Category: Uncategorized

  • The New Stem Cell Research for Hearing Loss

    Back in January, 2012, I talked to the research team at Children’s Memorial Hospital in Houston about the first human trials using stem cells to improve hearing. What follows is an article published in the Communicator:

    In my family, there are five generations of relatives who are deaf and hard of hearing. Every now and then, a discussion would come up among us—what if there was a non-surgical solution to restoring hearing?   I recently came across an article sent to me via my blog, about the first stem cell clinical trials being done in Houston, Texas.  I also came across an article opposing the research.

    I got in touch with the research team to find out more about using stem cells to restore hearing.  The idea of using stem cells to improve hearing first came about from a casual conversation between Linda Baumgartner and her husband, neurosurgeon Dr. James Baumgartner.  “Jim did a few other studies with stem cells for other issues and I asked him, ‘Is this something we can do for babies with hearing loss?’’ said Linda.  Jim was working on a trial using bone marrow for patients with traumatic brain injuries and he was intrigued with Linda’s idea so he did some research and talked to several researchers.

    Dr. Baumgartner came across previous research done in Italy which showed successful results using mice.  “The study used infant mice and exposed them to noise, antibiotics, or both– to create hearing loss,” he said.  “All of the mice were injected with human stem cells through the abdomen.  The damaged hair cells grew again—the nerves reconnected.  The cells from the human cord blood triggered the mice’s own hair cells to grow again.”

    The FDA approved a license for the first human trials on ten patients, ages six months to eighteen months.  Children’s Memorial Hermann Hospital in Houston, Texas and Cord Blood Registry(r) (CBR) identified two babies to receive the treatment.  The first baby, whose hearing loss resulted from CMV exposure, received the first stem cell infusion on January 23, 2012.

    I asked Dr. Baumgartner about the side effects from stem cell treatments and he assured me that the procedure had a strong safety record.   “Safety is our goal.  People  are often scared of stem cell research—they freak out,” he explained.  “Autologous blood, giving people back their own blood products, is safe.”

    Once the trial shows results with at least five infants, the team can request FDA approval for the second phase which will allow an increase dosage of stem cells.  The third phase would include double-blind random trials.   “I feel my hypothesis is strong and I’m hopeful we will get good results,” said Dr. Baumgartner.

    In a discussion with a friend, she revealed that she was scared about the potential success of the stem cell trials.  “It scares me to think that we would lose the beauty of deaf and hard of hearing people in the world.  The world would be so bland without that diversity,” she said.  “Think of how the world would be without the contributions of Beethoven… or Edison… or Vint Cerf—the father of the internet.  They are all deaf and hard of hearing and they contributed something valuable to the world.”

    My own feelings were very mixed on this.  I spent the last twenty six years getting really comfortable with myself after going from hard of hearing to deaf.  In sharp contrast to the teen who hid every sign of hearing loss, the teen who became deaf at nineteen learned to embrace a whole new world that included American Sign Language.  My world truly opened up after becoming deaf and I saw the change as a blessing.  I learned to embrace the gift I was given.

    I asked Dr. Baumgartner about research on families like mine—five generations due to a mitochondrial gene. My daughter will pass this gene on to her children.  He explained that bone marrow trials may be promising.  “Your own bone marrow won’t work. If you use a different person’s blood, one without the genetic cause, another person’s bone marrow would allow the organ of corti to repair itself,” he said.

    Talking to Dr. Baumgartner on the phone using an interpreter and learning about the possibility of growing new hair cells—like I said, this brought on mixed feelings. On one hand, there was the excitement at the possibility of progress, of being able to restore hearing.  I thought of my siblings—I know each and every one of them would jump at the chance of being able to hear again.

    I asked my daughter how she felt.  “I want deaf kids,” she said. “It makes me kind of sad to think of the world without deaf and hard of hearing people in it.”

    Yes, deep inside of me, there was a bit of sadness.  I believe the world is a more vibrant, colorful place with the tapestry of deaf and hard of hearing people who have crossed my path over the years.  I cannot imagine a world without them.

    Karen Putz is a mom of three deaf and hard of hearing teens.  She blogs at www.deafmomworld.com and www.deafhhcareer.com.

    Families who are interested in participating in the clinical trial can obtain more information at:
    http://www.cordblood.com/hearingloss

  • Financial Peace University with Deaf and Hard of Hearing Folks

    Last night, Joe and I discovered something new about each other.

    I’m the “Free Spirit.” He’s the “Nerd.”

    I’m the “Spender.” He’s the “Saver.”

    And it was time to learn some Financial Peace about it all.  Six years ago, we had no debt other than our mortgage and a car payment. Then we moved two blocks down into a bigger house. Then we lost our entire investment in a flower shop. The property taxes nearly doubled and our savings account dwindled.Then one kid left home for college.

    Sounds like a bad country song, doesn’t it?

    Then… instead of taking up knitting or some sensible leisure activity, I rediscovered my passion for a very expensive sport and started flinging twenty-dollar bills at every driver who would pull me barefooting.

    Uh oh.

    We signed up for Dave Ramsey’s Financial Peace University at our church along with several other deaf and hard of hearing folks. Meghan Vozzolo generously provided the interpreting:

    Over in Minnesota, Adan and Emily Burke are leading a Deaf Financial Peace University class:

    And over in Minnesota, they’re starting them at a young age:

    If you’re deaf/hard of hearing and interested in joining a Financial Peace University class:

    Adan Burke (Minnesota): adan(at)burkeconnect.com

    Karen Putz (Naperville, IL): karen(at)karenputz.com

    It’s time to live like no one else, so you can live like no one else.

  • Skiing in the 2012 Barefoot Nationals

    The 2012 Barefoot Nationals were held in the same place as last year at the Barefoot Ski Ranch in Waco, Texas. Even the heat was the same as last year, hitting 108 on one of the days.

    Since the doctor was adamant about waiting the full nine months after ACL surgery, I took it really easy over the summer and didn’t do anything new. I was pretty much happy to be able to stand up and make it down the lake.  I stood up a little too fast on my trick run, but the nice crew granted me a re-ride. My brace flew off, so we headed back to the dock to tape it. It didn’t matter– the darn thing flew off twice on both falls, leaving me with bruises on my left leg and a black eye.  Slalom wasn’t much better– the first run was okay, but I fell on the second run.

    Back to the drawing board to learn how to barefoot all over again for next year.

    But the best part of the tournaments is not the skiing, it’s the people. I’ve met so many people who inspire me and push me to new heights. They’re accomplishing amazing things with their lives.  I took a moment to grab a photo with Jim Boyette, the world’s oldest barefoot competitor:

    Jim is amazing– he’s been to every single Nationals since the first one in 1978. You can read more about him here:

    World’s Oldest Competitive Barefooter

    Jim Boyette, Still Competing

    Keith St. Onge and I were interviewed by KWTX TV Channel Ten and we had the chance to talk about his upcoming book, “Gliding Soles,” which will be released in September.  Keith and I spent the last two years writing this book together and we uncovered some amazing stories from his life journey and the lessons he learned along the way.

    The print version of the interview is here (the video portion was removed):

    Deaf Skier Overcomes Adversity

    A big thank you goes out to Phonak and HearingLikeMe, the company who made it possible to compete in tournaments. Another thank you goes out to Anytime Fitness Naperville, Badger Balm (they supplied the sunscreen and lip balm) and Tommie Copper.

    Next up is Women’s Week at the World Barefoot Center, where I’m hoping to accomplish a back-to-front instead of a back-to-splat:

  • Mary Clark, Missing Her Smile

    a href=”/wp-content/uploads/2012/08/20120825-082817.jpg”>20120825-082817.jpg

    The first thing I noticed when I met Mary Clark 23 years ago was her smile. We were in one of those dull, never-ending meetings which involved advocacy of some sort for our jobs, but after exchanging introductions, I knew there was something special about this gal. She was a quiet, gentle soul who had a way of speaking up which made everyone take notice.

    We bonded over our journey of becoming deaf as adults and we got involved with many different organizations. Our paths often crossed at meetings. Mary helped birth the Association of Late-Deafened Adults (ALDA) and I lead the West Suburban Association of the Deaf.

    We ended up pregnant at the same time. I gave birth to my first; she to her third daughter. As we watched our babies playing on the floor of her house and I sat there in exhaustion, asking her how she kept it all together when I was falling apart with just one kid. She threw her head back and laughed. “There are some days I just take it minute by minute.”

    When her middle child became hard of hearing, we bonded yet again; this time, we worked together to start a parent organization, Illinois Hands & Voices. She wrote the first grant which gave us funds to run our first Mom’s Night Inn. She spoke at the event, sharing her journey with straightforward candor and openness.

    I always looked forward to our lunches together. She was the kind of friend I could pour out my deepest thoughts and I’d get back a perspective I hadn’t considered previously or she’d dish out some practical advice.

    Last October, we met for lunch and had one of our most profound conversations about life… and the shortness of it all. “I’ve been happy, I’ve been sad, I’m ok with it all,” she said.

    Mary’s way-too-short life ended yesterday at 11:30 pm. I’m sad. Actually, I’m heartbroken. I know many others are too. She touched a lot of lives.

    Her smile will remain forever in my mind.

    There’s a tradition at the ALDA-Con where we stand in a circle, arm-in-arm during the last song of the night.

    Did I ever tell you you’re my hero?
    And everything I would like to be
    I can fly higher than an eagle
    Because you are the wind beneath my wings.

    This year, there will be a gap in the circle. We will miss you, Mary. You’re the wind beneath our wings.

    Wake:
    Thursday Aug 30th from 4:00pm until 8:00pm
    Service at 7:00pm
    Dreschler, Brown and Williams Funeral Home
    203 S. Marion
    Oak Park, Il

  • Would You Trade Passion for Hearing?

    “I don’t know what it’s like to be deaf, but I do know what it’s like when something is important to a person,” a new friend wrote. “I have a question for you, if God or man came up with a solution to restore your hearing, and in exchange you had to give up barefooting, which would you take? I’d bet the farm that you’d take the deal.”

    To this new friend’s surprise, I’d take the barefooting over restored hearing.

    You see, I’ve been deaf so many years now it is just a part of me. I’ve long moved past the stage of grief and into living. That doesn’t mean I still go through periods of time when I get down about the communication difficulties and wish for hearing. I had a lot of moments like that yesterday when I struggled to understand the conversations flowing around me at the barefoot tournament.  But to give up a passion? No can do. Now if I could have both, that’d be a different story…

    This week’s guest post over at Lipreading Mom explores the topic of why going deaf became a blessing for me:

    Why Going Deaf Was a Blessing for Me

    Special thanks to Shanna Groves for sharing my story.

    How about you– would you give up your passion if it meant being able to hear?

  • Speaking at the Social Media Breakfast in Madison

    I had the pleasure of speaking at the Social Media Breakfast in Madison, Wisconsin this morning on the topic of Social Media in a Specialized Niche.  A great group of people there!  (Photo courtesy of Anne Rubens)

    Here’s a summary of the event: Don’t Get in a Pissing Match with a Skunk 

     

     

    Photos from Bob at DiditDirect:

    In the afternoon, Paul Stokes and I took off for the river and spent the afternoon barefooting with Jes Laing.  Paul broke in his boat for the first time and we spent a few hours on the water.  Needless to say, I’m pooped!

    Jes does a toe hold:

    Paul regrips for a 360:

     

  • Todd Hlavacek, Software Engineer

    Todd Hlavacek software engineerTell me about your job, career, or calling. How did you get into this line of work?

    I’m a software engineer.  I knew back when I was a gangly teenager sitting in front of my Apple IIgs writing BASIC that I wanted to be in the computer field writing code.  Ever since that epiphany, I worked my butt off to get in the field.

    What is the best part of what you do?

    Solving the world’s problems.  🙂  Seriously, an analogy comes to mind here.  Think of Michelangelo working on the Statue of David.  He had a vision of what he wanted the statue to become.  The result of his hard labor was a beautiful statue.  It’s the same way I feel with my work.  The best part of what I do is I get something in the form of written requirements for a “problem,” and I work using some or all of the skills I have to get to the end result — a beautiful statue written in software code.

    What are some of the challenges?

    Admittedly, in a field like this, my deafness would be more of a hindrance, but fortunately, technology has progressed to the point where there are engineers, hearing, deaf and even blind, who do work remotely.  In order for them to do their jobs effectively as remote engineers, tools have to be utilized over the internet that I as a deaf engineer have benefited from greatly —

    1. Instant Messaging
    2. Go-To Meeting (similar to Microsoft’s old NetMeeting)
    3. Video Conferencing where other call in, and I can call in using Video Relay from home
    4. Smartphones — believe it or not — because now with the capability to text, IM and all on a smartphone, deaf engineers now can be a part of the “on-call” rotation with other hearing colleagues.

    One challenge still remains — face to face brainstorming and design meetings where my presence is needed.  I use sign language interpreting services for that.

    As I tell people when they encounter a deaf engineer — “Being Deaf only means that we use a different language than English to communicate orally and verbally, it does not of and by itself mean that we can’t do the job that any able-bodied engineer speaking a different language than English can do.”

    What was it like growing up/becoming Deaf/deaf/hard of hearing?

    Gosh, this is both an easy and difficult question to answer.  You see, I grew up with a deaf brother in a hearing family using Total Communication.  My mom never subscribed to the “oral only” or “Sign language only” methodologies.  She wanted to give my brother and I all tools from which we could utilize to be successful later in life.  Little did we both know growing up that we both would later use speech and sign language at one time or another throughout our lives wherever applicable — at home or at work.  I fought against one methodology and embraced the other.

    So, while growing up deaf was hard, I was fortunate in that I had a mother who fought for me.  I had access to other deaf/hard of hearing friends along with a good education.  So growing up was good, but not easy. Today’s deaf/hard of hearing children have it far much easier, I’d think, with a wide range of activities, organizations, and the like out there.

    What advice would you give a D/deaf/HH person who is looking for a job, career or calling like yours?

    I would say this:

    Number one, play around with the activities that will lead to your calling NOW instead of waiting until college.  Don’t just say, “I want to work with aeronautics” and sit and play games on your X360.  Find out all about aeronautics, do activities, etc.

    For example, I played with BASIC programming, along with other computer related stuff, back when I was a teenager — way before high school and through high school.  I knew right then it was for me.  I never changed majors in college.  The first major I went into was the one I graduated with.

    So, having stated that, if you are not sure but want to wait, don’t.  Find ways to do these activities, whether it be volunteering for a not for profit organization, or doing self-paced study online (there are plenty of them online these days), or taking community college classes.

    Number two, remember the saying:  “All work makes Jack/Jill a dull person” and conversely, “All play makes Jack/JIll an unhappy person.”  Find a balance in life between your pursuit of the calling and some play time.  Don’t sacrifice your social aspect in your relentless pursuit of your calling.  Don’t sacrifice your hard work by doing too much play time.  You’ll live for 80+ years, so be mindful of that.  You’ll find that your social life does in fact help you with your professional life, and vice versa.

    Number three, enjoy life.  Enjoy doing the work you want to do.  The day you stop enjoying it is the day you need to take a second look at whether the calling is for you or not.  I’ve been in this field for over 15 years now and I still feel the same excitement that I did the first day on the job.  I love what I do.

  • Top Ten Deaf Folks on Twitter

    top deaf on twitter

    Of course Marlee Matlin is number one!  What fun to be among this cool group of deaf folks:

    To Ten Deaf Folks on Twitter

  • My Hands & Voices Family

    I’m back home after five amazing days in Oregon for the 2012 Hands & Voices Leadership conference.

    We started off with our board meeting:

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    Hands & Voices has grown from four chapters to chapters around the world.

     

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    We opened the evening with a team building exercise to see who could build the tallest tower out of noodles and tape, with a marshmallow on top.  Hilarious fun!

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    The conference was located next to the beautiful Columbia River in Hood River, Oregon.  Breathtaking!

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    There are times when my heart gets tired of “battles” among communication choices and the constant advocacy which comes from this field.  But at the Hands & Voices conference, my eyes settled on a three-month old baby in the arms of her parents–one look, and passion and purpose comes flooding back.  If we can support just one family on this journey, we have given back.

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    Today, I’m up at Christie Lake, surrounded by five teenage boys.  Four of them in this picture are students from Rochester Institute of Technology.  All four are from different educational backgrounds and experiences.  They’re the results of the “choices” we make as families raising deaf and hard of hearing children.  But as I watched the boys crack jokes, laugh and talk about everything under the sun, I realize the bottom line– as parents, professionals and deaf/hard of hearing adults in the Hands & Voices family, it comes down to the same thing: we all want happy, well-adjusted kids.

    And it’s so much easier to navigate the journey with the support of one another.

  • Solution for Knee Pain: Tommie Copper

    I woke up early one morning before a speaking gig a few weeks ago and I couldn’t get back to sleep.  For once, I didn’t feel like reading or writing, nor did I want to get out of bed.  So I turned on the TV.  Well, there’s not much on in the wee hours.  I came across Montel Williams talking about a Tommy Copper compression sleeve.  I was intrigued, because the owner/inventor, Tom Kallish, created this product after a devastating waterskiing accident left him in chronic pain.

    I had my ACL reconstructed last December and in the middle of the rehabilitation process, I developed a rubber-band string of pain over the knee. This pain only happened when going up and down the stairs or doing squats.  In physical torture therapy, the therapists felt it was a tracking issue and the solution was to tape my kneecap over to the side.  This took pressure off the tendon/ligament and provided a little relief.

    I needed another solution, and I couldn’t get the Tommie Copper thing out of my mind.  After a few tweets, the company sent me a knee sleeve to try out. I also wanted to test it on the water as well.

    After the first day, I didn’t notice much difference, but I welcomed the additional support that the sleeve gave me.   By the second day, there was an improvement.  I could go up the stairs without having to hang half of my weight on the banister.  By the third day, I was sold.  The compression sleeve was very comfortable to wear and I often forgot that I was wearing it.  As the days went on, I noticed a marked improvement in the pain when going up and down the stairs.

    Yesterday was a real test– I forgot to put the sleeve on and left the house.  By the end of the night, my knee was aching after hitting the stairs. The sleeve is back on this morning.

    A big thank you goes out to the Tommie Copper gang– thank you for a great product!  It’s a product I’m definitely recommending to folks who are experiencing aches and pains.

    Tommie Copper Knee Sleeve

    And last week, during a filming for the documentary, I’m Fine, Thanks, I wore the Tommie Copper knee sleeve buried under a humongous brace.  I crawled out on the boom for two barefoot runs for the camera– and I had no pain while bending the knee.

    Now, if Tommie Copper comes out with a tie dye or water design, I’ll be stylin this summer!