Posts tagged ‘deaf child’

“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/

 

 

 

 

Yes, I DO have a husband!

I write so often about my adventures with my children that I rarely mention that I have a husband. I love him to pieces, and he is a hard worker and great with the kiddos.  The reason why I don’t write about him…well…he’s kind of boring and not very interesting to write about.

It is very important that we, as the couple that hold the family together, spend quality time with each other.  If we do not put each other first, raising children, especially children with disabilities, would be difficult.  We need bonding, relaxing time together, and we manage to get away for at least a night or two every month,

We went away last weekend to a little cabin we have in the woods of New Hampshire last weekend.  My dad actually purchased this cabin for us when Steven was only a year old.  We knew from his autistic-like behaviors that we were not going to be able to vacation as a family very well at any hotel unless it had padded walls, (which I think I’ve only seen in those motels advertised for sexual adventures!) This cabin is where we have vacationed as a family, swimming in the nearby lake, boating, tubing and water skiing, hiking in the woods, fishing, snowmobiling, making camp fires, and just relaxing as a family.  It has served us well through out the years, and my husband and I  now use it sometime when we get away.  I personally prefer a 5 star hotel, room service and a massage, but that is rarely in our budget…okay the truth is it is NEVER in our budget, so the cabin suffices.

My husband, bless his soul, loves to putter around the place fixing all the little things.  Last weekend he cleaned out the crawl space under the house and found lots of dead mice, who ate our mouse poison and didn’t make it out of the basement in time; we need longer acting mouse poison so they can make it home and die in front of their families.  My husband also found TERMITES.  The house is surrounded by woods with lots of dead trees littering the landscape. WHY would the termites choose our house to eat?  It’s not like it is warm in there because there is no heat.  Why are they drawn to eat the only thing they shouldn’t eat?  I’ve come to the conclusion termites are like children. They won’t eat the huge pile of spaghetti offered to them, but instead want to one by one eat the limited supply of meatballs in the pot. (However,unlike the termites, we won’t kill our children to save the meatballs.)

Without the kiddos with us at the cabin, I was slightly bored!   Of course, my husband and I make a lot of time for loving and such, but that still leaves several hours of the day where he is puttering around and I am bored. I am not a good “relaxer”.  I usually need to be doing something, (thus the reason I have 5 kids in the first place!)  Without cable television, I am forced to…do nothing.  I have no hobbies, and I don’t generally like to read books.  I have been adverse to reading ever since I started reading a Danielle Steel novel in 1982 and never got to finish it because the kids always needed something and I would have to stop mid-chapter.  So, there I was, sitting on the couch, actually feeling a little sorry for myself because I had nothing to do.  Then, VOILA!  I remember that my youngest daughter had downloaded games on my cell phone!  So, there I sat all weekend, playing Scrabble on my phone.  It was great!  I beat myself 53 times!  I was a happy camper!

I’d Give my KIngdom for a Manicure

I blogged a few times back about my son’s wedding.  For this wonderful event, myself, my husband and my two daughters Dinora and Marie flew out to California.  Due to unfortunate finances, (raising 5 kiddos is really expensive!) we flew out on a Saturday, attended the wedding on a Sunday, and flew home again on Monday.  We really only had Sunday to enjoy, and enjoy it to the max we were going to do!  Because the wedding was in the evening, Dinora, Marie and I drove off in the rental car looking for a place to get a manicure.  Although this was not a regular activity for us, it somehow seemed appropriate given the fact that this was my first born’s wedding!

The city where the wedding took place was upscale. We drove to the first place suggested by the hotel.  Manicures were $95, but they had no openings for us, (my GOD! Do people really pay that much?)  We drove to a second place, which was in an exquisite setting with a Greek God theme, statues, vines, flowers and fountains everywhere.  As soon as I saw the wine bar and the piano player off to the side, I knew that we were not going to be able to afford this place.  Fortunately, THEY did not have any openings either. We laughed because the Greek place would have been all wrong for us because Marie,who is deaf, could not hear the piano player and Dinora, who has had a problem with drinking, could not drink the wine.

We had begun to learn our lesson that one needs an appointment for a manicure as we went from place to place looking to have our “nails done”.  We actually turned this trek into a mission, laughing and joking the whole way. Finally, we all shouted with glee!  In among a little string of stores, there lay the pot of gold at the end of the rainbow…a storefront that read “Nails Pretty”.  YES!  NAILS PRETTY.  Just what we wanted.  We joyfully got out of the car and went into the empty salon where we were greeted by 6 of the most friendly Asian individuals I have ever seen. A manicure cost $15.  A “mani-pedi” was $25. The three of us decided to go for broke and ordered the works, our first “mani-pedi”.   The three of us sat in these large massage chairs while TWO people worked on us, one on our fingernails, one on our toenails. They washed and cleaned and massaged our feet and hands, a unique experience to say the least, and we laughed through the whole thing.   (Although I think Marie was also giggling at the feeling of the massage chair.)  It was SO MUCH FUN!!!

This experience taught me something about life. There are some things we have to do without due to finances.  But when we do get to do something special, it is a joy!  And I was especially joyful I got to enjoy it with my two best daughters!  Money doesn’t buy happiness, but a little bit of money can…

If you want to read more about my family and our experiences, (and contribute to the future manicure fund,) please check out The Apple Tree:  Raising 5 Kids with Disabilities and Remaining Sane”, an e-book sold at I-Books.

A Whole New Meaning to “Swimming with the Fishes”

I have been fortunate in that my mother loved to travel and she often took me and one of my kiddos “along for the ride.”  One of my favorite spots was Discovery Cove, part of Sea World in Orlando.  Discovery Cove offered a make believe coral reef with lots of beautiful fish swimming around and huge stingrays that would swim close and touch you. It was so amazing, and was as close to real snorkeling that I had ever been. With a life jacket, snorkel and mask on, Marie, (my 13 year old daughter who is profoundly deaf and has PTSD) and I spent the day swimming around, amazed at the many varieties of tropical fish. It was like being in another world.  In one spot, there was a glass wall and you could swim next to sharks.  Up until this point in my life, this was as close to real snorkeling, and SHARKS, that I would get! It was awesome!

Near the end of the day, Marie’s medication began to wear off as we had stayed later than I anticipated.  She began to get anxious, but she didn’t want to leave.   I told her one more swim around the coral reef and then we’d head back to the hotel.  As had been happening all day, a stingray came up and touched Marie on her leg.  In fact, she had been petting them for most of the day, calling them her “friends”.  For some reason, this touch was different than the rest.  She became frightened and had a full blown panic attack.  She started SCREAMING her high pitched scream and she was signing (in American sign language,) “The fish is going to eat me!” (Why the fish would think she were any tastier later in the day than earlier, I don’t understand.) To get away from the stingray, she climbed onto my back.  I tried to calm her down, but it was difficult to do sign language while trying to swim with a child on your back, and she was screaming so loud her eyes were shut and she couldn’t see what I was saying anyway!  By this time, we were halfway around the coral reef and as far from the shore as you could possibly get.  Marie decided she was not safe enough on my back because her toes were still in the water,  so she climbed up on my shoulders to get completely out of the water!  Unfortunately, that meant I’d have to sink UNDER the water for her to stay OUT of it.  I started screaming along with her.  (Albeit alternating choking with water and screaming.) She was truly frightened the fish was going to eat her and I was truly frightened I was going to drowned.

They have several life guards there and our dilemma was not hard to miss, with Marie standing upright and me bobbing in and out of the water choking. Because we were so far out, it took the lifeguards what seemed like an eternity to reach us.  When they got to us, Marie refused to let the lifeguards touch her, screaming and kicking at them.  (Good old Post Traumatic Stress Disorder shows up when you least expect it!)  What three of the lifeguards ended up doing was supporting me in the water while she continued to stand on my shoulders and scream. Of course there was a huge crowd of onlookers on the beach, some taking photos.  (We really were quite a sight!) Once on the beach both Marie and I collapsed into the sand.  The life guards asked if we needed to go to the hospital, but I was still breathing and Marie had stopped screaming and was crying quietly, so that meant we had both survived unscathed.  Well, maybe not totally unscathed, I’ve lost my wanderlust  for snorkeling!

 

If you are interested in reading more, I have written an e-book entitled The Apple Tree:  Raising 5 Kids with Disabilities and Remaining Sane  available at I-Books, Amazon, and Barnes and Noble.

I KNOW there is a heaven.

I generally try to write upbeat posts…that with whatever difficulties we have, there is always something good to find.  This post will be different than the rest…it will be about my younger brother’s death.  It won’t be upbeat, but there is something good that has come out of it.  I KNOW there is a heaven. Without a doubt.  Proof positive.

My brother, for those who are unfamiliar with my “life story”, was born during the Rubella days.  My mother somehow contracted German measles while she was pregnant with him and he was born legally blind, severely hearing impaired, (almost deaf by the time he died,) severely developmentally delayed, with a cleft palate.  His life with us is what taught me such tolerance for individuals with disabilities.  My brother was disabled, but he was a joy to be around.  He had simple pleasures that made him smile, and to me, he life was as worthwhile as anyone else’s.

He was wholly incorporated into our family life and he did everything with us.  When we traveled extensively, his favorite activity was paying the toll at the toll booth.  My father would drive up to the booth so Curtis’ hand could reach the booth, and give him the money to put in.  He took great joy in reaching out to feel the basket and put the money in.  I swear my father always took the turnpikes with tolls solely so Curtis could have fun paying.

Around the time I grew up and got married, Curtis developed schizophrenia.  The simple pleasures he had in life were replaced by demons and aliens telling him to do things.  Curtis, ever the obedient soul, started to wander the streets in the middle of the night doing what these voices instructed, and there came a time when my parents had to place him in a group home.  We were fortunate in the fact that it was a wonderful group home, full of caring staff, and they took excellent care of him.  Every Saturday my mother, my kids and I would pick Curtis up and take him out for the day, usually to the mall to walk around.  He loved malls, especially riding up and down the escalators and elevators.  To be so joyful doing something so ordinary was one of his gifts.

My mother, who was very spiritual and had several supernatural experiences,  passed away two years ago, in November.  (Note a reblog I’ve attached following this one entitled Angels Among Us.)  Although we missed her terribly, my children and I continued our outings with Curtis.  All of my children loved him and would often argue who would sit next to him, or who would be his sighted guide. Their immediate, natural attachment to him amazed me given his severe disabilities and his disfigured head.  (His head was flattened on the back and he had huge ears that stuck straight out to the side.  My daughter who is deaf gave him the “sign” name, one that usually highlights a person’s individual characteristics, of Uncle Ears.)

We continued to take him out and he appeared to have his same zest for life until October of last year.  All of a sudden, his skills began to decline. Numerous medical tests were done and he was determined to be perfectly healthy.  At the mall, although he always had shuffled along when he walked, his shuffling turned to dragging his feet, then losing his balance, then having to use a wheelchair to get around.  Again medical tests.  No medical reason for his decline.

I remember guiltily the last time I took him to his favorite mall.  He was in his wheelchair, but I left the footrests in the car, assuming he could pick his feet up or shuffle them along.  I knew I was in trouble when I purchased his favorite ice cream with strawberry sauce. Because  he had lost the ability to feed himself,  I spoon fed it to him. He started to spit it out.  He didn’t want it!  His favorite thing to eat!  I new I needed to get him to a hospital, but had to bring him back to the group home first because they had his medical records. When I tried to push the wheelchair, his feet stuck to the ground. He did not lift them or shuffle along.  They just hung there.  If I pushed it forward, his feet would get stuck under the wheelchair.  With tears stinging my eyes, I did the only thing I could do to get him out of the mall.  I turned around and pulled the wheelchair backwards.  I could hear the thump thump thump of his feet on the ground and I started to cry in ernest. I had to pick him up to put him in my car, and he slumped over to the side with only the seatbelt keeping him from falling over.  It was obvious he had declined to the point that neither I nor the group home could take care of him. We took him to the hospital where he was admitted and again found to have no medical problems so he was placed in a nursing home. It was difficult to find a nursing home that would take him due to his numerous scary diagnosis; deaf, blind, schizophrenic.  He ended up in a less than perfect quality facility.  Due to frequent attacks of anxiety, when I first visited him I found him in restraints and his hospital bed mattress on the floor.  They were concerned that he would fall out of bed, so the had removed the actual bed and just left the mattress. He was alone, and a tray of food uneaten, (unseen by him) was in the corner of the room. They would come in and poke and prod him, give him medicine and needles, never treated him like a valuable human being.  He could not hear what they would say, the needle would pinch him, a blood pressure cuff would take readings, the thermometer would be used to take his temperature, and all of this would come at him out of the darkness and he did not know what was going on.  No wonder he was anxious!

Recognizing that with the swiftness of his decline he did not have much longer to live, I made the decision to stay with him at all times. I had to preserve his dignity.  We had done all we could so he could live a happy, dignified life, I could not abandon him at the end of that life.  With my being there, he no longer needed the restraints. My husband valiantly cared for all of the kiddos at home while I took care of my brother.   I spent my days sitting in his private room trying to coax some food into him.  When he wouldn’t eat the food they gave him, I would bring ice cream, pudding, applesauce and other things I knew he would like. I would lay on the floor next to him and rub his back or his arm, like we used to do.  If he could not see or hear me, I am sure that he could tell by my touch that I was there.

Within a week, we knew that he was fading away quickly.  My brother, who despite his disabilities had been as healthy as a horse his whole life, was dying and there was no medical reason for it.  Then I learned the reason; on his last night, while I was rubbing his arm, he turned to me, opened his eyes so wide it seemed as though he could see me, and he said plain as day, without the almost unintelligible garbled speech he used to have, “Mom is calling for me.  I will be going to heaven soon.” Then he shut his eyes and never opened them again. He died exactly one year to the date as my mother.

Yes, there is a heaven.  I know because my brother told me.

For those who might want to read more about my incredible family, the e-book The Apple Tree:  Raising 5 Kids with Disabilities and Remaining Sane is available on Barnes and Noble, Amazon and I-Books.

Angels Among Us

First blogged January, 2010

My mother passed away several months ago and it has taken me this long to write about it.  She was the most wonderful mother in the whole world, (and I am not just saying that because that is what one is expected to say about their deceased mother.)  In addition to being kind and loving, she was also very spiritual.

I remember when I was four years old and we lived in Opalaka, Florida, right behind the Hialeah Race Track.  We had a cement swimming pool in the backyard which my father built, and next to it was a palm tree my mother had planted crooked so it was growing sideways.  I had a green parakeet whose name I certainly don’t remember, and I loved watching Howdy Doody and Captain Kangaroo on our little black and white tv with the rabbit ears antenna.  My brother was born one day in March, and life suddenly changed for our family.  My brother was born with serious disabilities due to Rubella Syndrome, (supposedly my mother had been exposed to someone with German Measles.)  With a cleft palate, he could not nurse or drink from a bottle, so he was fed by a large eye dropper. He could not such on a pacifier and he cried constantly.  He was blind and deaf and was obviously going to be severely developmentally delayed. My joyful childhood was suddenly overshadowed by a sadness of which I had never seen from my mother.  I would witness her throw herself across her bed and sob. A deep sadness enveloped our family. I looked at my little brother, who looked so innocent and little to cause such a fuss.

One day, when the sun was shining brightly and Curtis was asleep, my mother called to me to come sit in the rocking chair with her.  She squeezed me and held onto me tightly, rocking  and crying.  It was a different kind of crying, though.  A happy cry, if I could describe it as such.  From that day on, the gloom lifted from our house and I went back to living my happy childhood with my new baby brother.

Many years later, when I was a young teenager, my mother shared her experience of what happened to her that very day.  The doctors had been encouraging her to put my brother “away”, institutionalize him as was the custom in those days. “Forget about him,” they said, “You can have another child.”  She could not bear to make the thought of doing this.  Then, on that sunny day while rocking in her chair, she told me she was visited by an Angel, a beautiful, bright white Angel.  She told me she could feel the weight of the Angel’s hand on her shoulder, reassuring her that everything was going to be okay.  Although the Angel did not speak, she knew what the message was.  She did not have to worry anymore, her son would be fine, and he was.  He wasn’t fine in that he suddenly became perfectly healthy, but he was fine in that he has led a happy, fulfilling life. Clearly, she had been touched by something spiritual on that day to turn her torrents of tears into smiles of joy over her new baby.

Several years later, while camping high in the mountains, my mother woke up from her sleep and sat up in her sleeping bag.  She was joyous!  She told me she had been to see God, whom she described as a bright and beautiful. She said it felt real, not like a dream at all.  She was confused as to the experience because it seemed as though she was there to help a friend pass over into heaven.  She did not understand because of course her friend was healthy.  It was not until we returned home from vacation that she learned that this friend had died from a brain aneurysm on that very night at that very time.

My mother lived a life of  great happiness and contentment, always seeing the good in people.  Near the end, right before she died, I stayed with her 24 hours a day.  When we knew death was near, the nurses let me lie in bed with her and she passed away in my arms.  I don’t know what I expected when she died.  No…that’s not true…I expected to see some of what she had experienced!  I expected to see her pass into heaven!  I expected there to be some reaction from her body, some knowledge that her lifetime of spirituality would somehow, through osmosis, pass through to me.  But there was nothing.  She just stopped breathing. And there was nothing.

It took me a while to accept her death, and I became angry that there was no sign from God that she was with him.  Realistically I knew this was silly, but I was hugely disappointed.

Christmas time came soon afterwards.  As the parent of 5 children, I had this habit when the children were younger of taking a picture of their sleeping faces on Christmas eve.  As they aged, they hated the existence of these pictures!  (They were usually sucking on a “binky” at the time and girlfriends and boyfriends who saw the pictures in old photo albums would always go “Awwwwwwwwwwww, how CUTE,” the most mortifying thing that could happen to a teenage macho boy!)  This Christmas eve, filled with nostalgia, emptiness and sadness,  I again went into each of their bedrooms and gazed at their sleeping faces.  I was suddenly filled with a great sense of purpose and contentment, much like the type of contentment my mother might have felt when she felt the Angel’s hand upon her shoulder.  These were MY Angels.  These were my children who had endured so much when younger, either with their disabilities or with indescribable child abuse. They have not only survived, but they have THRIVED.  They are happy and loving and successful and they have bright futures as adults.  This is miraculous to me!

Another Prom Mis-Disaster

I wrote a while ago about the damage I did to my daughter, Dinora’s, prom dress eight or nine years ago.  I miscalculated my ability to hem such a delicate item (ON the day of the prom when she told me it was too long to go with her shoes…after weeks of my asking….) The hem was crooked and the dress was gathered in places it should be gathered! I was saved from the humiliation of being a terrible mother by a local taylor who miraculously fixed my mistake, leaving her prom dress in pristine condition.

Well, my youngest daughter, Marie, who is deaf,  is going to a prom next month.  This is the daughter who has always preferred to wear male clothing, even men’s bathing suits!  Her theory is, if she dresses like a boy, no one will think she is a girl, so no men will “bother” her…  She, of course, does not realize that at sixteen years old, she has developed in such a way that men’s clothing can no longer disguise the fact that she is a girl.

Marie had a talk with her counselor, and she actually decided she wants to wear a prom dress, which would be the first DRESS she ever wore.  She was mortified at the thought of a short dress, but warmed to the idea of a full length gown.  So, last weekend I took her shopping for a prom dress, every mother’s dream activity to do with her growing daughter. Again, my dream activity quickly turned to a nightmare, but then I was again saved from disaster.

The day started out fine as we went to the mall.  Marie led the way to a major store she knows I have a credit card to.  (Thus my laments that I “have no money” would be moot to her.)  The gowns were dazzling bright with sequins and frills, but not enough fabric to cover Marie’s “growing” body.  She ran from rack to rack, picking out modest gowns to try on.  Looking at the size 11s, I knew she was not going to fit into them.  In the dressing room, she kept asking me to help her zip them up.  I tried to explain to her they were too small, but she accused me of not helping her enough!  We had an argument in the dressing room and she flew out in anger.  We walked the length of the mall with her seething inwardly, when she spotted JC Penney, another store to which I have a credit card.  We found the prom gown section, and BLESS this store…they had gowns all the way up to size 19/20.  Marie, in her glory amongst the choices, found what she thought to be the perfect gown and they had it in her size.  It was white with rhinestones and layers of ruffles and her eyes glowed happily as she tried it on.  She looked like a bride and my eyes filled up with tears. I thought of the despair we felt as she left the previous store without a dress, and the joy we both felt as she found a dress to fit her.  I say thank you to those stores who have clothes of all sizes for teenagers, especially JC Penney’s, which enabled one sixteen year old girl who is deaf to move one step closer to her date at the prom.

My teenager talks on the phone…

I am so excited!!!!  As I sit here at the computer my teenage daughter is chatting with her friends.  They’ve talked about Justin Bieber, what they’re going to do after school, what color they are going to do their nails next, and the regular banter of teenagers.  It is music to this mother’s ears because it is the first time she has ever been able to talk to her friends.  Of course, she has her cell phone and she is able to text her friends, but this this the first time I can see the giggles and silly faces teenagers make when they are happy. My daughter is deaf, and she has just learned how to use the Sorenson Video phone. She can now see her friends and they can talk with American Sign Language!  At last, I have a “normal” teenage daughter!!!!

A kiss is a kiss is a kiss…

Showing my two youngest children, Angel and Marie, that l love them has always been a challenge.  I can tell Angel I love him 100 times a day, but he will never believe me because he feels unlovable (due to early childhood abuse.)  He has dissociative identity disorder (multiple personality disorder.)  Sometimes, this 210 pound young man will come and sit on my lap.   He is not 15 years old at the time, but three.  He will snuggle his head against me and I will put my arms around him, (although that is getting more difficult due to his size!)  Then I will sing the Song “All of you…”  Only my words are “All of you. I-i-i-i-i-i-i-i-i love all of you.  All of you, even your angry o-n-e.”  He smiles at this, because it is his angry part that feels so unlovable.  I can sing it over and over again, and he will smile.   The three year old in him believes I love him, but his angry part has been lied to many times before.

Marie has a different issue with my love.  She promised her birth mom that she would not love her “new” mom.  She is very resistant to kisses and hugs or any other signs of affection because she feels she is being disloyal, (She has expressed to me she cannot show me affection because if she sees her birth mother again, she will be very angry with her.)  So, we have survived on fist bumps and the “I Love You” sign in ASL.  However,  I have ways to show her affection in every day life.  For example, ever since she came to live with us at the age of seven, I have dried her off after her shower. This has involved sitting on my lap on the toilet seat while I hug her deeply with the towels on.  She melts into my lap and I can tell that she really enjoys it.  If I stop too soon, she will ask for more because she is “still wet”.  She is 13 years old now and I still towel dry her, (although she modestly wraps herself in the towels before I come into the bathroom.)  She still needs my love, even if she cannot accept it in the normal way.

Both children, however, get the biggest kick out of giving me one special kiss.  This is not an ordinary kiss, (so it would not go against Marie’s promise to her birth mom.)  This is a “let the dog lick them all over their mouths and then they run to me to give me an extra sloppy dog kiss”.  I make the obligatory “YUCK!” face, and they both convulse in laughter.  Ha ha!  They “got” me again.  Hey, a kiss is a kiss and I’ll take it any way it comes, even with dog slobber!

The Deaf Leading the Blind: “But I was just TALKING to her…”

My job is a social worker for children who are blind includes coordinating both a summer and winter program for the children with whom we work.  Last winter we went to an indoor water park during February vacation with about twenty-five children who are blind and “legally blind”.  The children had a wonderful time playing in the water park, on the slides, in the wave runner surfing area, and in the pool, as well as participate in the regular activities that we plan, such as playing bingo and dancing.  Getting together is a huge big deal for these children who are mainstreamed into regular classrooms in their neighborhood public schools where they might not ever see another student with a vision impairment.  I began this program twenty two years ago when my oldest son, who is legally blind, was six years old.

The winter program was a huge success!  Most notably for me, it was the first time my fourteen year old daughter who is profoundly deaf wanted to help out a group of younger girls who are blind.  Each girl had their own staff person who amicably allowed Marie to join their group to help with the little girls. 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 normally been obsessed with surfing at the wave runner attraction, and being a somewhat selfish young lady, I had expected she would help for a little while, but spend most of her time surfing. However, I was pleasantly amazed that she did not choose her own activity, but spent all of her time in the water park playing with the little girls, helping them on the slides, holding their hands to guide them around the park, showing them where the food was on their plates, and so forth.  She was having a grand time, and the girls all seemed to adore her.

On the last night of this program. Marie was seated at a booth with two of the girls and their staff.  One of the girls all of a sudden started waving her hands wildly in the air. Prone to seizures, her staff person asked her if she was okay.  She said of COURSE she was okay, 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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