“Now we know he’ll be OK on his own”— How the parents of a nine year old with vision loss were able to breathe easier again.

For the longest time, Julie and Jesse Hoskins did not think anything was amiss with their son, Lane, as he grew up in their loving home in Ewing, Virginia. Lane would go to school, see his friends and play video games like all the other kids. He could even go hunting without any issues.

It was when Lane was about seven years old that he began to show signs of blurry vision–, needing to sit very close to their large screen TV and complaining that he couldn’t see his schoolwork. Naturally, Julie took Lane to get glasses— but even with the glasses he was hardly seeing any better. Two prescriptions later, Julie and Jesse, at a loss, were referred to Dr. Sean Wadley, an ophthalmologist, in Knoxville, Tennessee, who diagnosed Lane with Stargardt’s disease, a rare genetic eye disease that prevents the retinas from providing sharp, central vision. It’s like macular degeneration for kids. By this point, even with his best eyeglasses, Lane only had 20/200 vision in his left eye and 20/400 in the right.

“His diagnosis of permanently reduced vision was very emotional for us as a family because our immediate thought was– how will he be able to live a full life or even drive someday?” Julie shared, candidly. “We didn’t know whether he would ever be able to have the independence an adult would expect to have.”

The Hoskins decided to enroll Lane in a private school so his teachers could better support his special visual needs. The teachers would print out his worksheets in a large font and Lane was provided magnifiers for his books and special software to enlarge the print on his computer screen.

One day, Lane’s grandparents when talking to their next door neighbor, found that he also happened to have Stargardt’s disease. The neighbor told them about his Ocutech bioptic telescope glasses that he had found so helpful. And he offered to let Lane try them on. Within seconds, Lane could read letters and numbers and see colors that he hadn’t seen in a long, long time. Julie spoke with Dr. Wadley, who immediately referred the Hoskins to Dr. David Armstrong, an optometrist who’s an expert in low vision care, so that Lane could be evaluated for Ocutech bioptics.

“As soon as Lane put on the Ocutech bioptics, his face lit up! He started giggling and laughing and looking at our faces and it hit me, that he hadn’t seen our faces clearly in who knows how long!” Julie recalled. “Dr. Armstrong even took him outside– without the new lenses, Lane said signs were just colors with white spots. But when he put the Ocutech glasses on, and Dr. Armstrong asked him what he could see now… Lane excitedly shouted, ‘It’s an exit sign!”

Dr. Armstrong was optimistic for Lane and the future that a bioptic could now pave for him. In a YouTube video where he shares Lane’s story, Dr. Armstrong explained that with his regular prescription glasses, Lane’s was almost legally blind. Today with his Ocutech bioptic, Lane is seeing 20/50— “a big improvement, and good enough to see just about everything.” Dr. Armstrong prescribed Lane the VES® Sport-II. He explained that Ocutech bioptics are available in a range of designs and powers, so that the low vision specialist can prescribe the one that’s most appropriate for the individual’s level of vision, which can vary greatly between individuals. There is no one Ocutech version that’s right for everyone.

With his new bioptic low vision aid, Lane, who is now nine years old, has returned to public school. Even just a few days into the school year, his mom was seeing a vast improvement in what he can do and how he feels, and she is so thankful for the opportunities that have now opened up for him.

“His being able to see the board again and his excitement to show off his bioptics and do his schoolwork like his friends— it means everything to me,” Julie explained. “The fact he was so young when he first started having trouble, it was hard to help because kids don’t know when something is wrong with their eyesight.”

Lane is excited to being back in public school, getting to see his friends’ and teachers’ faces, and feeling connected to everything. He loves that with his bioptic, he can watch movies like Fast and the Furious and play Call of Duty and see it all clearly. He can hunt again and go to the beach with his family and see the waves. For his parents, his laughs and giggles every time he sees something he hasn’t seen for so long melts their hearts.

“Before we found Ocutech, it was so depressing to worry about Lane, his independence and his future. Now, we know he’ll be OK on his own— something all parents want,” Julie summarized, passionately. “We’re just thankful to Ocutech for creating these aids that have been so helpful for our son.”

Ask your low vision specialist if an Ocutech bioptic might be right for you. For more information about Ocutech bioptics or for a referral to a low vision specialist visit www.ocutech.com. Complete the self-assessment form at https://ocutech.com/self-assessment-form/ to receive a reply from Ocutech’s experts about your special situation.


“She Became So Much More Curious”— How a visually impaired 15 Year Old’s World Suddenly Changed

Cheryl Jones didn’t know how to respond after taking her daughter, Leah, to yet another eye doctor to see why her daughter had so much difficulty seeing clearly, when the doctor told them “she’s probably pretending to have such bad eyesight so she can wear cool glasses like her friends.”

Her daughter— who was in fourth grade at the time— couldn’t believe it either.  She’d been struggling since kindergarten to see the board and her friends in her classroom. She had already been to eight specialists by the time of this visit and none could explain why she couldn’t see the TV if she sat on the couch with her parents. She always had to sit right up in front of the screen to be able to see anything.

It was a year later, at age ten, that Leah’s diagnosis was finally made. Upon walking into the room, the doctor saw Leah try to read the eye chart while tilting her head to the side. “He knew straight away what my daughter had—Stargardt’s disease”—a juvenile form of macular degeneration— “It was such a relief to finally know what was going on,” Ms. Jones recalled, thoughtfully.

Stargardt’s disease is a rare genetic eye disease that affects the macula, the central part of the retina that normally provides our sharp 20/20 vision. The disorder impacts about one in 10,000 people. Early on it may be very difficult for eye doctors to diagnose Stargardt’s Disease because the macula can appear normal for many years, prompting some doctors to think that the child might be fibbing. But eventually the macula does begin to change and the diagnosis can be made.

Understanding Stargardt’s Disease

Once her Stargardt’s diagnosis was made, Leah was introduced into the world of low vision aids—special equipment and software that enlarges print to make it easier to see and access.  But not that it was easy! Leah could be found in school rolling her heavy backpack, full of large print materials and bulky equipment like her electronic screen magnifier called a CCTV that has a special camera used to enlarge print. In each classroom, Leah would have to wheel her bag in and set up her equipment, and when she got to high school, it meant doing it sometimes eight times a day. And to get around school with her heavy rolling backpack, she’d have to use the school’s elevator requiring special permissions, forms and signatures— a parent’s nightmare.

“Her school librarian was moved to help us by adding a large print section in the library for Leah. Though it took a long time for Leah to finish reading each book, we felt that her gesture was so kind and sympathetic— it’s just one of many examples of how we’ve learned to navigate the challenges that Leah faces day to day,” her mother explained.

But about one month ago, Leah’s navigation through her visual impairment took a spectacular turn.


Leah was referred to Dr. Sonya Braudway, an optometric physician who specializes in low vision rehabilitation in Lakeland, Florida. Working at the Center for Retina and Macular Disease, Dr. Braudway demonstrated a pair of special eyeglasses designed for the visually impaired. These low vision aids, called Ocutech Bioptics, contain miniature telescopes that work like binoculars. In mere moments, Leah felt the ground shift under her feet.

“I’ve never seen her read an eye chart so fast,” Ms. Jones said, smiling. “Suddenly, my mother, my daughter and I all started crying, realizing the miracle that had just happened.”

Leah, whose vision is normally 20/400, can now see 20/60 with her special Ocutech bioptics— a reality made possible by her grandparents who purchased them for Leah when they saw how happy they made her.

“It’s like getting to watch her grow up again overnight,” her mother said. “She’s become so much more curious about the world, because now she can see it, just like any normal kid.”  And since her bioptic is focusable, she can use them to see better at any distance she needs including the TV, her computer, her Nintendo, as well as her art projects.

Low Vision Rehabilitation

Dr. Braudway has prescribed Ocutech bioptics for children many times before. “It’s one of the most rewarding things I can do,” she said.  “The impact that bioptics can have for children can be so profound. It helps them come out of their shell, and the smiles we see when they first begin to use it—oh my! It’s a shame that more families don’t know about this technology.  It can be so pivotal in their children’s lives.”

These days, Leah, now 15, attends Excel Christian Academy in Lakeland, Florida. She’s happily adjusting to her new life as an Ocutech user.  Whether it’s joining her classmates in the hallway instead of riding alone in the elevator, sitting between her parents on the couch to watch television together, finally getting to read signs, go shopping, see her friends and family— and even enjoying trips to the zoo where for the first time she can really see the sloths and giraffes in their pens— Leah is excited about what it all means for her future.

“Now we’ll find her looking at our old wedding photos hanging on the wall, staring at the wedding dress, the flowers and our family’s faces— seeing them all with quite literally a fresh pair of eyes,” Leah’s mother shared. “It’s amazing what a difference these glasses have made for her in such a short period of time; I’m not worrying so much anymore— she’s so much more independent and happy… [the way] every girl her age deserves to be.”

Ocutech bioptics are prescribed by Low Vision Specialists throughout the world.  To learn more about Ocutech bioptics, and whether you, your child, or a loved one might be a candidate contact Ocutech at info@ocutech.com.



Meet Aaron Paulk, a visually impaired competitive surfer.

His Ocutech bioptic low vision aid helped make it happen!

“My first dream as a kid was to be a US Navy Seal.” Says Aaron Paulk. “I enlisted in the Navy halfway through my senior year in high school in Indiana. Things were going along fine until my physical in boot camp found that I was losing vision due to a juvenile type of macular degeneration called Stargardt’s disease. That totally derailed all my plans as I was no longer eligible to join the navy or any service. I lost my dream, my vision, and my motivation at age 17 all at once. It was one of my hardest periods emotionally.”

“I lost my license and my independence,” he says. “And then I found Dr. Laura Windsor, my low vision specialist. She prescribed an Ocutech bioptic telescope—a miniature telescope built into eyeglasses that provide me with near-normal vision–and my life changed forever. It allowed me to follow my second dream, to be a surfer living in Hawaii, and I just placed third in the 2021 World Parasurfing Championships held in California December 7-11.

“Gosh where do I start with how my Ocutech bioptic has changed my life?” he says.  “I have been able to regain my independence and drive, which has helped me train harder and harder to now be one of the best visually impaired competitive surfers in the world.  Before Ocutech I couldn’t even see the surf in the ocean before I got in, but now I can check the surf and watch it through my Ocutech and get an idea of how the waves are breaking.  I wear my Ocutech at all competition events to have the ability to watch the competition and prepare for my heats.” 

Aaron wants to share his enthusiasm for using his bioptic with others. “The impact of my Ocutech has been so dramatic for me,” he says, “and I’m eager to do what I can to help inspire other people with visual impairments to adopt such great technology to help them follow their passions and achieve their dreams.”



“If It Weren’t for Ocutech, I Wouldn’t Have My License”— Julius Frierson is Seeing New Possibilities

Julius Frierson shuts the door to his car, parked on a street in the rolling hills of Ventura, California, with a grin— remembering how the license in his wallet and the ability to improve his vision was once just an impossible dream.

“I was considered legally blind ever since I was nine months old,” Frierson, a behavioral technician, explained. “Things were always hard for me— I was the kid who never saw the board in school, who needed special textbooks enlarged, the whole nine yards.”

Julius was born with macular scarring, a formation of fibrous tissue in place of the normal retinal tissue on the macula area, the central part of the retina, which normally provides our20/20 sharp vision. His condition is not very different than loss of central vision from disorders like macular degeneration or Stargardt’s disease. Julius’ reduced visual acuity made it hard for him to read print, see the blackboard, or see his friends’ and family’s faces. He was told that glasses, contact lenses, medication or surgery could not correct his condition.

Frierson recalls one mentor in his life who inspired him to keep his chin up, teaching him how to cross the roads even when his eyes couldn’t see the lights change.

For years, teachers at Frierson’s school would often follow Frierson home after school, ensuring the teen was walking home safely. He’d hear the cars whiz past and think about what it would be like to drive one— to see the road and feel the sense of independence he always wanted.

Many years later, that dream became a reality.

One day Frierson’s optometrist at Kaiser recommended special glasses called bioptics made by Ocutech.  Bioptics are miniature telescopes that are attached to regular eyeglasses. Just like binoculars, they make images larger and as a result easier to see. Ocutech bioptics enable the user to see much farther away. For example, if an individual can only see clearly to 5 feet away, a 4x-power Ocutech bioptic will let them see 20 feet away.

Frierson’s doctor fitted him for the VES-Sport-II, which is one of a range of Ocutech bioptic telescopes specially designed for the visually impaired to enhance a patient’s vision. They are focusable, so he could use them to see better at any distance he needed including the TV and the computer.

Of course, these types of special glasses aren’t cheap. But Frierson was determined to raise the funds to obtain hisOcutech bioptic and benefit from its life-changing potential.  He let his loved ones know of this opportunity to restart his lifeif he could onlyfindthe money to purchase the glasses.

It was then that his girlfriend set up a GoFundMe page, sharing Frierson’s intense and beautiful story. In just 24 hours, the money was raised to cover the cost of the glasses! The amazing support he receivednow unlocks memories Frierson holds dear.

Ocutech literally allowed me to see two to three times better [than anything I had used before],” Frierson shared, passionately. “As of now, my regular vision is 20/200 but with myOcutech, my vision is 20/40— and that is a drastic difference.”

It’s only been a little less than a year, but Frierson finds his future is suddenly clearer, in more ways than one.

With his Ocutech bioptics, Frierson can see the world the way his friends and family have always experienced it. He sees the scoreboard of sports games playing on the screens in his favorite restaurant. He reads the menu without help,and he feels the firm grip of the stirring wheel as he can now independently drive.

Frierson goes to concerts and doesn’t just hear the artist perform, butsees them—colors and all.

The license in his pocket, the car parked on his street, the ability to cross the road now with no one having to follow:it’s these little things—seemingly ordinary things—that ignite extraordinary joy for this Ocutech user.

“[It comes down to this],” Frierson said, smiling. “I simply cannot live without these glasses.”

To learn more about Ocutech bioptics, to determine if you might be a candidate for Ocutech bioptics, or if you or a loved are seeking a referral for a low vision specialist, contact Ocutech today at www.ocutech.com.


Briarna Dobson’s Journey with Stargardt’s Disease

Ocutech would like to thank Briarna for sharing her story with Stargardt’s and how she gained her independence back with dedicated parents, doctors and Ocutech bioptics!

I always get asked, “What do you mean you’re blind, you look so normal?” Most people find it difficult to comprehend that you can look normal but be partially sighted. We are taught there are three types of vision: perfect vision, vision that requires correction with glasses or completely blind with no vision. So, I do understand the confusion some have when I try to explain my vision.

Losing My Vision

I was born fully sighted and had no issues with my vision. When I was 8 years old, I started struggling to see the board. We went to the Optometrist and I got glasses for reading and seeing the board. I went back yearly for routine check-ups and it wasn’t till I was 13 years old that the optometrist found something at the back of my eye (my retina), we then went to the ophthalmologist in Tauranga, where they referred us for more testing at the Retina Specialist clinic in Auckland.  This was when we were told…I had Stargardts.

My parents were devastated. They saw all the obstacles I would be coming up against, would I be able to finish mainstream education? Would I be able to drive? Would I be happy? I, however, didn’t have the foresight to think of any of that. I could see alright for the moment and that was all that mattered. A few months later I understood completely how my parents felt that day.

What is Stargardt’s?

Stargardt’s Disease is a genetic juvenile condition. It affects the macula in the retina. This is responsible for colour and central vision. This results in the whole image not being sent through the optic nerve to the brain. My brain then fills in the missing pieces and compensates with my peripheral vision. The loss of vision starts with puberty and gradually continues to progress through the teens and adult years. As if puberty wasn’t difficult enough.

Losing My Sight and Independence

Growing up I was a very active kid, I got involved in all the sports, netball, volleyball, water polo, hockey, and dance, to name a few. With the loss of my vision that was taken away from me, I no longer was able to play those sports or see the choreographer in dance training. Then it came to the age where I was faced with “you won’t be able to drive.” My friends were getting their driver’s licenses; they were independent and could go off when they pleased. They could get around and did not have to rely on anyone else.  These days were dark for me, it just didn’t seem fair as I could not be independent and have the freedom that comes with it.

My parents are continuously working to find the best tools possible for me to live life as a normal teenager. They are always researching Stargardt’s Disease and keeping up to date with everything and anything that could benefit my condition and my life.  My Dad came across a video on “stuff.com” of a guy who was visually impaired that was granted his license with a special pair of glasses, he was also from New Zealand and we immediately got in touch with him. He explained how he got the glasses and who to contact.

Finding Hope and Learning I Could Drive!

My Dad got in touch with Peter Neuhauser and Anna Megaffin from the Hamilton Branch Bell Neuhauser & (Matthews) Optometrist. Peter sounded so hopeful and it was really promising.  Although I did not want to get my hopes up too high. 

We went to Hamilton and they ran a few tests. We were then given the best news of our lives – with these glasses (Ocutech VES-Sport II) I could obtain my driver’s license!

Photo of the VES-Sport II Bioptic Telescope
The Ocutech VES Sport-II

The glasses are ordered from America, so I started to study the road code like crazy and after a few months of waiting, the glasses arrived and the very next day, I took my learner’s license test in 13 minutes and got 35/35 correct.  I now have my very own licence.

It really was the best day and feeling ever!

The past 4 years have been the longest and hardest years of my life, but after meeting Peter, Anna, and the team, my life has completely changed in the best way ever and my dreams have come true!

I am so grateful for all they have done and my Ocutech Bioptics!