Alexander Graham Bell Association

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A life without limits for children with hearing loss

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Site title: Alexander Graham Bell Association – A life without limits for children with hearing loss
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Summer Rewind: Youth and Young Adult Programs In Full Swing!
Sep 8, 2026 · original
Lea en Español While summer is typically the time of year for everyone to slow down, it also provides an opportunity for new experiences. This summer, AG Bell hosted two events for youth and young adults with hearing loss. Here are some of the highlights from their adventures. Young Leaders Network Retreat By Jim Connor The Young Leaders Board recently hosted its 2026 Young Leaders Network Retreat in Estes Park, Colo. The retreat was held at the YMCA of the Rockies, about 1.5 hours from Denver International Airport. A total of 28 participants attended, and they came from all over the United States, Canada, and United Kingdom. On the first day, the attendees arrived at Denver International Airport and immediately bonded as soon as we hit the road to Estes Park. The event officially kicked off with introductions of the Young Leaders Board, guest speakers, and attendees. The first night’s a
There Is No Single Deaf Experience
Sep 4, 2026 · original
Lea en Español If you meet one person who is deaf or hard of hearing, you have met one person who is deaf or hard of hearing. It may sound simple, but it is one of the most important messages of Deaf Awareness Month. Hearing loss exists on a spectrum, and so do the experiences of the people who live with it. Every individual has a unique story shaped by their hearing abilities, communication preferences, technology choices, family support, educational experiences, cultural identities, and personal goals. There is no single path, no single perspective, and certainly no single way to be deaf. Some individuals use Listening and Spoken Language as their primary mode of communication. Others use sign language. Many use a combination of approaches depending on the situation. Some wear hearing aids. Others use cochlear implants, assistive listening technology, captions, or no technology at all.
Stories of Resilience After a Late Diagnosis
Aug 27, 2026 · original
Lea en Español In one of the 16 true stories collected for Late to the Party: Extraordinary Stories of Hope After Late-Identified Hearing Loss by Valerie James Abbott, Beth and Josh’s firstborn Alexis failed the automated auditory brainstem response (AABR) a few times before she was discharged from the hospital. By the time Alexis was three months old, Beth and Josh had participated in more than 20 different hearing health discussions with professionals who claimed they could assess her hearing. At the conclusion of each appointment, “none actually completed a hearing screen or diagnostic evaluation with a solid confirmation of no hearing loss. There were always excuses followed by: ‘I think she’s fine, but let’s reschedule and try again in a few weeks if you want to.’” Alexis was finally diagnosed with moderate to severe sensorineural hearing loss at age 4. This late identification pres
Global LSL Symposium Brings Us Together, Again
Jun 25, 2026 · original
Lea en Español On June 4 to 6, 2026, AG Bell welcomed attendees representing 18 countries to Arlington, Va., for our first in-person meeting since 2019. The vibes and energy could not be contained as old friends reconnected and new connections were forged. Highlights from the in-person meeting included networking sessions, interactive presentations, an active exhibition hall, and lots of hugs from old friends and connections with new ones. Live Learning Opportunities As with every Symposium, the educational advisory committee put together a terrific slate of presenters representing a wide range of topics, interests, and perspectives. What made the in-person presentations different was the opportunities for attendees to ask questions, meet presenters, and connect on a more personal level. This increased the amount of learning each attendee experienced. One attendee summarized their experi
Hiding the Holocaust: Memoir of a Deaf Daughter
Jun 11, 2026 · original
Lea en Español While Irene W. Leigh, PhD, was aware of her parents’ connection to the Holocaust, she didn’t know any details. Uncovering a shocking document led her on a path of discovery, ultimately leading her to write a memoir about their experience and its impact on her own life. Published April 21, 2026 by Gallaudet University Press, Hiding the Holocaust: Memoir of a Deaf Daughter is Irene’s ninth book. While the lifetime AG Bell member, who joined the Association in the mid-70s, is an experienced academic writer, this kind of personal writing was a “learning journey.” Currently Professor Emerita at Gallaudet University, where she is a former Professor and Chair of the Department of Psychology, Irene still has a private practice in psychotherapy and is involved in ongoing writing on critical issues related to individuals who are deaf and hard of hearing in the areas of mental health
Turning Uncertainty into Hope and Action
May 21, 2026 · original
Lea en Español Leah and Sophie Salzberg received cochlear implants three years ago. Not only are they thriving, but they inspired their mother, Jessica, to start a company, Heart of Hearing , to help other families. A Shocking Diagnosis The girls, who are profoundly deaf, are the eldest children in their family of six. They had typical hearing at birth and passed the newborn hearing screening test. There was no reason for concern until Leah was about 2 1/2 years old. That’s when Jessica noticed a delay in her speech development and started her in speech therapy. However, Leah wasn’t engaged during these sessions. Looking back, this isn’t surprising because the therapists were wearing masks as it was during COVID. At the same time, Jessica and her husband Matt noticed Leah wasn’t always responding when they called her name, especially in loud environments with a lot of background noise. T
Going The Extra Mile for Leo’s Education
May 19, 2026 · original
Lea en Español The lack of socialization during COVID-19 interfered with everyone’s educational journey, and for Leo, it caused difficulties when his parents wanted him begin developing Listening and Spoken Language. Leo was born with Usher Syndrome, which causes early vision loss and hearing loss. His family wasn’t new to this diagnosis however, since his older brother by four years, Luke, was also diagnosed with Ushers. The Listening and Spoken Language journey Luke successfully underwent convinced Leo’s parents to pursue the same with Leo. Leo was fitted with two cochlear implants to help with his access to sound. As Leo’s father William put it, they believed spoken language would “give Leo the best chance at hearing and communication.” The only dilemma, however, was transitioning Leo from the sign language to spoken language, at a time when the world was transitioning to virtual lear
Transitioning and Thriving: Liam’s Success in Mainstream Schooling
May 12, 2026 · original
Lea en Español The Academie Marie-Claire has always provided Liam with a welcoming learning environment. With a small class size, caring teachers, and a challenging academic curriculum, the bilingual private school has always helped Liam thrive. This kind of schooling was very important for Liam’s parents, especially when considering Liam’s Listening and Spoken Language journey. Liam’s hearing loss is genetic and progressive. By the age of 2, his hearing loss became profound and his parents decided it was best for him to receive bilateral cochlear implants. At the beginning of his education, his mom Sahar confided that it was hard to believe that Liam could speak. However, now he’s described as “so chatty,” and can communicate in English, French, Spanish, and Farsi. While the Farsi was family-encouraged, Spanish was added on as Liam’s third language, and bilingual learning in English and
Late to the Party
May 7, 2026 · original
Lea en Español Valerie James Abbott’s second book, Late to the Party: Extraordinary Stories of Hope After Late-Identified Hearing Loss , published on May 5, is a one-of-a-kind collection of true stories that illustrate what happens when hearing loss is identified later, outside of newborn hearing screening. And for Abbott, the topic is personal. Motivation As the parent of a late-identified child, Abbott’s experience was noticeably different from families of children who were identified through the newborn hearing screening process. Those families knew from the start their child had a hearing loss and were connected to the right tools early on, whereas families like Abbott’s had to figure it all out later. As a result of late-identification, Abbott’s daughter Bridget (Bridie) was developmentally delayed. “We were carrying guilt and panic and worry that just seemed different,” Abbott reca
Listen to Lisa! A Preschooler’s Advocacy Journey
May 5, 2026 · original
Lea en Español Lisa has never had a problem speaking up about what she needs. In fact, she can advocate for herself in a variety of different languages, including Swedish and English. This is because Lisa’s family is from Sweden, and after their move to Canada, she’s been adding another language to the list: French. With support from Résonance Montréal (formerly the Montreal Oral School for the Deaf), she’ll be able to continue voicing her concerns and even be able to explain her cochlear implants (CIs) in French! Lisa’s doctors knew she was deaf when she didn’t pass the newborn hearing test right after birth. Because she was tested so early, she was able to receive CIs as an infant as well! With her CIs, Lisa has engrossed herself in Listening and Spoken Language services as much as possible, and Résonance Montréal has been there for her every step of the way. Not only does the school f

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