Posts tagged ‘adoption’

The Truth about Reactive Attachment Disorder

I witnessed a conversation with the sister of a boy who had been adopted at the age of 2 years old after being abused by his biological parents. As an adult “he has always been in trouble with the law and has been in jail.” Upon hearing this, a deep sorrow enveloped me. I have such empathy for that child, having three of my own adopted at a later age. It was with a sweet naiveté that I had them join our family, believing that love can cure all. Despite our family’s best efforts, love did NOT cure all. To pretend that it did does a disservice to all of those families living with similar children. As brightly as I may portray our family, (and they ARE wonderful children whom I have never regretted adopting,) they have serious disabilities when it comes to social norms. They have reactive attachment disorder.
To quote from Wikipedia, “RAD arises from a failure to form normal attachments to primary caregivers in early childhood. Such a failure could result from severe early experiences of neglect, abuse, abrupt separation from caregivers between the ages of six months and three years, frequent change of caregivers, or a lack of caregiver responsiveness to a child’s communicative efforts. The AACAP guidelines state that children with reactive attachment disorder are presumed to have grossly disturbed internal models for relating to others”
I have worked hard to form attachments to my three youngest children, and, while I like to think that I am a “normal” mom to them, I have to admit that they may have difficulty controlling lying without remorse, stealing just because they want something, or acting out if they do not “get their way”. My son who has autism and RAD has always acted out, kicking the occasional hole in the wall or breaking a window. Such behavior can be tolerated as a child, but when that child becomes a young adult, such behavior is considered “domestic abuse” and “vandalism”. My youngest daughter with RAD sometimes would see something she likes in Walmart and slip it into her pocket, thus necessitating a trip to the manager to give it back. I like to think that such life lessons have sunk in, but I cannot guarantee that, as a adult, she wouldn’t resume just taking things she wants. My kiddos with RAD are chronic liars. I can tell they are lying by the vast amount of details in their stories. They didn’t just lose a school book on the way home, a masked man followed them all the way home, hid out behind the maple tree, jumped out at them when a car drove by and stole their book to use as material to start their fire. Their stories, which they steadfastly stick with, are creative and imaginative and complete lies, and lying is a typical behavior of a child with RAD.
I am convinced that their brains are wired differently. As infants and toddlers, they were not able to form emotional attachments with caregivers in order to feel secure. When their little brains were forming, and those energy cells which would turn into concepts of how the world works, theirs determined they could not count on anyone but themselves. They can be self-centered, unfazed by conventional ideas of right and wrong, and often willing to do anything to get what they want.
Dealing with such children is a life long challenge. I have done a fair job of instilling right and wrong in my children, not because they really believe in right and wrong but because, by habit, that is how we behave in our family. Yes, they love me, but let another “parent” come by who offers them a kitten, and their love will quickly switch. (True story…my daughter almost went to live with a couple who promised her a kitten!) Having the social skills to have real friends eludes them. RAD is a devastating disability which affects all aspects of their lives.
My heart goes out to all of those children out there who were unloved in their early years. It is NOT something they can just “get over”. I see people on tv who are arrested for this and that, and I hear their stories. 9 times out of 10, they were abused or unloved as children. I am convinced the loss of that initial security forever causes a permanent rift in the psyche that is contrary to the “norm”. To expect them not to be affected is naive.
Consequentially, a large percentage of people in prison were abused or neglected as young children, and I grieve their loss of “normal” lives, forever damned to seclusion from society as the result of their initial inability to form secure relationships in a loving family.
I apologize…this post is so unlike me, but I felt the need to discuss the issue.
Please join me in listening to my favorite song by clicking on the “Song by JJ Heller”. It is a song that addresses this very issue with a love that I feel in my heart. I hope you feel it also…

If you have time, please listen to my favorite song, “Love Me”, by JJ Heller. I have included the words. It never ceases to bring tears to my eyes…

Song by JJ Heller

“Love Me”

He cries in the corner where nobody sees
He’s the kid with the story no one would believe
He prays every night, “Dear God won’t you please
Could you send someone here who will love me?”

Who will love me for me
Not for what I have done or what I will become
Who will love me for me
‘Cause nobody has shown me what love
What love really means

Her office is shrinking a little each day
She’s the woman whose husband has run away
She’ll go to the gym after working today
Maybe if she was thinner
Then he would’ve stayed
And she says:

Who will love me for me?
Not for what I have done or what I will become
Who will love me for me?
‘Cause nobody has shown me what love, what love really means

He’s waiting to die as he sits all alone
He’s a man in a cell who regrets what he’s done
He utters a cry from the depths of his soul
“Oh Lord, forgive me, I want to go home”

Then he heard a voice somewhere deep inside
And it said
“I know you’ve murdered and I know you’ve lied
I have watched you suffer all of your life
And now that you’ll listen, I’ll tell you that I…”

I will love you for you
Not for what you have done or what you will become
I will love you for you
I will give you the love
The love that you never knew

Please note: links to purchase my book:

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

Amazon The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Nook/Barns and Noble

For Sentimental, Sappy Souls

On Columbus Day, my husband and I spent a wonderful day just driving around and enjoying the autumn scenery. I don’t know about you, but I seem to have an unusual sensitivity to the beauty in nature, and was once again overwhelmed by the beauty of the bright white and yellow streaks of sun streaming down through the white puffy clouds. Such a sight always encourages me as if reinforcing the fact that yes, there are clouds, and yes there may be rain, but that sun is still up there in the sky, overseeing it all, just waiting to break through and make things better. As an added visual treat, the sun shone so brightly on the tapestry of peak autumn leaves: oranges, reds and yellows, that I felt a need to wear my sunglasses, but with them on I would not be able to fully appreciate the effect of the over-the-top, gasp inducing colors. No photo, piece of artwork or beautifully sung song could have replicated the intensity of happiness that brought tears to my eyes and joy to my heart.
My husband and I sat, holding hands as he drove. There was no need to say anything. We were at peace, pleased to have such a respite after a hectic week of raising children and dealing with problems. We were in our own beautiful bubble, cell phones turned off so as not to ruin the interlude. It was a wonderful day!
Upon pulling into the driveway of our home, I spotted the two small maple trees which Marie had planted a few years ago. She had excitedly dug them up when they were fragile saplings with broken branches, and planted one on each side of the driveway. She had added gravel at the base of each, and attached a tall, straight, thin stick to keep them growing upright. I don’t know why I hadn’t noticed them before. I had NOTICED them, of course, but I had never really SEEN them. They had grown to be about four feet tall, straight and strong. My breath stuck in my throat as the brilliant, bright yellow leaves danced happily in the gentle breeze. They were a growing metaphor for my daughter, blossoming and beautiful and holding the promise of a bright future in their little yellow leaves. Despite once being fragile and broken, they would grow tall and amazing and fit perfectly in this world, reassuring me that my daughter, who was also once fragile and broken, would grow tall and amazing and fit perfectly in this world.

Under the “Dome of Silence”

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I am really dating myself, but my favorite tv show to watch when I was a child was “Get Smart”, a spy spoof where Maxwell Smart comedically played an agent who always “got his man”, even when he didn’t know how he did it! I relate so well to Maxwell Smart and his “methods”, because my life is been pretty much the same!
But their infamous concept, the “Dome of Silence” flittered through my mind recently in an unpleasant way, a way that made me change my thoughts in a major way.
My daughter, Marie, who is deaf, has been hospitalized again. For parents of children with severe psychiatric disorders, y’all know that hospitalizations are a recurrent theme, no matter how well a child seems to be doing. Life with such a child is full of peaks and valleys, and sometimes the valleys need a tune up. As conscientious parents, we probably all play the same game…do we visit every day? Do we bring food and drinks? Games? Puzzles? In other words, do we turn each hospitalization into a reward for being there?
My brother’s schizophrenia emerged when he was just emerging himself into young adulthood at the age of 18. This was a surprise disability on top of his already existing developmental, vision and hearing disabilities. As my parents aged, he eventually lived in a wonderful group home, but HE also needed “tune ups” in a psychiatric hospital, generally after an incident where the aliens told him to walk ten miles to the train station, or throw himself against the wall as punishment for some unknown offense. These hospitalizations were regular, and each and every time my mom would visit every day, bringing with her his favorite desserts, or a milk shake or ice cream sundae. Her heart ached to see him in the hospital so often, so she would sit there for hours with him, holding his hand or rubbing his back. It made her feel better to visit with him, and it made him feel better also. In fact, it made him feel so much better that the frequency of his “tune ups” increased. I learned as a young adult that being in a psychiatric hospital should not be rewarded with food and puzzles, or even with visitation every day.
I have tempered my need to mother my daughter with the need not to make inpatient hospitalizations seem better than the residential school in which she lives. Following my own instincts, which were reinforced by Marie’s social worker and psychiatrist, I have limited my visits. Yesterday, however, I changed my mind.
The hospitals have all been wonderful at providing ASL interpreters for at least 12 hours a day, which facilitates her conversations with nurses, social workers, unit workers and her psychiatrist. Marie does not, however, want to utilize the interpreter in conversations with other children. She tries to fit in with them, but does not understand what they are saying or laughing at. Being somewhat paranoid, (aren’t all teenagers?) she suspects they are laughing at her. She tries to join in, and they may include her for a few minutes, but soon the conversation continues over her head, and the children are once again laughing and joking and not including her. As I was leaving yesterday I witnessed this happening, saw the look of sadness in Marie’s eyes and noticed that she was holding back tears so as not to further embarrass herself in front of the other children. She looked so alone, and in reality she was. The other children were under a “Dome of Silence”. She could see them talking, gesturing and laughing, but could not hear or understand what they were saying. I don’t know why this obscure reference came to mind, but it did, and the visualization of it has changed my way of thinking. I realized that her isolation from others trumps the need not to reward her for being in the hospital. Nothing in the hospital could be a reward for her, as she is not part of the community as she is in her school. If anything, one would think she would be so adverse to being in the hospital that she would do anything in her power not to be hospitalized. Ah, the irony of that nostalgic “Dome of Silence.” I think I will visit for a few hours today and bring her a milkshake. We will sit there and “talk” in ASL and I will hold her hand like my mother did with my brother. She will no longer be sad and isolated, at least not during my visit…

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To read more about our life, here is a link to my book:

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Link to the Readers Digest review of my book:  http://www.rd.com/recommends/what-to-read-after-a-hurricane/

I Thought It Was the End of the World…Really!

I led a very eclectic lifestyle when I was a child, traveling around the country with a vagabond family. It was a wonderful life, made all that more meaningful by a mother who possessed a natural spirituality. We may not have gone to church Sundays, but our life was naturally filled with the presence of God.

Because I feel that I know you all, I am going to share a personal, life altering childhood experience. We were camping high in the mountains, a favorite spot for my father because he could sit and look out over the valleys and little towns below. For him, it seemed to minimized the stressors of life. How could life be so bad when the people were the size of ants and the lakes the size of large drops of water? For whatever reason, he seemed to feel safe in the mountains Things were good. Things were peaceful. We were content.

One night while I was sleeping, I was awakened by an extremely loud, earth shattering noise. My body shook with such a ferocity I thought I was going to fall out of my top bunk. Although it was later determined to be a nearby bolt of lightning, I will never forget how I felt immediately when I woke up; I thought it was the end of the world! I thought life as we knew it was over. My immediate reaction was such profound joy and love that my heart wanted to burst with happiness. I was deeply disappointed when I found out it was only thunder, and not a joyous entrance into the world beyond and an opportunity to meet God.

As a child who had never read the Bible or been “religious”, in retrospect it is surprising that my first thought was not fear at the concept of the end of the world but joy! It was not something I had learned about in catechism, or had even thought of before. My first feeling was automatic and unbelievable happiness and love. And it is that feeling that I carry with me to this day. For I know that the heart of that child so many years ago experienced a true and prophetic revelation…that God lives in the hearts of all of us, we just don’t always see it. Wouldn’t the world be different if we all knew, beyond a shadow of a doubt, that a joyous eternity awaits us? I was so very fortunate to have learned that at an early age…

It was Like Playing Leap Frog, but I Didn’t Get to Leap!

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I just returned from a four hour trip that should have taken me only two hours.  The day started out wonderfully enough…I drove up to see Marie and take her fishing. Last week she had birthday money and we spent two hours perusing through Dick’s Sporting Goods to get EXACTLY the right fishing pole, strong fishing line, (in case she catches a shark or something similar,) bobbers, lures, hooks and pretend “bait”  (yeh…like worms are really green with black speckles…)  I am pretty naive when it comes to fishing;  we live on a pond with tons of fish, so therefore all bodies of water have fish.  Driving around Marie’s school, we settled on a nice fishing spot that had some large rocks for sitting and many trees for shade.  It turned out we didn’t need shade for long because it became overcast and VERY cloudy, then began to rain.  This didn’t phase Marie, who is known for 4 season, all weather fishing on our pond at home.  Although drenched, she patiently fished, changing bait and lures several times to try to attract the appropriate fish for the area.  Although no fish saw fit to chow down on her line, fun was had by all. She was convinced that the fish could look up through the water at her hulking body and swam in the other direction.  She vowed to next time dress in camouflage gear. (It was only later that I learned that that particular “lake” was actually the drinking water reservoir for the area…no fish…and I was darn lucky all she was using for bait was plastic worms and tin lures!  EWWWWW if it was real worms!))

After dropping Marie back off at school, it started to pour out.  My good ole van isn’t always so good. In fact, it has an electrical short whereby if it gets splashed with water, the engine shuts off.  (It’s one of those things I should have had fixed, but WHO has the TIME?) If the engine has a constant flow of gas, it works okay even if it is wet.  However, if it slows down and there is no gas getting to the engine AND it goes through a puddle, the engine just stops.  Fortunately, I can hear when it happens AND the car keeps rolling on, so I have time to pull over to the side of the road into the breakdown lane.  Being in rush hour traffic AND in a torrential downpour wrecked havoc on the ride home.  When stopped in traffic, I’d put the car in “neutral” to be able to give it gas, shifting to “drive” again once the traffic started to move.  Of course, this did not always work, and often the engine would shut off and I would have to pull over again.  Although the traffic was very slow moving, and as far as I could tell my pulling to the side of the road neither inconvenienced nor blocked anyone, it was amazing the number of cars that would lean on their horns at me.  If I were paranoid, I’d think they were upset…but instead I just smiled and waved. What nice, supportive drivers! Fortunately, the car always started up again, and I’d pull back out into traffic, doing the “neutral”/”drive” dance in hopes that it would keep running. It didn’t.  Time and time again, lengthening the drive home to four hours, I’d pull over to the side of the road, and cars would pass me.  It was like playing leap frog, but I never got a turn to leap…

I think I’ll make time to have the car fixed tomorrow…

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To read more about our life, here is a link to my book:

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Link to the Readers Digest review of my book:  http://www.rd.com/recommends/what-to-read-after-a-hurricane/

“It Smells Like Flowers and Sunshine”

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Working this summer running an educational/recreational program for kiddos with disabilities, I have been giving my good ole, 12 passenger van with a wheelchair lift a run for its money.  Surprisingly, despite numerous past mechanical difficulties, it has become a war horse for transporting us throughout the state to many wonderful adventures!  Because it is an industrial type van, it supplies the children with a lot of extra bounces, creaking, twists and turns.  (It is good thing they are all snapped down into booster seats and seat belts or by now I would have many little dents in the ceiling from their bouncing heads.)  They laugh and screech and go “weeeeeeeeee” as though they are on a ride at an amusement park. (I dare say, some of the children have never experienced such excitement…)

Over the weeks, I have become somewhat lax in van cleanliness…food wrappers, discarded art projects, broken recreational items (such as water guns and deflated balls,) and, EWWWWWW, old clothing left by the children, litter the floor.  I KNOW it is not proper, but, somehow, I am so busy with the program arrangements, supervising the children and driving them back and forth from their homes that at the end of my 12 hour day, that I am too pooped to do anything but sit in my lounge chair at home and watch Judge Judy.  I did the only thing I could do under the circumstances…purchased a couple of cute, little, purple, sweet smelling air fresheners for the van.

The day after this ingenious addition, the children filed on one by one for a trip to the aquarium.  Many of them commented on the smell, including one little girl who is blind who remarked “Do you have flowers in the van?  It smells beautiful, like flowers and sunshine!”  Thus proving to me that those Febreeze commercials where people are put into smelly, messy enclosures really DO smell only the Febreeze!

But She was Just Talking to Her!!

Indoor Water Parks 1

My job includes coordinating both a summer and winter program for children who are blind and visually impaired.  Last winter our lovely little group of about 40 went to an indoor water park during February vacation. If you have never been to an indoor (or outdoor for that matter) water park, you are missing one of life’s most wonderful playgrounds with water slides for all ages and skills. My age may indicate I could manage the “black hole”, but my skill kept me in the kiddie area!  (Ohhhhh!  The KITTIE pool again!!!)   Lounging in the lazy river on a double tube was a great way for staff to keep an eye on their child without letting them float gleefully away amongst the throng of people enjoying the current. A huge water playground centered the park, with slides and little pools and tons of water play, including the huge bucket of water atop the structure.  Every so often, the bucket, filled with water, would tip over and the torrential water would come gushing down, soaking everyone as though…..well….as though a bucket of water was dropped on their heads. Because my daughter, Marie, was also on school vacation and she joined us, I chose this particular water park because it featured a surfing pool.  Marie LOVES to “surf”, and on every other occasion we have come to this facility she has spent the entire day doing so, waiting, nose pressed against the glass, at the door first thing in the morning to come in, and being the last one for the security guard to throw out at closing time.going to this water park.

My big surprise was that Marie wanted to help out a group of younger girls who are blind.  The girls had staff who amicably allowed Marie to join their group. Despite the fact that she normally communicates in American Sign Language, she somehow managed to be very sociable and get along well with everyone. Having such a strong love for “surfing”, my expectation was she would help for a little while, but spend most of her time surfing. Surprise of surprises!!!!  My wonderful daughter did not choose her own activity, but spent all of her time with the little girls, helping them on the slides, doing the “sighted guide technique” to maneuver around the crowded park, showing them where the food was on their plates, (using the clock method,) and so forth.  Marie was having a grand time, and the girls all seemed to adore her.

On the last night of this program. Marie was seated in the booth at the restaurant with two of the girls and their staff.  One of the girls all of a sudden started waving her hands wildly in the air, not just once, but she kept going! Prone to seizures, the medic ran over and asked her if she was okay.  Of COURSE she was okay, she said, she was just TALKING to Marie!!  The laughter started at their table and  soon circled around the room as everyone realized what she had said…she was signing to her, of course!!!!

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To read more about our life, here is a link to my book:

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Link to the Readers Digest review of my book:  http://www.rd.com/recommends/what-to-read-after-a-hurricane/

If the Washing Machine Eats the Socks, What Eats the Silver Ware?

We all know the adage that the washing machine eats socks, which is why they never come out in pairs.  I long ago gave up trying to match them, just buying plain black socks for the boys and hoping they kind of match.  Marie gets to feel in fashion because all of her socks are multi-colored with frogs, kisses, stripes and cats.  If she can get one stripe from one sock to match the color on the cat, then she has found a fashionable match!

My concern is our silverware.  When we first had kids, we started out with a full Faber ware set.  As we saw pieces disappear one by one, we had to replace the set several times.  (We now have 72 knives and six spoons left.)  We do not know where the silverware goes.  As far as we are concerned, we eat with it, put it  in the sink, in the dishwasher to be washed and then back in the silverware drawer.  It is not rocket science.  It IS, however, way too complicated of a system to work in our house.  For some reason, our silverware disappears!  One would assume that the washing machine/sock theory would work for the dishwasher and disappearing silverware, but, alas, that is not the answer.

Theory #1 is that ours is the “HOUSE OF THE DISAPPEARING SILVERWARE”, oooooooooh!  We sometimes stay awake at night imagining the silverware whisking away into thin air with a whoooosh here and a whooosh there, kind of like witchcraft.  (In the interest of full disclosure, my husband is not bothered by this and he sleeps soundly…)  In the morning, half of the forks are gone!

Theory #2 is that, somehow, the children are involved.  Maybe they take a paper plate of left overs to their bedrooms and the silverware gets thrown away with the disposable dish. I shudder to think of this dirty, tragic end to our fine and selfless silverware. They died in the line of duty, never again seeing the light of day…

Whatever the reason, and whatever the consequences we have put upon our children for not taking care of the silverware, it continues to vanish for no apparent reason. Long ago we gave up our concept that the ideal home has good silverware with which to feed our perfect little family. Currently, spoons and forks from the Dollar Store fill our silverware drawer.  The frustration of having to constantly replace good silverware is gone.  With that stress no longer on my shoulders, the result is a cheaper, flimsier fork.  Eating steak, which would potentially bend our new utensils, it out of the question. It doesn’t matter anyway…hamburger is about all we can afford.  We are so lucky that our budget matches our utensil selection!  Our hospitality skills are also hampered by the antics of our kiddos, so we are also lucky that no one in their right mind would come to our house for dinner, thus sampling our pittance silverware.  Isn’t it great how life does have a way of turning out perfectly?  We are so lucky!

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Link to my book

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Link to the Readers Digest review of my book:  http://www.rd.com/recommends/what-to-read-after-a-hurricane/

Cracker Jacks and Oranges: My Kids Have the Best Dad!!!

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I suppose I am prejudiced, because I picked him, but Raymond is a wonderful dad!  I am sure when we dated and eventually married sooooooo many years ago, he didn’t have a clue about the roller coaster ride we were in for.  Sweet little marriage with 2.5 kids, growing old together, holding hands and walking on the beach….forget that!  As the parent or foster parent to 19 children, we have spent our marriage trying to have a positive, loving impact on the the children who have passed through or are in our lives.  I am the flakier, impulsive, eternally optimist slob.  He is the more grounded parent, making sure we have enough money to pay the bills, the house is somewhat clean, and the meals are on the table.  He is like a big kid himself with the children…enjoying playing with them and gently bopping them on their beans when he tells them he loves them. He despises the lime light, and has asked me never to write about him in my blog…hopefully he will forgive me for this post.

During a recent visit to the grocery store, he demonstrated everything I love about him:

The store we shopped at was one in which the discounts are great, but the ambiance is lacking, as are the shopping bags.  This was his domain, as he does the shopping weekly. This is his life…no frills, just get down to business.

Filling the cart with basics, (pasta, spaghetti sauce, bread, cheese, eggs and milk,) he purchased enough to provide for our home as well as for our 2 young adult children who are struggling financially. Because I do not generally go grocery shopping with him, I did not know he did that. His sense of support for his children extends into adulthood. Even though they are out of the house, he is still their “go to” person for flat tires and a listening ear. When he listens, he takes things more serious than I do…for me, there is always a silver lining.  I will try to cheer my child up,  make her/him happy.  However, sometimes children just want to bitch that sometimes life just SUCKS!  He listens, commiserates, and gives them that affirmation.

Because he was shopping with a budgeted amount,  I was playfully reprimanded more than once for putting something in the cart that was not absolutely necessary.  However, he DID justify the expense to put in one special thing for each of our children; Cracker Jacks for Steven, fresh oranges for Dinora,  pasta salad mix for Angel and Lay’s Salt and Vinegar chips for me to bring on the weekend visit with Marie. Most importantly, while getting in line at the cash register, he reached over into a bucket of flower bouquets and spent time picking out the best one for me.  (Yes, he DOES buy me flower every week.)  Practical, loving and romantic.  Isn’t he great?

After filling our cart at the grocery store, despite a long line at the cash register, Raymond was patient.  So patient, in fact, that he let a woman with only a few items pass in front of him.  Smiling, he said “Go ahead of me, please. I’m in no hurry”.  He chatted with the cashier, expressing genuine interest, and he assisted an elderly woman in carrying her groceries to the car. He cares about others, strangers, anyone in need. Is it any wonder he has been a great father to our children?

Any set of parents will experience difficulties of varying degrees.  Raising children with disabilities magnifies those difficulties.  It is a huge financial strain, and any thought of retiring and spending our days walking on the beach holding hands is for naught.  Potential retirement savings have been spent on the care of our children, funding therapists who do not take our insurance, taking time out of work when they are hospitalized, transportation to hospitals and therapists out of state, and other expenses many parents would never dream of having. Quality time between Raymond and myself can’t be spontaneous, but needs to be scheduled. (Rest assured that romance is alive and well with us!) Family and friends are often not our best cheerleaders. (Is that a polite way to put it?)  The challenges have been huge, but Raymond’s support has never been greater.  He has rolled with the punches, as though having a screaming child rescued by paramedics from the side of ferris wheel during a PTSD episode, having a child with twelve personalities (and trying to get along with all twelve), spending the whole day at Disney World in a quiet cove of trees while our son who is autistic collects bugs and worms, never knowing whether to buy girl clothes or boy clothes for your daughter are normal parts of parenthood. It’s is just normal family life to him. And I thank GOD for that…because I could never do this alone…

 

 

 

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To read more about our life, here is a link to my book:

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Link to the Readers Digest review of my book:  http://www.rd.com/recommends/what-to-read-after-a-hurricane/

Miracle of Miracles: Turtle Tanks and Pony Tails

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My life raising kiddos has been full of excitement, as well as challenges. Steven has been my most difficult child to raise. The 7th child born to a woman who was mentally ill and addicted to crack cocaine and heroin, we took Steven home from the neonatal unit as soon as he was able to be released.  He was unbelievably “messed up”.  (Don’t you just love my knowledge of medical terms?)  He cried constantly, his whole body twitching.  Once I learned to swaddle him tightly in a baby blanket, keep the room dark, and talk in a whisper, he could tolerate my presence.  To touch him lightly would make him scream in pain, but cuddling him strongly, the deep pressure somehow calmed him.

Whether due to the drug exposure, or just because his birth mom was mentally ill, Steven exhibited extreme symptoms of ADHD, autism, bi-polar disorder, sensory integration deficit, obsessive compulsive disorder,severe anxiety disorder and learning disabilities.   (The whole concept of “diagnosis” is fraught with contradictions in my mind, as the “diagnosis” with which he was labeled were arbitrary, useless except for the benefit of getting special education services. We were fortunate to find a psychiatrist with vast knowledge of children born addicted to drugs, and he became our mentor.  Like myself, he does not not believe in labels, but in treating the symptoms.)

Steven has led an interesting life.  With his Asperger’s-like super knowledge of reptiles, and an uncanny natural love for children, he has shined in these areas.  He would be fascinated with the foster babies in our house, and his most favorite activity was sitting in the rocking chair by my side and rocking a little one.  He is, however,  unable to understand the concept of money, wear shirts with tags in them,  eat textured foods or adapt to an unexpected change in his schedule.  A strict, structured environment and predictable schedule has been the key to helping him manage every day life.

As any parent, I have thought a lot about his future and how he could possibly survive as an adult…

Then, a miracle happened…he found the perfect girlfriend to love him! Wonder of wonders!  Joy of joys!  I never thought is was possible, but the adage “there is someone for everyone” is true in his case!

Wonderfully patient Alexandra loves to keep everything controlled.  Where other young men would go running in the other direction at the sight of a young woman in strict control, for Steven, it was just what he needed!  She manages their time, his money, and their life together with strict precision.  JUST WHAT HE NEEDED!   They also have similar interests in reptiles, with Steven using his vast knowledge to ensure the safe upbringing of their many “pets”; three turtles in a tank, (recently caught in the lake behind our house, during one of their day long fishing adventures,) a small snake, a Chameleon and two lizards.  They are affectionate with each other, with Steven smiling brightly as she gives him deep bear hugs. The icing on the cake, as far as both of them are concerned, is her young daughter.  Again, where other young men would go running for cover, Steven goes running towards her sweet three year old daughter! He adores her!  This very large, 6 foot talk, husky, bi-racial, often scary looking young man who has an aversion to shaving, is like a loving angel with her daughter! He gently holds her hand to guide her when they are walking.  He plays Shutes and Ladders and Go Fish with her. He helps her pick out her clothes, (shirts without tags, of course!) Most amazingly, he has become her hair stylist, putting her hair up in braids and pony tails.  She loves showing off her new hair styles, proudly telling everyone that STEVEN did it, as they both stand there and beam happily!  She needed a dad to love, and Steven needed a family of his own. He adores Alexandra and she has a huge calming affect on him. And he has such a natural caring for children, and for Emily in particular, that it melts my heart every time I see the three of them together.  He LOVES them…an emotion I once thought he would never feel…as a boyfriend, (husband?), and father. Yes, he has found comfort in his own family…and has a content, structured, “normal” life.  Isn’t that amazing?????  Miracle of miracles!!

Is there no greater joy as a parent than seeing your child happy as an adult? Especially when you thought that may never happen…

 

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To read about Steven’s early childhood, here is a link to my book:

https://itunes.apple.com/us/book/the-apple-tree/id538572206?mt=11

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane

Link to the Readers Digest review of my book:  http://www.rd.com/recommends/what-to-read-after-a-hurricane/

Also, for just the cost of transportation, I am available to do presentations for your groups.   I can be funny on serious subjects…

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