Posts tagged ‘adoption’

Mother’s Day and Delayed Rewards

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Mother’s Day is a wonderful time to appreciate moms, step-moms, birth moms, adoptive moms, wanna be moms and women who love children. Bless you for making a difference in a child’s life! Don’t you get joy from seeing the joy in a laughing child, the shy smile of a child with twinkling eyes, and the serene look on their faces when they are sleeping?  Ahhhhhh……..what sweet little rewards of being with a child…

Most of us know, however, that it is VERY difficult to be a mom and sometimes the REAL rewards are far apart….

When my son Steven was in nursery school, it was a real challenge because of his autistic and ADHD problems. He had been born addicted to cocaine and heroine and his nervous system was “messed up” (my professional diagnosis.) Bringing him was a real challenge as he would kick and scream and cry, yet I did it because he could not hide out safely at home for his entire life with me vacuuming around him. At first, he would  spend most of the time in school hiding out in the “quiet tent”, playing with his plastic reptiles, sometimes soaking in the information from the teacher. Eventually, he sauntered out of his safe space to see what was going on.  He did not join the other children, but he was with them…a huge improvement.  Eventually, nursery school became normalized for him; part of his routine.  He would come home with his little projects; a paper flower, a painted snake, a play dough alligator.  I had learned not to make a “fuss” over these things, but to quietly tell him they were wonderful while his head dropped to his chest, eyes closed.  (He was not a child who could tolerate excitement of any kind.)  He survived two years in that classroom, and I wondered how he would act on “graduation day”, a celebration seemingly out of his tolerance level.  All of the children stood there in their little paper graduation caps, tassels dangling in front of their noses so they had to keep blowing them away.  All of the children except Steven.  The children sang a song, and thanked their moms and generally wowed the crowd with their antics.  All of the children except Steven.  The children walked in a nice, straight line to get their nursery school diplomas; all except Steven.  When all but one diploma had been handed out, the teacher walked over to where Steven was hiding under a chair, butt facing outwards. (If I had been smart, I would have sewed a smiley face on the butt of his pants, but, alas, I had been unrealistically hoping that he would join the other children in the graduation ceremony.)  The teacher bent down with the document and Steven’s  little hand reached out to grab it.  He quickly pulled the diploma out of sight.  Calm and cool under the seat, he had made it! Steven had graduated from nursery school without a tantrum, yelling or screaming.  He graduated in the manner he felt most comfortable, but graduate he did!  What a reward that was for me; I was a proud mother, indeed!

Diagnosed in elementary school with Dissociative Identity Disorder, Angel, has been very carefully placed in specialized classrooms.  Although intelligent and able to do grade level work, he frequently changes “parts”, (his word for his alternate personalities.)  His teachers and teacher aids, bless their souls, understand him well, and manage to educate him, even if it means repeating the same lesson because a different “part” was out that day, or giving his the test over because the “part” that studied for the test is not the “part” that took the test!  He has a baby part which necessitates him to just “veg out” in a large mushroom chair.  On those days, nothing was learned.  His condition has been kept top secret and no unnecessary teachers or others in the school know about it. Fortunately, he has been living a very “normal” life.  I have found one surprising benefit…he has a “Game Show Host” part.  I work with a recreational group of adults with disabilities, and every now and then we play Bingo or Family Feud. Angel, as have all of my children, regularly comes with me.  One day, he asked to be the moderator for Family Feud and his “performance” was beyond hilarious.  Usually a reserved child with groups, all of a sudden he channeled Richard Dawson! He went down the rows of “contestants”, gave each of them a peck on the cheek, and, while holding their hands in his, asked their names and a little about themselves.  The older women, who probably have not had much attention in their lives, giggled and smiled and blushed.  Then, Angel read each question with gusto, and made a “ding” noise when they got it right, and a loud buzzer noise if they got it wrong.  It was sooooooooooo funny because it was so out of character of the Angel that they knew.  This group of adult with disabilities, many of whom live alone on a minimum income with this once a week outing their only time out of their houses, were laughing hysterically that evening. Ever since then, they look forward to Family Feud and “Gameshow Host” Angel! What a reward for me to see Angel’s  give such joy to these wonderful people!

As a graduation present, my daughter, Dinora, and I took a trip back to her birth country in Guatemala.  She had done fundraising to assist with the opening of a soup kitchen in Antigua, and we were there for “opening day”.  We went shopping that morning, taking a little “putt putt” (2 wheeled open air taxi) into the village, giggling all the way as it bounced along. We bought flowers of all bright shapes and sizes, which stuck out of the putt putt on the way back, narrowly bopping passers by on the head. We spread the flowers out in front of  the  alter where a mass was to be said in honor of the opening of the facility. An overflowing crowd of people filled the make-shift pews, and it was a beautiful, emotional mass. Even though it was all in Spanish I seemed to understand every word, and I could certainly feel the emotion in the songs which the Indigenous Guatemalans sang.  After mass, people lined up for the food in their brightly colored clothing. There was my daughter, a young adult, behind the counter, dark hair pulled back into a pony tail, serving food with a beaming smile on her face showing dimples I never knew she had, (or perhaps she had never smiled so brightly.)  She was old enough and cared enough to give back something and help “her people” as she called them. I will never forget the sight of her…sweat on her brow, wiping her hands on her apron, making pleasant conversation in Spanish while smiling that amazing smile…   How could that sight NOT be a reward for a mom after years of raising a difficult teen?

Raising Marie has been the most difficult because of her many serious challenges.  When she came to us, she was street smart at the age of seven.(See post “All She did Was Scream and Say No! No! No!) She had no thought of danger and no social skills.  Although this may sound silly, one of my concerns was the fact that she would litter.  Get a drink; throw the bottle on the ground.  Have a piece of gum; throw the wrapper on the ground. Popsicle; stick thrown in the grass.    Repeatedly, I would have her pick it up and throw it away, explaining that we don’t litter in our family.  Marie could not have cared less…she did not want to be in our family anyway…  It took many months with us before she learned not to litter.  That’s why it shocked me when we were at the mall one day and she casually flicked the paper from her straw onto the ground.  My eyes widened, and just as I was about to ask her to pick it up, she bent down and picked it up, signing to me “I was just teasing you!  I know we don’t litter in this family!”  What a reward it was to hear her say that!  Finally, she felt part of our family!

My most favorite reward I saved for last.  For all of you parents, especially parents with children with disabilities, I will share that there has been no greater reward in my life than seeing my son, Francis, become a successful adult. Despite being legally blind, he has a college degree, is very successful in a job which he loves and through which he is benefitting others, and he recently married a great woman who not only loves him for the wonderful person that he is, but can also drive a car so he won’t have to take public transit to work any more!  There IS no greater reward for a parent; to know that the problems, fun, hard work, love, difficulties and dispersed joys of childhood have come together in a positive way. My son has officially “made it” to adulthood.  Now he can look forward to the rewards he will experience in raising his own children. Then I get the extra rewards of grandchildren!

To all of you mothers and others out there, Happy Mother’s Day!  Beyond the handmade cards, the flowers, the breakfasts and dinners out, and the gifts of the day, so many more rewards await you.  Sometimes you just have to be patient…

Another Daughter to Celebrate!!

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For those who know me, you may be sure that I am referencing a new foster or adoptive child. Not this time! This time, my new daughter is my son, Francis’, new wife.  She is wonderful and sweet and recently blew me away with the Mother’s Day Card she sent.  Separate from my son’s, she sent a beautifully designed Papyrus’ Mother’s Day Card with 3-D flowers and a lot of sentiment.  But the sentiment that was most important was what she wrote inside; “Thank you for being such a great mom and raising such a wonderful son!”  Isn’t it thoughtful?  I now officially have another “daughter” and she’s all grown up.  I didn’t have to  do a thing…

Easter reminds me of the Easter Bunny and the Easter Bunny reminds me of Santa…

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Easter.  Ham.  Easter Eggs.  Jelly Beans.  Marshmallow peeps.  Chocolate Easter Bunnies, (see picture.) AND the EASTER BUNNY!!

(Spoiler Alert:  Do not let anyone under the age of 7? 9? 12? read any further.)

 

I am sure that most of us of a Christian faith believed in the light, magical myths of the Easter Bunny, the Tooth Fairy, and Santa Claus.  Bah Humbug!

My realization that there was no Santa Claus happened on the day before Easter when I was seven years old.  Friends and I were playing hide and seek in our house, and my hiding space of choice was my mother’s closet.  I opened the door and plopped in…right on top of a cellophane wrapped Easter basket!  I could feel the jelly beans fall out, trickling down my legs, and the weight of my body squishing the basket with a sickening sound.  As the marshmallow peeps were flattened, my childhood fantasies vanished before my eyes!  It was only reasonable to assume if my mom pretended to be the Easter Bunny, then the Tooth Fairy and Santa Claus were also non-existent.

This was actually a good realization for me.  For many years I had questioned Santa’s fairness.  If he was omnipresent, then how did he not know what I wanted to Christmas?  Even when I sat on his lap and told him…repeatedly…and wrote letters…repeatedly…he still did not bring me that all important, desperately desired, Barbie Doll for which I had asked. The Santa who came to my house had always disappointed me.  Having parents who were obsessively frugal, Santa would bring me unexciting gifts…a new toothbrush, a t-shirt, hair ribbons, and small bottles of shampoo (which I later learned came from the times my father traveled for work and stayed in hotels.) One year I even got 3 pairs of underwear that were much too big, but, judging from the price tag which Santa had neglected to remove, they were on sale for an unbelievably low price!   As a child, I could never understand why my friends and classmates received wonderful gifts of not only Barbie Dolls, but Barbie houses, Barbie cars and tons of Barbie accessories.  They would receive many, and I longed to own just one… but it was not meant to be.  When playing with my friends, they were always kind enough to share “Midge”, Barbie’s “best friend”.  While I appreciated this, I still felt resentful of their good fortune.

It wasn’t until I realized that Santa Claus did not exist that I understood that my parents had purchased all of those “gifts”.  As my childhood revolved around my dad’s “crazy” obsessions, I suddenly understood the significance of the gifts.  It wasn’t that Santa didn’t love me, or that I was somehow less worthy than my friends, or even because my good behavior wasn’t appreciated, it was because our family life was very different than most other families. And I took some solace in the fact that my dad, on his work trips, was thinking of me when he brought home the shampoos.

The whole concept of “Santa” has been a difficult one with my children. My oldest son, Francis, who is blind, hated the thought of having a stranger he could not see come into his house on Christmas Eve.  It was the one night of the year that I let him lock his bedroom door.

One year, I made the huge mistake of hiding the gift of a Little Mermaid comforter set underneath Dinora’s bed.  When she discovered it, she became hysterical, screaming that Santa had been in her room and he could have hurt her!  (She was going through a particularly rough phase with PTSD where she was seeing apparitions of “Bloody Mary”, so her sensitivities to having Santa in her room were heightened.)   She was only five at the time, and the only way I could calm her down was to admit that Santa did not exist, which caused her to cry even harder at the loss of this icon.

Steven, with his autistic tendencies, never did admit that Santa existed.  He was used to his strict schedule, and gifts from a stranger were not a welcome change.  He would wake  up every Christmas morning, walk by the Christmas tree under which the gifts sat, go down to the kitchen to grab breakfast, and sit in the family room to watch The Animal Planet on television.  It was his familiar routine…he never did acknowledge or look at his gifts. (In fact, to this day I have the SAME bag of gifts.  I bring them out every Christmas Eve, and pack them up every Christmas Day, only to be brought out again the following Christmas.  It is very selfish to say, but I have saved a LOT of money by not buying him gifts!)

Angel, my son with Dissociative Identity Disorder, (multiple personality disorder) had a great time each year developing his very eclectic request for gifts to satisfy his many “parts”, male, female, baby, toddler and his appropriate age.  I am sure that not many other boys asked for a complete manicure set along with baby rattles, Superman and Spiderman toys, and a complete bow and arrow set, (don’t ask…)  The problem that developed was that Angel had finally begun to trust me, a conviction he had previously  not held in his four other foster placements. Everyone else had lied to him and let him down.  But here he was in our family with a family he could finally trust, a family that would not lie to him, a family in which he felt safe.  When he found out that Santa Claus was a lie, he felt devastated, furious, betrayed, conned, tricked and misled.  This lie has left an indelible mark on his life, one which he continues to discuss with a counselor.  Every single time I have gone into a therapy session with him, the fact that I am a liar comes up, and that lie is always about Santa Claus. While it is easy for us to say “just get over it”, for him, it has been impossible.   If only I knew then what I know now, I would have done things very differently.

Marie, I am embarrassed to admit, was a young teenager who STILL believed in Santa Claus.  Learning from my experience with Angel, I have never perpetuated this myth on her, but she came to live with us with this belief.   Because Marie is deaf and developmentally delayed, she had few opportunities to “heard” or learn that Santa is not real. This became very apparent to me last Christmas.  On Christmas Eve I put out the individual bags of gifts from “Santa”, which included one expensive item for each child, (a DVD player, Gameboy, camera and so forth.)   On Christmas morning, Marie woke up before all of us and deftly went through the bags, taking out all of the expensive items and putting them in her bag, leaving the other children with only minor items.  She excitedly showed me the wonderful bag of gifts Santa had brought; HER gifts, along with the valuable gifts from everyone else’s bag.  I was mortified to think she would be so selfish, and I told her so!  I told her that there was no Santa Claus and that I had bought the items and they were not all for her.  She tried in vain to argue with me that Santa left them all to her because she had been good, but both of us knew better…

So, this has been a long winded way of saying I DISLIKE SANTA!!!  While he may be a wonderful myth to many, for me and my children, he has been nothing but trouble. BAH HUMBUG!!!!!

The Easter Bunny?  Hey, SHE’S okay…

 

 

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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/

 

Sanitizer, Angry Birds, Locked Doors and Singing Toilets…What Do These Things Have in Common?

What do these things have in common?  They are “tools of the trade” for my daughter, the mother of a delightful two and a half year old!

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Things have greatly changed since my children were toddlers.  I am fortunate I never had to carry babies around in those heavy seats. I would not have been able to have more than one baby at a time, and I am sure I would carry it with 2 arms wrapped around it lest I drop it.  For the child’s own safety due to my clumsiness, I probably would have stayed home all the time! Our car seats stayed in the car and the babies and toddlers went straight into the umbrella stroller when we were out.  It was easy.  They could see the world, and my hands were free. Using the stroller also had the wonderful advantage in that when clothes shopping, they could be hung on the back of the stroller.  I had to be careful on clearance day, though, lest the weight of the clothing supersede the weight of the particular child in the stroller.  While I did misjudge several times, the stroller and the child would just fall back onto a nice, soft pile of clothing. I have such empathy for parents lugging the infant in the infant seat.  They look sooooooo heavy!

My daughter, Dinora, has child proof locks on her cupboard doors.  What a great idea!!!  I used to keep the poisonous soaps, sprays and cleaners on top of my refrigerator.  They were safe there, at least until Steven began to climb like a monkey!  Whoever thought of the lock on the cupboard doors was a genius!  Unfortunately, I am not genius level.  When I babysit for my grandson, I cannot figure out how to open the darn locks!  It appears that you have to use 2 hands to do so and my hands do not cooperate with each other.  During my futile attempts, my grandson stands there crying for his macaroni and cheese for supper, and I can’t get in the cupboard to get the box!  Those locks are childproof and grandmother proof! He doesn’t really mind, though, as he much prefers the pizza I order instead.

The other amazing “new invention” is a toilet that makes music when you pee in it!  (I am, of course, talking about a toddler potty.)  What a wonderful motivator for toilet training!  It is certainly be healthier than the M&Ms I used to give, and everyone within earshot can hear the delightful music and cheer the performer on!  The only downside leads to my next observation about toddlers these days; my daughter will need to get a different potty if her next child is a girl, who wouldn’t dream of peeing in a Superman potty.  With parents knowing before hand if they are having a boy or a girl, baby items now seem to be all girly or all masculine, with little in between, unlike in “my days” when babies wore a lot of green or yellow which would suffice for either.  I have never seen so many princesses and action heroes in my life! So much for sexism, I guess…

Imagine my surprise when my grandson climbed in my lap carrying an IPad and started to play a game of Angry Birds.  At TWO and a HALF years old he was independently using a computer!  But ANGRY BIRDS?He was lopping these little birds through the air to their deaths, feathers flying everywhere.  And giggling! This must be the training game for all of the fighting and war games that will come when he is older.

A final reminder of how much things have changed happened when Dinora, my grandson and I went out to eat breakfast in a restaurant.  While he played with child aps on the IPad, we had a lovely adult conversation with fussy interruptions.  (There were times when raising young ones that I would have died just to be able to drink a hot cup of tea without an interruption.)  At the completion of this wonderfully enjoyable meal, my grandson, whose speech is somewhat delayed, managed to ask his mom for some “sanitizer”.  I almost flew off my chair! SANITIZER?  What a word for a 2 year old! He dutifully put out his hands and she dutifully squirted the sanitizer, a beautiful fragrance of lilacs and honey. (Who comes UP with these combinations?)

Things are certainly different these days, with computer aps for toddlers, musical potties,  disposable training pants and bibs, sippy cups in all shapes and sizes, locked cupboard doors, and super hero and princess everything (sheets, toys, cups, dishes, silverware, hairbrushes, toothbrushes, shirts, pants, socks, shoes…you get the idea.) With the exception of having to tote an infant around in a car seat instead of in an umbrella stroller, these days of raising children seem like a lot of fun!  (Maybe it’s time for me to foster a few more…)

My husband must be a mind reader.  I just heard him faint…

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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/

A Miracle on St. Patrick’s Day!

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Okay, so the picture above is unflattering, blurry and goofy.  But do you see the miracle?  My daughter, a TEENAGER, for whom Reactive Attachment Disorder has been a major diagnosis, is willingly KISSING me!!!!! It has to be a miracle!  And my heart is happy and full on this Saint Patrick’s Day…

 

 

 

 

 

 

 

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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/

“All she does is screech and say No! No! No!”

 

The above description fit me perfectly.

Yes, me… perfectly.

Marie came to live with us at the age of 6.  She had been picked up off the street at 4 in the morning, barefoot, in her underwear, looking for food.  We took her in as an emergency foster placement because I knew American Sign Language and Marie was deaf. She looked like a wild animal…disheveled, matted hair, flaming eyes of distrust, so filthy everywhere that even an hour in the tub did not wash off all the grime.  Her teeth were dingy yellow, and her body was emaciated.  Being the “good” middle class mother that I was, I cleaned her as best I could and then I took her to buy some clothes.

In the store, she immediately disappeared.  I impulsively called her name, (as though she could hear me.)  When I finally found her, she was in the candy aisle, shoving candy bars into the pocket of her pants.  I screamed,  “No! No! No!”  She looked at me and ran in the other direction.  I finally tracked her down in the pet aisle, just as she was about to open the cage to the hamsters.  I screeched and said “No! No! No!”, and proceeded to grab her, pick her up, empty the candy bars in her pocket, and tote her back to the car without buying anything. If I thought this would teach her a lesson, it did not.  She was not used to buying anything, so she could not appreciate something she never had.

We ate out for lunch at McDonald’s.  Marie ate her sandwich and drank her milk and threw the wrapper and container on the floor.  No! No! No!

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The next day I gave her a stern talking to (“signing to?)  and told her that we were going shopping for clothes and that she needed to stay with me. As though THAT was going to work!  As soon as we got into the mall, a place she obviously had never seen before, she skirted UP the DOWN escalator, laughing with glee.  Mortified, I screamed and said No! No! No!  and then watched in horror as she slid down the banister of the escalator.  Big scream! No! No! No!  Home we went. 

Once at home, she got an orange to eat.  She grabbed the butcher knife to cut it and I screamed and caught her hand just as it was about to demolish the orange. No! No! No!

The next day we were going to take a walk to the library.  She broke free from the grip I had on her hand, and ran across 4 lanes of traffic. Scream! No! No! No!

Later in the evening, while watching television, Marie climbed onto my husband’s lap, where she attempted to rub his “private parts” and kiss him.  SUPER BIG SCREECH!  No!  No! No! Oh!  This child was so “bad”!  WHAT was I going to do with her?

At the end of the week, I went to Marie’s school where she was part of a dance performance.  I was glad to be able to be there, as her birth mother had never been seen at the school before.  I watched with pride as she danced and twirled, often sneaking a peak at me to see if I was looking.  When the dance was over, I saw her talking (signing) with another student who commented that Marie had a new mom, and how did she like her? Marie looked over at me for a minute and crumpled her nose, telling her that all I ever do is scream and say No! No! No! I was shocked.  I had never thought of it before, but she was right!  I was so busy chasing and correcting her that it would seem like all I did was scold her.  And what was I scolding her for?  For what I, as a middle class mother, think is wrong.  I had never taken into account that Marie had been raised to do all of those things…to steal food, to take what she wanted from stores, to litter, to be sexually promiscuous (at the age of SIX!) and to have no worries about safety, thinking she was invincible.  This young child, who had lived on the streets and managed to survive without any parental care, just parental abuse…WAS invincible! She did what she needed to survive.

I was so embarrassed. Embarrassed because I was judging her by my standards and not stopping to think of what her standards were.  I vowed never to scream No! No! No! again, but to explain things in a loving manner to her.

We do not steal.  If you want something, I can probably buy it for you.

We do not run into streets with cars, use butcher knives, or slide down escalators.  It is not safe.

We do not just throw garbage on the ground, but in our family we pick it up and put it in a garbage can.

And, most of all, there is no need to make money by being “friendly to men”.   We have plenty of money so you don’t have to do that.  And it is not fair that you had to do that instead of just being a little girl. And you never have to do that again.

Marie did not change overnight, but each time she would fall back onto old habits such as stealing or being unsafe, I would lovingly explain why she no longer had to do that.  She had a family that loved her and it was our job to keep her safe.

Then there was the time when, walking in the mall with a soft drink in her hand, she unwrapped the straw and threw the paper on the ground. My eyes widened, and she laughed when she saw my reaction.  “I was just teasing you” she signed.  “I know I don’t litter in this family….” 

No more screaming from me…

 

 

Link to my book  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 Have Raised My Children Right in The Most Important Area

I am sure that every parent questions how they have raised their children. I know I have.  I have not been strict enough in making them eat all of their vegetables and clean their rooms, (mainly because I don’t eat all of my vegetables and clean my room.) I know to some people  this is a major parenting faux pas.  However, I have raised my children right in the most important area…caring for others.

I volunteer with a recreational group of adults with and without disabilities.  We have a bowling league, then go out to dinner together, then have an activity at night, such as Bingo, Family Feud, or a visiting musician.  All of my children have come with me to this group,  starting with Francis when he was a baby and the group purchased a portable crib so I could bring him camping with us.  My children have been raised socializing with people with disabilities so that any disability is not knew to them.

Angel, my son with Dissociative Identity Disorder, has been my latest child to attend with me.  One of his “peeps” (as his calls his “parts’) I call the Game Show Host.  Angel is the one who calls the numbers for Bingo, or reads the questions for Family Feud.  He is hilariously similar to a game show host, right down to kissing the female “contestants” during a game of Family Feud. From the minute he starts an activity to the minute he finishes, we are all in stitches laughing.  Silly laughing.  Innocent laughing.  Heart beating fast with cheeks that hurt from laughing laughing. He is terrific, and I am so proud that he has learned to manage his disability in order to make others happy.

The happiest moment of all happened on Christmas Day.  All of our family festivities are on Christmas even, and Christmas Day is always a lazy one for us.  In fact, the children and I usually go to the movies.  Angel asked if it was okay if he invited a friend to the movies, and of course I said yes.  When we got there,  waiting for us expectantly, was Lisa, a 65 year old woman with a disability; the “friend” which he had invited.  She was dressed for Christmas…Christmas sweater, Santa Claus earrings, a Santa Hat and bright red lipstick. She was glowing as she hugged us all.  It seems that she has no family and had sat in her apartment alone for Christmas Eve.  Somehow Angel knew this, prompting his request that she come with us on Christmas Day.

We all laughed at the funny movie, and enjoyed a large popcorn, (mmmmmmm…movie theater fake butter popcorn!)  After the movie, we went out to a Chinese restaurant for dinner. (Duh!  Chinese restaurants are open…)  We had a lively conversation about anything and everything funny, and she beamed the whole time.  When we left her outside at her car to go home, she burst into tears.  She thanked us profusely. She said she was so lonely at Christmas, when everyone else had a family, that she had contemplated suicide because she had no one.  She said this was her best Christmas EVER!  Try as I might not to, tears slid down my cheek also.  Tears of sympathy for her and of pride for my son…a son who is seriously disabled himself, but who was still able to find the ability to care deeply for the feelings of this wonderful, lonely woman.

Yes, I have raised him right…

A Hug Award; My Kind of Award!

I am not one to generally accept awards.  I am pleased to receive nominations, but I do not generally post the award.  I strive to stay level headed and an every day person.  (Awards would tend to inflate my ego and I may start to sound “uppity”, which is not in my nature.)

However ,Michele Kearns who has the inspirational blog Joy Returns, nominated me for a very special award:

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The HUG Award© was initiated by Connie Wayne at A Hope for Today athttp://ahopefortoday.comwhich promotes hope, love, peace, equality, and unity for all people.

The HUG Award© is for people with an expectant desire for the world, for which they:  Hope for Love; Hope for Freedom; Hope for Peace; Hope for Equality; Hope for Unity; Hope for Joy and Happiness; Hope for Compassion and Mercy; Hope for Faith;Hope for Wholeness and Wellness; Hope for Prosperity; Hope for Ecological Preservation; Hope for Oneness

The HUG Award© recognizes and honors those who help keep hope alive in our current world, which is plagued by war, natural disasters, and economic recession.  They nurture hope, in any of the above areas (in italics),  by the work they do, or in their personal lives with things such as blogging, public speaking, charity work, etc.

The HUG Award© is for anyone, anywhere in the world, who meets the guidelines and wants to be nominated for the award. Please leave a comment on this page if you are interested in receiving this award, or if you would like to nominate someone else for the award.

The HUG Award© is for people who, without giving up or compromising their own religious, spiritual, or political beliefs, are able to nurture hope and respect the dignity of all people.

The HUG Award© is for those who, without bias or prejudice, use their resources and gifts to make the world a better place for everyone.

The HUG Award©is for people who have a hope or an expectant desire that the work or talents they use in things such as blogging, public speaking, charity work, etc., will make a positive impact on the world.

These people do not have to actively use the word “hope” in their work or creative talents.  They only need be conscious of their desire to make the world a better place for everyone.

These people use their available resources–a smile, a hug, a helping hand, a listening ear, a voice, time, money, possessions, education, personality, talent, websites and blogs—to make a positive impact on the world and make the world a better place to live.

The HUG Award© is not a website or blog award.  It can be given to people in your community, at your employment, at your place of worship, etc.  Please make sure they have a copy of these Guidelines, and please don’t forget to submit their names back to this site.

I am pleased to share this award with everyone who strives for peace and to make the world a better place.  Is it such an honor, and little ol’ me is humbled.

Lets Agree to Disagree…Mental Illness and Violence

I recently received a response from a blog colleague who’s beliefs are different than mine.  It is normal for people to have different views on things, and everyone’s views are welcome. This is my version of  agreeing to disagree…

Dear 5KWD, I wonder if you would have any insight on the following. After doing a smattering of research I learned that virtually every mass shooter on record was taking antidepressant psychiatric drugs when they “went off”. The news media and many posting here are examining the mental illness angle, but we know that depression, asbergers, etc, does not cause homicidal behavior. However, it seems very plausible to me that these FDA approved psychiatric drugs, which have known side effects, may be inducing this behavior. I think it’s the drugs, not the mental illness. This makes way more sense to me than the idea that sometimes formerly quiet, law-abiding people are randomly “going off” and shooting rooms full of children.  artandlifenotes.wordpress.com

 

I agree that every mass murderer may have been on antidepressants.  It would go along with my theory that they have underlying psychiatric conditions.  All of my adopted children are on psych meds.  My oldest daughter has attention deficit disorder.  Prior to medication, she couldn’t pay attention, she was flunking school, she couldn’t pay attention to read a book, and she developed sever anxiety over her inability to function “normally”.  Once on medication, (which includes an antidepressant,) she brought her grades up to straight A’s, attended college, and has a career in her chosen field.  I understand that some people would say that the side affects of medication would outweigh the benefits, she calls me from time to time to bring her medication to work because she forgot it, and she cannot concentrate to do her job. My middle son, who was born addicted to cocaine, has been diagnosed with a variety of mental illnesses, but I personally like to give him just one:  his brain and wiring is screwed up due to his prenatal exposure to drugs.  As an infant he would flail about and injure himself, he rarely slept, wouldn’t eat, and climbed out of his crib by 9 months old. (He couldn’t walk, but he could climb!) He would run around destroying anything in his path.  Without psych meds, it would have been impossible for him to attend school because he surely would have climbed out the bus window!  My youngest son, who was severely abused in his early childhood, has Dissociative Identity Disorder, (previously called Multiple Personality) a condition in which a child withdraws within himself/herself when abused, sort of “blacks out”, so to speak, but another part of the brain still feels the affects of abuse.  That other part remains in his “psyche”.  Hidden.  Buried. Showing itself from time to time in an angry, violent outburst, often requiring hospitalization. Without psych meds, he would not be able to function as well as he does.  He would be encompassed by deep depression and obsessive thoughts.  My youngest daughter has severe attention deficit disorder, and cannot sit still or pay attention without medication. Similar to my youngest son, she was abused as a child. Her hidden demons come back in Post Traumatic Stress Disorder, tearful, angry aggression, often on herself, but sometimes against others.  Without psych meds, she would not be able to function.  She still has PTSD and “episodes”, but they are far less frequent than when she was not on medication and it would be a daily thing.

I understand people have different opinions about psych meds, but in my family, without them, it would have been impossible for my children to live life “normally”. I know that there may be side affects, but the side affects are far less intrusive on their lives than their mental health issues. The doctor always goes over the possible side affects, and not a single child has ever indicated they bother them.

Regarding your concept of not believing the idea that sometimes formerly quiet, law-abiding people are randomly “going off” and shooting rooms full of children, again, I can only point to my own children.  Childhood abuse, even verbal abuse, and non-loving parents, can permanently harm a child’s developing psyche.  Permanently.  Even counseling and medication may not be able to fully quiet the demons hidden in a child’s brain.  My son, who is the sweetest, nicest, most generous boy, often displays his “angry part”, a part so vile and violent that it reminds me of Linda Blair in the Exorcist.  He is unrecognizable and so angry that violence surrounds him…sometimes resulting in a call to 911 for assistance with restraining and hospitalization.  For my daughter with PTSD, her episodes are more invasive.  The slight touch, smell, or thought can cause her to fall back into anger of abuse, and she dissociates and becomes violent.  She is not herself…well, that’s not true because even when she is having flashbacks she is herself, but the self as a young child being abused.  Regarding the randomness of violence, case in point:  she was recently arrested for “assaulting a police officer with a deadly weapon” when he charged towards her to get her to stop flailing about and screaming.  (She ripped a board off the wall and tried to ward him off.) She is living in a restrictive, “locked” facility with staff trained in behavior modification and restraints, but her behavior has horrified and shocked them.  It is not her fault, she cannot control it, but she is very violent.  Other people looking at her would never think such a sweet, friendly child could harbor such demons.

I know many people not exposed to individuals who are mentally ill to the serious degree of my children would find it hard to believe they just “snapped”.  No one never knows if a person who appears to be “normal and quiet” is really “normal and quiet” underneath.  I believe wholeheartedly that one has to have a mental illness, even if undiagnosed, to be a mass murderer. I believe no one in his/her “right” mind could possibly do such a thing!  Of course, this is just my one biased opinion.  I can understand, though, that there are different sides to every story.  Let’s just “agree to disagree”!

The Apple Tree: Raising 5 Kids With Disabilities and Remaining Sane by Linda Petersen.

Adoption Blogger Interview Project: Meet Ms. 20Stuff!

I volunteered to interview another adoptive parent, and I had the good fortune to meet Ms. 20Stuff who happened to have a friend who ran an orphanage in China…and the rest is history!  She has an amazing family, that is sure to grow even larger!


Please welcome her and her answers to my probing questions:

1)  Could you please let the readers know your underlying reasons for wanting to adopt, and why you specifically chose China.

We weren’t actually planning to adopt and didn’t have either any noble or heartbreaking reasons for wanting to adopting. We had been students preparing for a future of teaching at a university level and were “too busy” for kids. But a lifelong friend of my parents who runs an orphanage in Taiwan knew we were nearing our forties and still childless, and he persuaded us that we should apply for adoption. We did not know at the time that this small, private, government-approved orphanage only accepts about one in every thirty applications, or we would probably have been far more intimidated about starting the process! But we did start, somewhat reluctantly, and we stated in our application that we would take a child “with problems.” Apparently that willingness pushed us fairly high on the list, because only six months later and just two weeks after we’d moved to a different state for my husband to start his doctoral program, we received word about a five-week-old baby girl who was missing her left ear. We agreed to adopt her, then eagerly awaited photos! And less than six months later, just two days after Christmas (2007), we were in Taiwan and our precious little Pumpkin was in our arms.

We knew right away that we wanted a sibling for Pumpkin. I wanted a sister for her, but our orphanage director urged us to consider a boy, and I am so thankful he did. Two years later we were able to adopt ten-month-old Slick from this same orphanage, and he has been such a joy to us.

 

The first four or five months were not at all joyful to us, though — we were completely unprepared for Pumpkin’s over-the-top jealousy of Slick or for his waking up and crying once every two hours throughout the night. Crazy daughter during the day, crazy son during the night! It was a miserable time, and I felt that we had ruined our family by trying to have two children.

 

Just the same, in August of 2010, about five months after Slick came home, I happened to see two referral photos of Sunshine, a six-year-old girl with Cerebral Palsy in China,  on another adoptive mom’s blog, along with Sunshine’s story and a plea for someone to come forward and become this child’s family. I couldn’t help myself! I loved her and wanted to be her mother. I prayed for three months, and then at the end of October, my husband very unexpectedly said, “You know, our home study is going to expire — we should look at some agencies if we want to adopt again.” I told him about Sunshine, and we began her adoption the next day.

 

Then in August of 2011, our agency told us about Joy, a chronically ill 13-year-old girl about to “age out” of China’s orphan care system in just four weeks. I said I would advocate for her online and did so on our blog and Facebook, but no one came forward for her, so I asked if we could adopt her. Mr. 20Stuff then conducted a Hague-convention adoption in just three weeks! Oh. My. Word. Adoption of a special needs international child usually takes about a year, but through God’s mercy, the intervention of everyone from our adoption agencies to government offices on both sides of the water, and my husband’s heroic efforts, that adoption was completed in three weeks. I am still amazed! And did I mentioned that God provided every last dollar needed for Joy’s adoption? Even the airfare and hotel costs — everything came in within three days.

 

Mr.20Stuff flew to China without knowing whether he was bringing home one daughter or two, but within just a few days,  we rejoiced to learn that we would be bringing home two daughters, Sunshine and Joy. But within four days, Joy had become very angry about the adoption (imagine your child at 14 being taken away from everything she had ever known and sent to live with strangers from a different race and language far away from her own country). She raged and grieved and dug in for what was clearly going to be years and years of anger. I have no doubt even now that she was fully prepared to hate us for years. But I could see that she responded well and immediately to a particular type of personality in the women we knew at church, school, and elsewhere, and I saw that she was very intelligent and could be relaxed and happy and even sweet-spirited. As our home life fell apart around her misery, I began to imagine a “second chance” for her, a home with a mom who had that particular personality type that was so able to connect with Joy. Through one of our blog readers, God provided a second family for her after seven months in our home. She is now doing very well in her new home, and our younger three children are relaxing and returning to their “real” selves in her absence.

 

That’s our adoption story in a nutshell. :-) We do hope to adopt one or maybe two more, another boy and maybe a girl, but for now we are recovering from Joy’s time in our home and are content with just three children.

2)  How did you feel in that airport as you were waiting for your husband to get off the plane from China?

I felt quite apprehensive, because at that point I was well aware that Joy was bitterly unhappy about her adoption, and I wondered what on earth we were doing to our family. Still, I was convinced that this adoption was God’s will — He had shown us in multiple ways — and I still believe that. Joy’s second family could not have adopted her when she was in China and “aging out,” but they could adopt her once she arrived and had received citizenship and so forth. They are very, very clearly the right family for her. Of that I have no doubt at all. She has been in her new family for five or six months, now, and is happy and learning to be loved.

 

3)  Your children are amazed at the microwave and watch it go ’round and ’round.  What other American “inventions” have they found fascinating?

Yes, that was such a funny thing. Both Joy and Sunshine would stand and watch the microwave table turn. And it was through the microwave that we began to get a sense for Sunshine’s enthusiastic response to life. One day as I was setting the dining room table, I heard our little Sunshine shouting as she stood by the microwave, “Mommy! Mommy! Hot dog — BOOM!” She didn’t know how else to tell me that the hot dog had exploded in the microwave.

I think what has most amazed Sunshine has been the water park at the zoo. I have never seen a more grateful child in my life. She was utterly thrilled and thanked us over and over again for taking her.

4)  You mentioned in your blog that while shopping, buying additional clothes was beyond your financial [capability] at the time.  I think one thing readers may  not realize, unless they have adopted themselves, that there is an enormous financial cost to adoption before you even start the financial cost of raising these kiddos who, in your case, have disabilities.  Could you expand generally on this?

Yes, good grief! The “start up” costs for bringing in an older child are every bit as expensive as bringing in an infant: bed, bedding, dresser, clothing, shoes, books, toys, backpacks, etc., etc., etc.. In Joy and Sunshine’s first seven months with us, we spent about $10,000 in out-of-pocket medical expenses. Each girl had nearly two dozen medical appointments a piece, which included specialists of various kinds and a surgery for each of them. We were living on a single income, just my salary as a full-time lecturer at a university while my husband worked on his doctoral program (he’s in the dissertation phase), and we hadn’t done any fund-raising for the after-adoption expenses (very few families do), so it has been a tough year financially. Yes, adoptive families do struggle with the after-adoption expenses.

5)  What things have you done with your family that have been the most fun and least stressful?

Our children have especially enjoyed activities that we do together: taking walks, craft-time, going to the library, and so forth. This summer after Joy left, we were able to take Pumpkin, Slick, and Sunshine to the zoo and the water park on two occasions and this fall to a children’s museum, and they were thrilled with everything. They do have some physical, emotional, and behavioral challenges: cerebral palsy, severe astigmatism, hearing loss, Fetal Alcohol Effects, low muscle tone, poor articulation of speech, anxious attachment, sensory integration issues, etc., so time away from home can be challenging for them and for us. We are also unemployed right now while Mr. 20Stuff is working on his dissertation and I am staying home with our son, so family entertainment that requires admission fees or so forth can be a stretch for us. But God has provided for us, and we enjoy taking the kids places that delight and stimulate them.

 

Thank you, 5kidswithdisabilities, for interviewing us here at 20Stuff! We have not ever told our full story here on this blog, so it was fun to attempt to “write it in a nutshell.”

Thank you Ms. 20Stuff!  It was nice to “meet” your amazing family!  If anyone would like to get to know them more, the link to their blog is  http://20stuff.blogspot.com

 

To read more interviews of other adoption bloggers, go to http://www.productionnotreproduction.com/2012/11/adoption-blogger-interview-project.html

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