Tag: school

  • The Last IEP Meeting

    It hit me like a ton of bricks this week when the school counselor remarked, “This is the last IEP meeting for David.”   I looked at my son sitting next to me.  How did the time fly by so fast?  He was a little toddler when Joe and I sat in on his first IEP meeting.  David had just turned three and was diagnosed with a profound hearing loss just a short time before that.  I had attended many other IEP meetings as an advocate for other families, but it was a whole new ballgame to sit in the IEP meeting as a parent.

    One of the hardest things for me to do was to put him on the bus for a 45-minute ride to school.   It was hard to trust someone else to drive my child, hard to trust someone else to care for him and protect him.  I didn’t like the bus driver, a young man who seemed distracted.  My gut feeling kept telling me that something was wrong.  A few days later, I went to get David off the bus and spied a half-smoked cigarette on the floor.   That was the last time that bus driver picked up my kid and I requested an aide on the bus after that.

    David attended a school with a deaf program for three years.  In kindergarten, the supervisor came up to me and told me that they felt the best placement for David would be in his home school district.  I struggled with that view, because I grew up solo in the mainstream– I was the only kid with hearing loss all the way up until I met Shawn Haines in high school.  Then it was solo and a friend.  I didn’t want that for my kid.  I wanted to make sure he grew up with deaf and hard of hearing peers.  So at first, I balked at the suggestion.  Joe and I had days and days of discussion, wrestling with the decision.  Should we fight to keep him in the deaf program or should we try the mainstream option?

    Finally, we came to the conclusion that we would give the mainstream option a try, with the intention of putting him back in the deaf program if it didn’t work out.  From day one, I was determined to make sure he had a different experience than what I went through growing up.   Our subdivision had built a brand new elementary school right across the street from our house and it was just about to open up.  I went in and introduced myself to the principal, Randy Vanwaning.  That turned out to be one of the best moves, because Mrs. Vanwaning stayed on our side throughout the whole elementary school experience.

    There’s a saying that I learned at a MOPS (Mothers of Preschoolers) conference years ago:  “Bloom where you are planted.”  Once we decided that we were going to mainstream the kids, we kept that philosophy with us.  We made the best out of it.  I volunteered at the school and in the school library so that I could get to know the staff and the teachers.  I went into class and read books to the students using sign and voice.  I became involved with local playgroups and neighbors.  The school hired an interpreter whose parents are deaf.  Mrs. Mac is still interpreting today for Steven.  Mrs. Mac started an ASL club at the school.  The music teacher embraced sign in every single concert that the school put on and Mrs. Mac volunteered her time to teach the students one song per concert.  Many of the students signed the school song at assemblies.

    There were many experiences along the way that were challenging and it wasn’t always easy. I teamed up with Janet Des Georges to write The Myth of the Perfect IEP as a result of those challenges.  I often reminded myself that it would have been the same in any environment– it’s the nature of the journey and of life.   There were times when we questioned our decisions and explored options and considered changes.  One of the most difficult IEP meetings we ever had was David’s transition to high school.  A staff member felt strongly that we should keep him in the home district.  We felt differently– we wanted David at Hinsdale South, where he would have deaf and hard of hearing peers as well as a mainstreamed education.  We couldn’t come to an agreement at that meeting.  That was a meeting where tears were shed– I’ve had a few of them over the years with the three kids for different reasons.   We worked out that agreement and it paved the way for a smooth transition for Lauren as well.

    At David’s last IEP meeting, I sat and thought about all of this as I watched him talk about his experience at the “Explore Your Future” camp to the VR counselor and the district representative.  I sat in awe as I watched him share his views of what he wanted for his future– this little boy of mine has turned into a young man– when did that happen?   I thought back to preschool, and how he cried during the Christmas show that the teachers put on.   The teachers tried to encourage him to say his lines, but all he did was sit in his chair and cry while the other kids took turns saying and signing their lines.  I look back at that time and laugh, because I have a son who can get up on stage and put on a show now.  Go figure.

    For a long time, I was the parent teaching the child–guiding David through life and sharing what I wanted him to know.  Lately, I’ve been aware of how much the roles have shifted, I’m learning things from my son.  When we head to the gym together, he teaches me things about muscle development and he becomes my coach as he runs me through drills.  “Come on Mom, you have to do one more set”– which sounds a lot like the stuff I tell him at home:  “Clean the bathroom and sweep the living room.”  Just yesterday, he made a stir-fry dinner while I was glued to the computer and I was surprised at how delicious it was.  There he was, sharing his newly-made recipe with me and teaching me how to make a better stir-fry.

    I mentor families who are just starting out on the journey of raising deaf and hard of hearing kids and the beginning of the journey always seems so overwhelming, so impossible, so challenging.  “Hang on to every bit of time that you have with your child,” I tell them.

    Because before you know it, in the blink of an eye, all of a sudden, the last IEP meeting arrives and you wonder how it went by so fast.

  • Are You in the Deaf/Hard of Hearing Closet?

    For many years, I hid in the deaf/hard of hearing closet. I wasn’t comfortable dealing with the lone hearing aid that was given to me in fourth grade. During the school day, I hid the hearing aid under my thick hair and pulled off some impressive bluffing maneuvers. I would smile and nod along to conversations during lunch time and at recess.  I did so well that the teachers often told my Mom that I was getting along “just fine in the classroom despite my hearing loss.”

    When I look back at my early years in elementary education, I know that I had hearing loss long before it was diagnosed. I remember looking around after getting off the monkey bars, only to find all the kids lined up against the wall, ready to go back inside. I was the last kid left on the playground and I learned to calculate the time left at recess so I wouldn’t be the last kid in. I remember the kindergarten teacher coming over to tap me whenever nap time had ended. I quickly learned to watch the kid next to me and when they got up, I got up.

    In second grade, the teacher had a reading session and introduced the book, “Curious George.” I couldn’t get the word “curious.”

    “Erius George,” I repeated after her.

    No, she said. She repeated the word and then went on reading. I stared at the book, seeing the man with the yellow hat and the brown monkey. I had no idea what the book was about or the interactions between the man and the monkey. It wasn’t until I had my first kid and obtained a copy of “Curious George,” that I finally learned what the story was about.

    There are a lot of chunks of my life like that.

    I’m sure to my teachers, I appeared to be doing pretty good in school. In seventh grade, we had a class where we each took turns reading a paragraph out loud. I would calculate the number of students ahead of me, count the paragraphs in the book and figure out where I needed to start reading. Sometimes I would get lucky and see someone close to me reading with their finger on each word and if I listened, I could follow along with the words. Then when it was my turn, I’d start in on the correct paragraph.

    But inside of me, I know my stomach was churning and I was tense in trying to keep up. There were thousands of situations all through the school day, in after-school activities or on the playground where I was hyper-alert in trying to follow it all.

    I’m sure today, there are kids still going through this routine– this coping skill that gets them through the day as “normal” as possible.

    I can remember the day I came out of the deaf/hard of hearing closet. It was actually in college. I rode the bus with my hair pulled back in a pony tail and my hearing aid perched on my ear.

    And I didn’t care.

    For the first time in my life, I didn’t care who saw my hearing aid in public.

    That was a turning point for me.

    Over the years, I’ve met some people walking around with that closet around them.  Any talk about being deaf or hard of hearing is a painful thing. They know that elephant in the room is there and they step aside so they can talk around it.

    One only has to type in “deaf mom” on Google and they’ll quickly learn that Karen Putz and DeafMom go hand in hand. There would be no hiding the fact from a potential employer nor would I even try. Lately, I’ve been receiving emails from other bloggers, who share that they’re hard of hearing or deaf, but they don’t want to highlight that in their blogs for various reasons. Some feel that their hearing status has no bearing on their life. Others feel it’s a sign of weakness and they don’t want to share that.

    “I don’t hide it in person,” says Holly Kolman. “It’s just that the internet is forever.”

    After chatting with Holly, I learned that she had never published anything online about being hard of hearing. She was willing to discuss it for the first time online on this blog.

    “Life with a hearing loss means everything is harder,” she explained. “Almost everyone takes it for granted that people can hear…it’s like expecting someone with normal breathing to understand what asthma feels like–it’s impossible. It is very socially isolating. People think that you’re ignoring them when you don’t answer and they take it personally.”

    Holly recalled that some of her teachers did not understand what she was going through in the classroom. Over the years, they told her, “You hear what you want to hear.”

    I’ve been told that too. 

    In sixth grade music class, we had a test where everyone had to listen to a recording on tape and then write down the beat times.  The teacher noticed that I wasn’t writing anything down.  She tried to explain what I needed to do.  Again, I tried to listen along.  Again, there was nothing for me to write down. 

    The teacher was upset.  To this day, I still remember her words:  “Karen, you need to turn your hearing aid up and listen!” 

    I told my Mom about this incident and she marched to the principal’s office the next day and explained why I couldn’t follow the music.  The principal called in the music teacher and for some reason, he made me issue an apology to her.  I didn’t understand why, but there I was, saying I was sorry.  To substitute for the missed test, I had to write two 500-word essays on the piano and the guitar–over Christmas vacation.  While my friends were enjoying a break, I was writing reports.

    I think we’ve come a long way in terms of awareness, but I think we still have a ways to go to break down those closets that are still walking around out there.