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'I did quick eye test when glasses broke - days later I had surgery'
'I did quick eye test when glasses broke - days later I had surgery'

Daily Mirror

time05-06-2025

  • Health
  • Daily Mirror

'I did quick eye test when glasses broke - days later I had surgery'

Ashley Armstead, 34, was plagued by severe headaches after her reading glasses broke but when she went for an eye test a series of medical tests revealed something more serious What was supposed to be a routine eye check-up turned into a life-saving appointment for 34-year-old flight attendant Ashley Armstead after she broke her reading glasses. Ashley had been using reading glasses for years with no significant problems, but over two years, she noticed a worrying deterioration in her vision. ‌ The situation escalated when her glasses snapped and she awaited a new pair, leading to severe and persistent headaches that raised alarm bells. ‌ "In between getting new glasses my vision was becoming increasingly partial and I was having debilitating headaches all day and consecutive days," Ashley said. With her job and health at stake, Ashley didn't hesitate to arrange a standard eye examination. "As a flight attendant, that poses a major problem, so I inquired with my health care for an in-network eye doctor to just get a regular eye exam," she explained. "Then it was downhill from there." At the optometrist's, signs of swelling and irregularities behind her right eye were immediately apparent, prompting an urgent referral to an ophthalmologist on the same day. "That's when I knew it was real," said Ashley, from Maryland, USA. Further tests revealed a grave situation. She was diagnosed with neuroretinitis as her eye was detaching from the retina, coupled with dangerously elevated blood pressure. "On looking at my blood pressure and my eye, I was referred immediately to go to the emergency room," she disclosed. Following admission to the hospital, further tests, including a spinal tap, ultimately uncovered the root cause of Ashley's condition: Idiopathic Intracranial Hypertension (IIH). This condition involves an accumulation of excess cerebrospinal fluid (CSF) within the skull, exerting perilous pressure on both the brain and eyes. ‌ Ashley, who was already managing renal disease, now faced a daunting week ahead. This period would be marked by the painful process of fluid drainage, overwhelming fear, and the stark reality of potentially losing everything she had worked tirelessly to achieve. Yet, amidst this turmoil, Ashley experienced a glimmer of solace. ‌ "Oddly enough I had a small sense of peace because the things I was feeling and changed I noticed over some time, finally had an answer to it," she reflected. Ashley confessed to being consumed by fear and anxiety, given her limited history with serious ailments and her typically active lifestyle. The prospect of her life undergoing significant changes, coupled with the fear of losing her dream job, weighed heavily on her. The next critical step in her treatment involved undergoing emergency brain surgery. Ashley recalled feeling overwhelmed by the sheer volume of information presented to her. ‌ "All the information felt like it was just dumped on me," she shared. "From the spinal tap and drainage for an entire week, the next step was placing a Ventriculoperitoneal (VP) Shunt into my head." Despite the challenges of processing this information, Ashley's brain surgery proved successful. The VP shunt now effectively regulates the fluid build-up, redirecting it from her brain through a catheter that runs beneath her skin and into her abdomen. "Too much fluid can lead to increased pressure causing intense migraines and more severe potential damage such as stroke and vision loss and possibly much worse," she explained. "The shunt starts in my head and a catheter connects and extends down the side of my neck, over my collarbone and to my abdomen. ‌ "The fluid drains to my stomach and then nature takes its course." The ordeal took more than just a physical toll on Ashley; her self-image suffered greatly post-surgery. "I had dreadlocks that I loved and when I saw the area they shaved I immediately broke down," she said. "I felt like I was so ugly and I'd be this way forever." Ashley also opened up about battling depression and the difficulty of facing each day: "Sometimes I wouldn't get out of bed and I've broke down crying a few times when we were out in public because with the shunt i was having stomach pains and my wound was sensitive to everything." ‌ In the midst of her struggles, however, Ashley discovered a pillar of support in her employer. "I am a flight attendant for Delta and when I had to inform my manager what was going on, the first thing she asked was when and how were my parents coming and got them on the first flight out for my aide as I live in Ohio and they are in Maryland," she revealed. ‌ Two months on, Ashley is taking back control of her life: "I haven't had one migraine since the surgery, which I'm so grateful for. "A month after the surgery I was at about 85% back. Still working on strengthening my back and core because I was bedridden so long." While her recovery journey continues, her resolve remains steadfast. "My head is not 100 per cent healed, it's only been two months," she acknowledged. "But I am back working, running and lightly lifting weights. My mental (health) is stronger than it was before."

Nexalin Technology Reconstitutes Scientific Advisory Board with Leading Experts to Advance Alzheimer's Program Amid Encouraging Data
Nexalin Technology Reconstitutes Scientific Advisory Board with Leading Experts to Advance Alzheimer's Program Amid Encouraging Data

Yahoo

time13-05-2025

  • Business
  • Yahoo

Nexalin Technology Reconstitutes Scientific Advisory Board with Leading Experts to Advance Alzheimer's Program Amid Encouraging Data

HOUSTON, TX, May 13, 2025 (GLOBE NEWSWIRE) -- Nexalin Technology, Inc. (Nasdaq: NXL; NXLIW) (the 'Company' or 'Nexalin') the leader in Deep Intracranial Frequency Stimulation (DIFS™) of the brain, today announced the reconstitution of its Scientific Advisory Board (SAB) with the appointment of three renowned experts in neurology, neuroimaging, and neurodegenerative diseases. This move reflects Nexalin's strategic prioritization of Alzheimer's disease within its broader clinical development pipeline, supported by promising published data and internal data from studies involving its proprietary DIFS™ technology. Joining the SAB are Dr. Mingxiong Huang, Dr. David Owens, and Dr. Abe Scheer, each of whom brings specialized expertise that aligns with Nexalin's Alzheimer's-focused initiatives. The restructured SAB will play a pivotal role in guiding the Company's scientific direction, clinical strategy, and biomarker-driven trial design for neurodegenerative and neuropsychiatric disorders. 'This enhanced advisory board reflects our sharpened focus on Alzheimer's disease, and the high-caliber expertise of Drs. Huang, Owens, and Scheer aligns with our expanding research agenda,' said Mark White, CEO of Nexalin Technology. 'Their combined contributions will be invaluable as we advance Nexalin's technology through clinical trials designed to address one of the greatest public health challenges of our time.' Nexalin's Gen-2 SYNC and Gen-3 Halo™ headset delivers DIFS™, a proprietary waveform capable of penetrating deep brain structures implicated in cognitive decline and mental illness. Recent published articles and encouraging preclinical and early-stage human data suggest that DIFS™ may promote neuroplasticity and functional recovery in regions associated with memory and executive function. These findings have prompted the Company to intensify its focus on Alzheimer's disease, with the SAB's restructuring aimed at providing the scientific and clinical oversight required for this complex area of medicine. Scientific Advisory Board Members Dr. Mingxiong Huang is a globally recognized expert in magnetoencephalography (MEG) and neuroimaging, with over 25 years of experience developing and applying advanced imaging techniques to neurological and psychiatric disorders. He is Professor of Radiology at the University of California, San Diego (UCSD), Adjunct Professor in the Department of Electrical and Computer Engineering, Co-Director of the UCSD MEG Center, and a career research health scientist at the VA San Diego Healthcare System. Dr. Huang earned his Ph.D. in biomedical physics from Northeastern University and completed postdoctoral training in MEG at Los Alamos National Laboratory. He previously held faculty positions at the University of New Mexico before joining UCSD. His work has been instrumental in advancing MEG source imaging, integrating MEG with structural and functional modalities such as diffusion tensor imaging, and applying these methods to conditions including TBI, PTSD, stroke, epilepsy, and schizophrenia. He has authored over 90 peer-reviewed publications and received the Distinguished Investigator Award from the Academy of Radiology Research. Dr. Huang's deep expertise in brain imaging biomarkers directly supports Nexalin's mission to develop data-driven, non-invasive therapies for Alzheimer's and other neurodegenerative disorders. Dr. Abe Scheer served on the Company's prior SAB and brings more than four decades of experience in adult and pediatric neurology, psychiatry, brain injury medicine, and electrophysiology. Board certified by the American Board of Psychiatry and Neurology in both adult and pediatric neurology, as well as in brain injury medicine, Dr. Scheer has trained and held faculty positions at premier institutions including Columbia University, Cornell Medical College, Georgetown University, and the University of Pittsburgh. Dr. Scheer held the position of Director of Neurology and Stroke Services at Beebe Healthcare in Delaware for over 10 years. He is currently a neurohospitalist and neurointensivist at Bay Health in Delaware and maintains an attending role at MeadowWood Hospital in Delaware. Dr. Scheer has lectured extensively across the U.S. on neuromodulation therapies and was instrumental in launching the first vagal nerve stimulation and baclofen pump clinics in Lincoln, Nebraska. He has served in advisory capacities for leading device developers including Medtronic, Cyberonics, and Milestone Scientific. A passionate educator, he continues to teach medical students and residents while contributing to clinical advancements in both neurology and psychiatry. His expertise will play a critical role in supporting Nexalin's efforts to deliver innovative, non-pharmacological solutions for Alzheimer's and related disorders. Dr. David Owens serves as the Company's Chief Medical Officer and is a board-certified neuroradiologist and interventional neuroimaging specialist with more than 25 years of experience in brain and spine imaging. A graduate of Furman University and the Medical University of South Carolina, Dr. Owens completed residency and fellowship training at Emory University Hospital, where he specialized in interventional therapies for brain disorders before entering private practice. His expertise includes traumatic brain injury, neurocognitive disorders, and sports-related brain trauma. Dr. Owens is a nationally recognized leader in advanced imaging techniques such as diffusion tensor imaging (DTI) and functional MRI. Over the past decade, he has also conducted and contributed to clinical research on transcranial stimulation therapies for conditions including anxiety, insomnia, clinical depression, and chronic pain—particularly in the context of reducing opioid dependency. Today, he operates a national teleradiology consultation practice focused on outpatient neuroimaging and continues to serve as a strategic clinical advisor in emerging neuromodulation technologies. 'This is a critical moment for innovation in Alzheimer's treatment,' said Dr. Scheer. 'Nexalin's technology represents a novel approach to brain modulation that could complement or even exceed the efficacy of traditional pharmacological therapies, particularly in the early stages of disease.' The Company plans to initiate new Alzheimer's-focused clinical studies in the third quarter of 2025, incorporating cognitive testing, imaging biomarkers, and MEG-guided metrics to assess treatment efficacy and neural activation. The SAB will be instrumental in optimizing trial designs and ensuring adherence to regulatory standards and scientific rigor. 'I am excited to work alongside Nexalin's leadership and fellow SAB members to help guide the next generation of non-invasive neuromodulation therapies,' added Dr. Huang. 'The intersection of neuroimaging, brain stimulation, and clinical science holds enormous potential for treating neurodegenerative disease.' This SAB reconstitution underscores Nexalin's continued evolution as a science-driven company committed to transforming mental health and neurodegenerative disease care through advanced bioelectronic medicine. About Nexalin Technology, Inc. Nexalin designs and develops innovative neurostimulation products to uniquely help combat the ongoing global mental health epidemic. All of Nexalin's products are non-invasive and undetectable to the human body and are developed to provide relief to those afflicted with mental health issues. Nexalin utilizes bioelectronic medical technology to treat mental health issues. Nexalin believes its neurostimulation medical devices can penetrate structures deep in the mid-brain that are associated with mental health disorders. Nexalin believes the deeper-penetrating waveform in its next-generation devices will generate enhanced patient response without any adverse side effects. The Nexalin Gen-2 15-milliamp neurostimulation device has been approved in China, Brazil, and Oman. Additional information about the Company is available at: Forward-looking statements This press release contains statements that constitute 'forward-looking statements,' These statements relate to future events or Nexalin's future financial performance. Any statements that refer to expectations, projections or other characterizations of future events or circumstances or that are not statements of historical fact (including without limitation statements to the effect that Nexalin or its management 'believes', 'expects', 'anticipates', 'plans', 'intends' and similar expressions) should be considered forward-looking statements that involve risks and uncertainties which could cause actual events or Nexalin's actual results to differ materially from those indicated by the forward-looking statements. Forward-looking statements are subject to numerous conditions, many of which are beyond the control of the Company, including those set forth in the Risk Factors section of the Company's Report on Form 10-K for the year ended December 31, 2023, and other filings as filed with the Securities and Exchange Commission. Copies of such filings are available on the SEC's website, Such forward-looking statements are made as of the date hereof and may become outdated over time. Such forward-looking statements are made as of the date hereof and may become outdated over time. The Company undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law. Contact:Crescendo Communications, LLCTel: (212) 671-1020Email: NXL@ in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

Nexalin Technology Announces Closing of Previously Announced $5.0 Million Underwritten Public Offering
Nexalin Technology Announces Closing of Previously Announced $5.0 Million Underwritten Public Offering

Yahoo

time06-05-2025

  • Business
  • Yahoo

Nexalin Technology Announces Closing of Previously Announced $5.0 Million Underwritten Public Offering

Nexalin Technology, Inc. HOUSTON, May 06, 2025 (GLOBE NEWSWIRE) -- Nexalin Technology, Inc. (Nasdaq: NXL; NXLIW) (the 'Company' or 'Nexalin'), the leader in Deep Intracranial Frequency Stimulation (DIFS™) of the brain, today announced the closing of its previously announced underwritten public offering of 3,850,000 shares of its common stock at a public offering price of $1.30 per share. The gross proceeds from the offering to Nexalin were approximately $5.0 million, before deducting underwriting discounts and commissions and other offering expenses. Maxim Group LLC acted as sole book-running manager for the offering. The public offering was made pursuant to an effective shelf registration statement on Form S-3 (File No. 333-286711), previously filed with the U.S. Securities and Exchange Commission (the 'SEC') on April 23, 2025, and declared effective on April 29, 2025. The shares of common stock were offered only by means of a prospectus and prospectus supplement that form part of the effective registration statement. A final prospectus supplement describing the terms of the public offering has been filed with the SEC and is available on the SEC's website located at Electronic copies of the final prospectus supplement and accompanying prospectus relating to the public offering may also be obtained by contacting Maxim Group LLC, 300 Park Avenue, New York, NY 10022, or by telephone at (212) 895-3745. This press release does not constitute an offer to sell or the solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction. About Nexalin Technology, Inc. Nexalin designs and develops innovative neurostimulation products to uniquely help combat the ongoing global mental health epidemic. All Nexalin's products are believed to be non-invasive and undetectable to the human body and are developed to provide relief to those afflicted with mental health issues. Nexalin utilizes bioelectronic medical technology to treat mental health issues. Nexalin believes its neurostimulation medical devices can penetrate structures deep in the mid-brain that are associated with mental health disorders. Nexalin believes the deeper-penetrating waveform in its next-generation devices will generate enhanced patient response without any adverse side effects. The Nexalin Gen-2 15 milliamp neurostimulation device has been approved in China, Brazil, and Oman. Additional information about the Company is available at:

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