Global Healthy Living Foundation's CreakyJoints Arthritis Patient Community Takes Top Social Media Spot at European Rheumatology Conference
More than 62,000 people recognized CreakyJoints' Social Media Posts during EULAR in Barcelona
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EULAR, the European Alliance of Associations For Rheumatology, is Europe's largest arthritis medical conference, served as the platform for CreakyJoints' social media posts which received more than 62,000 views on Instagram, Facebook, TikTok, LinkedIn, YouTube, and others in less than a week.
'The total continues to grow,' said Ben Blanc, GHLF's Director of Digital Production and Engagement. 'We expect it to double within the next few weeks as more patients around the world tune in.'
Significant Reach and Engagement
The posts include 12 video interviews with leading rheumatologists, clinical researchers, patient advocates and health innovators covering cutting-edge topics shaping the future of rheumatic and musculoskeletal disease care, including shared decision-making, personalized medicine, PMR (polymyalgia rheumatica), CAR T cell therapies, digital tools, and health equity.
In addition to the interviews, GHLF presented two posters in the main hall:
OA Compass: An Online Decision-Making Tool Empowering Patients with Knee Osteoarthritis through Stories, Treatment Guidance, and Personalized Support.
Implementing a Digital Platform for Real-Time Collection and Integration of Patient-Reported Insights in Rheumatic Disease Management.
To access all of the content from EULAR 2025, visit EULAR 2025 Insights: Voices from the Global Rheumatology Community on the CreakyJoints YouTube channel.
GHLF's global social media presence includes a 17-show podcast network in addition to social media posts which reach approximately 4 million people each month.
'Being at EULAR reminds us why we do this work: when experts, patients, and advocates come together in the same room — or on the same screen — we learn more, push ideas further, and get closer to real solutions,' said Seth Ginsberg, Co-Founder and President of GHLF. 'This year's conversations showed how much progress we're making, and how listening to patient voices at every step is driving the next generation of care.'
About GHLF
The Global Healthy Living Foundation is a U.S. based, 501(c)(3) nonprofit, international organization whose mission is to improve the quality of life for people with chronic illnesses by advocating for improved access to health care through education, patient-centered clinical research, support, advocacy, and economic and policy research. GHLF is also a staunch advocate for vaccines. The Global Healthy Living Foundation is the parent organization of CreakyJoints®, the international, digital community for millions of people living with arthritis and their supporters worldwide who seek education, support, activism, and patient-centered research in English, Spanish, and French. In addition to arthritis and autoimmune disorders, GHLF supports dermatology, gastroenterology, neurology, cardiology, oncology, infectious disease, rare disease, and pulmonary patients through a host of different programs and activities which draw more than 700,000 patients a month to GHLF websites and create more than 10 million impressions a month on seven social media platforms. In 2024, GHLF had more than 1 million views and listens with its patient-centered audio-visual content, found on YouTube and podcast platforms. GHLF never asks the public for donations, receiving funding instead through governments, non-governmental organizations, foundations, industry, family foundations, and GHLF Co-Founder Louis Tharp. Visit www.ghlf.org for more information.
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Medincell: Half-Year Liquidity Contract Statement
MONTPELLIER, France--(BUSINESS WIRE)--Regulatory News: Under the liquidity contract entrusted by Medincell (Paris:MEDCL) to Rothschild Martin Maurel, the following resources were included in the liquidity account at June 30, 2025: 5 000 shares 1 145 177 € Over the period from 01/01/2025 to 30/06/2025, a total of : Number of executions Number of shares Traded volume in EUR Buy side 11,807 759,363 11,677,812.97 Sell side 11,343 758,413 11,671,875.50 Expand It should be noted that Medincell increased the funds allocated to the liquidity contract by €600,000 on 11 April 2025. At the time of its implementation on September 11, 2024, the following resources were included in the liquidity account: 8 824 shares 466 568.49 € About Medincell Medincell is a clinical- and commercial-stage biopharmaceutical licensing company developing long-acting injectable drugs in many therapeutic areas. Our innovative treatments aim to guarantee compliance with medical prescriptions, to improve the effectiveness and accessibility of medicines, and to reduce their environmental footprint. They combine active pharmaceutical ingredients with our proprietary BEPO® technology which controls the delivery of a drug at a therapeutic level for several days, weeks or months from the subcutaneous or local injection of a simple deposit of a few millimeters, entirely bioresorbable. The first treatment based on BEPO® technology, intended for the treatment of schizophrenia, was approved by the FDA in April 2023, and is now distributed in the United States by Teva under the name UZEDY® (BEPO® technology is licensed to Teva under the name SteadyTeq™). We collaborate with leading pharmaceutical companies and foundations to improve global health through new treatment options. Based in Montpellier, Medincell currently employs more than 140 people representing more than 25 different nationalities. UZEDY® and SteadyTeq™ are registered trademarks of Teva Pharmaceuticals. This press release may contain forward-looking statements, particularly concerning the progress of the Company's clinical trials. Although the Company considers that its forecasts are based on reasonable assumptions, any statements other than statements of historical fact that may be contained in this press release relating to future events are subject to change without notice, to factors beyond the Company's control and to the Company's financial capabilities. These statements may include, but are not limited to, any statements beginning with, followed by or including words or expressions such as "objective", "believe", "expect", "aim", "intend", "may", "anticipate", "estimate", "plan", "project", "will", "may", "probably", "should", "could" and other words or expressions of similar meaning or used in the negative. Forward-looking statements are subject to inherent risks and uncertainties beyond the Company's control which may cause actual results, performance or achievements of the Company to differ materially from those anticipated or implied by such statements. A list and description of such risks, hazards and uncertainties can be found in the documents filed by the Company with the Autorité des Marchés Financiers (AMF) pursuant to its regulatory obligations, including in the Company's document de base, registered with the AMF on September 4, 2018 under number I. 18-062, as well as in documents and reports to be published subsequently by the Company. Furthermore, these forward-looking statements only apply as of the date of this press release. Readers are cautioned not to place undue reliance on these forward-looking statements. Except as required by law, the Company undertakes no obligation to publicly update these forward-looking statements, nor to update the reasons why actual results may differ materially from those anticipated in the forward-looking statements, even if new information becomes available. The Company's updating of one or more forward-looking statements does not imply that it will or will not update these or any other forward-looking statements. This press release is published for information purposes only. The information contained herein does not constitute an offer to sell or a solicitation of an offer to buy or subscribe for securities of the Company in any jurisdiction whatsoever, particularly in France. Similarly, this press release does not constitute investment advice and should not be treated as such. It is not intended to address the investment objectives, financial situation or specific needs of any particular recipient. It should not be relied upon as a substitute for the exercise of your own judgement. All opinions expressed in this document are subject to change without notice. The distribution of this press release may be restricted by law in certain jurisdictions. Persons into whose possession this press release comes are required to inform themselves about and to observe any such restrictions. Appendices – Rothschild Martin Maurel from 01/01/2025 to 30/06/2025 DATE NB_BUY NB_SALE QTE_BUY QTE_SALE CAPITAL_BUY CAPITAL_SALE 02/01/2025 89 132 1,607 5,257 26,949.39 89,631.85 03/01/2025 65 61 2,170 2,570 38,343.90 45,900.20 06/01/2025 111 85 3,509 2,609 63,758.53 47,562.07 07/01/2025 135 116 7,131 4,281 126,432.63 75,688.08 08/01/2025 63 66 3,356 3,356 57,924.56 58,025.24 09/01/2025 86 52 3,965 1,715 67,167.10 29,103.55 10/01/2025 70 43 2,336 1,336 39,011.20 22,391.36 13/01/2025 110 76 2,580 2,830 41,899.20 45,987.50 14/01/2025 50 51 1,848 1,848 30,196.32 30,362.64 15/01/2025 57 55 1,708 1,708 27,891.64 28,011.20 16/01/2025 31 51 2,238 3,238 36,277.98 52,585.12 17/01/2025 42 51 1,063 1,813 17,199.34 29,424.99 20/01/2025 47 32 1,971 1,971 32,028.75 32,068.17 21/01/2025 243 133 7,060 7,560 113,736.60 128,822.40 22/01/2025 48 75 1,456 2,706 23,179.52 43,323.06 23/01/2025 59 53 2,014 2,264 31,962.18 36,020.24 24/01/2025 44 98 1,850 2,810 29,507.50 45,044.30 27/01/2025 47 54 1,495 2,535 23,979.80 40,990.95 28/01/2025 61 135 555 1,555 9,301.80 25,828.55 29/01/2025 254 161 16,266 10,766 269,852.94 177,208.36 30/01/2025 226 230 16,770 16,520 259,767.30 256,060.00 31/01/2025 51 96 1,340 3,188 21,064.80 50,211.00 01/2025 1,989 1,906 84,288 84,436 1,387,432.98 1,390,250.83 03/02/2025 45 95 2,511 2,413 39,046.05 37,811.71 04/02/2025 48 47 2,065 2,065 32,895.45 32,978.05 05/02/2025 45 59 1,100 5,100 17,644.00 82,263.00 06/02/2025 41 39 1,826 1,826 29,928.14 29,946.40 07/02/2025 82 31 3,387 887 54,632.31 14,227.48 10/02/2025 161 69 4,812 2,062 74,537.88 32,167.20 11/02/2025 49 62 3,412 2,512 51,760.04 38,132.16 12/02/2025 52 38 1,643 1,793 24,743.58 27,038.44 13/02/2025 92 80 3,027 1,527 45,072.03 22,843.92 14/02/2025 156 160 4,414 3,414 63,164.34 48,547.08 17/02/2025 91 128 2,886 4,886 41,183.22 69,967.52 18/02/2025 144 95 3,940 3,403 55,238.80 47,744.09 19/02/2025 243 265 12,992 11,529 177,210.88 157,370.85 20/02/2025 245 126 3,818 4,318 52,039.34 59,070.24 21/02/2025 96 92 2,295 2,372 31,212.00 32,354.08 24/02/2025 78 54 1,618 1,541 22,020.98 21,065.47 25/02/2025 125 79 3,641 2,141 48,388.89 28,432.48 26/02/2025 240 295 6,989 11,489 95,819.19 160,156.66 27/02/2025 172 119 4,575 4,075 65,422.50 58,476.25 28/02/2025 110 109 2,625 2,625 37,170.00 37,511.25 02/2025 2,315 2,042 73,576 71,978 1,059,129.62 1,038,104.33 03/03/2025 80 110 832 2,532 11,964.16 36,435.48 04/03/2025 174 129 6,650 4,450 94,762.50 63,991.00 05/03/2025 117 266 8,281 11,081 119,163.59 159,677.21 06/03/2025 92 62 3,934 2,134 56,020.16 30,537.54 07/03/2025 122 153 8,000 7,000 112,320.00 98,280.00 10/03/2025 105 100 10,000 8,000 137,800.00 110,640.00 11/03/2025 84 77 3,416 2,156 46,491.76 29,450.96 12/03/2025 34 96 1,951 8,560 27,040.86 118,641.60 13/03/2025 106 94 7,706 5,757 107,421.64 80,425.29 14/03/2025 81 60 7,716 5,016 107,406.72 70,324.32 17/03/2025 71 114 7,879 10,921 109,518.10 152,020.32 18/03/2025 64 78 11,612 14,940 165,819.36 213,940.80 19/03/2025 91 112 11,437 11,808 166,865.83 172,396.80 20/03/2025 42 46 5,941 6,000 86,916.83 87,900.00 21/03/2025 71 87 9,902 9,152 147,935.88 137,005.44 24/03/2025 88 30 9,351 5,001 140,171.49 75,015.00 25/03/2025 67 56 4,661 3,961 69,029.41 58,662.41 26/03/2025 25 73 4,004 7,003 59,979.92 104,904.94 27/03/2025 67 45 6,457 4,558 96,467.58 68,005.36 28/03/2025 52 65 2,768 6,668 41,298.56 99,753.28 31/03/2025 91 30 7,061 1,361 102,808.16 20,006.70 03/2025 1,724 1,883 139,559 138,059 2,007,202.51 1,988,014.45 01/04/2025 106 93 8,067 6,567 115,922.79 94,433.46 02/04/2025 84 103 6,275 7,275 88,979.50 103,668.75 03/04/2025 55 27 4,332 3,422 61,124.52 48,318.64 04/04/2025 44 37 2,700 2,810 36,801.00 38,216.00 07/04/2025 2 3 150 570 1,923.00 7,341.60 08/04/2025 38 56 2,213 4,043 29,875.50 54,701.79 09/04/2025 63 50 4,913 3,463 64,311.17 45,053.63 10/04/2025 82 52 4,514 4,014 60,893.86 54,108.72 11/04/2025 74 50 4,515 3,690 58,559.55 47,970.00 14/04/2025 27 72 1,575 4,900 20,868.75 65,219.00 15/04/2025 31 57 1,525 4,025 21,106.00 55,625.50 16/04/2025 71 106 10,148 10,148 142,883.84 142,883.84 17/04/2025 54 66 4,844 4,844 68,300.40 68,494.16 22/04/2025 62 86 5,796 6,796 82,766.88 97,182.80 23/04/2025 121 110 10,326 10,326 150,966.12 151,172.64 24/04/2025 105 110 8,794 10,794 130,590.90 160,506.78 25/04/2025 115 58 9,039 4,039 136,217.73 60,544.61 28/04/2025 77 88 8,327 9,327 124,571.92 139,625.19 29/04/2025 96 107 10,750 10,750 160,927.50 161,250.00 30/04/2025 100 92 10,209 10,209 155,380.98 155,687.25 04/2025 1,407 1,423 119,012 122,012 1,712,971.91 1,752,004.36 02/05/2025 46 84 4,802 8,802 73,614.66 135,286.74 05/05/2025 102 103 10,750 9,500 164,045.00 145,350.00 06/05/2025 130 98 9,918 10,418 151,348.68 159,395.40 07/05/2025 110 92 7,131 7,881 109,104.30 120,894.54 08/05/2025 69 85 7,463 7,463 115,377.98 115,601.87 09/05/2025 48 36 4,721 4,721 73,553.18 73,600.39 12/05/2025 142 132 11,275 10,775 169,914.25 162,379.25 13/05/2025 113 92 11,500 10,000 174,455.00 151,700.00 14/05/2025 45 53 1,041 3,041 15,781.56 46,314.43 15/05/2025 69 13 5,050 1,050 77,063.00 15,960.00 16/05/2025 26 60 1,981 4,981 30,071.58 75,611.58 19/05/2025 52 44 3,166 4,166 49,421.26 65,072.92 20/05/2025 135 114 10,628 9,628 164,946.56 149,522.84 21/05/2025 50 80 3,791 4,791 59,025.87 74,979.15 22/05/2025 113 69 7,466 6,966 118,186.78 110,411.10 23/05/2025 145 141 5,722 5,722 91,609.22 92,410.30 26/05/2025 152 144 10,400 7,650 176,904.00 130,126.50 27/05/2025 85 125 8,270 10,020 140,259.20 170,039.40 28/05/2025 204 176 12,204 11,704 201,610.08 194,052.32 29/05/2025 145 123 12,000 9,357 199,680.00 155,887.62 30/05/2025 141 137 7,853 12,496 130,988.04 208,183.36 05/2025 2,122 2,001 157,132 161,132 2,486,960.20 2,552,779.71 02/06/2025 201 128 13,078 8,078 216,179.34 133,690.90 03/06/2025 193 156 10,185 10,657 164,589.60 173,282.82 04/06/2025 102 88 9,000 7,278 144,450.00 116,811.90 05/06/2025 89 139 5,250 11,500 84,892.50 186,415.00 06/06/2025 106 59 8,810 4,864 143,603.00 79,477.76 09/06/2025 83 76 6,319 6,223 101,040.81 99,692.46 10/06/2025 109 104 9,407 7,449 151,546.77 120,152.37 11/06/2025 134 73 10,000 4,000 158,300.00 63,360.00 12/06/2025 124 84 7,676 7,676 119,899.12 119,745.60 13/06/2025 158 128 9,356 9,356 144,363.08 144,456.64 16/06/2025 137 148 12,930 14,249 200,415.00 220,717.01 17/06/2025 99 53 11,926 3,624 181,871.50 55,048.56 18/06/2025 30 132 2,050 14,683 32,533.50 233,606.53 19/06/2025 64 103 5,849 9,699 95,748.13 159,548.55 20/06/2025 148 113 11,114 10,114 187,270.90 170,724.32 23/06/2025 101 84 12,940 9,440 223,991.40 163,123.20 24/06/2025 91 71 8,216 5,353 138,193.12 91,803.95 25/06/2025 58 123 4,825 8,688 81,397.75 147,087.84 26/06/2025 71 48 7,843 6,302 132,076.12 106,629.84 27/06/2025 67 106 9,209 12,750 155,816.28 216,495.00 30/06/2025 85 72 9,813 8,813 165,937.83 148,851.57 06/2025 2,250 2,088 185,796 180,796 3,024,115.75 2,950,721.82 S1/2025 11,807 11,343 759,363 758,413 11,677,812.97 11,671,875.50 Expand
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Mauna Kea Technologies Enters Australian Market with Endotherapeutics Partnership
PARIS & BOSTON--(BUSINESS WIRE)--Regulatory News: Mauna Kea Technologies (Euronext Growth: ALMKT), inventor of Cellvizio®, the multidisciplinary probe and needle-based confocal laser endomicroscopy (p/nCLE) platform, today announces its entry into the Australian market by signing a new exclusive distribution agreement with Endotherapeutics Pty Ltd, a leading Australia-based distributor of cutting-edge medical devices, to bring the Cellvizio platform to Australian physicians. This strategic expansion comes as Mauna Kea experiences growing momentum for its CellTolerance application, prompting the company to open new geographic markets with strong growth potential. The three-year agreement grants Endotherapeutics the exclusive rights to distribute and promote the Cellvizio platform in Australia. As part of the market entry, a submission for Therapeutic Goods Administration (TGA) approval for the latest generation of Cellvizio products is underway. Mauna Kea Technologies has already been granted TGA clearance in the past and does not anticipate any hurdles in obtaining it again. The partnership will leverage the upcoming launch of the CellTolerance program with Professor Gerald Holtmann, MD, PhD, MBA, a leading Australian physician at Princess Alexandra Hospital in Brisbane, who is planning to acquire one Cellvizio for food intolerance applications. 'This technology brings hope of change for millions of patients suffering from food-related IBS symptoms,' commented Professor Holtmann. 'Cellvizio is truly unique in its ability to help identify the root causes of patient symptoms, enabling the creation of tailored diets. My entire team is excited to explore its full potential and improve the lives of our patients.' 'We're very pleased to partner with Mauna Kea Technologies to introduce Cellvizio to the vibrant Australian GI market,' stated Rob Curtin, Business Manager for GI at Endotherapeutics. 'The potential for Cellvizio and its key indications, particularly pancreatic cyst characterization and food intolerance detection is very significant.' Sacha Loiseau, Chairman and CEO of Mauna Kea Technologies, added: "We are thrilled to partner with Endotherapeutics, a premier distributor of cutting-edge medical devices and a trusted partner with deep roots in the Australian healthcare system. This partnership marks a key milestone in our international expansion strategy. As we see good momentum in the adoption of our platform, particularly for CellTolerance, we are taking key initiatives to expand our market reach in territories with strong growth potential.' *** About Endotherapeutics Pty Ltd Endotherapeutics is a leading Healthcare Technologies distributor serving customers across Australia and New Zealand, headquartered in Sydney, Australia. Endotherapeutics' mission is to improve healthcare and achieves this by supplying innovative healthcare solutions with the highest levels of service and support. To find out more, visit About Mauna Kea Technologies Mauna Kea Technologies is a global medical device company that manufactures and sells Cellvizio®, the real-time in vivo cellular imaging platform. This technology uniquely delivers in vivo cellular visualization which enables physicians to monitor the progression of disease over time, assess point-in-time reactions as they happen in real time, classify indeterminate areas of concern, and guide surgical interventions. The Cellvizio® platform is used globally across a wide range of medical specialties and is making a transformative change in the way physicians diagnose and treat patients. For more information, visit Disclaimer This press release contains forward-looking statements about Mauna Kea Technologies and its business. All statements other than statements of historical fact included in this press release, including, but not limited to, statements regarding Mauna Kea Technologies' financial condition, business, strategies, plans and objectives for future operations are forward-looking statements. Mauna Kea Technologies believes that these forward-looking statements are based on reasonable assumptions. However, no assurance can be given that the expectations expressed in these forward-looking statements will be achieved. These forward-looking statements are subject to numerous risks and uncertainties, including those described in Chapter 2 of Mauna Kea Technologies' 2024 Annual Report filed with the Autorité des marchés financiers (AMF) on April 30, 2025, which is available on the Company's website ( as well as the risks associated with changes in economic conditions, financial markets and the markets in which Mauna Kea Technologies operates. The forward-looking statements contained in this press release are also subject to risks that are unknown to Mauna Kea Technologies or that Mauna Kea Technologies does not currently consider material. The occurrence of some or all of these risks could cause the actual results, financial condition, performance or achievements of Mauna Kea Technologies to differ materially from those expressed in the forward-looking statements. This press release and the information contained herein do not constitute an offer to sell or subscribe for, or the solicitation of an order to buy or subscribe for, shares of Mauna Kea Technologies in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. The distribution of this press release may be restricted in certain jurisdictions by local law. Persons into whose possession this document comes are required to comply with all local regulations applicable to this document.
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Geneoscopy's New FDA-Approved Stool Collection Method Simplifies At-Home Colorectal Cancer Screening
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ColoSense is indicated for individuals aged 45 and older who are at average risk for CRC. It uses advanced RNA technology to detect biomarkers associated with CRC and advanced adenomas (AA)—precancerous growths that can develop into cancer if left untreated. As the only FDA-approved RNA-based test for CRC screening, ColoSense demonstrated 93% sensitivity for CRC and 45% sensitivity for AA in average-risk individuals. Among average-risk individuals aged 45 to 49, where CRC incidence is on the rise, the test demonstrated 100% sensitivity for CRC and 44% sensitivity for AA.* Despite the availability of multiple screening options, an estimated 44 million people aged 45-75 remain unscreened for CRC. 2 To help address a common barrier to stool-based screening, the updated ColoSense collection kit removes the need to scrape the sample. This improvement is expected to increase patient compliance, lower the rate of collection errors, and reduce the frequency of invalid samples. This ease of use can translate into fewer missed screenings and a greater overall impact on population health. 'To exceed 80% compliance for colorectal cancer screening, the patient experience for stool-based screening must be improved,' said Andrew Barnell, Chief Executive Officer of Geneoscopy. 'The new ColoSense test does that, offering patients everything they like about at-home, high-sensitivity screening, but now, with an easier collection process.' ColoSense is included in National Comprehensive Cancer Network (NCCN) guidelines, based on an evaluation of the strength of its clinical evidence and the robust science behind the technology. The test will be available through Geneoscopy's strategic collaboration with Labcorp, expanding access for providers and patients across the United States. ColoSense represents a significant advancement in noninvasive stool testing options, reinforcing the importance of accessible tools that help reach individuals who are less likely to undergo colonoscopy. About ColoSense ColoSense is intended for the qualitative detection of colorectal neoplasia-associated RNA markers and for the presence of occult hemoglobin in human stool. ColoSense is for use with the ColoSense Collection Kit, the ColoSense Test Kit, the ColoSense Software, and the following instruments: Polymedco iFOBT Analyzer; bioMérieux EMAG Nucleic Acid Extraction System; and Bio-Rad QXDx ddPCR System. ColoSense is a single-site test performed at Geneoscopy, Inc. A positive ColoSense result may indicate the presence of colorectal cancer (CRC), advanced adenomas (AA), or serrated precancerous lesions (SPL) and should be followed by a colonoscopy. ColoSense is indicated as a screening test for adults aged 45 years or older who are at the typical average risk for developing CRC. ColoSense is not a replacement for diagnostic colonoscopy or surveillance colonoscopy in high-risk individuals. Results from Geneoscopy's pivotal CRC-PREVENT trial were published in The Journal of the American Medical Association (JAMA). For more information, visit About Geneoscopy, Inc. Geneoscopy, Inc. is a life sciences company focused on developing diagnostic tests for gastrointestinal health. Leveraging its proprietary, patented stool-derived eukaryotic RNA (seRNA) biomarker platform, Geneoscopy's mission is to empower patients and providers to transform gastrointestinal health through innovative diagnostics. The company's FDA-approved ColoSense test uses a proprietary RNA-based platform to screen for colorectal cancer and advanced adenomas for average-risk individuals over the age of 45. In partnership with leading universities and biopharmaceutical companies, Geneoscopy is also developing diagnostic tests for treatment selection and therapy monitoring in other areas of gastrointestinal health. For more information, visit and follow the company on LinkedIn. References Luque JS, Wallace K, Blankenship BF, et al. Formative Research on Knowledge and Preferences for Stool-based Tests compared to Colonoscopy: What Patients and Providers Think. J Community Health. 2018;43(6):1085-1092. doi:10.1007/s10900-018-0525-x Hyams T, Mueller N, Curbow B, et al. Screening for colorectal cancer in people ages 45–49: research gaps, challenges and future directions for research and practice, Transl. Behav. Med, Volume 12, Issue 2, Feb 2022, Pages 198–202. *ColoSense identified 5/5 colorectal cancers and 37/84 advanced adenomas.
