for beginners: SLOW DOWN and SPEAK DECLARATIVELY. Mom is going to let me give her tips whenever she and Pamela are interacting so that she can support what we are doing.
Having to change as a parent and spend so much time planning and preparing can be draining. Being looked upon as the Adam's family when your cute little daughter is doing the Indy 500 around the church altar is no fun. I want to scream when told, "All she needs is a good pop on the hiney." Keeping our challenges in perspective keeps me sane. For example, think about how holiday planning changes for a family dealing with cancer. If one person attending Christmas dinner has a cold, you stay home! Pamela is mobile and healthy, so we do not have to carry around equipment or medical supplies. Over the years, as I saw Pamela becoming more and more resilient, I began to see that some day the holidays will get easier. And, I was right: Pamela had no problems this Christmas and told me she had fun as did Steve and I!















