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Found 80 results
  1. Content Article
    This paper in the journal RSC Advances aimed to track changes in chemical bonding taking place in PP meshes on the nanoscale via mechano–chemical processes. The authors used the novel and advanced spectroscopic characterisation technique secondary electron hyperspectral imaging (SEHI) to build high resolution chemical maps. Polypropylene (PP) surgical mesh is associated with serious clinical complications when used in the pelvic floor for repair of stress urinary incontinence or support of pelvic organ prolapse. While manufacturers claim that the material is inert and non-degradable, there is a growing body of evidence that asserts PP fibres are subject to oxidative damage. Material surgically removed from patients suffering with clinical complications has shown some evidence of fibre cracking and oxidation. It has been proposed that a pathological cellular response to the surgical mesh contributes to medical complications, but the mechanisms that trigger the specific host response against the material are not well understood.  The study presented key insights into the mechano–chemistry reaction of PP which can cause polymer oxidation, changes in molecular structure, crack/craze formation and the release of etched oxidised insoluble particles. SEHI, provided a new route to link the effect of localised stresses to reactions of mechano–chemistry within PP. The method of mechanical distension testing during hydrogen peroxide exposure followed SEHI image analysis could form the basis of an “early warning” system which has the ability to identify materials which are not appropriate for use as medical implants.
  2. Content Article
    This study, published in the International Urogynecology Journal, involved 18 interviews with women who had experienced vaginal mesh complications. Four themes were identified:perceived impact of mesh complicationsattitudes of medical professionalssocial support and positive growth. The impact of vaginal mesh complications were wide-reaching and varied, affecting many aspects of the participants lives including mental health, relationships and sexual intimacy. Authors conclude that a greater awareness would lead to better support for women experiencing mesh complications.
  3. Content Article
    The aim of this study was to investigate the potential role of transvaginal mesh bacterial colonisation in the development of mesh-related complication (MRCs).  An observational and exploratory study from Diedrich et al. was performed including 49 patients indicated for mesh removal and 20 women of whom vaginal tissue was retrieved during prolapse surgery as a reference cohort. The authors observed distinct differences in bacterial numbers and species between patients suffering from MRCs compared to a reference cohort. Bacteria were observed at the mesh-tissue interface in a biofilm. These results strongly support the potential role of bacterial mesh colonization in the development of MRCs.
  4. News Article
    An endometriosis sufferer has said her reproductive organs are so damaged by a three-year delay for surgery, it has affected her ability to have children. Claire Nicholls, 29, has been in pain for years with the condition - which involves tissue similar to the lining of the womb growing elsewhere. Ms Nicholls said she was passed from "pillar to post" and for 10 years, medical professionals did not seem to believe how much pain she was actually in. She has stage four endometriosis, which is the most severe and widespread. "The pain can be excruciating, at times I can't get out of bed and I have also had to attend the emergency department," she said. After opting to go private, her surgeon said he was unable to see many of her organs due to the amount of scarred tissue caused by the delay in surgery. "He told me the scarred tissue and adhesions were all around my organs... they couldn't remove it all as it could have damaged other organs including my bladder - it was just too severe," she said. Northern Ireland has the longest gynaecological waiting lists in the UK, according to a professional body. It is calling for two regional endometriosis centres. The report from the Royal College of Obstetricians and Gynaecologists found 36,900 women in Northern Ireland are on a gynaecology waiting list - a 42% increase since the start of the pandemic. Read full story Source: BBC News, 25 October 2022
  5. Content Article
    In this blog, Carl Heneghan, Professor of Evidence-based Medicine at the University of Oxford and Clinical Epidemiologist Tom Jefferson look at the long-term consequences of inadequate regulation and approval of pelvic mesh devices. They argue that regulators and health systems around the world failed to heed the early warnings, which lead to thousands of women being irreversibly harmed. They highlight that as early as 1999, a study of 34 women who had ProteGen mesh implants showed that 50% of mesh devices had eroded through the vaginal wall. Boston Scientific voluntarily recalled 20,000 devices as a result. In spite of this, the FDA continued to approve vaginal mesh devices, citing ProteGen as their predicate device.
  6. Content Article
    We often hear the mesh scandal blamed on poor surgeon skill. We also hear the argument that high use mesh implanting surgeons are likely to have fewer patients suffering mesh complications, than a less experienced surgeon. However, this study published in JAMA in October 2018, based on NHS data, shows that high mesh implanting surgeons produce the same or even more mesh complications compared to low volume implanters.
  7. Content Article
    Outpatient and daycase hysteroscopy and polypectomy (OPHP) are widely recognised methods for the treatment of endometrial polyps. There have been concerns regarding pain affecting satisfaction and tolerability of the outpatient procedure. Dr Bhawana Purwar and colleagues from the Royal Wolverhampton Hospitals NHS Trust conducted a service evaluation of their outpatient hysteroscopy and polypectomy (OPHP) and compared it with their daycase procedures. They concluded that the OPHP is cost-effective and efficient method with reasonable acceptability. It is well tolerated with remarkable success rates and excellent patient satisfaction. As compared to daycase group, it requires less time for recovery and sooner returns to work.
  8. Content Article
    Research paper by Toye et al. published in the Lancet on the experience of women reporting damage from vaginal mesh.
  9. Content Article
    In this opinion piece, Kath Sansom, founder of Sling the Mesh, looks at why an audit of pelvic mesh outcomes due to be published in April 2023 has again failed to capture the true extent of the harm caused by the procedure. She outlines why the approach taken by the Government and NHS Digital was flawed and why it is so important to understand both the proportion of women who have experienced harm as a result of the procedure, and the nature of their injuries and side effects.
  10. Content Article
    The OptiBreech project is a research study exploring the feasibility of evaluating a new care pathway for women with a breech pregnancy. About 1 in 25 babies are born bottom-down (breech) after 37 weeks of pregnancy. Women who wish to plan a vaginal breech birth have asked for more reliable support from an experienced professional. This aligns with national policy to enable maternal choice. In this video, Dr Shawn Walker explains why the combination of meconium and tachycardia, particularly in the first stage of labour, indicates increased risk in breech births.
  11. Content Article
    This report was produced by NHS Digital to investigate activity in the NHS in England surrounding patients who have had a procedure for the treatment of urogynaecological prolapse or stress urinary incontinence, including those where mesh, tape or their equivalents have been used. The report uses Hospital Episode Statistics (HES) data and was undertaken to help the NHS and others establish a clearer national picture of patients who have had these procedures. NHS Digital notes that these statistics are classified as experimental and should be used with caution. Experimental statistics are new official statistics undergoing evaluation.
  12. News Article
    The rising number of women who have caesarean sections instead of natural births is causing concern for the National Childbirth Trust (NCT). The trust, which supports women through pregnancy, childbirth and early parenthood, says it does not know why the rate of caesareans is increasing. One in four maternity services showed a caesarean rate of between 20% and 29.9%, and 2% of services had a rate of more than 30%, according to latest figures. The World Health Organization recommends that the acceptable rate is 10 to 15%. The maternity care working party, a multi-disciplinary group set up by the NCT, said there was an urgent need to address the problem. "A caesarean is major abdominal surgery," the working party said in a statement to a conference in London with the Royal College of Midwives and the Royal College of Obstetricians and Gynaecologists "Most women would prefer to give birth normally, provided that a normal birth is considered safe for them and their baby. It is important that health professionals' advice does not have the effect of denying them this opportunity without good reason." The working party is calling for data to be published on caesarean section rates and for obstetricians to justify in each case that the benefits outweigh the hazards. It also wants action to be taken to prevent any inappropriate use of caesarean sections. Belinda Phipps, chief executive of the NCT, said: "We know that in many cases caesareans are necessary for good clinical reasons. However, in our view rates have reached unacceptable levels and we want to know why." Read full story Source: The Guardian, 24 November 2022
  13. News Article
    A US Senate investigation into allegations that unwanted medical procedures were performed on detained female immigrants in Georgia has uncovered “a catastrophic failure by the federal government” to protect the detainees. A Senate hearing on Tuesday by the bipartisan permanent subcommittee on investigations (PSI), chaired by the Georgia senator Jon Ossoff, announced its findings on conditions and practices at the Irwin county detention center (ICDC). The ICDC, located in Ocilla, Georgia, housed detainees who shared accounts of poor treatment including gynaecological procedures that were “excessive, invasive and often unnecessary”. An account of what was occurring at the ICDC first came to light when Dawn Wooten, a nurse at the facility, acted as a whistleblower. Ossoff called the alleged unnecessary and sometimes non-consensual medical treatment and procedures disclosed in the 18-month investigation “nightmarish and disgraceful”. Ossoff said: “This is an extraordinarily disturbing finding, and in my view represents a catastrophic failure by the federal government to respect basic human rights.” The report detailed the harrowing account of an unnamed woman who was detained in the ICDC in 2020. The detainee describes how Dr Mahendra Amin allegedly removed a portion of her fallopian tube, a result of a dilation and curettage procedure she was not made aware of, and how Amin told her “she would never be able to have children naturally again”. Read full story Source: The Guardian, 15 November 2022
  14. Content Article
    In this blog, a woman who has suffered from severe pain and complications for 17 years due to transvaginal mesh shares her experience. She talks about how the device has changed her life, how her symptoms have been repeatedly dismissed by surgeons, and the variation she has witnessed between different specialist mesh centres.
  15. Content Article
    This report represents the views of organisations and experts who responded to the Department of Health & Social Care's call for evidence on its Women's Health Strategy. The call for evidence was released in March 2021. This report focuses on submissions received from 436 organisations and individuals with expertise in women’s health, including the charity sector (34%), academia (22%), industry (10%), clinicians (7%), professional bodies (7%), pressure groups (7%), NHS organisations (3%), parliamentary groups (2%), royal colleges (1%), local government (1%), think tanks (1%) and others (6%).
  16. Content Article
    This report by the Royal College of Obstetricians & Gynaecologists (RCOG) examines the real-life impact of long gynaecology waiting lists on women and on the wider health system. It highlights the problems that existed in accessing NHS gynaecology services before the Covid-19 pandemic, and reveals how the situation has become far worse due to the backlog of care: Gynaecology waiting lists across the UK have now reached a combined figure of over 570,000 women across the UK – just over a 60% increase on pre-pandemic levels Gynaecology waiting lists in England have grown the most in percentage terms of all elective specialties The number of women waiting over a year for care in England has increased from 66 before the pandemic to nearly 25,000 RCOG recognises that gynaecology has often been overlooked, and calls for the specialty to be given parity in recovery plans.
  17. Content Article
    In the 1790s, François Marie Prevost, a young French surgeon fresh from his medical training in Paris moved to Port-de-Paix, Haiti. “Of course at that time Haiti was France's most economically valuable colony”, says historian Deirdre Cooper Owens. “So there he began some experimental work on enslaved Haitian women, trying to perfect the caesarean section.” Prevost's sojourn coincided with the leadership of Toussaint Louverture, who had been born a slave, the fight for Haitian independence, and the abolition of slavery. And so Prevost left Haiti for Louisiana. “He moved to a little town outside of Baton Rouge, and began experimental surgery on enslaved women there, perfecting the caesarean section, and he did this in the 1830s, the era before the civil war that ends slavery.” It was also an era in which Louisiana surgeons were reluctant to attempt the experimental surgery on white women. Of the 15 caesarean sections done by Prevost and others in Louisiana between 1820 and 1861, all were performed on enslaved women. “At the time, in the 19th century, during the time of slavery, they couldn’t consent”, she explains. “But this is the really interesting thing: from the 1830s all the way to the 21st century, Louisiana has been in the top three states with the most caesarean sections on Black women patients…So what's going on, did all of these women need to have caesarean sections?”
  18. Content Article
    A woman who experiences pain during caesarean section under neuraxial anaesthesia is at risk of adverse psychological sequelae. Litigation arising from pain during caesarean section under neuraxial anaesthesia has replaced accidental awareness under general anaesthesia as the most common successful medicolegal claim against obstetric anaesthetists. Generic guidelines on caesarean section exist, but they do not provide specific recommendations for this area of anaesthetic practice. This guidance aims to offer pragmatic advice to support anaesthetists in caring for women during caesarean section. It emphasises the importance of non-technical skills, offers advice on best practice and aims to encourage standardisation. The guidance results from a collaborative effort by anaesthetists, psychologists and patients and has been developed to support clinicians and promote standardisation of practice in this area.
  19. Content Article
    CORESS is an independent charity, which aims to promote safety in surgical practice in the NHS and the private sector. CORESS receives confidential incident reports from surgeons and theatre staff. These reports are analysed by the Advisory Board, who make comments and extract lessons to be learned. Aiming to educate, and avoid blame, CORESS calls on surgeons to recognise a near miss or adverse event, react by taking action to stop it happening and then report the incident to CORESS so that the lessons can be published. Every month CORESS highlight's one of the cases reported for you to consider the issues raised and read the experts comments.
  20. Content Article
    In this blog Patient Safety Learning highlights the key issues included in its recent response to the Royal College of Obstetricians and Gynaecologists new draft guidance for healthcare professionals who are involved in providing outpatient hysteroscopy.
  21. Content Article
    This is the first Women's Health Action Plan published but the Government of Ireland, and it sets out women's priorities for their health. Women, their representatives and women's health professionals have influenced the development of the Action Plan by sharing their insights and experiences through listening projects and participation opportunities carried out by the Women's Health Task Force 2020-2021. The Action Plan responds to key issues that women raised, including faster access to specialist services, reputable sources of health information and enhanced healthcare experiences. Supporting documents and related reading are provided alongside the Action Plan, including information about the Women's Health Taskforce.
  22. Content Article
    This guide by The Eve Appeal and The Survivors Trust gives information about attending cervical screening for survivors of rape, sexual abuse or assault. It offers tips that may help patients feel more comfortable about their appointment. It is part of the #CheckWithMeFirst campaign to help raise awareness of the challenges survivors of rape, sexual abuse and sexual violence may face when accessing cervical screening.
  23. Community Post
    The comments below were all shared by members of Sling the Mesh in response to a call for the worst things that have been said to patients on their mesh journey. If you have had mesh surgery, please add your accounts of interactions with doctors and other healthcare professionals in this thread. Transvaginal mesh Hubby said "It’s really painful for her when we have sex." Dr replied, "Have you tried anal?" and then winked at my hubby. I thought my husband was going to punch the surgeon. My surgeon emailed me to attend mental well being therapy classes, as in ‘it was mind over matter’, for my pain and agony that I was suffering 12 weeks after insertion! You can only imagine my reply to her 😡 …10 weeks later she discovered under another general anaesthetic that the Mesh had cut right through my bladder! "You will have to learn to live with the pain… Drs are not miracle workers." Mine said, "l don't know why women over 50 want to have sex anyway!" Top urogynaecologist: "don’t worry you don’t have cancer" patting my knee. Surgeon said no way is it the mesh you are reading to much crap on the internet, it’s working that’s all you need to know. For a whole year, I was told by my implanting surgeon that the razor blade/ hot knife feeling cutting into me was all in my head… his registrar discovered that the mesh was cutting into my vaginal wall. When I questioned about the "tape " I was told it was not mesh & don't believe everything you read in Newspapers . Also my pain was in my head! It’s your menopause not the mesh 😡 “I just don’t understand why you have all this pain, Anatomically you look beautiful” followed by a laugh!! Mine told me I probably need hip replacements. Surgeon punctured my intestine during mesh surgery and said “well it’s probably good that happened because it caused you to rest in a bed for a month.” Uh… a hospital bed in which I almost died because he refused to admit he did anything wrong. My family had to demand an independent team come in and evaluate me… I would have been dead within hours if they hadn’t. I was SO relieved to find Sling The Mesh support group after hearing about it on the news (after the Cumberlege review) I wouldn't wish this sh*t on my worst enemy but I was SO glad to discover I wasn't going mad, its not all in my head, I wasn't the only person with complications. That evening I cried hard! Such a relief and source of support 🥰 What am I moaning about, your husband should be very pleased! I’m the only one to ever have anything wrong, it must be my body not the mesh! Your like a 21 year old down there now! Where would I start 🤔so many gems to choose from! .. one of my faves is.. "DO YOU HAVE ANY OTHER MENTAL ILLNESSES??" My surgeon told me that it definitely won't be the mesh that's causing my problems. I have learned since that he has received 6 figure sums from the mesh manufacturers for promoting it! I had a “specialist” that actually said to me “ look shit happens ..and it happened to you.” Don't be silly mesh doesn't cause leg pain. I have had 2 partial removals, drag my leg around daily, hip wear and tear, urine infections, have had E/coli infections in mesh with 7 times daily antibiotics. "It's all in your mind, maybe you need to speak to someone. " Yes a lawyer you fool. My surgeon said my mesh would last about ten years I asked what do we do then , he said we will worry about that when the time comes ! My urologist told me to stop looking at Sling the Mesh on Facebook 😂😂😂😂 and to believe the professionals!!! I stood up and walked out before I did him damage!!!😂 My surgeon said Chin up and have a glass of Prosecco. I was told "Surely it's a good thing when sex hurts a bit" After telling him for five years my new urinary issues were due to the mesh, I eventually got it removed due to erosion, but at my follow up being angry at not being listened to, he suggested I had PTSD and got referred to the psychiatric team! That is an insult to the poor people who do have it , I don’t I just had anger and vented it! One of the doctors at my surgery said “your to complicated, I cannot help you. Book another appointment to see somebody else” I was told that my GP practice could not help me as my problems are too complex. Looking at me, he said "I just don't understand how you could be in pain, I will refer you to a Psychiatrist". To my partner, he said "I've made her nice and tight for you". It’s your weight try exercise, when u can’t even walk. I asked my surgeon, is there a good mesh and bad mesh! He said there is NO bad mesh! Mine told me it was all in my head! That maybe I had a low pain threshold. My gynaecologist said stop 🛑 listening to the hype !!!!! 😡 Mine said, "You’re too fat for your hips." Has this all been brought on by the Mesh nonsense in the media!!! The first doctor suggested my problems were I needed more foreplay or a lubricant during sex after I said my husband feels something sharp when inside me!!! My original TVT had 'slipped'. My gynae surgeon said he would do a TVTO, a pelvic floor repair and a posterior pro-lift. At no point was the word mesh used and in my ignorance I thought he knew best, how gullible was I? It is in your head by so many over the years that you feel you are going mad 😡 as you know the pain your in. All in my head and then your too complex you must be imagining things you can’t be in that much pain. Your back has nothing to do with your vagina so how can your back pain be linked (female consultant). I have TOT mesh implant. Suffer with groin infection and fistula. After I had infection drained (unsuccessfully) I was seen by the gynaecologist, I mentioned that the infections were the mesh incisions in my groin ... he told me not to be silly .. that mesh is in the vagina not in the groin area .. he obviously only knew about tvt mesh not TOT.. I told him to go away and do some research... I didn't see him again!!!! I got told it’s not the mesh it’s were it should be and doing it’s job 😡. Also got told to stop looking and reading stuff in mesh groups as everything isn’t true 🤬 My surgeon said "Oh, so you are jumping on the Mesh bandwagon?" When I mentioned mesh because of my endless infections to yet another doctor at my previous surgery he said ‘as long as you’re nice, we look after people who are nice’. I was so taken aback I just couldn’t even answer- I’ve never been anything but nice through many surgeries and issues. I was told -“Nothing more we can do for you so will discharge you” Worst one was sent for testing STDs When we told my surgeon I could no longer have sex because it was too painful he said I had a duty to my husband so I should just put up with it. My husband was furious he said do you really think I could enjoy sex knowing my wife is in pain. My surgeon told me he had only one women with mesh had problems and she was "neurotic"... Surgeon Quote “you can’t be in that much pain its a standard operation ?” Surgeon Quote “ It must be sciatic pain, I’ll get an orthopaedic doctor to look at you and send you home!” Another mesh specialist “it’s blue and it’s eroded but majority of women are fine I don’t understand why you can’t walk anymore your infections and blood in urine must be due to a bladder infection!” Diagnosis in 2018 Mesh cut through obturator nerve, put in to lateral too tight, too much pressure on urethra and permanent pain and damage. I was treated in a very misogynistic way even though I have my husband present. Just ignored every time I mention it, no matter who it is. “You are an awkward patient…” "‘You're to old to have pain there." "It can't be the mesh causing you pain, I've inserted lots of these and your the only one who has complained!!" (2017) mesh inserted 2014. “You can’t believe what you hear in the news about other people having mesh problems, after all, I am the trained consultant…” 😥🤦‍♀️ It’s just the menopause, you will get used to it. “Your mesh is the gold standard, it is the old mesh that causes problems.“ “Your mesh just needs time to seed itself in.” “ I don’t know why you can’t have a sex life, there is enough room for a penis.” My implanting surgeon's response to my second visit following tvt implant was to take a cursory look in my vagina and pronounce all was fine. I have learned this response is common amongst patients who've had mesh complications. By this time I was peeing to the left and pooing to the right like some sort of sick trick. I likened it to turning up at A and E with a broken arm and the doctor not ordering an X ray. I later learned the mesh and resultant scar tissue had pulled my organs this way and that. I've just undergone my fifth and hopefully final operation to remove excessive scar tissue, small fragments of mesh after two full removals and perineum reconstruction. Surgeon suggested I see a shrink because he thought it was all in my head. “Go home and try to relax more” 😲 Neurologist -if you go see enough doctors you will eventually hear what you want to hear. There are so many shockers, but the worst has to be, "Prescription pads are expensive and patients like you are not worth the cost of a prescription" "It's all in your head nothing has snapped or eroded, you have to be patient with the incontinence settling down." GP listened to me telling her the unbearable vaginal pain I was going through feeling like glass cutting into me. She looked at me and said, "But why are you here today?" The cost of your catheters is too expensive for the NHS, we would like you to change to washable catheters 😲 It's all in your mind, you need anti depressants, and motivate yourself. A urologist that I had sought help from privately having walked out/discharged myself from care of implanting surgeon, "I sit on a board looking at mesh but I personally don’t believe any of this stuff you read on the internet . Mesh cannot cause such problems.“ “You must just have been coincidentally prone to interstitial cystitis and retention” Eye rolled as she said, “You shouldnt believe everything you read on the internet. Mesh is perfectly safe…” "This is a gold standard operation, it will be life changing." Well yeah, it was life changing but not in a good way. When I told the specialist how painful it was when my husband tried to put his penis in to have sex, he said , "Is he putting it in right?" We'd been married 36 years. I was told to massage it better My implanting surgeon said she "fixes up other surgeons mistakes" after putting mine in too tight and having to loosen it a year later. Mine told me I had a "good quality of life. Just to go home and get on with it." Surgeon said my operation was Tape is like a FREE TUMMY TUCK…” My favourite, "it’s your body that’s at fault!!!" “It can’t possibly hurt every time you urinate, that's an exaggeration surely.” Mine said, “Off the record, if you complain about this no-one will want to work on you in the future” Surgeon said, "If the mesh is still in place its doing its job" 🤬 I only brought it up to my surgeon once. He told me “not to believe I’m everything in the papers. Some women are just after a payout.” Surgeon said, “In 12 years I have never had anyone else complain so it cant be the mesh.” Blatant lie in 2016 as another patient at end of communication tether was busy putting warning flyers in his waiting room. Said in an abrupt tone, ”I doubt the pain is from the mesh it all stories from media and internet.” “You have been reading too much on the internet.” Well yes I have because from 3 days after the operation when I said something was horribly wrong you were telling me to go away and heal or that it could not possibly be the tape… thank goodness I googled TVT pain or I would never have found this group and thousands experiencing similar pain and disgusting treatment like me. Implanting surgeon “you’ll learn to live with it!” Consultant: "I've been to a conference and told some of colleagues about some of your problems and they said poor you, we're glad she's not our patient." "There's nothing there, it's not mesh!" Saw somebody else who could feel the mesh hanging out straight away. 😥 "It’s not mesh it can’t do this you’re wrong it’s your hip, go away and lose weight and exercise." Female GP after I’d read medical documents saying it can 😡 I was told I was having surgery with a dissolving hammock and medical records show no mention of MESH. "Oh it's you again!! I told you before it's not the TVT. You must be lonely or looking for attention." 😡 Surgeon said to stop listening to group (Scottish Mesh Survivors) as he was the expert with experience not a group of people who knew nothing!!! I asked why I was in so much pain and was told it was because I wasn't in a sexual relationship! "This has only ever happened to you. .... your body is to blame." Before I had my surgery (vaginal hysterectomy with anterior & posterior repair), the surgeon said he would sew me up "nice & tight" and actually winked at my husband!! Well, we haven't been able to have intercourse for 10 years since my op, despite physio, hormonal lubrication etc and I'm now on a waiting list (5 yrs so far) to see a sexual psychologist, cos it's all in my head of course. I ask him if the mesh he used was the same one they talked about on the tv program. He said no so I got him to write it down. When I got home I checked and it was the same polypropylene.. It’s got nothing to do with the mesh the pain is in your head 😡 My surgeons exact words to me, thankfully my husband was present... "I’m sick of all these women jumping on the mesh bandwagon. My surgery was a success. Your bowel is perfect. But if you think the mesh is to tight, I’ll open you up, detach the mesh from your spine, let it drop & put another piece of mesh over the top & reattach to your spine. You’ll be my first but I’ll give it a go!" Just to add, since removal of mesh I’m 80+% improved & my quality of life is really good. I was told I was one of the unlucky ones. He told me I needed to stop running all over the country trying to find a Dr who could help me even though He had not help me in five years. There is no cause for your pelvic pain! A pessary will fix you! Maybe stop going on social media! I’ve had a lot of problems since my removal of a TVT last August with extremely limited after care and no follow up appointments what so ever. When I did eventually get a telephone appointment I got upset because of the amount of issues I’ve had with no one to turn to for any help. Her reply was, "well you were warned that you could end up worse than before if YOU chose to go ahead with having it removed." My reply, "Yes I knew there was a risk of even more issues, as if I wasn’t having enough already… but what however was not explained was that there would be absolutely zero help with those issues if they did occur, no one to contact or answers to emails and voice mail messages…" She went very quiet after that. I was trying to find out if mesh had been used in my op & the surgeon said, "People see one Victoria Derbyshire program and panic." My female implanting surgeon told me she’d never had any problems with any other patients. She then told me it was a skin problem and gave me some cream then discharged me. She’d already discharged me and I asked my GP to go back and see her. My female GP kept telling me it was the healing process and to give it time. After months and months of me going back with pain and UTIs she started to get really sharp with me so I stopped going. Rectopexy mesh My surgeon said when I said my vagina was very tight and painful for intercourse that his wife would love an excuse like that not to bother. I got no referral elsewhere to investigate. Had no physical relationship for 11 years. Mine laughed in my face saying, "Don't be stupid I've done over 280 rectopexy surgeries and never once had a problem. This isn't mesh related." "If I take some of this out, you will HAVE to have a colostomy bag for life." No choice given. My implanting surgeon referred me to his colleague who was a pain specialist... the pain specialist said, "Its your periods you need to go into medical menopause." I was around 36 at the time. I was told it wasn't the mesh that was causing problems and to take ownership of situation. Mesh all removed now left with permanent stoma 😫😡 When I called my bowel specialist in agony and in desperate need of help. "Aww hun I wish i could just give you a hug." My GP said, "Some pain is unexplainable, you just have to live with it." 😡 Bowel specialist said you need rectopexy repair and don’t believe the hype about mesh. They said smoking was good for you in WW2... WHEN I QUESTIONED THE CHOICE OF MESH Hernia mesh On the day of my operation, the general surgeon didn’t want to do the removal, he denied my Physiomesh had been recalled in May 2016. I had to show the link on the government site, so my plastic surgeon believed my symptoms could be related to the mesh and agreed the operation was necessary. Mine told me these groups were filling our heads with rubbish. They are full of hysterical men and women. Was told I was the only one with these issues, never had issues like this before. Told me it was all in my head. Told mesh can't cause all of these symptoms. The groups have been the biggest support to me. I finally felt normal as in I wasn't alone. This wasn't in my head. It was a sigh of relief to find the groups. A hospital consultant said, "Hernia mesh can't cause these problems." (inflammation, autoimmune, joint pain, muscle pain, allergies, Lichen Sclerosis, etc.) "You're getting confused with vaginal mesh". "If hernia mesh were a problem, I would've heard about it and I've not seen one single case in my entire career... don't you think I would've heard if there were problems?" After I persisted in telling him the scale of the problem he then raised his voice and said, "You'll never prove it." And that spoke volumes! I guess he is still staying he has never heard of a single case. He also told me to stop believing what I read on the internet. “It’s not THIS mesh that’s on the news. THIS is a great product.” (The very next year THIS mesh was recalled).
  24. Content Article
    MP Emma Hardy and Sling The Mesh drafted a letter to MP Maria Caulfield for an update on mesh centres, waiting times and outcome measures. The letter was sent in January 2023 and the reply has been received this week and shared by Sling the Mesh.
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