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Meet Birmingham’s Nicole LaMont: Deaf, Scientist, Social Media Influencer

By Je’Don Holloway-Talley For The Birmingham Times Nicole LaMont was like any typical adolescent—fully functioning limbs, faculties, and all five senses. That changed for her at age 12. “It was roughly 3 a.m. when I woke up deaf. Kind of like when someone suddenly turns the TV off when you’re sleeping, so the sudden silence […]
The post Meet Birmingham’s Nicole LaMont: Deaf, Scientist, Social Media Influencer first appeared on BlackPressUSA.

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Nicole LaMont, is a medical laboratory scientist with an impressive social media following. She is also a former Miss Deaf Alabama. (Amarr Croskey, For The Birmingham Times)

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By Je’Don Holloway-Talley
For The Birmingham Times

Nicole LaMont was like any typical adolescent—fully functioning limbs, faculties, and all five senses. That changed for her at age 12.

“It was roughly 3 a.m. when I woke up deaf. Kind of like when someone suddenly turns the TV off when you’re sleeping, so the sudden silence wakes you up, … the silence jolted me,” LaMont recalled. “I first made some clicking sounds with my tongue and couldn’t hear it, so then I knocked on my nightstand and couldn’t hear that either.

“Then I thought perhaps I was dreaming and contemplated trying to go back to sleep and waking up for real—or running screaming to my mom. … Oddly, I wasn’t immediately panicked. I was more confused. I didn’t understand why it was so quiet.”

Doctors did not initially believe LaMont’s claim of deafness. She vividly remembers the trip to the emergency room and the worry etched on her mother’s face. “I saw multiple doctors and had tests done,” she said.

Eight months later and after dozens of tests, the cause behind LaMont’s sudden hearing loss was diagnosed. She had developed a rare autoimmune condition called neurosarcoidosis, which causes inflammation and abnormal cell deposits in any part of the nervous system: the brain, spinal cord, muscles, or peripheral nerves. LaMont’s bout with the condition resulted in bilateral deafness, meaning she was permanently deaf in both ears.

LaMont is a medical laboratory scientist for the Birmingham Veterans Affairs (VA) Medical Center, where she is responsible for performing scientific testing on samples in areas like microbiology, hematology, and urinalysis, as well as for reporting results to physicians. She also has an impressive social media following, with more than 65,000 followers on Instagram, 79,000 on Facebook, and growing audiences on YouTube and TikTok.

“I am still astonished by my following. The most popular videos that seem to get the most views are [the ones teaching] medical signs,” said LaMont, who answered her interview questions for this story via email.

“There are so many nurses and doctors who want to be able to have open communication with their patients,” she explained. “[As a member of the deaf community], it is such a relief when we see our nurses and providers attempting to make our visits less stressful and more inclusive.”

After being asked to teach American Sign Language (ASL) for many years, LaMont decided in October 2022 to post some fun, basic ASL videos on Facebook Instagram, and YouTube for family and friends. “Shortly thereafter, it took off and led me to the following and platform I have now,” she said.

Click to view slideshow.

Best of Both Worlds

At age 13, when LaMont learned that she wouldn’t regain her hearing, she had a procedure to get a cochlear implant (CI), which is a surgically implanted neuroprosthesis, or a device that is meant to replace missing biological functionality that might have been damaged as a result of an injury or a disease. It provides a person who has moderate to profound sensorineural hearing loss with sound perception.

“Without CIs, I am profoundly deaf and without any recognition of sound. With my CIs, while I am still considered profoundly deaf, they give me the ability to hear sound in the way I remember sound to be prior to my deafness. I do still miss some words here and there, but I have the best of both worlds,” she said.

Initially, LaMont rejected ASL. Her family tried to teach her at home, as well as encourage her to take classes at Auburn University Montgomery (AUM) and the Vocational Rehabilitation Service Blind and Deaf Division, which is made available through the Alabama Department of Rehabilitation Services (ADRS). Everyone in LaMont’s family took classes—except her.

“I was embarrassed to sign in public,” she said. “I was getting bullied in school. My so-called friends were now mocking me and would throw up fake sign language in my face to tease me.”

To make matters worse, LaMont was also humiliated before a classroom of her peers by her own teacher.

“I had always completed my work early and would doodle and draw while sitting in silence because I was deaf and had no interpreter, and [the teacher] got mad at me for looking down at my notebook. … He complimented my drawing skills and then made me go stand in front of the class.

“[When I got to the front], he covered his mouth with his hand, so I couldn’t read his lips, and said something. Then he uncovered [his mouth] and told me to repeat to the class what he just said. I just stood there mortified, and then I burst into tears. … This was just a few months after I had woken up deaf,” LaMont remembered.

Importance of Representation

Instances such as those taught LaMont the importance of representation and advocacy for those with special needs. She doesn’t remember many positive hearing-impaired role models during her adolescent years, which can be a crucial time for preteens and their sense of identity.

She does, however, recall the impact of Disney’s “The Little Mermaid” series and a three-part episode titled “Wish Upon a Starfish,” during which Ariel, the mermaid and main character in the franchise, meets what LaMont perceived as “a Black mermaid at the time, but she was really Latina. … Her name was Gabriella, she had a purple fin, my favorite color, and she was deaf. She used very accurate ASL in the cartoon, and that was my first time seeing a deaf person, let alone [a deaf] person of color portrayed on TV.”

Eventually, LaMont saw that deaf wasn’t a bad word. She embraced ASL and became fluent in less than four weeks after taking classes at Gallaudet University (GU), a private federally chartered university in Washington, D.C., for the education of the deaf and hard of hearing.

She earned a Bachelor of Science degree in biology, from GU in 2008, a Bachelor of Science degree in medical laboratory science from AUM in 2016, and a Master of Science degree in clinical pathology from the University of Alabama at Birmingham (UAB) in 2020.

During her collegiate years, the Montgomery, Alabama, native would become Miss Deaf Alabama (2009–2011), Miss Black Deaf D.C., and Miss Black Deaf Student Union.

“My platform was to bridge the gap between the deaf and hearing communities,” said LaMont. “[Using my platform], I advocated for accessibility to entertainment and for other public settings to have open [captioning, which are permanently visible on the screen], and closed captioning, [which can be turned off], in movie theaters, waiting rooms. … I also encourage hearing parents of deaf children to strive for open communication for their children using ASL, in addition to whatever hearing devices the family feels fit their child’s needs.”

“Hearing devices are wonderful, but they are technology and man-made,” she added. “ASL is always going to be there and won’t fail. It won’t run out of batteries and does not depend on external energy other than the physical.”

Science and Medicine

LaMont always seemed destined to become a laboratory scientist. The Birmingham resident has a twin sister, Monique, and an older brother, Mikal.

“My older brother was always mixing potions and really into science. He had his own little microscope and everything, and I followed everything he did,” said LaMont. “I’m one of the very few people who can look back at her 5-year-old diary and see that a dream became reality. In my earliest writing, I wrote, ‘I’m going to be a scientist.’ I was naturally drawn to shows like ‘ER’ or anything that had to do with medicine.”

Science and medicine run in the family. LaMont’s mother is a retired psychiatric nurse practitioner, and her twin sister followed in their mother’s footsteps and is a psychiatric nurse practitioner who also has served in the U.S. Air Force. Her maternal uncle is a retired nurse anesthetist, her grandmother is a retired registered nurse, and her cousins on her dad’s side are in the medical field.

“I’ve always been surrounded by those who study medicine,” she said.

In addition to being surrounded with science and medical experts, LaMont was influenced by a law enforcement professional. Her father is a retired controls worker, who operated and maintained the security and integrity at a detention center via the security system located at the central control facility. At retirement, he was a control worker for the juvenile courts in Montgomery.

“That’s why we were such good kids,” she joked.

You can learn more about Nicole LaMont via social media on Instagram (@signingwithnicole) Facebook: (https://www.facebook.com/nictwin1), YouTube (@ndlamont01) and TikTok (@nictwin1).

 

This article originally appeared in The Birmingham Times.

The post Meet Birmingham’s Nicole LaMont: Deaf, Scientist, Social Media Influencer first appeared on BlackPressUSA.

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LIHEAP Funds Released After Weeks of Delay as States and the District Rush to Protect Households from the Cold

BLACKPRESSUSA NEWSWIRE — The federal government has released $3.6 billion in home heating assistance after a delay that left states preparing for the start of winter without the program’s annual funding.

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By Stacy M. Brown
Black Press USA Senior National Correspondent

The federal government has released $3.6 billion in home heating assistance after a delay that left states preparing for the start of winter without the program’s annual funding. The Low-Income Home Energy Assistance Program, known as LIHEAP, helps eligible households pay heating and cooling bills. The release follows a shutdown that stretched 43 days and pushed agencies across the country to warn families of possible disruptions.

State officials in Minnesota, Kansas, New York, and Pennsylvania had already issued alerts that the delay could slow the processing of applications or force families to wait until December for help. In Pennsylvania, more than 300,000 households depend on the program each year. Minnesota officials noted that older adults, young children, and people with disabilities face the highest risk as temperatures fall.

The delay also raised concerns among advocates who track household debt tied to rising utility costs. National Energy Assistance Directors Association Executive Director Mark Wolfe said the funds were “essential and long overdue” and added that high arrearages and increased energy prices have strained families seeking help.

Some states faced additional pressure when other services were affected by the shutdown. According to data reviewed by national energy advocates, roughly 68 percent of LIHEAP households also receive nutrition assistance, and the freeze in multiple programs increased the financial burden on low-income residents. Wolfe said families were placed in “an even more precarious situation than usual” as the shutdown stretched into November.

In Maryland, lawmakers urged the Trump administration to release funds after the state recorded its first cold-related death of the season. The Maryland Department of Health reported that a man in his 30s was found outdoors in Frederick County when temperatures dropped. Last winter, the state documented 75 cold-related deaths, the highest number in five years. Rep Kweisi Mfume joined more than 100 House members calling for immediate federal action and said LIHEAP “is not a luxury” for the 100,000 Maryland households that rely on it. He added that seniors and veterans would be placed at risk if the program remained stalled.

Maryland Gov. Wes Moore used $10.1 million in state funds to keep benefits moving, but noted that states cannot routinely replace federal dollars. His administration said families that rely on medical equipment requiring electricity are particularly vulnerable.

The District of Columbia has already mapped out its FY26 LIHEAP structure in documents filed with the federal government. The District’s plan shows that heating assistance, cooling assistance, weatherization, and year-round crisis assistance operate from October 1 through September 30. The District allocates 50 percent of its LIHEAP funds to heating assistance, 10 percent to cooling, 13 percent to year-round crisis assistance, 15 percent to weatherization, and 10 percent to administrative costs. Two percent is used for services that help residents reduce energy needs, including education on reading utility bills and identifying energy waste.

The District’s plan lists a minimum LIHEAP benefit of $200 and a maximum of $1,800 for both heating and cooling assistance. Crisis benefits are provided separately and may reach up to $500 when needed to resolve an emergency. The plan states that a household is considered in crisis if it has been disconnected from energy service, if heating oil is at 5 percent or less of capacity, or if the household has at least $200 owed after the regular benefit is applied.

The District’s filing notes that LIHEAP staff conduct outreach through community meetings, senior housing sites, Advisory Neighborhood Commissions, social media, posters, and mass mailings. The plan confirms that LIHEAP applicants can apply in person, by mail, by email, or through a mobile-friendly online application and that physically disabled residents may request in-home visits.

As agencies nationwide begin distributing the newly released funds, states continue working through large volumes of applications. Wolfe said LIHEAP administrators “have been notified that the award letters have gone out and the states can begin to draw down the funds.”

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Seven Steps to Help Your Child Build Meaningful Connections

BLACKPRESSUSA NEWSWIRE — Swinging side by side with a friend on the playground. Sharing chalk over bright, colorful sidewalk drawings. Hiding behind a tree during a spirited game of hide-and-seek. These simple moments between children may seem small, but they matter more than we think

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By Niyoka McCoy, Ed.D., Chief Learning Officer, Stride/K12

Swinging side by side with a friend on the playground. Sharing chalk over bright, colorful sidewalk drawings. Hiding behind a tree during a spirited game of hide-and-seek. These simple moments between children may seem small, but they matter more than we think: They lay the foundation for some of life’s most important skills.

Through everyday play, young children begin learning essential social and emotional skills like sharing, resolving conflicts, showing empathy, and managing their emotions. These social skills help shape emotional growth and set kids up for long-term success. Socialization in early childhood isn’t just a “nice-to-have”—it’s essential for development.

Yet today, many young children who haven’t yet started school aren’t getting enough consistent, meaningful interaction with peers. Research shows that there’s a decline in active free play and peer socialization when compared to previous generations.

There are many reasons for this. Children who are home with a parent during the day may spend most of their time with adults, limiting opportunities for peer play. Those in daycare or preschool may have restricted free play, and large classrooms can reduce supervision and social coaching. Some children live in rural areas, are homebound due to illness, have full schedules, or rely on screens to fill their playtime. And for some families, finding other families with young children to connect with isn’t easy.

While these challenges can feel significant, opportunities for connection still exist in every community. Families can take simple steps to help children build friendships, create a sense of belonging, and strengthen social skills. Here are some ideas to get started:

  • Storytime sessions at libraries or local bookstores
  • Community offerings such as parent-child workshops, art, music, gymnastics, swimming, or sports programs
  • Weekly events at children’s museums, which may include art projects, music workshops, or science experiments
  • Outdoor exploration, where kids can play with peers
  • Local parenting groups that organize playdates and group activities
  • Volunteer opportunities where children can participate, such as pet adoption events or packing meals at a food bank
  • Classes for kids at local businesses, including hardware, grocery, or craft stores

Some of these community activities are free or low-cost and give kids the chance to build friendships and practice social skills. Parents can also model positive social behavior by interacting with other parents and encouraging their children to play with their peers.

These may seem like small moments of connection, but they can have a powerful impact. Every time your child shares a toy, plays make-believe with peers, or races a friend down the slide, they’re not just playing—they’re learning the skills that build confidence, empathy, and lasting friendships. And it’s good for you, too. Creating intentional opportunities for play also helps you strengthen your own network of parents who can support one another as your children grow together.

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#NNPA BlackPress

Seven Steps to Help Your Child Build Meaningful Connections

BLACKPRESSUSA NEWSWIRE — Swinging side by side with a friend on the playground. Sharing chalk over bright, colorful sidewalk drawings. Hiding behind a tree during a spirited game of hide-and-seek. These simple moments between children may seem small, but they matter more than we think

Published

on

By Niyoka McCoy, Ed.D., Chief Learning Officer, Stride/K12

Swinging side by side with a friend on the playground. Sharing chalk over bright, colorful sidewalk drawings. Hiding behind a tree during a spirited game of hide-and-seek. These simple moments between children may seem small, but they matter more than we think: They lay the foundation for some of life’s most important skills.

Through everyday play, young children begin learning essential social and emotional skills like sharing, resolving conflicts, showing empathy, and managing their emotions. These social skills help shape emotional growth and set kids up for long-term success. Socialization in early childhood isn’t just a “nice-to-have”—it’s essential for development.

Yet today, many young children who haven’t yet started school aren’t getting enough consistent, meaningful interaction with peers. Research shows that there’s a decline in active free play and peer socialization when compared to previous generations.

There are many reasons for this. Children who are home with a parent during the day may spend most of their time with adults, limiting opportunities for peer play. Those in daycare or preschool may have restricted free play, and large classrooms can reduce supervision and social coaching. Some children live in rural areas, are homebound due to illness, have full schedules, or rely on screens to fill their playtime. And for some families, finding other families with young children to connect with isn’t easy.

While these challenges can feel significant, opportunities for connection still exist in every community. Families can take simple steps to help children build friendships, create a sense of belonging, and strengthen social skills. Here are some ideas to get started:

  • Storytime sessions at libraries or local bookstores
  • Community offerings such as parent-child workshops, art, music, gymnastics, swimming, or sports programs
  • Weekly events at children’s museums, which may include art projects, music workshops, or science experiments
  • Outdoor exploration, where kids can play with peers
  • Local parenting groups that organize playdates and group activities
  • Volunteer opportunities where children can participate, such as pet adoption events or packing meals at a food bank
  • Classes for kids at local businesses, including hardware, grocery, or craft stores

Some of these community activities are free or low-cost and give kids the chance to build friendships and practice social skills. Parents can also model positive social behavior by interacting with other parents and encouraging their children to play with their peers.

These may seem like small moments of connection, but they can have a powerful impact. Every time your child shares a toy, plays make-believe with peers, or races a friend down the slide, they’re not just playing—they’re learning the skills that build confidence, empathy, and lasting friendships. And it’s good for you, too. Creating intentional opportunities for play also helps you strengthen your own network of parents who can support one another as your children grow together.

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