Archive for the ‘disabilities’ Category

Differences

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Occasionally with my morning tea I play on the website Game Duel. This international site has all of the regular games for free; solitaire, Crazy 8s, Yahtzee and so forth. After waking up, I enjoy playing against other players as a semi-introduction to the social world, (before I actually have to be wide awake and sociable in the real world.) This morning, while playing Crazy 8s, my other two opponents were texting in Russian. Although they were surely texting trivialities such as “good morning”, “here comes a bad card”, and “nah nah nah nah nah nah”, my heart was immediately struck with fear. In this era of terrorism, and growing up in an age when the Russians were our enemy, I was irrationally frightened they were planning an attack on the US or something else negative. Worse yet, that they could tell who I was through my computer.

Prejudicial.

When driving through the Deep South in the early 60s, my father would take Route 302 instead of the highway, (which may or may not have been built at that time.) As a child, I was frightened at the attitude towards African Americans. There were “white” and “colored” signs above the bathroom doors, with a significant disparity between the two. I heard the local folk call the African Americans the “n” word, and talk down to them. Their attitude frightened me, and I could not understand why they would do such a thing.

Prejudicial.

When my brother was born with Rubella Syndrome with a massive cleft palate, developmental delay, hearing impairment and vision impairment, my four-year-old little self loved him to pieces. Not being familiar with all of the intricacies of babies, he looked just fine to me. As we grew, other people’s reactions to him upset me. They often recoiled as though in horror and I would wonder why. Other children called him the “r” word and point and laugh. Through the eyes of my love for him, I didn’t see anything funny about the situation. His mouth may have looked a little funny, but didn’t they see the glorious gleam in his blue eyes?

Prejudicial.

When my great aunts would visit from Michigan, they would sleep in my room on the big double bed and I would sleep in a cot in my parent’s room. They were elderly, but still had a lot of spunk. My mom would take them dancing at the senior center where they would dance with gusto to their favorite line dances. They were very affectionate women with my family and between themselves. I thought nothing of their holding hands while watching tv, but others talked in hushed whispers. It wasn’t until I was an adult that I realized that Aunt Mina and Aunt Betty were gay, and that they had to hide their “gayness” in the confines of our home because others in the community wouldn’t understand, thinking there was something wrong with them.

Prejudicial.

Fast forward to our adoption of Marie at the age of 7, who was deaf and had been severely abused. She was a wild one; untamed, disrespectful, destructive, stealing things at the store, and begging from strangers when given the chance. (I learned to stay by her side and intervene before she even got close to anyone unfamiliar.) She refused to wear girl clothes, insisting on wearing boy’s underwear, pants, shirt, shoes and socks. (This caused a slight problem at McDermott Pool, which had a strict “no shirt” policy 15 years ago. Because she insisted on wearing boy’s swimwear, she obviously needed a shirt!) She would tell everyone, (in sign language,) that she was my son. At her annual check up at the age of 8, she tearfully asked her pediatrician if he could sew a penis on her. As a very sympathetic doctor, he understood that her needs were different than other children’s. He gently took slim her hands into his big ones, and looked into her deep blue eyes, (which darted back and forth between his face and myself, who was interpreting what he said in ASL for Marie.) He said that it was possible to sew a penis on her, but that she had to wait until she was fully grown to make that decision. Relieved that at least it was a possibility in the future, she was consoled. In the meantime, she could continue to be a boy without the extra attachment. Since that time, with intense counseling, she confessed she only wants to be a boy was so that men wouldn’t hurt her. She continues to dress and profess to be male, but is not interested in getting the proper anatomical equipment. Her choice of male attire, now plumply filled out in the bust area, has been cause for concern for many. For her, and many other actual transsexuals, life is met with stares and disapproval.

Prejudicial.

My ever-optimistic brain would like to think that people have such negative reactions for the same reason I was fearful of my Russian opponents this morning; because they don’t know any better. If only everyone would just accept people as they are; to be valued and respected for their uniqueness….

 

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My Children Are Just Like Me

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My children who are adopted are of mixed races, which has instigated a lot of joking over the years about how much we are like each other. I remember shopping at Walmart with my daughter, Dinora, when she was about 6 months old.  Sitting in the infant seat, she exhibited every characteristic of a child of Mayan Indian heritage.  The woman in front of me turned around and looked at her, then looked at me, then looked back at her. “She certainly must look like her father!” she said, in kind of a huff. Incorrect, of course, she was just like us.

Three of my children have brown eyes, just like me! Two have blue eyes, just like their dad! Amazing, just like each other!  All of us love ice cream, especially cookie dough, which was hard to keep in the freezer, even though I would hide a carton way in the back under the pork chops, figuring the children hated pork chops.  They didn’t hate them enough to look behind them to find our special treat.

Swimming is something we have in common, (mostly because we live on a lake.) Dinora was able to swim by the age of 18 months old. She used to jump off the side in the deep end of the community pool with me. Everyone was shocked, saying it was dangerous for her to be so deep. But she was so tiny that even if she jumped off the lower end she still wouldn’t be able to touch the bottom, so what was the difference? My son, Francis, was on a swim team, and won a medal for the fastest swimmer.  Steven spent most of his time by the water, pretending to be the Crocodile Hunter with the ability to swim quite far if he saw one of his prey. Angel was a great swimmer, as was Marie.  Many a time Marie and I would take floats and swim back and forth across the lake.  (Okay, so using float was cheating, but the comradeship was worth it.) Hubby, I, and all of my children,  are natural swimmers, just like each other!

Three of my children are creature lovers, anything from earth worms to boa constrictors to the every day dog, cats and bunnies. It is as though any living creature is a fascination to them, handled with care and put back into their “natural environment”, a special expression of Steven’s. One day, while camping at six years old, he found a common garter snake, hunting it down as only Steve Irwin, the Crocodile Hunter, could do.  On his haunches, he followed the snake through the rocks and eventually wrangled it onto a stick. By then, a crowd of children had gathered, squealing, “A snake!  Yeeeewww.  A snake! Steven gently showed the snake, saying “Isn’t she a beaut?  Look at that great color that can hide in the forest. Nature is amazing!”

With the exception of me and their dad, everyone loves scary movies. Okay, so maybe they aren’t like us in this manner as hubby turns away anytime he sees blood or monsters on tv and I hide under a pillow anytime I hear eerie music. We can’t ALWAYS be the same!

We all love to go apple picking, to see the colored leaves in the autumn, to watch a sunset at the beach, to swim in the waves, and to help those less fortunate.  Francis was building houses with Habitat for Humanity despite his blindness and Dinora raised money for a soup kitchen in her native Guatemala.  We all worked on making sandwiches which would be delivered to Cross Rhodes. With all of these similarities, of COURSE we are related! And so we have built MY family…

Now they are building theirs. Francis has a three year old daughter who physically looks JUST LIKE HIM, (minus the vision impairment!) Dinora has a young daughter and son who physically looks JUST LIKE HER. And Steven has a three year old who physically looks JUST LIKE HIM, massive head of kinky, curly hair and all! Angel is in touch with his biological family who physically look JUST LIKE HIM. All of the similarities we fostered as a family cannot compare to the fact that their flesh and blood look similar to them. But that is not what they focus on. They bond over similarities…Steven’s daughter really loves animals and strawberries, she MUST be his daughter! Dinora’s son is great at drawing and her daughter is a little diva, enjoying make-up and nail polish, (so much like her diva mom.) Francis’s daughter loves vanilla pudding and swimming in the waves in California! Go figure!

The truth is, family is not what is built by flesh and blood, but by common interests, tastes, morals and a whole lot of love. Of COURSE we are all related, we are a family!

 

‘Twas Once a Child

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My daughter, Marie, has reached adulthood, having graduated from a residential program that had services for both her deafness and her mental health issues. This is the age of worry for any parent, especially one with so many challenges.

When she came to live with us at the age of seven and we were told she was “just deaf”, we could not have properly prepared ourselves for the roller coaster ride of a life she, and we, would have. She was a wild child, blonde hair askew, eyes angry, mouth so hungry she would hoard food under her mattress. She was very angry she had been removed from her mother, (for doing unspeakable acts which shall remain unspoken.) Despite providing her with a healthy, well cared for childhood, Marie’s disposition had been preformed. She would lie, steal, beg strangers for money, and reject all of our efforts to parent her. A hug and a kiss would throw her into a fury. Discussing our parenting situation and our need to show her love, she reluctantly let us “fist bump” her. Years later she apologized and told us her birth mom made her promise not to hug or kiss us, and that we really wouldn’t be her parents. It took us many years of fist bumps before she would accept a hug, and many years more before she would let us kiss her. She is now a young adult, and freely hugs and kisses us if the mood suits her. She shows genuine affection and appreciation, the highest reward any parent could expect from an original wild child.

Although Marie can be very capable, she has been unable to live in a non-structured setting because of her unstable bouts with Post Traumatic Stress Disorder. For those unfamiliar with this life altering condition, it is experiencing horrific memories so acutely that one becomes “in the moment” of prior abuse, crazed eyes staring back as though at her accusers, ready to defend herself with flailing arms and legs and gnashing teeth. An ambulance ride to the hospital and sedation was the only thing that could bring her out of her experience. It has always been especially tear inducing, (for me,) when at the hospital, with her hand in restraints, she would wake from the sedation, look around, and finger spell (ASL) asking me where she was, having had no memory of the event. Next she would say her throat hurts, (from screaming, no doubt,) and ask for a Popsicle, which she would skillfully eat while still in restraints.

Marie is now formally an adult. A lot of planning has gone into finding an adult home for her, one that would be staffed 24 hours. My calling all possible supported living programs in our state began about a year and a half ago. With the dual diagnosis of deafness and mental illness, no program would accept her. Many of the programs who may have had prior experience in working with her, never even returned my calls.

After working closely with the Department of Developmental Disabilities, whose frustration and efforts equaled mine; they were able to establish a placement for her that has far surpassed our expectations through a program used to dealing with adults with more severe developmental disabilities. They had no prior experience with a young adult with both of Marie’s difficulties, but once they learned there was someone in such need, they stepped right up and took on the challenge.

Marie now lives in a cute, little house on a nice residential street. As described by those on the show “House Hunters”, this one would be described at “Retro”, with bright yellow tile, a front door carved with circles, and a front porch with wrought iron table and chairs. Neighbors bring over cookies and wave to each other on the street. There are three bedrooms in the house, and she is hoping that a housemate will join her soon. She insists that her house buddy like to watch scary movies, (VERY scary movies,) and, most of all, must not be allergic to pets. Marie has a guinea pig that is usually perched on her chest with both of her hands gently stroking the lucky animal, a calming activity that works for both her and Oreo, who is black with a white center, of course.

Marie is thrilled to be able to go shopping for food she likes, not necessarily the food I have cooked for her. She is no longer in school, so work activities will happily replace the classes with which she used to have such frustration. She has directly chosen the things that she would like to do during the day, throwing out suggestions I would have thought unobtainable.

Marie has always loved to ride horses but gets frustrated that when we go, her horse needs to be tethered to another due to her deafness. She recently began an activity at a horse farm that facilitates riding for children with disabilities. For such children, the riding is therapeutic, but the horse walks slowly. Marie’s job is going to be to trot the horses at the end of the day because the horses themselves get bored walking slowly. What better job than that for someone who loves to ride horses?

Marie’s penchant for all animals has earned her a spot working with “disenfranchised” cats and kittens, that is, homeless felines. She will clean the cages, feed them, and then “show them off” like Vanna White highlights the letters on “Wheel of Fortune”. Oreo will be jealous, I’m sure, so Marie will have to wash the cat scent off before she returns home.

At this point in her life, Marie is feeling very good about herself and her care for others. She has signed up for a Meals on Wheels route, and all of those hugs she didn’t give in her early years will undoubtedly be dispensed ten times over among her lunch recipients.

As a mom with a daughter for whom life experiences didn’t start out well, I am so thrilled that in her adult life she will be doing the things she enjoys with people who will support, encourage and appreciate her. What more could any parent ask for?

 

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To read our story raising Marie and her four siblings, please purchase my book, The Apple Tree:  Raising 5 Kids with Disabilities and Remaining Sane. It is on sale on Amazon and Barnes and Noble. Thank you for your support!

Come On, Friend!

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One of the joys of being a grandparent is spending fun time with my grandchildren. Sometimes on Saturdays my granddaughter, Rose, and I go to the Play Place at Burger King. She has so much energy that the climbing, jumping, crawling, swinging, hiding and chasing meets her activity level head on. However, the most amazing behavior coming from this innocent little tot is her ability to consider everyone her friend.

Rose, whose speech is delayed, is very large for her age of three, chunky and sturdy, but not overweight. She has a head of wild, curly hair that overwhelms her face. When other children talk to her, she cannot answer questions about her name, how old she is, or other ordinary questions children ask. Instead, she will gleefully look them in the eye, motion to them, and say, “Come on, friend,” as they inevitably run off to play together.

Rose adjusts her behavior to the age and temperament of her friends. Older boys, who would not generally want to play with a toddler, will play “tag” with her, thinking they can outrun her. Giggling, she runs beyond their speed limits with her long legs, chasing them into a corner where she tags them, and she steps back so they can run off and the game can begin again.

If Rose is playing with someone smaller than herself, her whole demeanor changes. She smiles and gently motions them along, skillfully helping them up to the next level, patting them soothingly on the back, and encouraging them with “Come on, friend.”

Rose has the most fun playing with someone her own size. They generally take turns playing “follow the leader”. Laughter streams from the Play Place as everyone is having fun.

Rose does not discriminate between friends, and merrily plays with anyone. One day a boy with obvious ADHD was running, skipping and jumping in a disorganized manner throughout the play area. Rose joined him, step by step, copying the same things he did, laughing uproariously.

Another day, an older girl who was non-verbal with an obvious developmental delay, became her friend. Rose joined her, playing on the outskirts. She copied her; jumping and twirling like her new friend. Every now and then, this girl would make a pleasant noise and Rose would repeat it in a singsong manner, taking her friend’s hand and saying, “Come on, friend,” as they did their dance.

Anytime one of her playmates leaves, Rose runs over to wave and say “Bye, friend,” then looks around for another friend to call her own. If no other children are in the Play Place, she will come and sit with me to have a drink of water and relax a little bit. Sometimes she will stand up and look into the Burger King dining room to see if any potential friends are eating their lunch. “Friends?” she says quizzically, putting both hands up in asking the question. As soon as another child enters the play area, Rose jumps up, runs to them, pats the child on the back saying, “Hi, friend!” as they go off to play.

This past Saturday, I heard screaming coming from the upper level of the play area. Not screaming as though she were hurt, but screeching that affected everyone’s eardrums. The boy with her was screaming also, in unison. Standing on my tiptoes, I saw the boy hit Rose, and Rose hit him back. This screaming and hitting went back and forth a few times before Rose heard me calling her to come down. Generally obedient, Rose was soon by my side where I reminded her that she should not hit or scream. She looked at me with her innocent, big brown eyes, pointed up and said “Friend?” who had continued screaming while his dad sat nearby and played on his cell phone. Reinforcing my rule for Rose that SHE could NOT scream or hit or we would leave, she wasted no time in darting her eyes around the room to find another friend, and soon ran off to play with someone else.

I learned two very important life lessons from Rose that day. She could learn proper behavior, and choose not to engage in misbehavior, even if it was hilarious fun for her at the time. More importantly, she was accepting of all children, and modified her behavior to deal with their differences. What a wonderful society we would have if we all could accommodate those different than ourselves; not just “accepting” them, but actively interacting with them and providing a positive relationship.

Come on, friends, we wait to greet you!

Try a Sip of Greasy Wine

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My usual low level of frustration has been tested this week. Anyone who has an adult child with disabilities can understand fully the parenting that goes beyond the age of eighteen. Steven, my wildly impulsive, curly haired son, who was born addicted to heroin and cocaine to a mom with severe mental health issues, has a brain that does not function quite right, especially in the responsibility and common sense areas. His highly valued license was suspended last year for failure to pay for a ticket. After many prompts, in January I led him to the Licensing Board to pay the fine. He then had to take this paper to the DMV to get his license reinstated. He went at least eight times, both when I took him and when he ventured into the crowds himself alone. The fact is, he does not have the ability to sit still or wait for more than 10 minutes before getting agitated, so he had been unable to get his license back. The DMV has wonderful accommodations for individuals with physical disabilities, but wouldn’t it be great if there were a quicker line for those with severe attention deficit hyperactivity disorder. The only incentive for Steven to delve back into the commotion of DMV came when a police officer pulled him over and dispensed a ticket for driving without a license. Off he went back there, late in the day, to get his license. (He was quite excited that he only had to wait 30 minutes, but because the facility was closing shortly, the workers were all working at warp speed to be able to get out of work on time.)   The most frustrating news came in the mail today; a notice that his license is suspended again because he did not pay the most recent ticket…

My son, Angel, seems to be a very good driver, although he is quite fussy about needing to have his car in perfect working and cosmetic shape. Two years ago, he had borrowed my car and, when stopped at a red light, was hit so hard from the back that he was accordianed right into the car in front of him. His injuries were mostly mental, with our insurance having to pay for the damage to the car in front of him, (is THAT fair?) along with the newly instilled fear that he could be killed at any time. My injury was that the insurance only paid for a fraction of what we had paid for this older car, certainly not enough to purchase a reliable car again. It was so frustrating trying to make the best purchase for a minimal amount of money!

About a year later, when he again borrowed my elderly car, the engine literally blew up on him. Again, not his fault. Again, insurance paid a fraction of what we had paid for the car. We searched and searched and found a very old, one owner who only drove it to the church, mint condition car with all of the bells and whistles. (Heated seats! Sunroof! Stereo surround sound!) It was a miracle to be able to purchase such an awesome car for the amount of money we had, and I had truly enjoyed driving it. I say “had enjoyed” because this car, also, has become one of Angel’s victims. This week, while turning with a green light, another car ran a red light and “T-boned” him. He does have some injuries, especially emotional due to this most recent brush with death. My injury is the loss of this “perfect for the money” dream car, the third one in three years. My driveway is again empty.

So last night, trying to squelch my frustration, hubby and I had wine with dinner. I’m not a big drinker, but somehow the occasion called for it. Sitting back sipping it daintily, the ice chips tinkled on my lips. Half of the glass was gone before I noticed an odd, greasy taste. Looking at the ice, what looked like blobs of butter clung to them. Butter? How could that have happened? Hubby’s eyes shot open wide and he ran to the freezer. Because we had corn on the cob the night before, he had put the butter in the freezer, a technique to keep the butter from melting while putting it on the cob. Unfortunately, he had left the butter in the ice tray where it sunk to the bottom of the ice and was ground up to make the greasy ice chips in my wine. I sighed; couldn’t make this stuff up!

Like a Breath of Fresh Air

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I’ve always dreaded the long winter months with all that cold and ice, but noticed recently that if I am dressed in a warm jacket with scarf, hat and gloves, the cold doesn’t seem to be as horribly frigid as remembered.  In fact, as I walked out our front door this morning with a temperature 23 degrees, a healthy dose of brisk air filled my lungs. It was a pleasant surprise.  The frigidity that swelled in my lungs really felt like the proverbial “breath of fresh air.”  It awakened me and I became acutely aware of my in and out breathing, (a technique for stress reduction that had previously eluded my abilities.) With the awareness of the winter chilliness inflating my innards, somehow the weight from the pre-holiday stressors leaked out.

Deep chilly breath in and out…my Thanksgiving turkey may have been dry, but hubby’s awesome smashed potatoes, squash and apple casserole, and pumpkin pie more than made up for it.  Why had I cared about the turkey?  With enough gravy, it was edible!

Deep icy breath in and out…the stress around the Thanksgiving table, with warring factions of children, became a thing of the past. As stressful as it was, there was nothing I could do about it. They are grown children who no longer reflect my beliefs but maintain their own truths and temperaments.  In one way, it is a relief to have them on their own, no longer my responsibility.

Deep arctic breath in and out…driving on Route 2 pre-New Year was an experience in hurry up and wait, and wait, and wait.  (Same experience trying to drive through Apponaug.) In retrospect, I did get to listen to beautiful Christmas music that I wouldn’t have had the time to do otherwise, plus traffic is now back to normal.

Deep frozen breath in and out…digging in the basement for the Christmas tree and decorations hidden under a pile of summer clothes, as well as putting the tree up with a minimal, scattered ornaments with no help from the children was a disappointment, but any reminders of such is now back in the basement, carefully put away to be easy to find next year. Out of sight, out of mind.

Deep bitterly cold breath in and out…buying the perfect gift for each was a concern, but the exhaling of cool, clean air convinced me I had the best of intentions and, in reality, there WAS no “perfect” gift, not one that I could afford anyway!

Deep frosty breath in and out…keeping the house clean through New Year’s Day while my son, his wife and daughter visited from California was a very hard challenge for me, making me anxious with every dropped tissue, spilled milk or spider spotted sitting up near the ceiling.  Pure stress, but throughout it I was still able to appreciate their company and enjoy their visit. Next time we will be going to THEIR house.

As enjoyable as the holidays were, the individual stressors had slowly added up inside me, preventing perfect New Year joy and relaxation. Perhaps I had finally accomplished the ability to use deep breathing as a relaxation technique. This was the first time I appreciated breathing in the frozen wintry weather, but it won’t be the last. On this cold, brisk day of January, that all changed.  It was like a breath of fresh air!

 

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Please consider purchasing my book, The Apple Tree:  Raising 5 Kids with Disabilities and Remaining Sane.  Thanks!!!!

Termites Aren’t so Bad

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My oldest son, Francis, was born “legally blind”. His visual acuity stabilized at 20/400. (In layman’s terms, what a fully sighted person could see 400 feet away, Francis could only see blurrily at 20 feet.) He used his hearing so well that it was easy to forget that he had impaired vision, but every now and then something humorous would happen to remind us!

One Friday night when he was about three years old, he entered the living room as my friend and I quietly sat amongst the pillows on the couch, munching away on buttered popcorn, and watching “Dallas” on television, (our ridiculously favorite TV show at the time.) He toddled toward where we sat and without hesitation climbed onto my friend’s lap.

“Why, HELLO there!” she exclaimed excitedly, since Francis had previously been very shy with her. He looked startled and then began to cry hysterically. He thought that he had crawled onto my lap! He could see well enough to distinguish that there were 2 figures on the couch, but was unable to focus on the differences of our faces. From that moment on, when he entered a room, he would say “Hi, mom!” and I would respond, “Hi, sweetie!” so he could tell from afar which figure I was. At the age of three he had already learned to make accommodations for his vision loss.

He made similar accommodations when he started. He loved going and had many playmates but seemed to develop a deep friendship with a little boy named Eddy, whom I had not yet met because his mom dropped him off at a later time. Francis would come home and tell me that he and Eddy played with blocks or outside in the playground or cleaned the hamster cage together. I was not only excited that he was actually telling me about his day at “school” but relieved that he was able to socialize and make friends.

One morning my lazy body did not want to get out of the comfy bed on time, so he was driven to school much later than usual. I accompanied him into the building and saw the entire class sitting on the floor listening to their teacher read a book. At first glance, the sea of toddlers looked like a blur of Caucasian, light haired children. Francis scanned the room with his limited vision, spotted Eddy, and walked over to sit down next to the only African-American child in the class. Francis was one smart kid…for his best friend he chose the classmate who was easiest to pick out!

Francis had a wonderful, normal nursery school experience, with one notable exception. The school invited an exterminator as a guest speaker who regaled the class about the abundance and peril of termites munching on the wood of houses. Francis came home terrified at the possibility of having them in our basement. I had never seen him so anxiety ridden and he developed problems falling asleep and nightmares. After about a week of this, I finally asked, “WHY are you so afraid of such tiny bugs?” He burst into fearful, explosive tears. “TINY????” he replied. “THEY ARE HUGE!”

Driving through Providence, RI, Francis had previously seen the only termite of his young life, the famous “Big Blue Bug” atop a building on Route 95, which is 928 times the size of a regular termite. No wonder he was so petrified! His understanding was that termites that large roamed throughout his basement and were eating his house! After I stopped laughing, it was explained to him that the Big Blue Bug by the side of the road was a joke and that termites are tiny. Then his dad and I took him downstairs, searched and confirmed that our house was, in fact, termite free. Happy dreams were his again.

 

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If you want to read about Francis’ hugely successful life, including skiing, captaining a sailboat, obtaining a Ph.D. from Cambridge University, and eventual career as a high level manager at a famous Silicon Valley computer company, please purchase my book, The Apple Tree: Raising 5 Kids with Disabilities and Remaining Sane through Barnes and Noble or Amazon.

Mothers, Help Your Sons Grow Up to be Fathers…

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My oldest son, Francis, grew up amongst a caravan of foster brothers and sisters. Specializing in newborns and infants who had been affected by prenatal drug exposure and addiction, our family was usually comprised of my husband and myself, Francis, his sister, Dinora, who had been adopted from Guatemala, and one or two foster babies. Despite the fact that Francis is severely visually impaired, he played an active role in child care, frequently holding a little one, feeding a bottle and changing diapers. When going to the mall, he and his sister would proudly push the double stroller. (With the 2 of them, he could be a pusher without having to see where he was going…) Throughout his childhood, sixteen foster babies lived with us, and caring for them was just a fact of life.

Francis is now an adult with a Ph. D. from Cambridge, a well paying dream job, a wonderful wife and a cozy home complete with a grill for grilling steaks and a lawn to mow. And, as of three weeks ago, a newborn baby. My week spent with his little family renewed my faith in the power of what is learned in childhood. Without even knowing it, I had trained Francis how to be a good father! He bundles his little girl up in a baby blanket, like I had bundled up those babies who were going through withdrawal. Newborns like being in a tidy bundle because they arrive with strong startle reflexes and without much control of their arms and legs. By pulling her arms and legs in close and securely wrapping a blanket around her little body, baby India can feel safe and secure. When she is awake and alert, Francis rocks her and sings songs to her, songs that he heard me sing so many years ago: “Itsy Bitsy Spider”, “Hush Little Baby,” and “The Wheels on the Bus Go Round and Round”. Even though she couldn’t possibly know the songs, the sound of his voice quiets her, and these songs are easy to sing. When he is expertly changing her diaper, he plays “This Little Piggy” with her toes, gently pulling her feet to his mouth to kiss. He exaggerates the “wee wee wee home” by tracing his finger from her toes to her chin, tickling her slightly before kissing her forehead. And while she sits in his arms on the couch, ready for bed, he reads her books with very large print; “Goodnight Moon”, and “Five Little Monkeys Jumping on the Bed”.

On the evening before I left to fly home, he looked over at me and thanked me for giving him the opportunity to practice on all those babies years ago. All of his friends are having babies now, he said, and they are all in a tizzy. Because of the practice HE had, he is a confident parent and not at all nervous with India. I realized that by being a foster parent to infants, I was not only caring for little ones, but also nurturing parenting skills in my oldest sons, skills that will ensure he will be an awesome father!

I have repeated this post from last year. His adorable baby is now a year old, and his father’s day skills have continued to flourish!

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If you are interested in reading other stories about Francis, please purchase my book on Amazon.

With the Wind Just Flying Through My Hair

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Like many of you when driving, my mind races with thoughts of things I have to do, problems to solve, errands to run, crisis to deal with and so forth. Yesterday was different. As I was driving on a back road to get to a client’s home, I found myself following a gentleman, (or gentlewoman as I couldn’t tell; the only clue being the gray hair on the back of his/her head.) Because it was an awesomely beautiful day after a horrendous winter of being snowbound, the top to the MG convertible was down, sunlight shining happily on the occupant. Looking at the car, I recognized it as similar to the one bought with my own money when I was a teenager. My pride and joy that was purchased with my dad, a gentleman who did not generally interact with people, including me. Buying that car bonded us in a way that still brings tears to my eyes. The fact that HE always wanted such a car and possibly was living vicariously through me didn’t dampen my extreme love for him, even when he borrowed it for a joyride himself.

I loved driving my little MG, especially with the top down, and joyful memories flooded back to me while following the car. That was a happy, carefree time in my life. Not that I have regrets about anything I have done since then, including dealing with five difficult children, but remembering being young and without worries induced a sense of euphoria. My current thoughts and worries disappeared, and I became one with that little car. Instead of a stranger driving it, I imagined it was me. My own windows were rolled down so the wind was flying through my hair. My radio was playing songs from the 70s, turned up very loud so it could be heard through the whoosh of the wind. I sang along to the songs, surprised the words came to me so easily. And I was innocently, thoroughly happy without a care in the world.

When the car turned off onto a dirt road, I wanted to scream “No! Stop! Let me follow you!” but of course I didn’t. Instead, the happiness of this memory was etched in my mind. It still gives me a warm glow when I think about it, and I am smiling as I type this.

My thought is; it is easy to get overwhelmed with every day problems and issues. Making time for ourselves may be almost impossible. Look for unexpected joys and happiness, a grandfather walking down the street holding onto a toddler’s hand, the sunlight streaking through the clouds, the flowers bright and blooming, or an old memory that strikes you at unexpected times and makes you smile. Sometimes we have to make our own happiness in unconventional ways, but we all need to have joy in our lives. You just have to look for it.

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The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane
Authored by Linda Petersen
The link to the book:
https://www.createspace.com/5321986?ref=1147694&utm_id=6026

That Disability Line Looked Awfully Tempting!

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Needing to get a picture ID, Marie and I went into the black hole named the Registry of Motor Vehicles. Despite many years of revamping, that place can still take 4 hours to navigate. It was with this background that I bring up the option of the line for people with disabilities. Actually, there WAS no line. Tempting. MMMMMMMM. Marie has a disability. Teaching her to be more independent, I was actually only accompanying her while showing her that SHE can maneuver through the system. Without parental assistance, she really DID have a disability. But I have raised my children not to see their disabilities but their abilities. She may not talk or hear, but, armed with all of the appropriate paperwork filled out and the certificates of existence she needed, (birth certificate and social security card,) she has the capabilities of writing what she wants to say and reading back what the other person writes to get her ID herself. She can function as fully as a non-deaf teenager in the registry. And that meant she was fully capable of waiting in line like everyone else.
There have been many times in life that a disability line looked tempting, especially handicapped parking. What parent of a child with a disability hasn’t dreamed of getting that front row spot. Granted, many parents of children with disabilities DESERVE that front row spot, but not us. My kiddos can walk fine. No need to park there, even if the only other spot was a half mile away. But it certainly was tempting…
Just like that line at the registry. After about an hour of snaking through the regular line, the disability line looked awfully lonely. Marie could just zip in there and be done with it. But Marie isn’t disabled. She can communicate fine, just differently than others. She does not need a special line.
And such is our life. To let the children think they can use a disability line to get through life would be unfair to them. They have been raised to know they can do everything anyone else can do, they just may have to do things differently. No disabilities here!

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The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane
Authored by Linda Petersen
The link to the book:
https://www.createspace.com/5321986?ref=1147694&utm_id=6026

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