Posts Tagged ‘ stress incontinence ’

Teresa Hughes: Demanding Answers and Raising the Profile of Vaginal Mesh Injuries in the UK

Nov 5th, 2012 | By
Teresa Hughes: Demanding Answers and Raising the Profile of Vaginal Mesh Injuries in the UK

Teresa Hughes, 61, a resident of Liverpool, England, and mother of two, has made so much noise about defective vaginal mesh that last year she was profiled in the UK paper, The Daily Mail. It started: “Thousands of women have been left severely damaged as a result of an implantable ‘sling’ operation to treat problems
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Deb C Suffering: Stress Incontinence Mesh Injuring Women Too

Oct 10th, 2012 | By
Deb C Suffering: Stress Incontinence Mesh Injuring Women Too

 February 3, 2012. That was the day that Deb Contestabile says her health took a downturn from which she has still not recovered. The 46-year-old mother of two boys led a predictable and comfortable life with her husband of almost 22 years who owns a machine shop. They have busy lives with the two boys
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J & J Execs to be Deposed About Vaginal Mesh – What Did They Know – When Did They Know It

Jul 29th, 2012 | By
J & J Execs to be Deposed About Vaginal Mesh – What Did They Know – When Did They Know It

July 29, 2012 ~ Johnson & Johnson’s new CEO is on the hot seat. Alex Gorsky must show up to provide a videotaped deposition concerning the upcoming Ethicon transvaginal mesh lawsuits pending before a New Jersey Superior Court. Ethicon is a wholly owned subsidiary of Johnson & Johnson. The decision to require Gorsky and two
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Consumer Alert- Walks Like News, Quacks Like News- Must be News? Wrong

Jun 19th, 2012 | By
Consumer Alert- Walks Like News, Quacks Like News- Must be News? Wrong

Op-Ed – June 19, 2012 ~ Editors Note- * -As someone who worked in the mainstream news for 25 years I know how it used to work. That was before the 500 channel universe and all eyeballs abandoned newspapers to go online. But the profitable business models for news – both print and broadcast –
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We hope you find this a helpful resource. National News Editor, Jane Akre, began MDND with the hope of providing the latest news, information and perspective from the regulatory, industry and patient point of view, something that goes under-reported in much of the coverage of medical devices. The public is just now becoming aware that many devices do not undergo the same scrutiny as prescription drugs and are instead grandfathered in under an FDA loophole that has gone largely unchanged since the 1970s. As a result, patients become the post-market clinical trial subjects, and many suffer devastating and permanent injuries.