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Unique Wellness Brings NASA Technology to Senior Care with Its Advanced Briefs

Unique Wellness Brings NASA Technology to Senior Care with Its Advanced Briefs

Wellness Briefs, Pull-Ups, and Underpads deliver industry-defining absorbency, comfort, and dignity through engineered InconTek® technology
BROOKLYN, NY, UNITED STATES, July 7, 2025 / EINPresswire.com / -- When astronauts travel to space, even the most basic bodily functions require innovative solutions. NASA's answer to managing hygiene during long missions was the Maximum Absorbency Garment (MAG)—a high-capacity, multi-layered brief designed to keep astronauts dry and safe during spacewalks. Now, that same engineering excellence is helping transform incontinence care for millions of older adults through Unique Wellness, a U.S.-based healthcare brand committed to bringing space-age innovation to everyday life.
At the core of Unique Wellness' award-winning product line—Wellness Briefs, Pull-Ups, and Underpads—is its proprietary InconTek® technology, inspired by the MAGs and used by NASA. This multi-layered core system is designed to absorb up to 87 ounces of liquid, reducing leaks, preventing skin breakdown, and significantly lowering the number of daily changes required.
With this innovation, Unique Wellness is redefining what it means to provide effective, dignified incontinence care. As the global elderly population continues to rise and more than 25 million Americans live with incontinence, the demand for premium hygiene products has grown rapidly.
For seniors, caregivers, and healthcare professionals, Unique Wellness offers a solution that combines performance with compassion.
Wellness Briefs: Designed with maximum absorbency in mind, these briefs minimize overnight changes, eliminate common issues such as leakage and foul odor and are suitable for both mobile and bedridden users. Wellness Briefs feature a 3-per-day change system to reduce up to 70 percent in product use over regular brands, which also saves a lot of time, cost, and laundry.
Wellness Pull-Ups: These provide the same advanced absorption in a more flexible, underwear-style design. For active seniors seeking discretion, comfort, and mobility, Wellness Pull-Ups are the perfect option. Whether running errands or relaxing at home, users experience the confidence of leak-free protection.
Wellness Underpads: Meant to be used on beds, chairs, and wheelchairs, these protective pads provide another level of protection. Their absorbent core and soft, breathable materials help maintain cleanliness and skin health in both clinical and home settings.
Wellness Brief® Softistico™ Pack: The latest in the Unique Wellness offering of incontinence care range, the Softistico ™ Pack is a luxury solution, elevating comfort and performance. The Softistico ™ is developed with extra-soft, breathable materials, facilitating all-day wear to deliver maximum comfort for sensitive skin. It is also the first-ever breathable adult diaper with secure tape tabs (not Velcro) and a resealable landing zone, allowing for easy adjustments and a custom fit.
Conventional incontinence products often require 6-8 changes daily, resulting in caregiver burnout, higher expenses, and user discomfort. InconTek® changes the equation. Its layered core system draws liquid away from the skin and traps it deep inside the brief, keeping users dry for up to 8 hours. This innovation not only boosts comfort but also supports skin integrity by reducing exposure to moisture and bacteria.
Combined with advanced odor control, the technology ensures users remain comfortable, confident, and dignified throughout the day and night. Whether in a hospital, long-term care facility, or private home, Wellness products provide a dependable, high-performance solution that prioritizes both user health and caregiver efficiency.
Unique Wellness designs its products with both clinical professionals and family caregivers in mind. Reduced changes mean fewer interruptions, better sleep, and more time for care.
'The only product that lets my dad sleep through the night without interruption.'
— Caregiver, Illinois
'I've tried many brands. Nothing compares to the absorbency and comfort of Wellness Briefs.'
— Home Healthcare Nurse
Key Benefits:
Sustainability: Fewer changes = less waste and lower environmental impact.
Skin Health: Dermatologically tested and breathable materials reduce rashes and pressure sores.
Cost Efficiency: Fewer changes result in reduced monthly product usage and caregiving time.
Odor Control: Built-in odor-neutralizing layer ensures long-lasting freshness.
Caregiver Relief: Simplifies routines and reduces the physical and emotional toll of caregiving.
About Unique Wellness
Unique Wellness is a leading name in adult incontinence products, dedicated to enhancing lives through scientifically advanced, medically inspired solutions. Headquartered in Brooklyn, New York, the company has built a reputation for reliability, compassion, and innovation.
All Wellness products are developed with user dignity in mind and are trusted by healthcare providers, caregivers, and families nationwide. With its NASA-derived technology, Unique Wellness is proving that space innovation can solve Earth-bound problems—one brief at a time.
About Unique Wellness
Unique Wellness is a leading name in adult incontinence products, dedicated to enhancing lives through scientifically advanced, medically inspired solutions. Headquartered in Brooklyn, New York, the company has built a reputation for reliability, compassion, and innovation.
All Wellness products are developed with user dignity in mind and are trusted by healthcare providers, caregivers, and families nationwide. With its NASA-derived technology, Unique Wellness is proving that space innovation can solve Earth-bound problems—one brief at a time.
Anurag Srivastava
EBIZON CRAYON INC
email us here
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About Avexitide Avexitide is an investigational, first-in-class glucagon-like peptide-1 (GLP-1) receptor antagonist that has been evaluated in five Phase 1 and Phase 2 clinical trials for post-bariatric hypoglycemia (PBH) and has also been studied in congenital hyperinsulinism (HI). The U.S. Food and Drug Administration (FDA) has granted avexitide Breakthrough Therapy Designation for both indications, Rare Pediatric Disease Designation in congenital HI, and Orphan Drug Designation for the treatment of hyperinsulinemic hypoglycemia (which includes PBH and congenital HI). Avexitide is designed to bind to the GLP-1 receptor on pancreatic islet beta cells and inhibit the effect of GLP-1 to mitigate hypoglycemia by decreasing insulin secretion and stabilizing blood glucose levels. In PBH, excessive GLP-1 can lead to the hypersecretion of insulin and subsequent debilitating hypoglycemic events. In two Phase 2 PBH clinical trials, avexitide demonstrated highly statistically significant reductions in hypoglycemic events. These events can lead to autonomic and neuroglycopenic symptoms that can have a devastating impact on daily living. About Post-Bariatric Hypoglycemia (PBH) Post-bariatric hypoglycemia (PBH) is a condition that is estimated to affect approximately 8% of people in the U.S. who have undergone the two most common types of bariatric surgery, sleeve gastrectomy and Roux-en-Y gastric bypass (approximately 160,000 people in the U.S.). PBH is thought to be caused by an excessive glucagon-like peptide-1 (GLP-1) response leading to hypoglycemia and impaired quality of life. PBH can cause debilitating hypoglycemic events associated with inadequate supply of glucose to the brain, known as neuroglycopenia. Clinical manifestations can include impaired cognition, loss of consciousness, and seizures. PBH is also associated with a high degree of disability that can result in major disruptions to independent living. There are no approved therapies for PBH. About the LUCIDITY Trial LUCIDITY ( NCT06747468 ) is an approximately 75-participant, multicenter, randomized, double-blind, placebo-controlled Phase 3 clinical trial evaluating the efficacy and safety of avexitide in participants with PBH following Roux-en-Y gastric bypass (RYGB) surgery. The Phase 3 trial will be conducted at approximately 20 sites in the U.S. Participants will be randomized 3:2 to receive either 90 mg of avexitide subcutaneously once daily or placebo. The trial includes an up to six-week screening period, including a three-week run-in period, and a 16-week double-blind treatment period. Participants who complete the double-blind period will be eligible to enter an open-label extension (OLE) period with a duration of 32 weeks. The primary efficacy objective of LUCIDITY will evaluate the FDA-agreed upon primary outcome of reduction in the composite of Level 2 and Level 3 hypoglycemic events through Week 16. Safety and tolerability will also be evaluated. About Amylyx Pharmaceuticals At Amylyx, our mission is to usher in a new era of treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are currently focused on three investigational therapies across several neurodegenerative and endocrine diseases in which we believe they can make the greatest impact. For more information, visit and follow us on LinkedIn and X. For investors, please visit Forward-Looking Statements Statements contained in this press release regarding matters that are not historical facts are 'forward-looking statements' within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, Amylyx' expectations regarding: the potential of avexitide as a treatment for PBH; expectations regarding the timing for recruitment completion and topline data readout of the Phase 3 LUCIDITY trial of avexitide in PBH; and expectations regarding timing for potential commercialization of avexitide. Any forward-looking statements in this press release and related comments in the Company's earnings conference call are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Risks that contribute to the uncertain nature of the forward-looking statements include: the success, cost, and timing of Amylyx' program development activities; Amylyx' ability to execute on its regulatory development plans and expectations regarding the timing of results from its planned data announcements and initiation of clinical studies; the risk that early-stage results may not reflect later-stage results; Amylyx' ability to fund operations, and the impact that global macroeconomic uncertainty, geopolitical instability, and public health events will have on Amylyx' operations, as well as the risks and uncertainties set forth in Amylyx' United States Securities and Exchange Commission (SEC) filings, including Amylyx' Annual Report on Form 10-K for the year ended December 31, 2024, and subsequent filings with the SEC. All forward-looking statements contained in this press release and related comments in our earnings conference call speak only as of the date on which they were made. Amylyx undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law. View source version on CONTACT: Media Amylyx Media Team (857) 320-6191 [email protected] Lindsey Allen (857) 320-6244 [email protected] KEYWORD: UNITED STATES NORTH AMERICA MASSACHUSETTS INDUSTRY KEYWORD: HEALTH CLINICAL TRIALS RESEARCH PHARMACEUTICAL SCIENCE BIOTECHNOLOGY SOURCE: Amylyx Pharmaceuticals, Inc. Copyright Business Wire 2025. PUB: 07/13/2025 05:00 PM/DISC: 07/13/2025 05:00 PM

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