Author: Karen Putz

  • Yesterday’s Field Trip– Deaf and Hard of Hearing Advocacy Day

    Yesterday, my son David took a field trip to attend an annual “Deaf and Hard of Hearing Advocacy” day. This event is the brainchild of Katie Ward, a supervisor of a program that serves deaf and hard of hearing students in Lockport, Illinois. There were 104 students attending and about 20 parents. Most of the students attend their local schools and some of them attend specialized programs for deaf students.

    Earlier in the year, the students were encouraged to share a story about their life and the different ways that they advocate for themselves. Unfortunately, David’s itinerant teacher forgot to share that information with us so we weren’t able to participate. David’s good friend, Aubrey Millar, won an award as a semi-finalist for her wonderful powerpoint presentation.

    This year, there were nine deaf and hard of hearing adults who shared a bit about their life– their careers, travels and advocacy tips. There was a financial advisor, a marketing specialist, vision teacher, village trustee, physical education teacher, band director, network administrator, stay-at-home mom and an audiologist. Each of them had the same message to share:

    “Don’t let anything stop you from acheiving your dreams.”

  • It’s No B.S. Mom, I Love You Too!

    I grew up in a family with five generations of hearing loss. My Great-Grandfather, Grandmother, my mom and all of her siblings were deaf or hard of hearing and none of them knew sign language. All of my siblings have hearing loss as well as my children and one niece.

    My mother’s hearing began to decline in her twenties. All of my brothers and sisters were born hearing and one by one, we each lost our hearing. My oldest sister was three years old when she fell, hit her head and instantly became profoundly deaf. My parents sent her off to live with my aunt and she attended Central Institute for the Deaf, an oral school. My brother Dennis was 36-years-old when a wooden beam fell on him at work and he woke up in the hospital two days later with a severe hearing loss. My sister Jeanie began to lose hearing in her 20’s and a few years ago, she slipped on a rug and became profoundly deaf.  My brother Kenny has a mild hearing loss that began a few years ago from a fall while barefooting.

    I came along 10 years after the last sibling was born. When I was five, I was diagnosed with a moderate to severe hearing loss. I muddled along in school, receiving a hearing aid in 4th grade and speech therapy. Because I “functioned” so well and was able to keep up my grades, I was pretty much lost in the system. Teachers lavished praise on the “girl with the hearing loss.”  My loneliness was often overlooked.

    My life stayed this way all through my school years. I made friends with a select few who could look beyond my hearing loss. In high school, I met another girl, Shawn, who also wore hearing aids and we became fast friends. We each shared the horror of dealing with group situations and the anxiety that came with it. We learned to adapt so well that some of our friends had no clue that we wore hearing aids. (I never wore my hearing aid outside of school or during the summer.)  Of course, we missed out on the punch lines of many jokes while laughing along with the others.

    When I began attending classes at the local community college, I started to fear that I had no future ahead of me. I had interviewed for several jobs, but no one had the courage to hire me or deal with my inability to use the phone. I took one job as a dishwasher at a local restaurant and earned money mostly by babysitting. The future began to look pretty bleak. The few guys that I dated weren’t good marriage prospects. I began to wonder just where I was headed.

    On a whim, I decided to transfer to a college that had a program for deaf and hard of hearing persons. My mother reluctantly supported my decision. She was afraid to see her last baby go off to the great unknown. How in the world would I cope at a university when I could barely get by at the community college?

    Just before going off to college, I was water skiing on my bare feet and I turned to cross the wake. I fell hard, and for the next few days, I kept feeling like I had water in my ear. I had become profoundly deaf.

    Going off to college turned out to be a blessing. At first, it was quite a culture shock. I was living on a co-ed floor with people who signed so fast that it was intimidating. Little by little, I was transformed. Slowly, I was introduced to a Deaf life to the point it felt like “coming home.” I was in a world where hearing didn’t matter. It was a world where, if I missed the punch line of a joke, someone would kindly sign it over again until I could join in the laughter. Of course, occasionally I encountered: “Sorry, train gone!”

    My mother and siblings began to see a new person blossom in front of them. I introduced them to a TTY, and a new, accessible world began to open for them. My mom admitted that she wished she had known more about sign language while we were growing up so that we could have had access to interpreters.

    When my oldest son became deaf, my mom began to ask how to sign certain things. It made me smile to see my 70-year old mom signing to my kids. One of her favorite signs was the sign for “I love you,” which is made with the thumb, forefinger and pinky finger extended and the two middle fingers bent downward.

    Every time we got into the van to leave to go home, Mom would flash her “I love you” sign. There was only one problem though…

    Mom would occasionally forget and leave the thumb bent inward, which turned the sign into “B.S.”

    It is quite a picture to see Mom flashing her “B.S.” sign when we are pulling out of the driveway. It always puts a smile on my face.

    It’s no B.S., Mom. I love you too!

  • The Dog, Interpreters and an SOB Conference

    On Saturday, I arrived home from a baseball tournament to a note on the door:

    “Dear Mom, Kaycie ate the chocolate peanut butter cups. I’ll tell you more when I get home.”

    My daughter and her friend had gone to the movies. I found the nearly empty tub of Trader Joe’s chocolate peanut butter cups in the garbage. My heart stopped for a minute. The twelve-ounce tub was full when we left. But Lauren’s friend had a certain penchant for those Trader Joe chocolates. She was known to polish off the entire tub in a weekend. Was I panicking for nothing?

    After a quick call to the vet, I realized that I needed to play it safe. Chocolate, in large doses, is toxic to a small dog. Two hundred and forty eight dollars later, I learned that Kaycie had indeed polished off the entire tub of chocolate. It took her a day to recover from her ordeal.

    Two hundred and forty eight dollars.

    Which leads me to the reason why I need to convince Liz Strauss to give me a discount to the upcoming SOB Conference:

    I spent my registration money on my dog!

    Now, if that isn’t enough to convince Liz that I deserve that $100 discount for the upcoming SOB Conference, I’m betting that as blogger who happens to be deaf, I’ll be able to add a unique aspect to the blogging discussions that will take place on May 12th. For me, the internet is a visual medium and occasionally I encounter podcasts or videos that are not accessible to me or the millions of other deaf and hard of hearing users on the web. Perhaps I can add an “eye-opening” perspective as to how to make blogs accessible.

    I want to thank Liz Strauss and the SOB team for agreeing to provide interpreters for the upcoming SOB Conference. I’m looking forward to being able to fully participate in the blog discussions.

    After I get my $100 discount, of course.

  • Friday the 13th– My Lucky Day

    One year, my father handed me an envelope with money inside for my birthday. Years later, I cannot remember the amount of money that was inside, nor the year that it was given to me. But I saved the envelope inside my nightstand for years. Typed on the outside was this little poem that my Dad wrote:

    Karen

    Friday the 13th, a suspecious day
    But you came along and I say;
    It’s hard to believe but it’s true
    Wish we had two just like you.

    Your Mudder, Fodder and everybody else.

    Years later, when I was in college, I couldn’t wait for the weekends to head home or to ahem, party with my friends. One day, out of the blue, my mom sent me a package. Inside was a plaque:

    Hang on, Friday’s coming!

    After spending yesterday bawling at yet another IEP meeting (I’m sure I have a reputation in my district as an emotional mom, nevermind that I can advocate for someone else like a Piranha!), I’m just glad that today’s Friday, and the 13th at that. I’m heading to work this morning then out to lunch with a friend.

    The best part of all– there’s actually a glimpse of spring today!

  • Custom Greeting Cards by a Deaf Designer

    Jill Stark, another mom who is deaf, runs a business designing customized greeting cards. Jill has an amazing eye for design and her cards are beautiful. If you’re looking for a customized wedding invitation, greeting card, birth announcement–she’s the gal to go to.

    The design you see above is one of the samples from her site: Jilizart.

  • A Snowy Easter

    We headed up to Christie Lake on Saturday and as soon as we arrived, it began to snow. There was already an inch or two of snow on the ground. My brother and my nephew had put the pier in the water the weekend before. If you look closely at the photo above, you’ll see a swan gliding on the left.

  • Published in Another Book!

    Yesterday, a flat package arrived in the mail. I tore open the envelope and found the book, Don’t Cut Me Again! True Stories About Vaginal Birth After Cesarean (VBAC) Edited by Angela Hoy, owner of Booklocker and Writer’s Weekly, the book is a collection of birth stories centered around women birthing vaginally after previously having a cesarean birth. About a year ago, I had submitted the story of my youngest son’s homebirth. My two older children were born via cesarean. The story is included in the book, along with pictures of my kids.

    Angela also runs a VBAC blog here: Angela’s VBAC Blog.

    A few months ago, I received my copy of On The Fence: The Hidden World of the Hard of Hearing, written by Mark Drolsbaugh. I had submitted a chapter in that book as well, highlighting my experience of growing up hard of hearing and becoming deaf.

    Someday, in my lifetime, I’d like to write my own book.

  • Passing on some Success Secrets


    I’ve been tagged by Stephen at Adversity University to share some daily success habits. The Daily Success Secrets started over at Today Is The Day. The idea is to list five or ten “success” habits that you follow on a frequent basis.

    Wake up grateful.This is a relatively new habit of mine. On most days, I tend to wake up with a mental list of things to do for the day. I am learning to replace this with thoughts of gratitude.

    Do something nice for someone else. My mom taught me this one– she often helped neighbors, baked something for someone or lent an ear when someone needed to talk. Spread some good stuff, and the good stuff will come back to you.

    Maintain a balance. Life gets crazy at times. It becomes tough to maintain a balance in all areas of life. However, when things are out of balance, then the success of other habits begins to shift. I’ve learned to let go of some things or create new habits to maintain balance.

    Enjoy life. If you’re not having fun, laughing, loving someone or enjoying life– then what is it all for? Every day, every moment, is a gift.

    And the ultimate recipe for success:

    Follow the Happiness motto. Back in high school, an itinerant teacher gave me a small plaque that said: “The grand essentials to happiness in this life are something to do, something to love, and something to hope for.”

    I’m tagging my friend Groovy next!

    Goovy’s Ruminations

  • A Quick Vacation and Back to Reality


    This past weekend was a whirlwind of activity. On Friday night, David’s friend Aubrey stayed overnight and I drove the two of them to a local junior high to meet up with their dodgeball teammates for the day. June Prusak, the youth director at Chicago Hearing Society was driving the team up north. Fourteen deaf and hard of hearing kids were entered in a tournament at the Schaumburg Park District.

    The kids had a blast at the tournament and David headed home with another friend for a sleepover. I was busy packing up a suitcase for our trip to the Dells. My neighbor Barb came over with her kids and we ordered some lunch.

    On Sunday morning, we picked up David and took off for Wisconsin. The trip is an annual tradition for me and my friend Sue and our families. Sue and I met at Northern Illinois University. We became roommates and close friends, sharing pregnancies together and raising deaf and hard of hearing kids. Our kids are close friends as well. Sue has five kids (two step-children) and all of the kids get along great.

    This year, we headed out to the Wilderness Resort. I was surprised to see how much the resort expanded from our first visit years ago. The place now has three waterparks with a variety of water rides. The adults spent time in the indoor/outdoor hot tub (with grown up drinks) while the kids roamed. This was the first year we could really kick back and let the kids take off. Such a bittersweet feeling– to enjoy the freedom on one hand but also realize how our kids have sprouted wings too soon.

  • “Through Deaf Eyes,” And Through My Own

    Yesterday was one of those crazy days. My parents and sister came in from Michigan and my cousins came in from Maryland and Missouri. My brother and his family joined us for dinner. All of us are deaf or hard of hearing with the exception of a few. We had a great dinner of my mom’s famous lasagna and Red Velvet cake aferwards.

    After dinner, a friend of mine and another guy installed a new videophone system in my office. I am starting a new job and wanted to make sure that I had several videophone options to rely on. If you’re not familiar with a videophone–it is a webcam that is hooked up to a tv or monitor and an interpreter shows up on the display. I use a phone to talk directly to the person I’m calling (or who is calling me) and the interpreter interprets/signs what is being said. The conversation is almost seamless for me with very little lag time.

    When 9:15 p.m. rolled around, I suddenly realized that the PBS Special, “Through Deaf Eyes” had already started. My mom and one of my cousins joined me in watching the show. It was definitely an “eye opener” for them.

    While watching the documentary, I found myself taking a few trips back in time. When I graduated from college (just yesterday, ahem!), I started a deaf senior citizens group and often spent time with older deaf persons who shared what their life was like while growing up. They shared stories of traveling great distances to see their friends, only to find out that no one was home. An older woman shared the same thing on the PBS show. When they showed the early TTYs,(early phones for deaf people), which were big Western Union teletype machines, I thought back to the calls I made on the last few teletype machines that were still working less than twenty years ago. Today, my TTY machine is collecting dust on my kitchen counter. I now use a captioned phone and video phone to make my phone calls.

    The documentary also featured the National Theatre of the Deaf and that took me back to my college years when I attended a show for the first time. I knew very little sign language back then and could not understand any of the theatrical American Sign Language that was flying across the stage. I remember leaving that play feeling quite lost and empty– I was still dealing with becoming profoundly deaf and learning a new language. The same thing happened when a band called “Foxfire” performed– I couldn’t follow any of the music or the signing. I’ve since learned that for me to enjoy any musicals or plays with ASL, I have to turn off my hearing aid and immerse myself in the ASL. Otherwise, if I attend a concert, I obtain an interpreter who can interpret with an emphasis on English so I can match the sounds going in my ear.

    I was happy to see the variety of communication modes on the show because there’s truly a diverse population of deaf and hard of hearing persons. I was surprised however, not to see an interview with an adult or family using Cued Speech as several of the families that I know use this method of communication.

    My cousin is heading home today and plans to enroll in an ASL class. I look forward to teaching her all the naughty words in sign.