My Children Are Just Like Me

 

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!

 

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‘Twas Once a Child

 

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!

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!

Why Is It That…

 My morning commute to work should be 17 minutes according to the GPS. That time is based on the average number of red lights along the way, as well as traffic slow ups in a few areas. I generously leave myself 20 minutes of drive time. Most days, my body is in my chair at work, computer turned on, by 9 am. On those more important days, such as an early meeting with a patient or a work committee, every traffic signal along the way glares “stop”. They turn red JUST as I get to them. Every one. Some of those red lights at the big intersections seem to be several minutes long, adding precious time to my commute. Why is it that on the most important days, traffic seems to be heavier, more acutely elderly are driving at a snail’s pace, and there are an abundance of red lights?

     Eating out is a wonderful experience Hubby and I get to do once a week. Saturdays are especially important because many local restaurants serve Prime Rib, a favorite of mine, especially while on a low carb diet. There’s nothing better than eating a huge, Flintstone size, piece of meat. (I apologize to all vegetarians, but I am what I am….) Hubby and I settle into a comfy booth with the seat still warm from the couple sitting before us. We leisurely chat a little bit, telling the scurrying waiter we are in no hurry, mentally savoring the meal that is about to come. Except it doesn’t. The restaurant is out of Prime Rib. OUT? How can that be? My patience is tested when I am told they had a “run” on this mouth-watering hunk of meat and none was left for me. Why is it that when I am most looking forward to a meal, the restaurant is out of it?

     The days of nice summer weather have been a delight, and I had splurged on a few summer dresses for work. Ah…the warmth of the sun on my skin, the sunlight making my eyes squint, a dress swishing around my legs and a bounce in my step. Except for that one day last week, where the temperature was in the 60s and it was rainy and glum. I wore my favorite dress that day to add something positive to the dreary atmosphere. It would have worked out fine except the dress was sleeveless and I shivered all day. Why is it that we are tricked into wearing summer clothes when the temperature is more of autumn?

     Why is it that…

…when you wear sandals, there are socks a-plenty, but when you wear regular shoes, there are no matching socks to be found?

…when you meet someone from your past and you try to introduce him/her to Hubby, you can’t remember his/her name?

…you can be happily playing the penny slot machine at a Casino for an hour, and when your $20 runs out, you leave the machine, only to observe someone else sit in your spot and win the jackpot?

…when you search and search and can’t find your glasses, they are right on top of your head?

…when you need to sign a check, the only writing implement in your purse is a Sharpie?

…when you are just getting into an interesting article, it ends….?

 

 

 

 

 

 

Try a Sip of Greasy Wine

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!

Just Like a “Call the Midwife” episode

 

For some odd reason, I love the show “Call the Midwife”. Every conceivable scenario for “birthing babies” (obscure reference to “Gone with the Wind”) is explored. For this reason, I will be sharing the birth of my brother.

I got swept into the drama of childbirth at the tender age of four, an early memory that was etched into my tender brain. Several months before my mom was supposed to go to the hospital to get her new baby, my dad ushered both of us into the car, handed me a very large bag of Hershey kisses and dropped me off at my grandparents. My grandparents were not your usual huggy kissy type, but the standoffish, can’t stand kids type. So I sat there alone in their oven of their Floridian sun porch, eating Hershey kisses and watching Captain Kangaroo and Howdy Doody on their tiny tv. As the chocolate melted, it was imperative to eat them right away, which, of course, I did! Covered in melted chocolate, I was able to enjoy the taste for quite a while afterwards, licking my fingers and scooping up melted spots from my dress.

When mom came home from the hospital, I jumped up and down in excitement to see my new sibling. Mom was not her cheerful self, but managed to open the blanket to show me my new brother. I had never seen a new baby before, so I thought this one just wasn’t done yet. He certainly was tiny! His baby blue eyes were tenderly open, but in the middle of his face was a gaping hole where his nose and mouth should be. Still had to grow in, I thought in my childlike innocence. He had these huge ears that stuck straight out. He was going to be able to hear everything with those ears! He was a fine looking baby!

In my childhood innocence, and before post-partum depression was a diagnosis, it seemed odd that my mother spent all of her time in bed, crying softly. She picked Curtis up to feed him with an eyedropper, but most of the milk dribbled down the side of his mouth spot. Her tears would continue to fall, and I could tell she was upset because he didn’t seem to want to drink the milk. When she laid him down for his long daily naps, he would make mewing noises like a cat. I thought it was cute until learning later that he was crying.

My childhood was turned upside down. My loving, sweet mom changed. There were no more of her tender kisses and words of encouragement. She didn’t want to play games with me, or go for one of our walks around the block. In her place was a stranger.

I was brave and tried to take care of myself, but my heart ached at the loss of my mom. She spent all of her time in bed, sleeping or quietly crying. She continued to try to feed Curtis, but most of the time the milk spilled out and she would put him down again for a nap, where his mewing was heard constantly. Sometimes, when she was asleep, I would pull a chair next to his cradle and unwrap Curtis, letting his tiny fingers hold onto one of mine. I would sing songs my mom sang to me, and sometimes he would stop mewing. Time would go by with me sitting there, stroking his bald head and telling him the story of The Three Little Pigs and Goldilocks and the Three Bears. I would be pleased with myself if he would go to sleep and not mew. He looked so peaceful and sweet!

A few weeks after Curtis was born I was sitting in the living room eating out of a cereal box and watching “Lamb Chop”. The sound of the rocking chair in my mom’s room indicated she was again fruitlessly trying to calm Curtis as he mewed. Her room suddenly brightened, as though she had turned on a million lamps. Streams of light spewed out the door of her bedroom into the living room. It was curious and strange, but I was just a kid and saw new things every day, it was no big deal. Returning to watching my favorite lamb puppet sing and dance, I was annoyed that the streams of light made it difficult to a see the tv.

From that time on, the sleeping/crying mom was replaced with my real mom. Carrying Curtis out of her room for the first time, she came over and gave me a kiss and told me she loved me. My own heart softened, and tears started to slide down my cheeks in relief. I had been brave and tried to take care of myself, but having someone else care for me was much preferred.

Mom and I went to the hospital so she could learn how to feed Curtis better. They showed her how to thicken the formula so it would not spill out of his mouth spot. She learned to squeeze little amounts in and wait for him to swallow it. Soon, both Curtis and mom got the hang of it, and he was happily gobbling down the formula. His mewing, which we had become accustomed to, stopped. As weeks went by, he gained weight and I was sure he smiled at me. Of course, it was hard to tell because he had such a strange mouth spot, but his eyes twinkled in such a way that I could tell he was smiling. What a lovely new baby brother!

Fact #1: My brother had been born with Rubella Syndrome, and was hearing impaired, legally blind, severely developmentally delayed and had several physical deformities. He was born this way because when my mother was pregnant, she came in contact with someone who had German Measles. Thankfully, a vaccine was invented to prevent this disease, which can harm more than the carrier.

Fact #2 It was years later that my mom explained what happened that day when the bright light filtered out of her room. She had been rocking mewing Curtis, herself crying and uncharacteristically cursing her life and the life of her deformed, newborn son. Unexpectedly, she was engulfed in an unbelievably bright light that emitted the feeling of unconditional love and encouragement. It washed the sadness out of her, and seemed to tell her everything was going to be all right. She knew it to be a Divine Being, and this experience changed her life, and mine, forever.

 

 

To read the life story of Linda’s sweet brother and Divinely amazing mother, along with her own passion for caring for children with disabilities, please purchase her book; The Apple Tree: Raising 5 Kids with Disabilities and Remaining Sane. It is available on Amazon and Barnes and Noble.

 

A Mom is Forever

    Saturday, I was perusing the bargains at JC Penney’s, picking out a deeply discounted cute grey sweater to ward off the cold while waiting for the spring that I know is supposed to arrive any day now.

     While waiting in the long line, which moved incredibly quickly, I admired the clothes on the counter ready to be purchased. They were in pastel colors, the colors that are supposed to look best on me according to my “color chart”. Of course, I never buy the appropriately colored clothes because the deep discount bargain rack is my go-to shopping place, where pristine, professional looking, pastel colored items are rarely hidden. Thus my wardrobe consists of the browns, the blacks and the grays.

     On the cashier’s counter lay two different colors of pants, a light pastel peach and a business-looking tan. The peach colored sweater had three quarter length sleeves and pearl buttons on the neck and down the front. A matching, sophisticated shirt, obviously of wrinkle-free material had a crisp collar and matching pearl buttons on the sleeve. The clothes screamed success and professionalism, and were obviously not from the bargain rack.

     The woman for whom the clothes were being purchased was about my age, with hair dyed a honey blonde and a middle aged waist holding up a pair of jeans. What struck me most was her relationship with the woman standing next to her. The two of them were giggling conspiratorially, pointing at the clothes with a look of accomplishment, arms gently around each other’s waist. The other woman was much older, with similarly colored hair and body frame. They kissed lightly, among their smiles, and as they walked away with the precious bagged items, they seemed to bounce on air. It struck me that it was a daughter and her mother, with the mother buying her daughter some clothes for her work. As old as the first woman was, her mom still wanted to care for her and buy her the perfect clothes. It was probably a special occasion and they had the pleasure of shopping together to purchase the perfect gift, a joyful adventure for both mom and daughter.

     This scene ignited such an emotional flash back for me that I almost cried out. That could have been my mother and me if she was still alive. For my birthday, she would always take me shopping to buy two wonderful outfits that I would not have been able to afford otherwise. They would be in my perfect colors, and we wouldn’t care if they were on sale or not. We would go out to lunch at local restaurant and share a piece of cheesecake for dessert. It would be a special mother/daughter day, where my mom, eventually in a wheelchair as she aged, would still be my mom, maternally caring for my needs, an emotionally bonding experience for both of us.

     My mom passed away a few years ago. My heart is conflicted with joyous memories along with a deep sadness that hurts my heart. I sit here typing this with tears in my eyes, trying not to let them fall. Mother’s Day this year was especially meaningful. Only now, with her permanent etching upon my soul, do I really appreciate the things she did for me. I wish I could tell her I love her one more time…

 

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

With messy hair and an ear to ear grin

One of my favorite cartoons as a child was The Jetsons. The portrayal of the future was colorful and amazing; cars flew around in the air and people chatted to each other on videophones.  Contemplating the “picture” phone, I shuddered with dismay.  I would NEVER want to talk to anyone on such a device, picturing myself answering with my hair askew, clothes rumpled and dirty dishes in the sink in the background.  If and when it was invented I would never use it, thank you anyway.  My regular phone would do just fine!

Who could have imagined then that one day we would chat on videophones as a normal part of life.  The first time it became significant to me was when my daughter who is deaf went away to school. Using a video monitor, we could chat in American Sign Language, which is SUCH a visual language.  Not only are the hand gestures important, but this special language includes facial and body gestures. For instance, she could sign “school okay”, with a facial grimace and thumbs down sign or with a smile that indicated “okay” was synonymous with “good”. Not to mention the fact that ASL is a visual language that cannot be conducted on a regular phone, and regular mom/daughter conversations would have been impossible. With modern technology, she can call anyone anywhere and an interpreter on her screen would interpret her words for the hearing person she called and sign back what the other person said.  Several times she has ordered pizza from Dominoes in this way, pleased with herself for her independence. She has had the great fortune of using this method for telephone communication during her lifetime.  How much more difficult would it have been had she lived 10, 20 years ago.

The other wonderful advantage of video chatting is being able to be a grandmother to my California son’s 2-year-old daughter.  We have been visiting with her by phone since she was about 6 months old.  I’d sing nursery rhymes and Papa would pretend to tickle her belly.  We were there as she developed, rejoicing in each new little trick she’d learn. When we see them twice a year at Christmas and for her birthday in May, Lailya readily runs into our arms for hugs, sticking her belly out so Papa can tickle it and sitting on my lap so the 3 Little Pigs story can be told in person. After all, she KNEW us because we graced her living room for games and songs every Sunday evening.

With my son being so far away, these visits were also parental support for him. He was very proud to be able to share his daughter with us, beaming with happiness when we told him what a great job he was doing as a dad and what an amazing daughter he has. He would ask our opinion on toilet training and how to get her to eat more vegetables. We were a family and chatting with him made the distance between us immaterial.

Now when I think back to the Jetsons and my aversion to using a video phone because my hair might be messy, I laugh.  Yes, this past Sunday, while singing, talking and laughing with Lailya and Francis, my hair WAS a mess.  I also had on a bathrobe because it was almost time for bed, (due to the 3-hour time difference between us.) With an ear to ear grin, enjoying our granddaughter’s antics, suddenly what we looked like wasn’t important at all.

The Hospital Vacation

An unexpected vacation came my way last week via a trip to the local emergency room when I experienced severe pain radiating from my shoulder down to the tips of my puffy fingers. The ER receptionist immediately had me whisked away in a wheelchair for a cardiac work-up, (not a recommended way to beat the line, but it was nice not have to wait!) The orderly swished me by all the cubicles so fast I did not have time to be nosy and glance in to see what everyone else’s commotion was about. The thing about the ER is that is houses REAL people with all their unglamorous appeal. No high heels or make-up. Unruly hair which obviously had not seen a comb in some time. Morning crustiness still in the eyes, line of drool down the side of the mouth. Bra-less, face contorted into an ugly grimace of pain, posture slumped over..and that was just ME, I could only imagine what everyone else looked like!

Once admitted to the cardiac ward, the nurses got right to work hooking me up to all kinds of do dads and thing a ma jigs. Their cheerfulness belied the seriousness of their work. I was comforted not only by their reassurance but also by the toasty, warm blanket that soon enveloped my body. Once the morphine took away the pain, I was a happy camper and willing test participant. Wheee! Off with another orderly for another test. Lay still like a sardine in a tiny metal tube while it sounded like the room was crashing all around me? Piece of cake. Electrodes super glued to my breasts? No problem, I wasn’t using them anyway. X-rays this way and that? Show me how to pose. (Those 5 modeling classes I took as a gawky teen finally came in handy!) Then there was the added adventure of being maneuvered, gurney and all, back to my room, bumping in and out of the elevators, around other patients and gurneys, and trying to fit through slim doorways all the while piloted by friendly orderlies. It was reminiscent of trying to scooter through Disney World with my daughter last May, and I tried to hide my silly smile lest the orderly think I was not in my right mind. (And, yes, the morphine was still working.)

Once back in my room, taking my blood pressure and poking and prodding for blood tests and glucose monitoring became commonplace at any time of the day or night. What an amazing staff of nurses and CNAs whose job it was to wake me only to poke me with a needle to capture my blood, and to do it all pleasantly when I felt less than pleasant for them having to do it. Although I tried not to be too crabby at them, my roommates were often less inhibited and grumbling was commonplace. Still, the staff smiled and carried on with quiet reassurance, seemingly immune to the barrage of complaints.

The most exciting thing for me was “room service”. Yes, “room service”, just like in a fancy hotel! Armed with an actual menu, I called down to the kitchen and my custom order would find its way to my bedside table. How amazing! Being a person obsessed with food, this was the highlight of my vacation. (Well, that and not being home to have to clean my house.) I carefully selected each meal; scrumptious omelet with tomatoes and onions, muffins and fruit, macaroni and cheese and broccoli with custard pudding, pot roast with salad with cake for dessert! Yum! It all sounded as good as I am sure it tasted, IF I were ever able to eat it when it arrived! Unfortunately, my food delights were delivered while I was away for one test or another. Imagine…meals being interrupted by medical procedures! What kind of vacation is that? The nurses offered to heat it up for me or to get me something else, but this seemed to be a silly request with all the important medical stuff that they had to do. When they took their jobs, I am sure that “waitress” was not in the job description.

Fortunately, it was the kind of vacation where the primary focus was my health; where what was going on INSIDE my body was more important that what I put INTO my body. With the utmost professionalism, the staff were unwaveringly pleasant, reassuring and kind. My medical care was top notch, and I was soon sent on my way home with expert instructions for the next chapter in my medical care.

Nothing could beat my hospital “vacation”. Next time I really want something as frivolous as a hot meal, I will go to a restaurant!The

Crosswalks, people, CROSSWALKS!

 

My son, who lives and works in Silicon Valley, delights us in discussing the progress of Google’s “cars that drive themselves”, which can regularly be seen toting along the streets in his neighborhood. Being blind, he has a special interest in this new technology, (although UBER has provided a suitable stop gap in the meantime.) A report on the self-driving cars shows that in the history of trials, there have been 4 accidents; 3 were someone else’s fault and 1 was the car’s fault, but technically the car was right.  Because it had been programmed with the rules of the road, the car was following the law, but it was a law Californians routinely break and of which the programmed car had no knowledge. Currently, the Googlers are working on programming the car for these types of idiosyncrasies.

My car, which routinely FOLLOWS rules, almost caused an accident this morning when fellow Rhode Island drivers followed their own rule idiosyncrasies; IGNORING CROSSWALKS. Somehow it appears that most drivers think their CARS have the right of way and the white stripes on the ground are decorative, not meaningful.

A lovely, older woman, clinging to hold her coat shut against the frigid air, gray hair flailing about in the wind, was waiting on the curb in front of a crosswalk.  Drawn in at first by the sight of her, then by the crosswalk that loomed in front of her, I stopped my car. The car behind be, which had been tailgating, came within a hair’s breadth of hitting me, evidenced by the car’s screech and swerve up onto the curb, sounding it’s horn so loud I thought it was foggy and I was a boat in the bay. Once that car had settled with one wheel on the sidewalk, the startled woman boldly took a few tentative steps in front of my car to begin her crossing adventure. She stood in front of my car while 1,2,3,4,5,6,7,8 cars quickly passed by without pausing at all and the fog horn sounded again behind me. Finally, the 9^th car stopped after he had correctly slowed down seeing the crosswalk.  Looking over, I saw the driver smile and motion for the petrified woman to continue to cross.  She tentatively shuffled her little elderly feet in front of him. Coming from the other direction, and with advance observation of what was happening in front of them, the cars in the opposing 2 lanes stopped to allow her to successfully complete her daring adventure. She shuffled more quickly, head down, hair flying, coat flinging open. When she triumphantly stepped onto the sidewalk on the other side, my heart, which had sunk into my stomach, slowly rose to its normal position. On my way I went, encouraged on by the sound of the fog horn once again.

The near miss accident intrigued me.  Have I gone the way of the Google self-driving car which follows the law but can still cause an accident?  Or was everyone else who didn’t stop following the way of the recalculated Google self-driving car which make accommodations for laws which are routinely broken? Either way, my assumption was the driver-less car would have been more observant on obeying a law which allows a frail, grandmotherly type woman to live a few years longer by allowing her to cross the street safely.

 

 

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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