Showing posts with label telling young children about disabilities. Show all posts

Teaching Dr. Self

Parents of kids with O.I. are often referring to "the scream." This is the noise that sends our parents scurrying to our side and then whipping out the bag of old splints and bandages that appears out of thin air. It is not the same cry you hear when a toddler is getting a booster shot, and it isn't the same heartbreaking wail when a child's hopes are crushed at the toy store. It is part shriek, part cry, part scream, and all of it is directed at a sliver of wispy gray-white that no one can see until hours later on the x-ray. And even then it is sometimes invisible.
There comes a time when the scream doesn't serve so much as an "alarm" for our caretakers because we realize for ourselves what has happened -- we begin to recognize that the pain is coming from a broken bone, just another fracture. And instead of "the scream" we are then able to say "I just broke a bone.."
So when is that moment? How can caretakers or parents help kids develop that recognition? How do kids with O.I. become better aware and more knowledgeable of where a fracture is? How do we know how 'badly' it is broken? Or even how many places the bone is broken in?
There are a few tips that can help make the experience a little less frightening and a little less uncertain ---

Structuring the Suddenness: 
Warning: Just because you are raising a "Dr. Self" doesn't mean medical opinions should be ignored! 

  • It is always most important to listen to the child! Or become acutely aware of where their hands are gripping, or which limb has become oddly limp and unused. Just because you may have heard a crack coming from there, doesn't mean that may be where the bone is broken!
  • Let the child hold the broken bone as much as possible - particularly during the transition before going to the doctor's. I know that from my own experience it is difficult for parents to not want to rush in and 'fix' everything themselves; however, knowing how the broken bone feels to us, where it is, how tightly to hold, what position to rest the broken arm in are all small details that begin to build our awareness of our bodies. The body is learning even when things may be breaking down.
  • Know which questions to ask. At the time of a fracture, especially for an O.I. fracture, "how did this happen?" Might be one of the first two questions that are on the tip of your tongue. But think about it!! The child has O.I.!! And most of the time, especially for young children, we aren't always aware of how the bone suddenly broke. From my experience, I used to become extremely frustrated with school nurses who would ask me "how did this happen? What happened?" before they would assess where the injury was. It doesn't help the O.I. child when you are trying to figure out the "how and why's" while they are in pain; in my experience in fact, it only made me feel worse. Instead figure out "where does it hurt?" "What hurts?" "How much does it hurt?" "Can you wiggle your fingers?" "Does your leg feel numb?" Thinking about fracture prevention is important, but not until after you have taken care of the incident at hand first!
  • Let the child be a part of the 'grown-up' discussion. This might be difficult because the fine line between protecting and shielding are so often blurred. However seeing the x-ray, listening to the doctor talk with my parents about healing time, and becoming 'naturalized' to the language and vocabulary all became useful tools to becoming self-aware of my body. Of course no parent wants their child to hear the doctor say "healing might take about 5 months.." but the reality of it is that we begin to connect the pain to healing-time that is required. It is a difficult connection to describe in words, but understanding that my arms heal faster than my legs or that my ribs take about 2-3 weeks to heal have helped me become better equipped at assessing my own physical abilities.
  • Routine. No one likes the idea of breaking bones becoming a routine. But because of the frequency of these incidents the truth is that there is some kind of routine to each of our own fracture management procedures. Whether the child fell off a trampoline, broke a clavicle, or sustained a bruise to the bone -- try to keep some semblance of order in the chaos. I know, I know many of you are thinking Sandy, you just wait until YOU have a kid with O.I and THEN you try doing this..but growing up I have appreciated the order in which my parents dealt with broken bones. It helps to know that small instances in life that can quickly be turned upside down are not reasons to feel despair. It helps to know that just because you broke a bone doing something your brother does all the time doesn't mean you were wrong to do it. And it helps to watch that no matter how badly things feel anything can be righted once again!  



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Going to School (Part 1) - For Moms & Dads of O.I. Children K-5

Soon you will be sending your child to school; for some of you it will be just another year and for others it will be your first time! This first entry is geared for parents and tomorrow's post will be geared specifically for the students. Note - The content below is most appropriate for those attending K-5; I wrote a separate entry for those Transitioning to Middle School 


For Moms & Dads: For the younger crowd their school day is chock full of activity and movement: There's circle time, Phys. Ed, show & tell, story-time, free-play, sing-a-longs, and everyone's favorite: snack time & recess... all among a roomful of twenty or more children. Of the details that I do remember from elementary school I certainly don't remember ever sitting still (though that might just be me...) The jostling, running, squirming, chattering, singing, and constant movement of the school day for younger children is fun! And while I am no educator, I know that all the silly games and sing-song chants has its own educational purpose. However, all of this joyful commotion might prove to be a dangerous environment for a young child with brittle bones. I'm sorry to say but your journey of growing gray hairs and worry lines has only advanced to all new levels.

Just as with any other aspect of an O.I.'ers life precautions should be taken in school. Should you make a presentation to your child's class about O.I.? Will there be 'social consequences' for your child if you "make a big deal" out of the O.I.? Should you ask the teacher to assign a "helper buddy" for your child? What happens when a fracture occurs? (Because we all know they will...) What if there's something going on during the day that is physically uncomfortable/painful for your child - will he or she feel comfortable addressing the situation? These and many other questions are probably whirling around your head, especially if your child is just beginning their school experience! 
Before I get into the tips for The Mom & Dad readers, let me just say one thing: You Cannot Always Be Hanging Around The Classroom, And Nor Can You Go Poking Your Head In The Door Every Five Minutes. (Regardless of what grade your child is in!!) It's distracting, embarrassing, annoying, ... and really? Do you really want to be known as that parent? Aside from all of that though, one of my favorite parts of school was the fact that I WAS away from mom, dad and the rest of my family (sorry guys, the truth hurts). It was a time for me to, on some level, manage myself! My 12+ years in the classroom taught me skills in independence, and it was a time when I could feel like a 'normal' kid. 

Helping the School Handle...Well, Everything
(I can't possibly cover everything a parent might be worrying about in the tips below, so if you have any further questions never hesitate to email me at oi.perfect@yahoo.com Chances are, if you are wondering about it then so is someone else!)
  • Whether you choose to make a presentation on O.I. to your child's class or not the decision should be based 99.9% on what your child says, and how s/he feels. If you have a particularly shy child this could be good and bad. While s/he might feel that this is a good route to take so that they can feel safe, they might also feel totally embarrassed! On the other hand, if your child is shy - a presentation will basically be introducing them to the entire class while a parent is present. Kids who are not shy, well... if they feel comfortable with the idea then, why not?
  • If you go with the presentation idea (I have taken this route a handful of times) these are some things to definitely include: Compare the fragility of the bones to something everyone can relate to i.e. an egg shell, or glass. Telling young kids that "Sally's bones will break if you push her or if she falls.." doesn't paint an accurate picture in the minds of a young child. If you have old casts lying around share them with the class! Depending on the severity of the O.I. remember to mention that fractures can happen for the simplest of reasons i.e. a cough or a sneeze. Explain the purpose of the wheelchair, the walker, and leg braces if necessary. In the past I have told my classmates that my leg braces are like shin guards they might put on if they play soccer or hockey, and they basically serve the same purpose. When the time comes for questions and answers, allow your child to answer as many as possible!
  • If your child uses a manual wheelchair and a walker during the school day make sure that there is an easily accessible place for the equipment. Whether it's by the teacher's desk (where other students are not allowed to go) or somewhere in the nurse's office, medical equipment should be stored in a safe & accident-free zone
  • There are lots of picture books about young kids in wheelchairs who go to school; if it's appropriate you can ask the classroom teacher to choose one of them to read and discuss with the class. These discussions, when handled well, will not focus on your child in an awkward way but instead allow everyone to feel inclusive; and if your child feels comfortable s/he will contribute to the discussion in a very natural way
  •  Have a Fracture Plan. I know that many parents these days have "break bags." If you feel the need to make one that is for in school use only and if you are comfortable with the teacher or school nurse putting a temporary splint on then train them as appropriate. I will admit that my parents never allowed anyone in the school to touch me. If a fracture happened in school I was quickly taken out of the classroom by my classroom aide (or put in an isolated area in the classroom) and my mother was contacted
  • Make sure that you get all the necessary doctor's notes that will be needed to authorize the school to give your child pain medication. This also includes directions from your child's orthopedic or physical therapist about appropriate physical activities, exercises, and most importantly: what should not be done
  • If your child has a classroom aide see if you can meet this person before school begins. This will allow time for your child to get comfortable with the person who will be "the one in charge" and it will also give you time to help train the person if necessary. Things like how to pick your child up, how to put leg braces on, how to fold the wheelchair, and what to do when there is a fracture. This might also be a time to talk to your child's aide about things your child likes to do for fun; sometimes these activities can be done during recess with friends, or when your child is sidelined during Phys Ed due to an injury. Over all, the more comfortable and the better your child knows his or her aide the better the school-day experience will be!
  • One tip that helped my comfort levels throughout elementary and middle school was that my closest 2 friends were always going to be in the classroom with me. I might not know which teacher or which classroom I would be in, but I could always count on a few familiar faces to goof around and bond with. I'm actually not sure who was in charge of this arrangement (whether my parents or my school teachers), but I'm sure if you asked the classroom teacher about it for the following year something can be arranged. 
  • There were countless times when my parents would get into arguments with the school nurses. They would insist their medical knowledge trumped how well my parents knew me and how to manage my fractures. At times school administrators would look at my parents in disbelief if my mom came to school to put a sling on my arm and then sent me back to class, "You're not going to take her to the doctors right NOW?! But there's liability! We can't risk her getting hurt even more!" "She's fine. It's not a big break, she isn't crying, we will go to see Dr. Shapiro right after school. She can't miss out on learning.." Expect that these conflicts will happen. Be patient but most of all be firm with where you stand and what you know! 

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