Showing posts with label special needs kids. Show all posts
Showing posts with label special needs kids. Show all posts

Sunday, January 23, 2011

Special Needs Kids Arrive, No Patron Saints or Guardian Angels Included

I don't know if Erma Bombeck ever had a special needs child, and I am not one to pick bones with the dead. Overall she presents a nice image of the mother of special needs child, but some of it comes dangerously close to the kind of sentimental claptrap I have been railing against for years. At the end she says:

And what about her Patron saint? asked the angel, his pen poised in mid-air.

God smiles, "A mirror will suffice."


For a woman with less emotional wherewithal, more than a mirror is needed. Bombeck assumes that all mothers of special needs moms will somehow all be strong, and, once the shock wears off, she will do just fine. The shock, anger and grief diminish over time, but they never really wear off.

I remain haunted by an event that took place almost ten years ago. Kid O was invited to a birthday party, her first and last. My husband stayed home with the baby Kid Q, and off Kid O and I went. Her classmate's family lived on the second floor of an old walk up apartment. The apartment was dark. The apartment was packed with people, however, a mix of the dad's family and the mom's family. They had hired a clown to entertain the ablebodied kids while the two disabled kids were largely ignored, tucked away on the couches in the living room. Both kids, KId O and her classmate, A, very much wanted to be included. Despite the fact that their son was celebrating his fifth birthday, there was no joy in that apartment. A's dad was a very angry man. A's mom looked really sad and resigned. My heart went out to her. Even as she was surrounded by family, her sadness was very apparent. A wore AFOs and so he could stand but only with assistance. No one seemed interested in helping the birthday boy join in the fun. A's dad wanted me to join him in his anger and resentment. I would not.

As these two five year olds sat in the recesses of the apartment, A's dad turned to him and said, "I don't know why we hired a clown. We already have you." I filled with grief for the son and for the mom to be saddled with such a horrible man. How could he be so unkind to someone who depended on him so? I understood the resentment at being denied what everyone else had to seemed to have: a "normal" child. What I couldn't understand was A's dad lashing out at him in such a cruel and public way. A may have been only five, but he understood that he was far from what could be desired in a son.

I could also not understand the obliviousness of the rest of A's family. I suspect, sadly enough, that A's mom felt too downtrodden to ask them to see to it that the birthday boy was included, and A's dad was too filled with rage to care. It was A's birthday, and he was being ignored by his entire extended family. I could not fault the clown. She was just doing what she was asked to do, and that was entertain the kids. She largely had them participate in races such as she could in that cramped apartment. I motioned for the clown to come over. She had those banner ribbons that kids so enjoy, and I figured that, at the very least, these kids, with assistance, could play with those. She gave me a ribbon banner and she gave one to the birthday boy. And for a few moments on that dreary day, those two kids were part of the fun. Kid O lit up when I placed the banner in her hand and helped her wave it around.

While it's comforting to think that all special needs kids go to strong women with great senses of humor, it doesn't align with reality. Even with family and friends around, a parent can feel horribly alone and left to despair. The grief is real. The anger is real. The sense of betrayal all the more so. If, as Erma Bombeck wrote, special needs children do not come with patron saints or guardian angels, then God, assuming there is one, has some explaining to do. At the very least someone needs to explain to me where to go and get one, like so many triple A batteries so I can get recharged.

Raising a special needs child can be exhausting, especially when a child is severely disabled. Everything needs to be done for them. That's becomes even more demanding as a child gets older. At the very least I could do with a guardian angel who could lend a set of hands to make the work lighter. Kid O is probably around 70 pounds and around five feet tall. She is not a passive sack of potatoes when she is carried from her wheelchair to some other chair in the living room, for instance. She may cooperate or she may kick and bare her teeth as if she were going to bite me. She may also scream or shriek. She is not passive, to say the least, and, frankly, I have yet to know a child or young adult of any age who is. Kid O has little autonomy, so it's understandable that she may choose to express herself in various physical ways.

While it's true I am patient, have a great sense of humor and at least a little bit selfish, I still have times when I feel I just cannot move another inch. I cannot imagine what it would be like for someone who doesn't have my inner strength. Having any child is not for the faint of heart, let alone one who turns out to be a special needs kids. Parents of "normal" kids have enough challenges, let alone parents of kids with special needs. And sometimes people who have "normal" kids crack, too. You read about it in the papers. 'Cause kids are kids first, and they disabled or have special needs second.

My mom, the pragmatist though she is, has this odd romantic streak about marriage and children. Everyone should get married, and everyone should have kids. Kids can be wonderful, but, as any honest person will tell you, they are a lot of work. And some people are not cut out to be married let alone have kids. We all have curves thrown our way as we go through life. We cope the best we can with challenges. Some cope better than others. Whether this is through attending a support group or going to therapy or actually having good family and friends to support us, it's important to have someone or something. And that even includes God. I don't believe in God, but I do not ever knock those who have faith. Sometimes, though, none of that is enough. Some people simply are ill equipped to deal with life, and a special needs kid may be the thing that sends them over the edge and into the chasm.

What many of us need and seldom get is the support of that elusive village. Families are spread out. Friends work. People often have their own problems. Often we don't ask those with extra burdens how they are coping or if they need anything. Too many parents flounder about. They feel overwhelmed. Perhaps they are embarrassed to ask for help or don't know where to go to ask for help. Or they think they ought to suck it up and go it alone, even as they are going down for the third time. And taking their child with them. Solutions that may seem obvious to someone else is not necessarily obvious to a parent right in the middle of trying to figure out why this child came along and turned their lives upside down. Many times we know what the solutions are. We just don't always have what it takes to bring those solutions about.

If I cannot have a village, then I'd at least like to sometimes have an extra pair of hands. Or maybe someone with wings.

Tuesday, April 13, 2010

What Holmes Said to Watson

What Holmes Said to Watson

Sherlock Holmes said to Watson, "you see but you do not observe." Watson was chagrined, to say the least, to hear this pronouncement, but Holmes did have a point. Many medical practitioners and special education educators presume they know more than a child's parent. They will feign humility, "you are the parent, you know best," and then proceed to tell you how, no, they really know better. It's offensive. It's disrespectful. it's maddening. In all likelihood, most parents will not question what a school psychologist or a principal says to them. I myself have done my share of shrugging off my intuition even when it's screaming at me, because, well, why would the principal, for instance, lead me astray?

I should have insisted on having Kid O transferred from her first school to her second school when she was five. The principal persuaded me to have her stay a third year even though that didn't feel right to me. "Her next teacher has raised her own special needs kids." There are special needs kids and then there are special needs kids. This woman raised two kids with a congenital disease, which, if you didn't know them, these kids would come across as "normal". This teacher had no idea how to teach Kid O or how to really communicate with me.

As the year dragged on, my heart sank deeper and deeper. Became increasingly clear to me that the teacher, principal and educational psychologist were intent on labeling Kid O as severely to profoundly mentally handicapped, although, at the time, i didn't really understand that was what they were doing. What I did understand that it didn't matter what they saw, they would find a way to dismiss it or deny any observations to the contrary. When my husband and I presented them and the rest of the staff with a video showing Kid O taking yoga instruction, we were told that this evidence was inconclusive. And, over the years, any evidence that might negate the original diagnosis of severely to profoundly handicapped would be squashed. Any pleas I might have to really look into Kid O eyes and see the intelligence there would routinely be dismissed as coming from a desperate mother who was simply in denial. Anyone who really knows Kid O has been able to observe her intelligence, her focus, her tenacity, and, above all, her wicked sense of humor. But no friends, family or outside therapists have opinions that count for anything, and so, with few exceptions, Kid O has had very little in the way of an actual education.

Monday, April 12, 2010

Preferring Paris

There's a story that makes the rounds on email and other places about preparing for a birth, or as the analogy goes, a trip to italy, only to land in Holland. Out go all the Italian lessons. Stuck with Gouda and herring. Apologies to Holland. There are many fine museums in Amsterdam, and, of course, there's always Delft. There's an inherent snobbishness built into the whole idea of choosing Italy over Holland, and, by analogy, that somehow the special needs child is going to be lacking. Can't get much more insulting than that. Truth be told, I don't want to be in either Holland or Italy. I'd rather be in Paris.

Our daughter is neither Paris nor Holland nor Italy. She is a kid first and special needs kid second. She has a wicked sense of humor. She can tantrum with the best of them. And, so, neither all good or all bad. Just different. Of course I would give anything if she could speak or stand or walk. But she can't. Makes it more challenging. But. Not a disappointment. Would I give anything to hear her say, "I love you, Mommy?" Of course I would. But that doesn't make her lesser. The only way she could possibly be lesser would be if I were a shallow person who cared only about "how it would look" to have a special needs child. There are some parents like that, sad to say, but I am not one of them.

It does take some adapting. There is a kind of initial complaint. A whine, if you will. A question of, but why isn't she precocious like those other kids? A persistent why me? Notice, not why her? Why me? It's natural to be a bit self-absorbed when bringing a child into the world especially when so many of us buy into the"perfect child" brand, and, yes, it is a brand. That is why it's so hard to accept someone less than perfect. There is a desire to consult the brochure. Or ask the travel agent. "But you didn't tell me..." When a child is born with special needs there's no customer service to complain to. One just has to deal.

The reaction snowballs. It's not just your reaction. Or your spouse's reaction. It's the entire extended family. Awkward pause. When Kid O was born, she was a preemie. Only 3 lbs, 8 oz. A sister in-law recommended a friend of hers who had been a nanny to a preemie. The difference is that baby had been in the NICU for six months and was essentially "normal" despite her premature entry into the world. Kid O was and remains intense. What we didn't know was that her nervous system was disorganized. After few days of helping me out, the friend passed her off to me as if she were a football and bolted. I didn't even have to ask, "are you coming back?" I knew she wasn't. And so began a largely lonely journey.

Kid O and I weren't in Paris or Holland or italy. We were in unchartered territory. Not even the medical experts were able to explain to me how to care for her. The more senior pediatrician of this one practice insisted, for instance, that she couldn't possibly be teething at two months. But she was. And in more pain than most. The pediatrician we saw in that practice could not explain to me why she had painful bowel movements. If a person has weak abdominal muscles, that is what will happen. The woman who did the preemie follow up insisted I take Kid O to get her hearing tested. The exam turned out inconclusive. Not because she was hearing impaired but because she was unable to turn her head to indicate that she had heard a sound. I tried to tell the woman in charge of the clinic that Kid O had very acute hearing. A short time later, I removed Kid O from the preemie follow up program. I sensed that the research they were conducting was going to be flawed because they were really bad observers.