2011 Fall Parent Workshop

On October 22, 2011, BC Hands & Voices held its 3rd annual Fall Workshop at BC Family Hearing Resource Society in Surrey. It was an honour to have Angela Clancy, Executive Director of the Family Support Institute, lead the workshop. The focus this year was on the brothers and sisters of our children with hearing loss. Parents listened to a presentation and took part in discussions on how to build healthy sibling relationships within their families and meet each child’s own unique needs.

Angela shared with the group some valuable insights into sibling dynamics and offered practical tips to employ at home. She included endearing personal anecdotes about her own experiences, growing up with a brother who has special needs. Two “seasoned” parents, April Cowley and Anja Rosenke, were each invited to speak of their journey in raising their children when one is deaf or hard of hearing. Throughout the day, attendees joined in the dialogue by sharing their own colourful stories with the group, which complimented the subject material presented by Angela. The opportunity to learn from Angela Clancy as well as from other parents that day proved to be an empowering combination for all.

Setting the stage for the day’s discussions, Angela began with the idea of becoming travellers to each other’s worlds and to utilize this perspective in communicating. For example, I must be sensitive not to impose “my world” when I’m visiting “your world”. There will be time to visit “my world” afterwards. It was a strong message and a positive one, establishing how important it is to honour and respect each person’s viewpoint and ideas. Upon this premise we can teach our children to tell their stories and talk about their feelings, thus opening up the channels of communication and strengthening relationships.

Along those same lines, the concept of active listening was a common thread throughout the day’s talks, as listening is the first step to establishing communication. Clancy spoke of being “physically present”, demonstrating body language that is open and accepting, being attentive and hearing the person out. As parents, it is important not only to model this ourselves, but to teach our children these important social skills as well.

Helping our children become proficient communicators first means teaching them to hear each other, and naturally age appropriate approaches need to be considered. One parent suggested the “Bug and Wand” technique whereby the children face each other and take turns telling the other “It bugs me when (you do such and such)”, followed by “I wish (you would…)”. A simple and visually strong technique, I have already found success in prompting my 4- and 6-year-old children to use it at home!

Angela also touched upon some of the concerns that brothers and sisters may internalize as siblings to a child with a disability, such as embarrassment, a sense of isolation, resentment, an obligation to care-give and worry about the future. Again, the idea of building strong open lines of communication with the siblings to address and work through such feelings is imperative.

As parents, we need to provide a safe environment for siblings to open up about negative feelings or to ask tough questions about their brother or sister’s disability. In other words, if the sibling feels embarrassed and “wishes their little brother wasn’t deaf”, our role is integral to expelling the guilt or fear from these thoughts and make it ok for siblings to air their feelings.

Clancy stressed that families should keep having conversations so resentment doesn’t build. Having said that, she also pointed out that we should explain to our children that while it’s ok to be mad at your brother/sister, it’s not ok to say mean things or to blame the disability. That is something that he/she cannot change. It’s a non-negotiable and teaching respect between siblings is key.

Another issue that came up was the role that brothers and sisters often play in translating for their Deaf/HoH sibling. Sometimes they do it out of necessity, but in other cases the sibling instinctively takes on this responsibility. Angela spoke from personal experience when she added that this can be a lot of pressure for a child to assume. She suggested that families “bring others into the circle” by teaching those who interact with your Deaf/HoH child – even extended family members – some of the main signs your child uses, and if speech isn’t intelligible, what certain sounds or phrases represent. Clancy recommended we give the sibling a choice in how much and in what fashion they want to participate, but not to impose expectations. This too is an ongoing conversation to have.

Some of the other take-away ideas Angela presented centered around conflict resolution and problem-solving between siblings – topics relevant to any familial household on any given day. These included reminders for parents to set clear expectations surrounding acceptable behaviour, to give consequences and ensure follow-through. Involving your children in the process of setting ‘house rules’ or assigning chores can be powerful (what do you think is fair?). And finding solutions together means that children will not only feel involved, but also be accountable.

Of course with any household decision-making or settling of disputes, parents should ensure that the Deaf/HoH child is included in the conversation. Sometimes, this calls for restructuring the environment so that information is accessible to that child. First and foremost, have them be present. Take steps to provide the information at their level of understanding. Employing visual aids like a calendar, a flow chart with pictures or an experience book about `Yes/No Behaviour’ can be highly effective.

When children face disagreement, Clancy cautioned against stepping in too soon and stressed the value in allowing children to learn to work through their differences independently. Several times throughout the day, talks came back to the idea of treating the child with the disability ‘just like the others’; that is, levelling the playing field between siblings. Within reason of course, parents should try to suppress the impulse to protect or shelter the child with the disability at times and let them work it out for themselves.

Studies have shown that siblings of children with disability often develop strong qualities of tolerance and compassion. They may be more certain about their own future goals – both personal and vocational. Children who grow up with a brother or sister who has special needs are often more aware of the consequences of prejudice and orient themselves towards humanitarian interests as adults. Certainly, they develop an increased understanding of others.

And it all starts at home. Adopting an attitude of acceptance and pursuing it through open communication is clearly a foundation for building strong, trustful and positive relationships between siblings within the family. As parents, the task is ours – the opportunity is ours – to shape our home environment and guide our familial interactions to that end. A final thought to contemplate is a term that Angela mentioned that day: DIVERSABILITY over DISABILITY. We are more alike than different after all.

Thank you to all the attendees, volunteers and board members who helped to make the day such a success.

BC Hands & Voices also wishes to extend a big thank you to Angela Clancy for helping us navigate this part of our journey in raising our children.

We’d like to express our gratitude to the following organizations for their financial and/or in-kind support:

  • Preferred Interpreting 
  • BC Family Hearing Resource Society
  • BC Early Hearing Program
  • BC Children’s Hospital Family Support Groups/ Networks Funding Committee
  • Gwyn Morgan & Patricia Trottier Foundation
  • Family Support Institute

 

Want to learn more about The Family Support Institute, BC Hands & Voices or sibling relationships? Please check out the following links:

 

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A Whole New World

When I was two years old I was diagnosed with a severe to profound hearing loss. I was the first deaf person my parents had ever met. Decisions had to be made, and my parents made the best decisions they knew how for me at the time: they fitted me with hearing aids, enrolled me in speech therapy, and chose to mainstream me.  My main mode of communication with my world was through speech, and through lip-reading.

Growing up, I never really complained much about my hearing loss. Truth is, I didn’t spend much time thinking that I had one. I lip-read fairly well, and save for an FM-System and my hearing aids, as well as hearing resource teachers, I didn’t really see myself as any different than my peers. I really wanted to fit in with the world I was in, which was the hearing world and the only world I knew of at the time. There were times when I would be assertive, like if I was to watch a movie, I knew to ask for closed captions, and I knew to explain to people that I was lip-reading them. (The lip-reading part got me friends in school, especially when people realized it was an extremely useful tool in eavesdropping, but one I tried not to participate in too much – people deserved their privacy.)

I did okay in school – I excelled at reading, writing and social studies, but in math and science I fell behind. I was an okay student, and I did what I had to do to get by. I did love school, but I never looked forward to it, simply because it was both frustrating and exhausting in terms of how much work it was to keep up to hear.

My frustration was at an all-time high when in high school, my hearing loss took a turn for the worse and I was no longer getting by on my own:  my hearing that I had couldn’t support me anymore. It was at that point an interpreter was assigned to me. Having a sign language interpreter there was the first time I really accessed everything I had been missing out on – PA announcements, movies that weren’t captioned, what students were saying in the back of the room. Although at the time I was not fluent in sign language, I understood everything my sign language interpreter was saying (she signed a mixture of ASL and English); I really believe that people who are hard of hearing or deaf are amazing adapters and that our brains autonomously adjust to things we know will help us communicate.

After high school, I enrolled at the Youth in Transition Program provided by the Provincial Services for the Deaf and Hard of Hearing, where I met other deaf youth who signed and had a counsellor who supported me in my educational pursuits. It was then that I learned about Gallaudet University – the world’s only school for the deaf and hard of hearing teaching exclusively in American Sign Language (ASL). It is thanks to my hearing resource teacher in my final years of high school and the Deaf community in Vancouver who supported and encouraged me in my pursuit of immersing myself in ASL that I drew the courage to transfer to Gallaudet University.

Gallaudet isn’t like any other place I’ve ever gone to. For me, it encapsulates everything that Aladdin and Jasmine were singing about in their movie, about a whole new world. Especially the part about no one to tell us “no”, because at Gallaudet, everything is completely accessible, on a level I never knew was possible. Gone are the days of PA announcements being inaccessible – they’re done on a TV screen in sign language. Everything is taught in Sign Language directly, and the class discussions that were always hard for me to be a part of suddenly become engaging and entertaining, everyone signing.

One of my fondest memories of Gallaudet is one of the first days of classes when I transferred in and the teacher had announced we were watching a movie. I unconsciously raised my hand to ask the question I had been asking my entire life: is the movie closed captioned? After I asked, I caught myself in a smile as everyone around me looked at me and laughed with me: of course it was. This was a school where everyone was like me. Where we weren’t “hard of hearing” or “deaf” or “disabled”, we were students having our dreams come true, within a world that wasn’t stopping us. Teachers actually know you by name, and the biggest class size I’ve had was with 20 people.  I’ve become a better public speaker because so many of our classes require presentations where we receive feedback and support from both teachers and peers.

It’s been said that an education isn’t worth a great deal if it teaches you how to make a living, but not how to make a life (unknown). At Gallaudet, I find this has come to be true. Gallaudet’s teaching doesn’t end when classes are over, it stretches on, to the cafeteria lunches and dinners where you can engage with your peers in accessible communication and sometimes out -of- this-world debates. The typical late night college study sessions consist of music – songs are signed in ASL combining both worlds into one. Fire alarms that consist of flashing lights instead of sound, proving you don’t always need to hear in an emergency.

Before Gallaudet, I was an average student, never really putting the time into school to excel. At Gallaudet, however, that all changed. I’ve joined a sorority. I’ve taken amazing classes like the BioPsychoSocial Aspect of HIV/AIDS. I have been on the Dean’s List for several semesters and have won several scholarships. I even got to participate in a federal internship.

I care about my education now, because it’s accessible to me and I have people around me who challenge me daily without a language barrier. I met one of my best friends through the Honours Program at Gallaudet, and we continuously push each other to become better scholars as well as people; she’s now pursuing her doctorate degree, and every time I’m not sure I can do it or I start to doubt myself, I remind myself that she has set the bar higher and that I should too.

I have met some of the most incredible people at Gallaudet. They have taught me patience, kindness and resilience. When I have doubted myself, they were there, picking me up, encouraging me in a way that I have never had before, because they know what it’s like to both hear, and to not. Sometimes, no explanation is necessary, because they’ve been in my exact shoes before. And they inspire me, because for the first time in a long time, I know that I’m not alone.

My time at Gallaudet is coming to an end, but I won’t forget the lessons I’ve learned and I cherish every moment I have spent there. I don’t simply feel like I’m leaving a college, I feel like I’m leaving a home. Gallaudet has instilled in me a pride for being deaf and hard of hearing. I take comfort in knowing that I have been to a whole new world, one that is filled with beautiful hands and beautiful dreams, and the knowledge that nothing is impossible if you know how to make a life and not just a living.

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Crash Crawly’s Family Fun Day

BC Hands & Voices is organizing a Family Fun Day at Crash Crawly’s Adventure Playground in Coquitlam on Sunday, March 4th, from 10am to 1pm. This event is for families with hard of hearing ordeal children and teens and CODAs (children of deaf adults), along with their parents.

Fun Activities for the Whole Family

Soft Play: Climb, crawl, and slide for way through our maze – do you dare conquer the black slide?

Toddler Area: “Comfy Land Area” for children three and under.

Ball Pits, Train, Jeeps

Laser Tag: An updated Egyptian theme “Valley of the Kings” feature two stories, a mirror maze, bridges, lookout points and more! Great for teens.

Ballocity: Two floors with six ball blasters, a ball dump, a ball volcano, and a ball vacuum.

RSVP Required

Register by Sunday, February 26th. Online registration at chhaparents.bc.ca or register by calling or texting 604-684-1860.

Cost is only $3.00 per person, and that includes all Crash Crawly’s activities. Drinks and snacks are available for purchase at the concession.

ASL interpreters will be provided.

Crash Crawly’s Flyer – 2012
Crash Crawly’s Flyer – 2012 – Chinese Version

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Join Us For Our 2011 Fall Workshop

Hosted by BC Hands & Voices and Guide By Your Side

Presented by: Angela Clancy, Executive Director of the Family Support Institute

English Printable Flyer
Chinese Printable Flyer

Meeting the needs of everyone in the family can be a challenge – especiallywhen one or more of the children are deaf or hard of hearing.  This interactive workshop will focus on identifying common issues that arise with siblings, as well as strategies, ideas, and resources to help deal with them.  Topics will include:

  •   The needs of all children
  •   Sibling relationships
  •   Parenting strategies (active listening and overall effective communication)
  •   Dealing with conflict
  •   The benefits of growing up with a brother or sister who is deaf or hard of hearing

There will also be time throughout the day for families to socialize and share information with one another informally.

Saturday, October 22nd, 2011 from 10:00 am-3:00 pm.
BC Family Hearing Resource Centre
15220 – 92nd Ave., Surrey (click for map)

Childcare will be provided at no cost – children must be pre-registered.

ASL interpreting will be provided.

Language interpreting may be available for families who do not speak English.  Resources are limited, so please contact us ASAP if you know of a family that requires interpreting.

REGISTER by Wednesday, October 12th using our online form.

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The Best Fit for One Family

2012 photo Joy“Baby Sign Language is all the rage nowadays!” I exclaimed to myself as I finalized my order on Amazon.ca for Baby Sign Language books and DVDs. I was six months pregnant, and like any other new (and nervous!) mother, I had spent massive amounts of time on an endless quest for information, tips, and latest trends in parenting. I aspired to raise an imaginative and articulate child, and often fantasized of someday having a conversation with my toddler where he or she would tell me stories about their day at preschool, and I was especially looking forward to hearing the ones drawn from the imagination. All my research seemed to suggest the same concept to “Introduce language to your child at an early age.” So it was then that I made the decision to commit to ensuring that my child would be in a language enriched environment, be it spoken or visual.
My DVDs and books had finally come in, I was excited! About five minutes into watching my first DVD, I was already confused. The woman on the television seemed to just be making random hand gestures, and I thought to myself, “This is all supposed to mean something?!” I made sure I knew the basics… “Milk,” “Diaper,” “Bath,” “More,” and “Sleep.” I felt that was enough visual language to let my child know I was making an effort to communicate. Besides, I thought that making sure that I constantly spoke to my child would still be promoting a language enriched environment. Alas, like any other impulse online purchase, the books and DVDs collected dust.
Early Halloween morning, Teanna was born, and she instantly had me wrapped around her tiny little finger. Yes, I was smitten, and I wanted to give her the world. She was a tiny girl, yet in spite of her petiteness, it was already apparent that she had a big and captivating personality. Even as an infant, she seemed to be extremely observant, her eyes wide, a naturally curious expression, and her head constantly turning as if to absorb everything going on in her surroundings. I spoke, sang, and signed the very limited amount of signs I knew with my daughter. She smiled and giggled no matter what I did, she was a happy child, and I, a sleep deprived but nevertheless happy mom. At 8 months old, she signed “diaper,” and when checked, had actually needed a diaper change. I was floored, to say the very least – my child was communicating! At 10 months, she had learned to sign “sleep,” and I would have to gloatingly say that bedtime was always such a breeze. I loved her, and I was happy, but there was a part of me that felt like there was something that was not quite right.
By the time Teanna had turned a year old, she was happy and healthy as ever. However, there still seemed to be some sort of disconnect, a gnawing feeling, if you will. I have had suspicions regarding her hearing since she was born, and it was not until she was 19 months old that she was officially diagnosed to have been profoundly Deaf in both ears. It was a rough and emotional experience, and not only had I felt like I was mourning the loss of something very important, but I was also lost as to what to do next. It was an overwhelming time, filled with so much information from a multitude of resources. It was a time for life-altering and time sensitive decision making, and frankly, I had begun to feel so numb from it all, that it felt like I was simply being carried along the chain of events.
Teanna had immediately gotten fitted for hearing aids, and I felt it was the best decision to choose an intervention program where both a Sign Language Instructor and Speech Language Pathologist would be available. Having an actual instructor for American Sign Language (ASL) made learning it easier. I discovered just how visual the language is, as most of the signs are reminiscent of the English word definition. It definitely was not just a “bunch of random gestures” made in an effort to convey a thought. ASL is an actual language, with grammatical rules that needed to be followed. As much as I found the learning process enjoyable, it took some time for me to feel comfortable using it, even with the instructor. However, as unnatural as it felt, I knew that it would benefit my daughter, so I made an effort to sign with her as much as I could when it was just the two of us. There were many aspects of ASL where I felt slightly awkward. One example being the use of very pronounced, almost exaggerated facial expressions. Raised eyebrows when asking a yes or no question, a furrowed one when asking one that needed a more detailed reply. Pursed lips when describing something that is small, and saying “cha!” with eyes wide to describe something large. It was a time of adjustment.
As with most languages, ASL was accompanied by a culture of its own, the Deaf Culture. Throughout my journey, I have come to learn that Deafies are a very warm and welcoming bunch. I was noticing Deaf people everywhere! I would muster up the courage to approach them in restaurants, at the mall, and I had even found a church that had a Deaf ministry. I had mastered signing, “Hi, my name is Joy. I saw you signing, are you Deaf? I have a daughter who is Deaf, and I am learning Sign Language very slowly.” When a Deaf person sees you making an effort to communicate in their language, their eyes light up, and they are more than willing to sign extra slowly, or even try and speak to have a conversation with you. It was a great feeling when I saw that I, a hearing person, could have a sensible conversation with a Deaf person. In the Deaf Culture there is Deaf Pride, which states that a Deaf person can do anything except hear. I found the culture to be extremely interesting, and begun to immerse myself in it at my own time. I read books, articles, and websites – I wanted to be educated, after all, this IS my daughter’s culture.
Teanna received a Cochlear Implant in her right ear in the Winter of 2009. She currently goes to a preschool where both Deaf children, and children of Deaf adults (CODA’s) attend. In school, the teachers both sign and speak. She receives Speech Therapy every day, and is showing steady progress, as she is currently babbling and making great efforts to speak certain words. She is also recognizing various words that she hears. Her Sign Language skills continue to impress me, she is becoming quite fluent, and at times I feel like I am starting to trail behind. Through Sign Language I can see that she is clever. “I want juice, please,” she asked me one day. “I don’t have juice for you right now, just water,” was my reply. She held up a grape that she was snacking on and signed, “Ok, there is juice inside the grape,” then ran off to play. Through Sign language I can see that she has a sense of humour, she jokes around and I know what types of things she finds funny. Currently she has many imaginative stories involving slapstick comedy. Through Sign Language she is able to voice her emotions, recall past events, and express what she hopes to do in the future.
Personally, the decision to give my daughter a combination of the Cochlear Implant, speech, and American Sign Language is what works for us. There is no doubt that it keeps the calendar pretty full, but it also poses plenty of perks. Teanna will be bilingual, and I feel that she is able to receive the best of what being Deaf and hearing has to offer. Growing up, I lived an expatriate childhood, and I would constantly be reminded that it is important to “remember my roots.” I believe that the decision to educate and involve ourselves with Deaf Culture is giving my daughter a solid foundation as to who and what she is. It is a fact that I am raising a Deaf child in a world that is predominantly hearing. Being involved in the Deaf Community gives her a sense of belonging, and surrounds her with people with whom she shares something in common. I believe it is this involvement that will give her a strong sense of self, thus giving her the confidence to venture out into the hearing world. Teanna will be faced with having to make various decisions about her life as an adult. With the foundation that I am laying out for her, I strongly believe that I am giving her all the tools she may need, no matter which path she chooses. I too, am preparing myself to be in a position to support her decisions. When she was born and I held her for the first time, I knew I wanted to give her the world… Now, she has both the Deaf and hearing worlds at her fingertips.

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Fun in the Sun! End-of-Summer Informal Get-Together

A great chance to socialize and catch up! Wading pool and playground – bring a picnic lunch and blanket. Cancelled if it rains.

Grimston Park in New Westminster – 19th St. at 7th Ave.
Look for the orange and blue balloons.

www.newwestpcr.ca/parks/community_parks/grimston_park.php

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Hard of Hearing Teenaged Fiddler Travels to Scotland

By Teresa Kazemir

Our son Jesse traveled to Scotland this past summer – he is a  fiddle player with the North Shore Celtic Ensemble, and they  participated in the Aberdeen International Youth Festival for  12 days in July and August.  It was an intense, exciting experience for the  20 teens that went – they all had a fantastic, if  exhausting,  time.

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Jesse is hard of hearing and wears two Bone Anchored Hearing Aids (BAHAs), so there were a few things to consider when  planning the trip.  For one thing, we made sure the chaperones knew that he would not wake up in case of fire, as he  would not hear the alarm.  Chaperones and other kids in his  flat were told that in the case of a fire, someone would have  to go into his room and wake him, and so Jesse made a point  of not locking his door when he was sleeping.  In fact, even  though he has a vibrating alarm clock, Jesse tends to fall back  to sleep after it wakes him up (teenage boys can really  sleep ), so there were a few occasions when his friends had  to wake him up for breakfast.   

Jesse also made a point of packing his dry aid kit – we have  found that in some places the air is more humid (especially if  we are camping and staying in a tent), and that causes problems with his hearing aids.  Storing the aids in the dry aid kit  each night helps with this.  Jesse also took it in case his hearing aids got wet – it rains a fair bit in Scotland.    

One security guard questioned Jesse about his hearing aids  when going through security at the airport.  Jesse is quite  practiced at talking to people about his hearing aids and hearing loss, and once he explained, they did not hassle him any  further.  I think it helped that Jesse was not at all defensive,  and was quite happy to explain.

There were some situations during the trip where Jesse found  it difficult to hear – he managed OK in the cafeteria, but the  cabarets we attended each night (where different groups performed for each other) were VERY loud.  It was so loud that  no one could hear, though, so Jesse was not alone.   

Jesse also found that each concert venue where they  performed was different, and there were a few places  where he had a hard time hearing the guitar (which is  critical when you are playing as part of an ensemble,  and the guitar sets and maintains the beat).  The musical directors of the group are very respectful and  understanding about Jesse’s hearing loss, but they  don’t necessarily know when Jesse is having a hard  time hearing. It’s his responsibility to let them know,  and then they make any necessary adjustments. When Jesse was new to the group, he was hesitant to  speak up, but as his confidence has grown, he has  become much better at advocating for his listening  needs.  There were two or three times this trip when  he was able to adjust where he stood so he could  btter hear the guitar through the monitor on stage.

Another challenge was the fact that participants  came from all over the world.  Many people spoke  English, but with a whole variety of accents.  This  typically presents a challenge for people with hearing  loss, but Jesse actually found that he could understand most accents quite well.  He did struggle with the flight attendants from Air France, who had very  strong French accents.  He found he used the same  strategies as everyone else – listening carefully, asking the person to repeat, or asking a friend for clarification.

Overall, Jesse’s hearing loss did not really cause many  problems for him on this trip. Preparing ahead of  time definitely helped (talking with chaperones, packing the dry aid kit).  The challenges a person encoun* ters when travelling certainly vary from person to  person, depending on their hearing loss and other  factors, but one key strategy is to be proactive and be  prepared.   Other than that, perhaps the best tool is a  sense of humour – a smile and a laugh certainly help  to smooth things over when an instruction is missed  or something is misheard.

As a parent (and chaperone) it was really good to see  how independent Jesse has become, and how he can  use strategies to compensate for things he might be  missing.  I have chaperoned on several trips over the  years (ensemble trips and school trips) and have  found it to be a wonderful way to help the other kids,  teachers, leaders and parents learn more about  Jesse’s hearing loss.  There are oUen nice, natural  opportunities for people to ask me questions that  they’ve never quite got around to asking.   So, Scotland was great, Jesse now has the ”travel  bug”…and I am confident that his hearing loss will not  hold him back.

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Posted in Families to Families, Newsletter - Apr 2011 | Comments Off on Hard of Hearing Teenaged Fiddler Travels to Scotland

Spring Picnic at Clayton Community Hall

Our third Annual Spring Picnic will be another opportunity to meet other families with children who are deaf or hard of hearing, ages 0-5.

Saturday, May 28th 11:00 am to 2:00 pm

Clayton Community Hall (on 70th Avenue near 184th Street in Surrey)

(click for map)

  • Meet at the shelter near the playground – look for the blue & orange balloons!
  • Bring the whole family and a potluck dish to share (beverages will be provided).
  • Don’t forget your blankets & lawn chairs. We will move into the hall in case of rain.
  • Fun for the kids! Face painting, crafts, parachute games, races & playground.

Please RSVP by Wednesday, May 25th to info@bchandsandvoices.com or phone us at 604-552-2254. Please include your names, the age(s) of your child/children, and what you would like to bring.

For those that live outside the Lower Mainland, We have a grant from BC Children’s Hospital to help pay your travel expenses to come to our event!  It will not cover flights, but would certainly help with ferry fares, gas, etc.  Please contact us to find out more details.

Download a printable version of this announcement

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Blossoming in Kindergarten

CaitlinThree years ago when our daughter Caitlin was 18 months old, she barely spoke ten words. We were concerned about her development so we took her for a hearing test (no screening was available when she was born). It turned out she had permanent mild to moderate sensorineural hearing loss. She was fitted with hearing aids within two weeks and then began intervention a month later. In my sadness, one big concern was whether she would be able to enter kindergarten in our neighborhood school with the young children she already knew. But, three years later, after consistent hearing aid use and weekly intervention, she was ready to go to our local school with her friends.

In the spring before Caitlin turned five, both her preschool teacher and speech and language pathologist thought she was ready to go to Kindergarten that September, but I was nervous about how it would all go. She is a late November baby, was still quite shy/quiet in group situations and she had just managed to learn her capital letters after hours of practice. To make matters worse, we had watched Caitlin struggle through the years with new concepts like learning her colours and the names of her extended family members. I was so worried that the new concepts in Kindergarten would take her a long time to master.

What put our minds at ease was we knew she would receive tons of support. Back in the spring, Caitlin’s preschool teacher (coincidentally a mother of a hard of hearing teenager) referred us to a hearing resource teacher in our school district. We had a meeting in May and started planning her IEP (individualized education plan) with the professionals who would be working with Caitlin. The hearing resource teacher also arranged all the paperwork designating Caitlin such that she would receive as much support as possible. This designation led Caitlin to share a full time specialized education assistant (SEA) with another boy in her kindergarten class. In September, I attended an IEP meeting with the SEA, the classroom teacher and the hearing resource teacher. We spent an hour talking about goals for Caitlin and set three goals connected to her speech, listening and independence with her FM and speaker system. We were told she would be the only child with a hearing loss in her school, which was worrisome. But she spoke well and was very social in small group situations, so we hoped for the best as she embarked into Kindergarten that fall.

Caitlin’s classroom was (happily) small and carpeted, creating an easier listening environment. In addition, the room is bright, colourful and full of books and toys. Overall, the classroom is stimulating but there are predictable routines. The hearing resource teacher works with Caitlin for an hour each week for a one on one session on the IEP goals we set. Also, the classroom teacher uses a sound field system to amplify her voice for all students (so she is very used to wearing a microphone). Caitlin’s FM system patches in reasonably well. The hearing resource teacher even spoke to our hearing aid company and arranged for a dynamic sound field system that matches even better with Caitlin’s FM – so Caitlin is receiving excellent sound quality.

With all of these accommodations and supports, Caitlin has done better than I ever expected. She loves learning her letters and quickly picked up her lower case letters. She is very independent and enjoys picking out original and fashion forward outfits in the morning before school and putting on and connecting her FM when she arrives at school. She looks forward to “special helper day” when she gets to bring something from home in a box writing the first letter of each object on the outside. In September had to help her; by November she chose three items (two frogs and a bird) independently. I looked on the front of the box and she had written “FFB” all by herself – wow, what progress! Caitlin started the year as a very quiet child and did not share her thoughts, but the teacher now tells me that she offers answers during circle time. Caitlin loves making play dates and plays well with others.

The best moment was in December at the Christmas concert. Each class from Kindergarten to Grade Four sang two songs. When I watched our older son in that concert last year, I couldn’t even imagine Caitlin standing up there. If she could be dragged up there, I imagined her standing, head down and silent. Instead, to our delight, Caitlin confidently walked onto the risers, and faced forward, head held high. She sang the songs with joy on her face. She didn’t just sing – she shouted and I sat in my chair and smiled from ear to ear.

Our little girl has blossomed into a fully communicating, happy student who is succeeding in school. We have a long way to go yet (she needs to learn to read and understand math and of course so much more) but I definitely feel much more confident. The support to make sure that the many small things are in place that all add up to helping her succeed has been amazing, and Caitlin has thrived.

Read this article in PUNJABI
Read this article in TRADITIONAL CHINESE
Read this article in SIMPLIFIED CHINESE

Posted in Newsletter - Apr 2011, Newsletters | Comments Off on Blossoming in Kindergarten
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