Posts Tagged ‘vaginal mesh doctor’

FDA Approves Over The Counter Medication For Overactive Bladder, Vaginal Mesh Helpline Reports

Written by Vaginal Mesh Helpline on . Posted in Medical News and Your Vaginal Mesh, Vaginal Mesh News

At the Vaginalmeshhelpline.com we are always looking for new information to help our readers injured by the vaginal mesh. Many women have had the mesh implanted for urinary  incontinence. We just found this online and are sharing it. The FDA has  approved  Oxytrol for women.  This is an over-the-counter Oxytrol treatment for overactive Bladder. Of course we suggest discussing this with your doctor.

January, 25, 2013 — The U.S. Food and Drug Administration today approved Oxytrol for Women, the first over-the-counter treatment for overactive bladder in women ages 18 years and older.

Oxytrol will remain available for men with overactive bladder by prescription only.

Overactive bladder is a condition in which the bladder squeezes too often or squeezes without warning. Symptoms include leaking urine (urinary incontinence), feeling the sudden and urgent need to urinate, and frequent urination. Overactive bladder affects an estimated 33 million Americans, the majority of whom are older women.

Oxytrol for Women contains oxybutynin, a medicine that helps relax the bladder muscle. Oxybutynin belongs to a class of drugs known as anticholinergics. It is the first drug in this class to be made available over-the-counter for treatment of overactive bladder.

Oxytrol for Women is a patch that is applied to the skin every four days. The patch delivers 3.9 milligrams of oxybutynin per day.

 

“Studies demonstrate that over-the-counter Oxytrol for Women is a safe and effective treatment for overactive bladder,” said Shaw Chen, M.D., Ph.D., deputy director of the Office of Drug Evaluation IV in the FDA’s Center for Drug Evaluation and Research. “Women should make sure to follow the Drug Facts label and consult their doctor if their condition does not improve.”

 

Oxytrol for Women’s safety and effectiveness for over-the-counter use were established in more than 5,000 subjects participating in nine studies. Overall, results from these studies showed that consumers can understand the information on the label, properly select whether the product is right for them, and use the drug appropriately.

Side effects reported during clinical studies were mild and included skin irritation where the patch was applied, dry mouth and constipation. A leaflet with tips to help manage overactive bladder will be provided with the product.

Oxytrol for Women is marketed by Merck, based in Whitehouse Station, N.J.

Source: FDA

Posted: January 2013

FDA Approves Botox For Urinary Incontinence, News For Vaginal Mesh Complications

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News, Vaginal Mesh Stories, Vaginal Mesh lawyers

The Vaginal Mesh Helpline is keeping you up to date on all news related to vaginal mesh lawsuits, Incontinence and vaginal mesh complications and trial updates. This new FDA approval of Botox for urinary incontinence is very interesting. Many mesh victims are seeing incontinence return with the vaginal mesh failing and falling apart.  This news on Botox may be of interest to our vaginal mesh readers.

January 18, 2013 — The U.S. Food and Drug Administration today expanded the approved use of Botox (onabotulinumtoxinA) to treat adults with overactive bladder who cannot use or do not adequately respond to a class of medications known as anticholinergics.

Overactive bladder is a condition in which the bladder squeezes too often or squeezes without warning. Symptoms include leaking urine (urinary incontinence), feeling the sudden and urgent need to urinate, and frequent urination.

When Botox is injected into the bladder muscle, it causes the bladder to relax, increasing the bladder’s storage capacity and reducing episodes of urinary incontinence. Injecting the bladder with Botox is performed using cystoscopy, a procedure that allows a doctor to visualize the interior of the bladder while Botox is being injected.

“Clinical studies have demonstrated Botox’s ability to significantly reduce the frequency of urinary incontinence,” said Hylton V. Joffe, M.D., director of the Division of Reproductive and Urologic Products in FDA’s Center for Drug Evaluation and Research. “Today’s approval provides an important additional treatment option for patients with overactive bladder, a condition that affects an estimated 33 million men and women in the United States.”

Botox’s safety and effectiveness for this new indication were established in two clinical trials of 1,105 patients with symptoms of overactive bladder. Patients were randomly assigned to receive injections of 100 units of Botox (20 injections of 5 units each) or placebo.

Results after 12 weeks showed that patients treated with Botox experienced urinary incontinence an average of 1.6 to 1.9 times less per day than patients treated with placebo. Botox-treated patients also needed to urinate on average 1.0 to 1.7 times less per day and expelled an average of about 30 milliliters more urine than those treated with placebo.

Treatment with Botox can be repeated when the benefits from the previous treatment have decreased, but there should be at least 12 weeks between treatments.

Side Effects.

Keep in mind that this could be beneficial or prove to have complications down the road.

Common side effects reported during clinical trials included urinary tract infections, painful urination, and incomplete emptying of the bladder (urinary retention). Patients who develop urinary retention may need to use a catheter until the urinary retention resolves. Patients being treated for overactive bladder with Botox should not have a urinary tract infection and should take antibiotics before, during, and for a few days after Botox treatment to lower the chance of developing an infection from the procedure.

Botox is manufactured by Allergan Inc. based in Irvine, Calif.

Vaginal Mesh Trials Have Begun. Vaginal Mesh Lawyers Ready

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh Lawsuits.

The Vaginal Mesh Helpline is keeping you updated on  new news regarding the Vaginal Mesh lawsuits. The vaginal mesh trials have begun. We are waiting, watching and hoping for justice for the thousands of women injured by all these Prolene mesh implants. The stories of pain and suffering we hear on a daily basis are horrific.

We must reach out to all women with a vaginal mesh to push you to file your vaginal mesh lawsuit now.

Have You Been Rejected By A Lawyer Due To Statute Of Limitation Issues?

Call the Vaginal Mesh Helpline. We may be able to get a lawyer for you. Yes, there are statutes of limitations for your state but, there are aspects of the law that may bypass these.  We do not want anyone to be left out. If you have been told by a lawyer that you do not meet “his” criteria do not give up. Call us and get another opinion. There are so many lawyers after mesh victims and as the trials proceed new allegations, criteria and injuries will start to be revealed. What was no 6 months ago maybe yes now. Do not give up hope and call us today.

You Must File Your Vaginal Mesh Lawsuit Now.

The vaginal mesh lawsuits are being filed against five separate manufacturers. They are Johnson & Johnson’s Ethicon division, Coloplast, American Medical Systems, C.R. Bard, and Boston Scientific.

Vaginal Mesh Lawsuit Settlements

The first vaginal mesh trial against Johnson & Johnson  has begun. In March, the nation’s first trial involving an Ethicon mesh lawsuit concluded in the New Jersey litigation, with the jury awarding more than $11 million to the victim, including $7.76 million in punitive damages. (Gross v. Gynecare Inc., Atl-L-6966-10, Superior Court of Atlantic County, New Jersey).

File Your Vaginal Mesh Lawsuit

If you have not filed your vaginal mesh lawsuit or have been rejected by a law firm based on His “criteria” or statute of limitations call the Vaginal Mesh Helpline today, We may be able to get you a vaginal mesh lawyer and a vaginal mesh doctor.

Vaginal Mesh News Update

A Joint Status Conference is scheduled for May 23rd regarding the thousands of transvaginal mesh lawsuits pending in U.S. District Court for the Southern District of West Virginia. The lawsuits have been formulated into five MDLs, which are entitled: In Re: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2325; In Re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation, MDL No. 2326; In Re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2187; and In Re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2327.

Vaginal Mesh Bellwether Trials Set For 2013, File Your Vaginal Mesh Lawsuit

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh Information, Vaginal mesh Lawsuits

Thousands of women with horrific and life changing side effects from vaginal mesh implants nationwide will begin to see justice in 2013. The bellwether trials are set to begin and you must get justice. If you have not retained a lawyer for your mesh lawsuit you must di it right away. You cannot wait. Women nationwide must stand as a group and every single one must file the lawsuit to get justice for all women. It is not about the money but, the message. Justice must be sought.

Bellwether trials involving vaginal mesh lawsuits will be in the news for 2013 and may well be the largest lawsuit of 2013.

Bellwether trials are set to begin in 2013 for the vaginal mesh which has caused severe injury to 1000's of women. Our vaginal mesh lawyers are  actively filing lawsuits in the mesh litigation and looks forward to the steps toward justice for women across the USA. Wome of all ages have been harmed. The youngest we have heard from is 33 and the oldest 87. These are daughters, wives, sisters, mothers and grandmas.

These bellwether trials will help  determine  how juries will  rule in similar actions.

Vaginal Mesh Bellwether Trials
These trials will take place in four multidistrict litigations underway in U.S. District Court, Southern District of West Virginia.  C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2187”) will begin on February 5, 2013.

American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2325”) will begin on December 3, 2013. Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2327”) and Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2326).

Important vaginal Mesh Alert

The first trial for Ethicon vaginal mesh lawsuits will begin  in January 2013 in New Jersey Superior Court, Atlantic County division,

Judge Joseph R. Goodwin of the United States District Court in West Virginia presides over not one multidistrict litigation, but four, all involving transvaginal mesh lawsuits.

  • Johnson & Johnson’s Ethicon division,
  • Coloplast,
  • American Medical Systems,
  • C.R. Bard,
  • Boston Scientific.

Judge Goodwin ordered C.R. Bard’s bellwether trial date to be February 5th, 2013. C.R. Bard specifically faces an MDL comprising 600 lawsuits. Avaulta Mesh’s MDL bellwether trials are scheduled for the same month.

Judge Carol E. Higbee, who presides over a sixth transvaginal mesh multidistrict lawsuit in New Jersey, set  trials to begin in November.

If you have not filed your vaginal mesh lawsuit you must do it immediately. Once the trials begin knew knowledge and facts will begin to be revealed and more injuries will mean many of the cases that may have been rejected will be viable. If a lawyer has rejected your mesh lawsuit due to some sort of decided pre-trial criteria you may still have a chance once the proceedings develope and injuries become apparent. We suggest you contact us right away if you have been rejected by a law firm to get a second opinion.

 

 

Vaginal Mesh Lawsuit Information, National Campaign Launched

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

The Vaginal Mesh Helpline has Launched a vaginal mesh lawsuit outreach campaign to keep women updated and informed on the progression of the transvaginal mesh lawsuits. There are still wome with complications from the mesh that do not know about the vaginal mesh lawsuits. The lawsuits are proceeding as a part of a consolidated multi district litigation. Most of the mesh lawsuits are being heard in West Virginia. The  vaginal mesh federal and   state lawsuits are growing  as 1000′s of filings  against the vaginal mesh manufacturers proceed and the number continues to grow as more and more women stand up for themselves against the manufacturers  who caused them so much pain and suffering. Federal vaginal mesh lawsuits have been consolidated into four multidistrict litigations (MDL) based on the manufacturer they’re filed against. Vaginal mesh MDL pretrial proceedings are moving in full force with Chief Judge Joseph R. Goodwin, United States District Court, WV, has set a trial date. As of October 2012, the number of suits filed against each manufacturer continues to increase rapidly:

  •        AMS- American Medical Systems
  •        Johnson & Johnson’s Ethicon division, Gynecare
  •        Boston Scientific
  •        C. R. Bard Avaulta
  •        Coloplast recently added

Now would be the time to retain a vaginal mesh lawyer.

We do not want anyone to be left out. Women have suffered from these mesh implants and the Vaginal mesh lawsuits are one way to let manufacturers know you demand justice. Both you and your spouse have suffered injuries.  The  marital bond has suffered due to mesh erosion and many men have suffered injury as well during sexual intercourse. By the time all the facts come out it will be shown that 100′s of thousands have been harmed.

Manufacturer Updates

Boston Scientific transvaginal mesh lawsuits, as well as  several other transvaginal mesh litigations are currently pending in the Southern District of West Virginia,

Speak to a female medical social worker and get help guidance and support.

The Vaginal Mesh  Helpline is here ready to help you and your spouse, mother, sister, grandmother and all injured by these manufacturers who put profits over harm.

Vaginal Mesh Lawsuit Alert, The Vaginal Mesh Proceedings Have Begun

Written by Vaginal Mesh Helpline on . Posted in Vagiinal Mesh Class Action, Vaginal Mesh News

Do You Have a Vaginal Mesh Lawsuit? Do You Need a Mesh Lawyer?

The vaginal mesh proceedings have begun as a part of the two primary MDL's in West Virginia and New Jersey. Vaginal mesh lead counsels are gearing up and dates have been set.

The  vaginal mesh federal and   state lawsuits are growing  as 1000's of filings  against the vaginal mesh manufacturers proceed and the number continues to grow as more and more women stand up for themselves against the manufacturers  who caused them so much pain and suffering. Federal vaginal mesh lawsuits have been consolidated into four multidistrict litigations (MDL) based on the manufacturer they’re filed against. Vaginal mesh MDL pretrial proceedings are moving in full force with Chief Judge Joseph R. Goodwin, United States District Court, WV, has set a trial date. As of October 2012, the number of suits filed against each manufacturer continues to increase rapidly:

  •     1,697 cases filed against AMS
  •     1,725 cases filed against Johnson & Johnson’s Ethicon division
  •     1,114 cases filed against Boston Scientific
  •     1,256 cases filed against C. R. Bard

July 2012, the first case presented to a jury resulted in a $5.5 million damage award in California state court, for a woman who experienced complications where her Bard Avaulta mesh sliced through her colon, causing her to undergo at least eight additional surgeries. Additional lawsuits are scheduled for trial in federal court beginning in February 2013.

The Vaginal Helpline is in full gear to locate any woman with a Prolene mesh filed after 2002 in states where the Statute has not run out.
 

How To Choose Your Vaginal Mesh Lawyer, Vaginal Mesh trials Have Begun

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh lawsuit Lawyer, Vaginal mesh Lawsuits, Vaginal Mesh News

The vaginal mesh lawsuit has moved into the action stage. If you have been injured by a vaginal mesh the time to act is now. The statute of limitations for some state have run out. As the trials poceed and the facts come out it will be more important to have your lawsuit filed and with a law firm that understands the entire MDL process. Differemt criteria may start to develope and if you are not with the correct firm you may find a case rejection letter in your mailbox. Not all firms are using the same critieria. The stiffer the criteria becomes the more important the  firm you choose is. Some have much broader criteria then others. Some law firms want it clean and easy. They do not want more then one mesh implant, only one mesh with one manufacturer, no additonal surgeries or complications, no pressing merdical conditions and a variety of intricate criteria based on the way they see the case and the financial implications for the settlement. Other law firms are using a much wider criteria and still others are taking a case in a state where the statute is over to the state of the manufacturer.

Another important issue is how are your calls and concerns responded to. If your first and only contact is with a paralegal or "screener" that person is your contact person. That is the person that may be your only contact. They must understand the mesh and the suffering you have gone thru. If they can help you find a doctor I would give them an extra plus in the yes category. If they take your case strictly based on prior medical records wothout a doctor intervening on your behalf regarding your current situation it may be harder to prove your case. The best situation for you is a doctor who says it is the mesh and you need a revision of better yet, mesh removal. Having a good doctor is not only good for your case but, a medical necessity.

As the lawsuit proceeds more questions regarding your rights will develope and you will need answers. Interview the first line person.

That may be the most important person. Ask: Who will be my contact person? Has this lawyer ever done any mass tort cases? Has this lawyer been involved in the litigation of cases involving dangerous drugs and devices that harm women? What cases? To what degree?

Will my case stay with you? If it will not under what circumstances will it be referred to another firm? Remember, the MDL lawsuits will require your vaginal mesh lawsuit litigation taken to trial by one of the lead counsels. But, your lawyer can file the case and be the end of the line for the filing process. Do you need a lead counsel? Not everyone can be alead counsel. Some of the best lead counsels have inattentive, insensitive screening staff who really do not understand the mesh litigation at all. Some insensitive staff may  become very strong with you if you even raise the issue of switching lawyers.

If I do not feel my lawyer's staff is senstive to my concerns can I switch?

Yes, you can and there is no financial loss to you at all. If any law firm tells you otherwise they are just wrong and using tactics to keep you with them. That alone should be a sign to reconsider.

The most important thing is that you feel comfortable with the law firm, that they have mass tprt and MDL experience and do know the difference between an aut accident and dangerous drug and device fenseral case. They are not the same. The local lawyer you may pick for the highway accident may not be right for a mass tort. They may have no experience in mass torts and have no intention of wrking your case. They are looking for an experienced mass tort lawyer to send your case to. It may be the next guy that advertises on T,V who they do not even know.

In mass tort cases like the vaginal mesh lawsuit, local may not be the best move at all.  This is an MDL and is only being consolidated in certain states in front of a certain judge. It is not being heard in every state. It may never be litigated in your state. Local is just not all that important.

Fike you lawsuit right away and use care in selecting your vaginal mesh lawyer.

 

   
 

Botox New Hope For Urinary Incontinence, Vaginal Mesh Helpline Reports

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

The Vaginal Mesh Helpline will keep you updated on all the most recent news. Our vaginal mesh network of lawyers is filing mesh lawsuits on behalf of women with a failed Prolene mesh. The mesh was used for urinary incontinence in 100's of women.

Published on Saturday 15 September 2012 21:02

Botox injections may help women with urinary incontinence, The Daily Telegraph has today reported. The newspaper said that injecting the muscle-freezing toxin into the wall of the bladder can have a long-lasting impact on overactive bladder syndrome, a major cause of incontinence.

The newspaper’s story is based on a UK medical trial that investigated whether the paralysing properties of botox were effective at reducing the symptoms such as frequently using the toilet, feeling an urgent need to urinate, and leakage in patients with overactive bladder syndrome.

The trial featured 240 women who had not responded to medical treatments for overactive balder syndrome. The researchers found that women who received the botox injection experienced these symptoms significantly less frequently than women who received a dummy injection of saltwater. However, women given botox were more likely to get urinary tract infections.

The results of the study indicate that botox may be effective in treating a common and upsetting health condition. However, if it does get adopted into use in this way there are several other treatment options (including lifestyle measures, bladder training exercises and medication that would be considered first. Botox may be considered as an option only if these treatments fail, and the benefits would have to be considered in relation to its potential harms.

 

Where did the story come from?

The study was carried out by researchers from the University of Leicester and was funded by the Moulton Charitable Trust and the women’s health charity Wellbeing of Women.

The study was published in the peer-reviewed medical journal European Urology.

The Telegraph covered this study appropriately, covering the study size and design, as well as the treatment benefits and harms.

 

What kind of research was this?

While it is hard to gauge the true scale of the problem, research suggests that around 13% of women in the UK may have some form of urinary incontinence. Although many conditions and factors can cause urinary incontinence, one major cause is overactive bladder syndrome. The condition is marked by uncontrolled contraction of the bladder that results in an urgent need to pass urine. While this can lead women to need the toilet frequently, some also experience a form of leakage called urge incontinence.

An overactive bladder can be a cause of urge incontinence, which is when urine leaks at the same time or just after you feel an intense urge to pass urine. Urge incontinence differs from stress incontinence, where the pelvic floor muscles are too weak to prevent urination. This causes urine to leak when your bladder is placed under pressure from actions such as coughing or laughing.

This was a placebo-controlled randomised controlled trial that examined the effectiveness and safety of using botulinum toxin (botox) as a treatment for overactive bladder syndrome. A randomised controlled trial is the best way to measure the effectiveness of a treatment, as the randomisation process helps to ensure that any patient characteristics that may influence the outcome have an equal chance of appearing in either treatment group. This allows researchers to be confident that any observed effect is due to the treatment under study.

 

What did the research involve?

The researchers enrolled 240 women with bladder muscle overactivity, or overactive bladder syndrome, that had not responded to previous treatment. The women were randomly allocated injections of either Botulinum toxin A (botox) or placebo (saltwater) into the wall of the bladder. Women with another common type of incontinence, stress incontinence, were not included in the study.

The participants kept a diary over three days, recording the number of times they:

    emptied their bladder
    felt an urgent need to empty their bladder
    experienced an unintentional passing of urine (or leakage)

The women also completed a questionnaire that assessed their quality of life, as overactive bladder syndrome often has a significant negative impact on patient quality of life.

The researchers conducted follow-up sessions with the women on average at six weeks, three months and six months after treatment. They assessed differences in the frequency of the above three symptoms between the two treatment groups. They also compared quality of life scores, treatment complications and time until troubling symptoms returned between the two groups.

The researchers used appropriate statistical methods to assess differences in frequency of symptoms between the two groups.

What were the basic results?

There were 122 women allocated to the botox treatment group and 118 women allocated to the placebo group.

The researchers compared the outcomes in the botox and placebo groups at the six-month follow-up. They found that in any 24-hour period women in the botox group:

    emptied their bladders less often: 8.33 times versus 9.67 times, a difference of 1.34 (95% confidence interval [CI] 1.00 to 2.33, p=0.0001)
    experienced fewer leakage episodes: 1.67 versus 6.00, a difference of 4.33 episodes (95% CI 3.33 to 5.67, p<0.0001)
    experienced fewer episodes of urgency to urinate: 3.83 versus 6.33, a difference of 2.50 episodes (95% CI 1.33 to 3.33, p<0.0001)

Almost a one-third of women in the botox group (31.3%) developed bladder control (or continence) following their treatment, compared to 12.0% in the placebo group (Odds Ratio [OR] 3.12, 95% CI 1.49 to 6.52, p=0.002).

However, urinary tract infection was reported at least once during six months by a one-third of women in the botox treatment group, compared to 10% in the placebo group (OR 3.68, 95% CI 1.72 to 8.25, p=0.0003).

Those given botox also reported greater difficulty emptying their bladders, which required self-catheterisation to remove their urine: 16% of the botox group compared to 4% of the placebo group (OR 4.87, 95% CI 1.52 to 20.33, p=0.003).

 

How did the researchers interpret the results?

The researchers concluded that injections of botulinum toxin A into the bladder wall is an effective and safe treatment for overactive bladder syndrome in women who have not responded to previous treatment.

 

Conclusion

Urinary incontinence can be a distressing and problematic condition, and although we cannot be sure of the number of people affected, research suggests it is surprisingly common.

While there is a range of potential treatments and ways to manage urinary incontinence (including medication, bladder training, lifestyle changes and surgery) not all people respond to them, and they can have problems. This randomised controlled trial provided good evidence that botox injections may be a useful treatment option for women with incontinence due to overactive bladder syndrome that has proven difficult to treat with other methods.

The researchers say that the relief of symptoms reported by the participants was considerably better than those who used oral anticholinergic drugs. These drugs act on the nerve supply to the bladder and are the standard medical treatment used for this condition. They add that other randomised controlled trials have reported similar effects.

The researchers say that since they designed their trial, other studies have published results that support using a lower recommended dose of botox for this type of treatment. Therefore, it is unclear if the same results would be found at this reduced dose. They also say that their study recruited participants with severe cases of overactive bladder syndrome, and that it is unclear if the treatment would be as effective in less severe cases.

It is important to note that the study participants did not have stress incontinence, which is a common cause of urinary incontinence. Therefore, the results of this study cannot be generalised to all women with symptoms of overactive bladder or incontinence, but can only be applied to those with diagnosed overactive bladder syndrome (or detrusor overactivity).

Botox is not routinely used by the NHS in this way, but if it were then it would probably be considered as an option only among women who have required specialist referral for their condition. This would be given after they had tried other treatment options first, which may include lifestyle measures and bladder training exercises in addition to oral medications. If these treatments fail, the benefits of botox would have to be considered in relation to its potential harms.

Vaginal Mesh Lawsuit Lawyers Florida, Helping Florida Women Get Justice

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh Information

Vaginal mesh lawsuit lawyers of Florida including: Belle Glade, Boca Raton, Bonita Springs, Boynton Beach, Bradenton, Cape Coral,  Clearwater, Coral Gables, Coral Springs,  Daytona Beach, Deerfield Beach, DeLand, Delray Beach ,Fort Lauderdale, Fort Myers, Fort Pierce, Fort Walton Beach, Gainesville, Haines City, Hallandale Beach, Hialeah, Hollywood, Homestead, Immokalee, Jacksonville,  Key West, Kissimmee, Lakeland,  Largo, Melbourne, Merritt Island, Miami, Miami Beach,  Naples,  New Smyrna Beach, Ocala, Orlando, Ormond Beach, Palm Bay, Panama City, Pensacola,  Plant City, Pompano Beach, Port Charlotte, Port Saint Lucie, St Cloud, St. Petersburg, Sarasota, Spring Hill, Starke, Tallahassee, Tampa, Tarpon Springs, Titusville, Venice, Vero Beach, West Palm Beach, Pensacola, Winter Haven, and Winter Park are filing lawsuits on behalf of Florida women suffering from the various Prolene synthetic mesh devices.

Hundreds of  Florida women have been implanted with various vaginal mesh devices. These include mesh for uterine prolapse, bladder prolapse, bowel prolapse and urinary incontinence. We have special concerns for our seniors.  Calls coming in from children and grandchildren concerned for their loved ones who are suffering and withdrawing.  They are alone and cannot actively help themselves. We have heard from children with mom's in their eighties with a mesh and we wonder what doctor would put such a product in a woman of this age.

The mesh can be life threatening for our Florida senior women. Infection and bladder or bowel perforation can lead to very severe medical complications. Infection in a senior population can result in the body becoming septic which can be fatal. Our senior woman with these mesh devices are suffering and must have justice. Naby of them have given up and cannot get the correct medical care. We are here to help.

If you have a grndmother, mother, or wife with a mesh who is suffering you must reach out an help. Call the Vaginal Mesh Helpline and we will help you locate a doctor. many seniors come from an era where sueing is unheard of. It is up to you to reach out on theor behalf and encourage them. All wome of all ages must come forward to stand up against these manufacturers.

We are here to help. Call the Vaginal  Mesh Helpline for help with complications from these vaginal mesh and baldder sling implants.

C.R. Bard's products include:

  •       Pelvitex
  •       Pelvisoft
  •       Pelvilace or Pelvicol
  •       Utrtex
  •       Uretex TO
  •       Uretex TOO2
  •       Uretex TOO3

Gynecare/Ethicon/Johnson & Johnson products include:

  •    Prosima
  •    TVT Exact
  •    TVT Abbrevo
  •    TVT Retropubic System
  •    TVT
  •    TVT Obturator
  •    TVT Secur
  •    Gynemesh PS
  •    Prolift
  •    Prolift+M

AMS's products include:

        AMS MiniArc Precise Single-Incision Sling
        AMS MiniArc Single Incision Sling
        AMS Monarc Subfascial Hammock
        AMS In-Fast Ultra Transvaginal Sling
        AMS BioArc
        AMS Sparc Self-Fixating Sling System
        AMS Elevate
        AMS Perigree
        AMS Apogee

Boston Scientific products include:

        Boston Scientific Arise
        Boston Scientific Pinnacle
        Boston Scientific Advantage Fit
        Boston Scientific Lynx
        Boston Scientific Obtryx
        Boston Scientific Prefyx PPS
        Boston Scientific Solyx

Tyco Covidian (which manufacturers the Tyco Covidian Duo and Mentor ObTape)

The mesh lawyers are filing lawsuits for Florida. Florida Statue of limitations is still within a timely period to file. However, do not wait as

Tennessee, Kentucky and Louisiana women are past the statue to file already. This is not sometyhing tp put off till later.

 

 

Vaginal Mesh Launches Nationwide Outreach, Vaginal Mesh Lawyers Applaud

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh Helpline reports that  a women has finally had enough and protests the vaginal mesh. The Vaginal Mesh Helpline and vaginal mesh lawyers applaud. Perhaps this will become a trend and we will begin to see protests thru-out the country. and is being offered to our readers.
The Vaginal Mesh Helpline is gearing up for what they feel is a second round outreach to some of the largest cities in the United States. "We expect a new wave of T.V ads by lawyers after the election and we are ready."" Women see lawyer ads on T.V and they have alot of questions".Says the helpline medical social worker."They want to speak to someone they feel safe and comfortable with and they call us".

The vaginal mesh lawsuit proceedings have begun" We want all women covered and we want them to get medical and legal help", the helpline representatives tell us. "We have the staff and capacity to help women by offering support and guidance"."They just feel more comfortable with a  social worker then a law firm"

The outreach is a massive undertaking for the Vaginal Mesh Helpline. Their mission is clear and they are ready. They expect to be adding 5-10 new cities a week until they have the major cities in the U.S covered.  The helpline is seeking all women who have not filed their vaginal mesh lawsuit "to stand up and seek justice"

The first round Vaginal Mesh Outreach projected reach the following cities to be:

New York, N.Y.,
Los Angeles, Calif., http://www.vaginalmeshhelpline.com
Chicago, Ill.,
Houston, Tex.,
Philadelphia, Pa,.
Phoenix, Ariz,.
San Antonio, Tex.,
San Diego, Calif.,
Dallas, Tex.,
San Jose, Calif.,

Second vaginal mesh Outreach Campaign

Jacksonville, Fla., http://www.vaginalmeshhelpline.com
Indianapolis, Ind.,
San Francisco, Calif.,
Austin, Tex., http://www.vaginalmeshhelpline.com
Columbus, Ohio,
Fort Worth, Tex.,
Charlotte, N.C.,
Detroit, Mich.,
El Paso, Tex.,
Memphis, Tenn.,

Third round of Vaginal Mesh Outreach

Baltimore, Md.,
Boston, Mass.,
Seattle, Wash.,
Washington, DC,
Nashville,
Denver, Colo.,
Louisville,
Milwaukee, Wis.,
Portland, Ore.,
Las Vegas, Nev.,

Additional Vaginal Mesh Lawsuits Outreach

Oklahoma City, Okla,
Albuquerque, N.M.,
Tucson, Ariz.,
Fresno, Calif.,
Sacramento, Calif.,
Long Beach, Calif.,
Kansas City, Mo.,
Mesa, Ariz.,
Virginia Beach, Va.,
Atlanta, Ga.,
Colorado Springs, Colo.,
Omaha, Nebr.,
Raleigh, N.C.,
Miami, Fla.,
Cleveland, Ohio,
Tulsa, Okla.,
Oakland, Calif,.
Minneapolis, Minn.,
Wichita, Kans.,
Arlington,,