I underwent a TVT operation about 5 years ago. Just over a year ago
during another operation it was found that the tape had moved and is now very close to my bladder, it actually touches the bladder when it is
full. I now need this removed as it may penetrate the bladder. Has anyone else had this problem and if so what is the outcome?
I am putting this off as i am very worried that my bladder may be damaged during the removal,although i have been told that i should have this removed asap! and that it will be a major operation with 4 weeks in hospital. I feel that i should have been warned of this risk before i underwent the original operation, but i was not! Please does anyone have any knowledge of this particular problem.
Many thanks
Mrs. M. Gardener.


Dear Miriam,
Please contact me. I have the same problem. You are right to be concerned. The edges of the tape are very abrasive and the tape itself has grown into your native tissue. Removing the tape will cause a lot of harm to the healthy tissue around it.
My doctor has been removing the tape from inside my bladder for almost 5 years now. He has managed it conservatively and not removed it completely, just the portion that is actually in the bladder.
I have filed a product liability lawsuit against Ethicon, Inc, Gynecare and Johnson & Johnson in the United States District Court for the Southern District of Florida.
Lana C. Keeton, Plaintiff Pro Se vs.
Ethicon, Inc. (d/b/a Gynecare Worldwide) and Johnson & Johnson, Case #06-21116-Civ-Ungaro-Benages.
It is set for trial for October 1, 2007.
I have reports from an expert witness that the edges of the tape are defective. Please contact me at miamiblog@bellsouth.net I will be happy to send you a copy of the reports to show to your doctor.
Be sure to see an expert urogynecologist before you take any action. I look forward to hearing from you.
Lana
Lana,
Is your law suit a class action or are you on your own? There are many attys filing class action lawsuits against Mentor which I found out about by going to site--Mentor TVT removal.
Hi, I had TVT surgery in 1907 and as a result have pain so terrible that I can't have sex with my husband. Pelvic exams are torture as well. I have a worse incontinence problem now than before my surgery. Believe me being in Depend diapers is grim. They are expensive, unconfortable, and a permanent wedgy. I live in Canada and I want to join a class action suit. Recently, I did some research, but can't find any class action suits in Canada. Can I join your law suit? Can I start my own? Please help me as I don't know what to do next!
I too am In Canada and I would love to talk with you.. I am in Ontario where are you from? I am so frustrated with our health care system and how they don't know what to do with this mesh.
Please email me I would love to talk more.
fashions@mountaincable.net
Hi I am in England and woul like to start a class action suit against the manufacturers here. Can you tell me how your class action suit is getting on in the USA. Regards Christine
I had the TVT placed 8 weeks ago. I had to be readmitted to the hospital 3 days and 3 emergencry room visits later. I had a 2nd surgery to remove a softball size hematoma from the perineum area with a 3 inch incision in the vaginal wall. I have had trouble with the TVT from day one. I am seeing a different surgeon this Friday to see about having the TVT removed. I have had pain since the day of the surgery and there is no way I could have a speculum exam much less relations with my husband since the procedure. I have told my family and friends that I would have rather endured the trouble of leaking than this! Think twice before having it done!!! I would be interested in learning of any class action law suits as well.
I wish anyone else the best of luck with their post procedures!
Sincerely,
Beth
Dear Beth,
You need to have it removed. If you are having this much trouble now, it will continue. Please be VERY careful what doctor removes the mesh. The second surgery can be worse than the first if the surgeon does not have the surgical skill.
You need to see a highly qualified urogynecologist who has A LOT OF EXPERIENCE REMOVING MESH. There are some urogynecologists who claim they are very good at removing mesh who are not, particularly some who have websites proclaiming their skills.
I recommend you join Medical Mesh. Write me at miamiblog@bellsouth.net for further information on joining the group. We help each other find doctors and support each other through the misery that is mesh.
Also, go to www.truthinmedicine.us.com for more information on our efforts to stop this from happening to others.
All the best, blessings, Lana
Lana Keeton
President & Founder
Truth in Medicine Incorporated
1521 Alton Road, #198
Miami Beach, FL 33139
truthinmedicine@bellsouth.net
786-566-7780
Any info on what I can do about insurance? I had insurance at the time of ALL 3 of my surgeries and now, once again, I have more of the mesh erosion... which I didn't even understand was an issue for so many women! My doctor (who is now retired) NEVER said a word about this, even the exposed mesh he removed 4 months after the original surgery. (Dec 06) Now, I feel awful, have a husband who is worried about the "wire" feeling inside me when we're intimate, and I have had 17 kidney stones since the surgery. Anyone else in this same boat? I am afriad my bladdar will fall out, never be intimate with my husband, and have erosion with other organs. Please help! I am in Washington state and have no where to turn.
~Angee.
Hi
I have just read you are from England. I am too. I have had lot's of problems since I had the operation last May.
They finally sent me for a cystoscopy test last week only to be told I have TVT erosion seen at mid urethra. Also bladder inflamation GREAT!
The doctor tried to speak to the consultant but he had gone home. I'm just waiting!
Having read the reviews I feel very nervouse - it does not make for good reading. I only hope it comes out with out a problem, but where do they go from here?
And more importantly what about me!!!
I would like to hear from you
Hello - I am so very sorry to hear about your problem. I could not have the mesh removed as it was inserted 8 years ago and it has grown into the surrounding tissue. My new gynae did however say that he would not undertake this procedure if the mesh had been inserted more than 6 months before. So if yours was done 8 months ago maybe its too late to have it removed.
So the only procedure open to me was to have the erosion removed by laser I had this done 6 months ago and it has eroded again. So I will have to go back into hospital to have it redone!!!!
I can see this continuing for the rest of my life and its very depressing. However, the laser procedure is far less invasive and less risky than mesh removal, and in any case they can never remove the whole mesh.
If you need to contact me again for any details of surgeons etc please do so. I am not in England at the moment but can always respond to your emails.
With kind regards and good wishes
anonymous
PS I am attempting to start a class action in the future plus I am seeing if I have any legal redress against the surgeon who inserted it in the first place
PPS Have a look at the UK website meshupmesh.org They are very supportive.
Hi Christine,
It was so good to hear from you. It's such a help to hear from someone who has had the same problems I am now having to go through.
After the operation and all the complications, the consultant put me on Kentera patches for three months, which gave me disturbed vision.
I'm not sure whether it was the cystoscopy I had the other day or withdrawl symptoms from the patches but I have had a rotten few days, feeling sick & swimmy.
When I last saw the consultant the plan was:
To start me on a brand new drug just out! don't know the name as I was to give time for the letter to get to my G.P, then book an appointment to see her.
Next was to organise an appointment for the cystscopy. I then recieved a cancellation appointment. That's when I found out about the erosion.
I'm now waiting to see what the plan of action will be. I'm really pleased I found this site as at least I'm better informed to have a 1 to 1 discussion with the consultant so we can cover all the options and do what is best for me.
I'm only 57 this condition has made a big impact on my married life, hobbies travel it just spoils everything ! I hate having to wear pads with a passion.
When you had the laser was there any improvment in your condition ? I'm guessing not! as it's a fix rather than a cure! Are you on any medication now & does it work?
I will keep you informed as to what happens next!
Thank you for your support
When I had the laser treatment I was sympton free for about 5 months - It was wonderful. Apparantely not everyone erodes again. The surgeon who did the procedure had done 5 before me and only one had re eroded. Its rotton luck and if it had happened in two years I might have thought, well fair enough, but 6 months feels like too much bear.
Anyway, there is nothing I can do. It'll be like this for the rest of my life
Keep in touch
Christine
Hello Angee, Sorry I did not write back sooner. The notification went into to my spam and I just read this today. Please contact me at truthinmedicine@bellsouth.net. I will help you to find a doctor. You may need to have all of it removed. The original scarring of your tissue into the mesh from the first surgery will probably keep your bladder from prolapsing. Just take one step at a time. The first step is to find a skilled urogynecologist (preferably a pelvic floor repair specialist) who has a LOT of experience removing mesh. You may have to travel out of state. What a shame the doctor was less than candid with you about the real situation. There are good doctors with ethics who are out there helping women (and men) like you.
All the best, blessings, Lana
Lana C. Keeton
Founder and President
Truth in Medicine Incorporated
1521 Alton Road, #198
Miami Beach, FL 33139
e-mail: truthinmedicine@bellsouth.net
website: www.truthinmedicine.us.com
blog: www.theladyisachamp.blogspot.com
Just wanted to let you know that I had every doctor I went to tell me that
I could not have my mesh removed and looked at me hopelessly...I did my
research and found a doctor at University of Michigan remove mine last
May after having it there for almost 5 years.....very complicated, but
she goes slow and does the job.
Hi and thanks for the information. Could you tell me the name of your doctor and can you tell me where your mesh had eroded.? Mine has eroded into urethra and i have been told that if I attempt to have it removed I will need urethral reconstruction.... It doesnt bear thinking about .
Thanks Christine
DEar Lana - Can you tell me how your lawsuit went in 2007 and why you chose to sue the manufacturers instead of the Doctor that inserted the mesh?
Thanks Christine
There is now a class action lawsuit filed in Canada against Johnson & Johnson for the Gynecare Surgical Mesh. Contact Stevensons LLP Barristers, Toronto Ontario, 416-599-7900 Ext. 226 Attention Margaret Lover, Litigation Law Clerk and Assistant for Lauren B. Black and Daniel McConville. email mlover@stevensonlaw.net
Good luck!
Hi, I would like to hear about your TVT problems, as I feel all alone. My gynecologist is sending me to a urogynecologist in Halifax, but I haven't got the appointment yet. I had one urologist say that everything is fine. Well if that is the case why do I have so much pain when I have sex or a pelvic exam? I am really scared that they are going to carve me up to get the tape out. After the TVT surgery I was in horrible pain for 3 months and now my incontinence is worse.
It really sucks to be in adult diapers. Is there any way out of this mess?
Hello,
I had my TVT surgery here in Sydney NS back in September, of course, it was botched. I was then "forgotten" by the doctor who performed the procedure, while he went on vacation. I knew the day after the original surgery that something was wrong and was dismissed. I couldn't sit, stand, I had more infections than i can count, i couldn't control my bladder. Intimacy with my husband was non-existent and hasn't been since September, which is frustrating to say the least.
I went to my family doctor and requested a referral to Halifax NS. I was lucky, I was in Halifax Oct 27 to see a urologist, unfortunately, it was too complicated for him to do anything to repair/remove. He referred me to another urologist in Halifax. I was back the first week of November. This 2nd urologist basically specializes in complications. I refer to him as "the Cleaner". He is wonderful! I'm not saying I'm perfect, yet :), but I'm so much better than I was.
The doctor in sydney that performed the procedure basically severed my urethra as he inserted (installed sounds so mechanical) the mesh too tight and it eroded into my urethra, thus severing it over the 6 week period post op. The doctor in Halifax removed the original sling, did urethral reconstruction and re-did the sling, without the mesh! The surgery was complicated and long, but my urologist was patient and more importantly, knew what he was doing. I'm not leaking if I cough or sneeze, i do have an issue as far as control, (if i need to urinate, everyone get out of my way, i'm coming through :)) My corrective surgery was done in December, i'm still healing, I think i'm one of the lucky ones. I've had infections, abscesses that had to be drained on my labia (ouch), a catheter for 3 weeks (over the christmas holidays, ho ho ho, i "lovingly" referred to the bags as Freddie - my leg bag and Freda - my purse), 12 staples across my lower abdomen.
I'm not out of the woods yet, and won't be for a long time. My urologist is confident i won't need anymore surgeries for a long time. I just hope he's not retired by then :)
I know this is a serious situation, but I think my sense of humour, and the support of my husband and family are helping me get through it. Please, if you have someone to talk to, talk to them. Don't be afraid or embarressed. It can be depressing as well, i was warned of that by my urologist in hali. And it has been depressing. I'll admit, I've been taking a mild anti-depressant med to help cope. this has been the worst 6 months of my life, but we're strong and we'll all get through it. All i wanted was to be able to play hopscotch with my daughter and jump on the trampoline with my son, I didn't think that was too much to ask, but if you don't have the right doctor, maybe it is. Ask questions and lots of questions if you or someone you love is contemplating having the TVT sling procedure done, don't take it lightly. it was pitched to me like an infomercial - 45 minute procedure, day surgery, 3-4 days you'll be better than ever.
But again, I've been lucky...the doctor on the other hand won't be once the college of physicians and surgeons get my complaint :)
Yes indeed there is a lay firm to help us here in Canada,I have filed,something has to be done,the tvt has ruined lives,,,
Hi Christine,
I had my tvt surgery in September 2009. I knew asap something was wrong. My mesh also eroded into my urethra to the point of severing my urethra. I was adament the mesh was not staying inside of me. I requested a referral to Halifax and found a wonderful urologist who was able to remove all of the mesh. I did have urethral reconstruction as well and a new sling in place. It wasn't easy. This was all done 1 1/2 weeks before christmas. I have 2 little ones that couldn't understand why mommy had to be away for 1 week and then to come home in the state that i was, wasn't pretty :( It was one the most difficult times of my life...I was lucky because the mesh was only in me for 2 1/2 - 3 months. my urologist was surprised i was having problems so soon after, but when he examined me, he then realized why it had to come out asap and why i was having so many problems so soon. The pain from the mesh was unbelievable, I couldn't sit, stand, or walk for any length of time, no control over my bladder...i thought i was going crazy (perhaps I am for having the procedure done in the first place...)
Take Care,
Lori
Kathy,
Have you heard anything on your referral to the uro in Halifax? I have the name of the best in the country who is in halifax. He did my mesh removal surgery in dec, along with urethral reconstruction and sling replacement. If it wasn't for this doctor, I don't know where i would be right now.
Take Care,
Lori
Read you story,really not fit what us as woman have to go through,Iam in nl and have been through hell since 07,no end in site,what is the name of your,dr? I really need someone else!anyone would be better than what I have for a dr,pain,pain ,pain,thats all I feel any more ;(.....snowflake,,,
Hi Snowflake,
So sorry to hear about another victim :(. I don't want to provide the doctor's name over the internet without his permission, please send me an email and I will be more than happy to send his name your way. He is an amazing doctor! my email is meshsurvivor@hotmail.com
Look forward to hearing from you.
Lori
Reading these comments, I am now very concerned. I too have a TVT, inserted in January 2009 with anterior vaginal repair, and at the 6 week checkup voiced my concerns to the consultant that I was still in a lot of pain, thought the tape had been put in "wonky" and was constantly wetting myself (which did not happen before the op!). In August 2009 I underwent a posterior repair for bowel prolapse and he was hoping that would "pull the bladder up" and sort things out. He did not do either of the ops but passed it over to a collegue on his team. Here I am some 16 months after the first op, still having to dash to the loo, wear tennaladies all the time, unable to work and thoroughly fed up. I am going next Tuesday for a urodynamics test, then day surgery on 14th April so he can look inside the bladder to see if it has been damaged. Had I known what I'd be going through I would never had had the TVT done! But looking back, the stress incontinence was getting unbearable so I acted on what I thought was good advice. I suppose it's good to know I'm not alone!
hi i had the tvt surgery in 2006 then the urologist sugested that i get a sling procedure bad idea i had pain every day and i went from having to use pads to not being able to urinate setting down i had to stand up and turn left and right to find the spot to urinate. my urologist keept acting like the pain and problems were all in my head after several surgeries the problem was not gone,so i went to the university of michigan hospital where i found a urologist that knew just where to touch i keep telling the doctors that i felt a ring like thing in my vaginal aria and that every time i set down and moved i would get severe cutting pain well this uroligist whent in and removed the tvt, it was where is shouldn't have been, the doctor removed a lot of tissue too. the cutting pain is gone but the vaginal pain and urinating problem is not. i have an appointment to see urogynolocy specialist next month i pray this doctor can take care of my vaginal pain.
good luck with your surgeries don't give up
bea
I am from WA state as well. Have you received any help??? I had a TVT in '05 and am miserable...
If anyone has any further information, please contact me. I am having surgery to remove the tape in June. The tape has slipped, was on too high, and the tape has grown INTO my ureathra. It has to be removed as it has bunched up also. they thought it was a bladder stone. I get many UTI's and was quite ill a short while ago with e-coli infection. Most interested in having something to tell my doctor, who says he has not seen or heard of anything like this. I have no great problem with incontinence, for some reason. The doctor wondered how I urinated at all!!
Thanks
Hi,
I am also in England and had the TVT operation about three years ago, since then l have had recurring soreness in my vagina with the outer lips also sore and swollen. I also have a lump on the wall of my vagina which l assume is something to do with the TVT op?
sex is painful and it seems as though there is an obstruction which l assume is the swelling/lump on my vaginal wall? I have been to various GP's an gyno's in and outside of my area and none seem able to help me, none have suggested that my problems are anything to do with the TVT op, it is my husband who thinks my problems started after the TVT op? I am still not sure if it is the TVT that is giving me the problems but having read other peoples letters on the subject l suspect it is. Having read your letter could you contact me on my email (meshmess@yahoo.co.uk) and give names of doctors that could help and any other useful info you may have. l tried the UK website you suggested but could not find it, does it exist? Thanks for any help you can give.
Jacky
Hi I'm from England and have been in constant pain since Feb2007 is there an action group or support group I can contact or join. I'm frightened and desperate.
Does anyone know if there is an active class action lawsuit in the USA? I had a TVT mesh implant in 2003 and 2 corrective surgeries. Ongoing infections and pain.
Lori,
My 1st surgery was May 25, 2005, my procedures were: abdominal sacral colopexy, retopubic urethropexy(burch procedure), paravaginal repair, cystoscopy, posterior repair. My 2nd surgery was Jun 30th, 2005, lower bowel slipped out of mesh. I have never felt right since that operation, I feel nauseated all the time, stomach is bloated and sore to touch. I have pain in my back, hips, groins. I have problems urinating and it smells strong when I do. My bowels dont seem to be working right now and I'm just sick, anyways. My husband and I are planning on moving to N.S. as soon as our house sells. Would it be possible to get the name of the Dr. in Halifax that took out your mesh. Im trying to feel confident about this move, knowing there is a Dr. there that I can get to take out my mesh.
Thank you so much, I totaly appreciate it. My email address is-ljryder@rock.com. I presently live in Alberta. Will be waiting patiently for your reply. Thanks!!!!!!!!!!!!!Lois
is this a personal law suit or can others join? I guess i need to find out which company made the TVT materials used in me. Please let me know what to do.
Hi Annon,
I am also from U.K. and I am having problems even contacting other people on this site, or am I doing something wrong. I had a TVT in 2004, I am in big trouble now as I can't even sit down, I think mine has erouded into my vagina, I am getting no help here in the U.K. How about you? are you also looking for a decent honest surgeon here. I can tell you who Ive been to up to now to save you money and also who did this to me, if you reply.
Best wishes.
At age 39 a mid-urethral polypropylene sling placed in 8/2007 during cystocele repair. I was unable to void from the get-go. The ob/gyn referred me to a urologist who has told me my abd, anal/rectal pain, pelvic pain and throbbing pubic bone was not related to the mesh. I have had to self cath to void multiple times a day. She finally thought the mesh needs a little snip. I went to another doctor as I felt frustrated that she found no relation between my other pain and the mesh. This doctor says I need the mesh out, I agree. Now when I am able to pass stool clumps of thready string material comes out. I see a GI doc in two days. I'm terrified I will need a bowel resection. Does anyone know what the mesh looks like when it erodes through the organs or has anyone experienced this?
Terrified in SLC
Christine I was wondering how you are getting on and wanted to know if you had a sling inserted TVT or mesh to support prolapse. I seem to remember you had yours done by professor Cardozo like me. I am scheduled to have mine removed by suzie Elneal on 16th november and she seems positive she can remove all except end. Not sure now whether I have sling or mesh. Can you help
Anne
hi i am from england uk i am having mine removed after i had a bit taken out but my incontinence returnd so i had another one put in .it was worse then the first one .had it shaved .but now am going in to hav it removed .i have been told that if my simtoms come back i can be considerd for a sling made from my muscle sounds better than the mesh .just dont no wat to expect wen it gets removed can any one tell me pleas thank you
Hi, Ann
How long have you had your tape in? you say you are having it removed. I have had mine in since 2004. I have seen three seperate consultants in the last three months. One of them was the Gynecolegist who I was under at the time, He told me it could'nt be removed after all this time and didnt even examine me, this was privately, he also said how can it affect your vagina? Then next person has just looked for other things and has'nt even mentioned the tape, he did a CT scan which showed a cyst on the overies, so next a CA125 blood test also negative, no mention of the tape. The next person who is in London which involved a painful long train journey told me I have a bladder prolapse into my vaginal wall, every other surgeon I have seen has denied this except one. Sadly this last surgeon has sent me a bill for a clamida test for £56 in spite of the fact I havent been able to have sex for three years, I had also told him I had every test done at a V.D. clinic in september again, just in the hope they had missed something previously. I am in despair as each time I go to see someone new here about the TVT tape, they just look for other things. I was alright before the tape was put in and now I cant sit down or drive, or do my garden bend down, swollen bottom and stabbing pains in my vagina and bottom, constant discharge and pains in my legs and intense burning. This has been going on since last May with no relief the only thing that helps a little are piritan allergy tablets. You say you are seeing someone who is removing your tape can you tell me who? so I can go too. I dont know if you can send a private email on here, but if you know how I will give you my phone number and email address. I am going to the U.S.A. next although I have private medical insurance here, up to now it has been useless, the surgeon in U.S.A is pretty sure its the tape causing these problems and so am I. After all I managed to live a fairly active life and had two children before the TVT and I didnt have a bladder prolapse either.
I also have pain along with lots of other health issues that developed after my tvt sling procedure. Now depressed and in constant pain do not know who to go to for help. I would like to have it removed but don't know what the outcome issues would be. Also who would be a doctor in hamilton, toronto area that has experience with this?
Could you please give me the name of your Dr. you mentioned from the U of Michigan. My grandmother's doctors are saying they can't remove all of her mesh and she is in constant pain. She desperately needs to find a doctor who will at least try.
Thanks!
Katie
katiejones981@gmail.com
Hi Jaque,
I want my TOT removed as I am in a lot of pain. I live in the UK and would appreciate it if you could send me the names of surgeons you have visited to date and if you have found one to remove it.
Thanks very much!
I too have a nightmare to share. I had my TVT mesh operation in 2006, soon after I began having bladder infections - Month after Month-, pelvic pain and intense pain during sexual intercourse. In 2010 I had an operation to remove mesh. Specialist informed me that mesh had attached to bladder and she anticipated that removing would cause further complications. Currently, I'm in a worse situation than the beginning - leakage so bad that I constantly have to were protection.
I would like to know how I can join this class action suit.
Hi. I had a TVT in May 2011 in Halifax and shortly after started having suprapubic pain.
At the six week mark the urogyne gave me an injection of solumedrol and lidocaine but that only increased the pain to the point I didn't want to move. It has settled but I still have pain after walking about the house for 10 - 15 mins.
I would love to speak with one of the ladies who went to Halifax and find out who "the cleaner" was because if this doesn't get resovled after my next visit, I'd like to got to someone else who could help me live pain free.
Thanks (Another)
Kathy
Had a TVT just 2 weeks ago already had infection, was not told of all these poss problems I'm reading about on this website, I was looking the procedure up because I have this nagging feeling that all is not well, I'm not a stranger to surgery, but I get the feeling that things just feel too tight, I'm struggling to urinate! and to open my bowels is just torture! I feel like I want the toilet all the time, but when I go nothing is there! the vagina seems to be under pressure! anyone out there know if this is normal at this stage
Karen newman
Cheshire Uk
Age 52
Hi,
had my TVT in april, was fine until a couple of months ago, groin pain and now erosion on the left side of my vagina wall, is there any happy ever afters on here, i feel very angry that even though I work in theatres, I didn't get the possible pitfalls of this dangerous procedure!!
Hi Christine - I had a TVT tape inserted approximately 2 years ago by Prof. Cardozo I am now told by her National Health unit that I have chronic bladder lining infection (after bouts of cystitus and a cystectomy) and should take a 3 months course of Norfloxacin. As I like to play sports I am wary of taking this medication as it can cause rupture of tendons - have you taken it? Also of course, I hate the thought of taking anti-biotics for a prolonged period. Can you advise what surgeon you subsequently saw in UK rather than Cardozo?
I had no problems of this sort before I had the TVT tape inserted and bitterly regret it
Kind regards - Julie
Hi i am having my TVT procedure in Nov 30 2011by dr. buckly from north york general hospital, after reading all the comments i am thinking twice about having this procedure done, has anyone had this procedure recently, as I am looking and most of the women have had it done 2005-2009......Is there still a law suit in toronto.....are there still problems? can someone help?
thanks
Rachel
I had a TVT procedure done in September 2010 and have had groin pain, left leg pain down to my foot and pain for both my husband and I during sex, which we've given up on for a few months now :o( It turns out that the tape has eroded into my urethra and I am to go for surgery to 'loosen' the tape and have my urethra 'reconstructed'. Why can't they use our own muscle tissue to do this, rather than this invasive, foreign object? Not a happy camper.
hi i had my tvt done at the end of july 2011 worst thing ever done pain is awful on a lot of painkillers i allso self cathertrise bladder sensation lost since op . and cant wee i live by alarms to remined me to go .waiting to have it removed .there is also a great web sit called tvt mum take a look
take care elaine
I understand you had the mesh removed after a few months, had reconstruction on your urethera, and a new sling put in. I had a tvt done a few days ago, and I am quite frightened by what I am reading about using mesh. What did the doctor do to find out that your mesh was erroding? How was your urethera repaired, and what did they use when you had a new sling put in? I am very afraid that my mesh will also errode, and what I have heard is that if it is inside you for too long (6 months or so), then it is nearly impossible to get it out. I am wondering if I should have it removed immediately before any damage is done, and have a new sling put in. I just dont know what else they use if they dont use mesh. My operation went well, and I feel fine now physically, but maybe am starting to panic a little because of everything I am reading. I have read so many sad stories, and it is really disheartening.
I understand you had the mesh removed after a few months, had reconstruction on your urethera, and a new sling put in. I had a tvt done a few days ago, and I am quite frightened by what I am reading about using mesh. What did the doctor do to find out that your mesh was erroding? How was your urethera repaired, and what did they use when you had a new sling put in? I am very afraid that my mesh will also errode, and what I have heard is that if it is inside you for too long (6 months or so), then it is nearly impossible to get it out. I am wondering if I should have it removed immediately before any damage is done, and have a new sling put in. I just dont know what else they use if they dont use mesh. My operation went well, and I feel fine now physically, but maybe am starting to panic a little because of everything I am reading. I have read so many sad stories, and it is really disheartening.
I understand you had the mesh removed after a few months, had reconstruction on your urethera, and a new sling put in. I had a tvt done a few days ago, and I am quite frightened by what I am reading about using mesh. What did the doctor do to find out that your mesh was erroding? How was your urethera repaired, and what did they use when you had a new sling put in? I am very afraid that my mesh will also errode, and what I have heard is that if it is inside you for too long (6 months or so), then it is nearly impossible to get it out. I am wondering if I should have it removed immediately before any damage is done, and have a new sling put in. I just dont know what else they use if they dont use mesh. My operation went well, and I feel fine now physically, but maybe am starting to panic a little because of everything I am reading. I have read so many sad stories, and it is really disheartening.
I live in Montana but am originally from Michigan. Can you tell me the Doctor's Name at U of M? Thank you in advance and so happy you have found relief from this nightmare.
I live in Montana but am originally from Michigan. Can you tell me the Doctor's Name at U of M? Thank you in advance and so happy you have found relief from this nightmare.
Dr. Fenner at U of M.
I would appreciate any information on qualified doctors for removal of TVT please contact uklady100@gmail.com
DONT Do IT, please.
if your from NS and had this TVT please email me gailchaisson@eastlink.cathanks