Close Menu
    Facebook X (Twitter) Instagram
    Trending
    • Top ten A real income Black-jack Casinos inside United states to own 2025
    • Best Position Sites Uk 2025 Enjoy Real cash Online slots
    • Black-jack Online for real Currency: Top 10 Local casino Internet sites in the 2025
    • Пин Ап
    • Chatbots in healthcare: an overview of main benefits and challenges
    • What is Google Bard? Everything you need to know about ChatGPT rival
    • 7 Top Machine Learning Programming Languages
    • Casinoland Gambling establishment Evaluate Japanese
    YYC Times
    • Home
    • Latest News
    • Trending Now
    • Updates
    YYC Times
    Trending Now

    Mom raises funds for ‘robotic legs’ for daughter with rare disease

    YYC TimesBy YYC TimesFebruary 26, 2023Updated:February 26, 2023No Comments6 Mins Read

    Breadcrumb path hyperlinks

    1. Information
    2. Native information

    Amanda Levesque’s daughter Ariana is one in every of lower than 70 folks worldwide recognized with GNB1 syndrome

    Mother Amanda Levesque and her daughter Ariana, who has a rare condition called GNB1, in Calgary on Sunday, February 26, 2023.
    Mom Amanda Levesque and her daughter Ariana, who has a uncommon situation referred to as GNB1, in Calgary on Sunday, February 26, 2023. Darren Makovichuk/Postmedia

    Article content material

    At seven years previous, Ariana Levesque has seen extra medical doctors, specialists and therapists than most individuals will see in a lifetime.

    Commercial 2

    This advert has not but loaded, however your article continues under.

    Calgary Herald NewsConnect Powered by Postmedia Network

    REGISTER TO UNLOCK MORE ARTICLES

    Create an account or log in to proceed your studying expertise.

    • Entry articles from throughout Canada with one account
    • Share your ideas and be part of the dialog within the feedback
    • Get pleasure from further articles per thirty days
    • Get e-mail updates out of your favourite authors

    Article content material

    However after a profitable trial final yr, her household hopes a Canadian firm’s so-called “robotic legs” will in the future assist the younger Calgary lady stroll on her personal.

    Calgary Herald Headline News Banner

    Signal as much as obtain day by day information from the Calgary Herald, a division of Postmedia Community Inc.

    By clicking the enroll button, you comply with obtain the above e-newsletter from Postmedia Community Inc. You’ll be able to unsubscribe at any time by clicking the unsubscribe hyperlink on the backside of our emails or any e-newsletter. Postmedia Community Inc. | 365 Bloor Avenue East, Toronto, Ontario, M4W 3L4 | 416-383-2300

    Thanks for subscribing!

    A welcome e-mail is on its approach. When you do not see it, please verify your junk folder.

    The following problem of Calgary Herald Headline Information will probably be in your inbox quickly.

    We encountered an issue signing you in. Please attempt once more

    Article content material

    Identified at two years previous with a uncommon genetic situation often known as GNB1 syndrome — one in every of solely two Canadians and fewer than 70 folks worldwide recognized to have the illness — Ariana has spent her total life out and in of medical doctors’ places of work and recovering from surgical procedures associated to the uncommon illness. The illness has brought on Ariana extreme mobility issues – she normally will get round in a wheelchair – together with epilepsy and delayed development.

    Whereas her mom says Ariana is functioning cognitively on the similar degree as her friends, she has to work a lot more durable than others her age to study common motor expertise.

    Commercial 3

    This advert has not but loaded, however your article continues under.

    Article content material

    “She’s such a decided little lady — like she’s a firework,” mentioned Ariana’s mom, Amanda Levesque. “When she actually will get going, she actually places her thoughts to it and works actually arduous. She has achieved many issues within the 5 years since we had her prognosis.”

    Robotic-assisted stacker helped Ariana throughout examine

    After years of trying and attempting each remedy and remedy accessible, Amanda thinks she’s discovered an possibility that might be an vital step in her daughter’s journey to studying to stroll.

    On Sunday, two days earlier than Uncommon Illness Day on Feb. 28, the household launched a GoFundMe marketing campaign to assist elevate cash for a robot-assisted walker, constructed by Ontario-based firm Trexo Robotics.

    The machine—which gently pushes mobility-challenged kids’s legs with a correct gait, offering train and coaching—was an extremely great tool for Ariana throughout a College of Calgary examine funded by the Alberta Kids’s Hospital Basis, which study expertise and its advantages.

    Commercial 4

    This advert has not but loaded, however your article continues under.

    Article content material

    We apologize, however this video couldn’t load.

    The robotic legs, even over a brief trial interval of three months, have been an enormous success for Ariana. The household and researchers have been amazed by her progress.

    “After coaching within the Trexo, even earlier than she completed her coaching interval with us, she was in a position to stroll along with her (hand) walker or throughout the room,” mentioned Dr. Elizabeth Condliffe, the principal investigator of the examine performed by the college’s Pediatric Onset of Neuromotor Impairment Lab.

    “So which means that she has gained the power to do extra train herself. She gained the power to navigate her setting.”

    Seven-year-old Ariana Levesque was diagnosed at two with an incredibly rare genetic disease, GHB1 syndrome.
    Seven-year-old Ariana Levesque was recognized at two with an extremely uncommon genetic illness, GHB1 syndrome. Photograph offered by Amanda Levesque

    Condliffe says she expects the analysis to seek out gadgets like Trexo “neuroplasticity-inducing” means they may assist folks like Ariana have skills they did not have earlier than, even after they’re not utilizing the gadget. She additionally famous that you will need to embrace uncommon circumstances, like Ariana, in additional common research.

    Commercial 5

    This advert has not but loaded, however your article continues under.

    Article content material

    “What is absolutely related is the general operate she has and never her particular prognosis,” Condliffe mentioned. “We are able to embrace folks with uncommon ailments on this examine, and I truly assume that is crucial to do.”

    ‘She was so proud’: Household desires to purchase their very own machine

    As Ariana’s trial got here to an in depth and the Levesque household bid a tearful farewell to the machine, they’re in search of assist to lift the $50,000 to purchase a Trexo of their very own.

    “My coronary heart simply melted to see her being part of it in a complete completely different approach. She was so pleased with herself,” Amanda mentioned.

    “After seeing what simply three months did with that Trexo, I actually hope that I can present that chance for her.”

    With Ariana presently recovering from reconstructive remedy on her hips earlier this month, Amanda says they’re beginning at “sq. one” by way of her rehabilitation. The household hopes the system could also be step one on a path to permitting Ariana to in the future stroll on her personal.

    “The Trexo might be the important thing to getting her out of a wheelchair,” Amanda mentioned. “(It is) now such a vital time for her. It is form of a make-or-break second.”

    mrodriguez@postmedia.com

    Twitter: @michaelrdrguez

    Share this text in your social community

    Commentary

    Postmedia is dedicated to sustaining a full of life however civil discussion board for dialogue and encourages all readers to share their opinions on our articles. Feedback could take as much as an hour to look on the location. We ask that you simply preserve your feedback related and respectful. We have enabled e-mail notifications—you may now obtain an e-mail while you obtain a reply to your remark, there’s an replace to a remark thread you comply with, or when a person you comply with feedback. Go to our Neighborhood Pointers for extra data and particulars on alter your e-mail settings.

    Be part of the dialog

    Commercial 1

    This advert has not but loaded, however your article continues under.



    Source link

    Previous ArticleAlberta RCMP press charges against man involved in police shooting
    Next Article Alberta company raises funds for Calgary man in Turkey helping injured siblings
    YYC Times
    • Website

    Related Posts

    Trending Now

    TC Energy pipeline rupture sparks wildfire near Edson, Alta.

    April 17, 2024
    Trending Now

    Hearing on whether terrorism charges to be tossed to resume Wednesday

    April 17, 2024
    Trending Now

    Alberta businesses balk at federal budget’s capital gains tax increase

    April 16, 2024
    Add A Comment

    Leave A Reply Cancel Reply

    Categories
    • 1
    • AI News
    • Latest News
    • Trending Now
    • Updates
    Categories
    • 1
    • AI News
    • Latest News
    • Trending Now
    • Updates
    • Privacy Policy
    • Disclaimer
    • Terms & Conditions
    • About us
    • Contact Us
    Copyright © 2024 YYCTimes.com All Rights Reserved.

    Type above and press Enter to search. Press Esc to cancel.