Camp Lejeune

Contaminated Water at Camp Lejeune?

From 1953 through 1987, military staff, family members, and civilians who served, lived, or worked at Camp Lejeune may have been exposed to industrial solvents, benzene, and other toxic chemicals in the drinking water at the base. Reservists and guardsmen may also have been exposed. We are currently still taking clients for Camp Lejeune lawsuit settlements with zero up-front fees for any legal representation unless we win your claim.

Camp Lejeune Toxic Water
Settlement Explained

During the years 1947-1987, water supplies at Camp Lejeune (North Carolina) were found to be contaminated with a number of hazardous chemicals linked to a range of serious health conditions, including cancer, birth defects, ALS, and other potentially life-threatening injuries. On May 15, 2023 — New study from Major Medical Peer Review Journal links solvent in water to Parkinson Disease Risk in Camp Lejeune Veterans.

Over one and a half million people lived at Camp Lejeune within this time period: active duty and former military service members, families, non military staff, and others

If you, a family member, or a loved one has suffered health effects due to the water contamination at Camp Lejeune, you may be eligible to participate in the Camp Lejeune Water Contamination Lawsuit.

Camp Lejeune, a United States Marine Corps base in North Carolina, experienced significant water contamination issues between the late 1940’s through 1980s. The drinking water at the base was found to be contaminated with toxic chemicals, primarily volatile organic compounds (VOCs) like trichloroethylene (TCE), perchloroethylene (PCE), benzene, and other compounds. The contamination resulted from leaking underground storage tanks, industrial activities, and improper waste disposal practices at the base.

The contaminated water at Camp Lejeune posed serious health risks to military personnel and their families who lived and worked at the base during that time. Exposure to these chemicals has been linked to a range of adverse health effects, including various forms of cancer, birth defects, and other health problems.

The extent of the contamination and its impact on the health of people at Camp Lejeune were not fully understood until the late 1980s and early 1990s, when investigations and studies revealed the severity of the issue. Since then, efforts have been made to clean up the contaminated sites, and affected individuals have sought compensation and healthcare assistance through various legislative measures, such as the Honoring America’s Veterans and Caring for Camp Lejeune Families Act of 2022.

Requirements to file a successful Camp Lejeune claim:

If you, a family member, or a loved one has suffered health effects due to the water contamination at Camp Lejeune, you may be eligible to participate in the Camp Lejeune Water Contamination Lawsuit. The US Senate passed a bill in 2021-2022 called Camp Lejeune Justice Act of 2021.

Round up

Need Help Filing a Roundup Lawsuit?

Roundup is a widely used herbicide containing the active ingredient glyphosate, designed to control weeds and unwanted vegetation. In recent years, several studies have concluded a link between glyphosate exposure and an increased risk of developing certain types of cancer, particularly non-Hodgkin’s lymphoma. Consequently, numerous Roundup cancer injury lawsuits have been filed against its manufacturer, Monsanto (now owned by Bayer), alleging failure to provide. adequate warnings about potential risks and safe usage instructions.

Roundup Cancer Lawsuit

If you or a loved one has been diagnosed with cancer linked to Roundup use, it’s crucial to act quickly. Time limits, known as statutes of limitations, apply to Roundup cancer injury lawsuits, making it essential to seek legal counsel as soon as possible.

Contact us today for a free, no-obligation consultation to discuss your case eligibility and explore your legal options. We have been working on Roundup Cancer Cases for over 7 years and have unfortunately worked with thousands of people that suffered from a roundup weed killer injury and over 77% have already been compensated for exposure to Roundup.

Complete the 2-minute Roundup Cancer Survey on the right and one of our highly trained legal representatives will call you back immediately to assess your eligibility.

Although studies dating back to the 1980s raised concerns about Roundup weed killer’s ingredients, nothing was done until about 8 years ago. Bayer will remove Glyphosate from residential Roundup beginning in 2023, but we are still left with a formula that many researchers say is harmful. The courts are listening. At its core, Roundup’s formula is dangerous, and it is fueling current lawsuits. Although Bayer has already paid billions of dollars to settle most of the older claims, victims continue to come forward and significant settlements are being awarded to them.

Understanding Roundup
Cancer Injury

You (or a loved one) were diagnosed with Non-Hodgkin’s Lymphoma, B-Cell Lymphoma-Cell Lymphoma, Chronic Lymphocytic Leukemia (CLL) Hairy Cell Lymphoma.

You(oraloved one) were diagnosed with Non-Hodgkin’s Lymphoma, B-Cell Lymphoma-Cell Lymphoma, Chronic Lymphocytic Leukemia (CLL) Hairy Cell Lymphoma.

You (or a loved one) used Roundup at your residence at least 10 times.

You (or aloved one) used Roundup at your residence at least 10 times.

You (or a loved one) used Roundup as part of your (or a loved one’s) occupation.

You (or aloved one) used Roundup as part of your or aloved one’s) occupation.

You (or a loved one) used Roundup for agricultural purposes.

You (or a loved one) used Roundup for agricultural purposes.

Talcum Powder

Talcum Baby Powder Cancer
Lawsuit Claims

Welcome to our comprehensive resource on Talcum Powder lawsuits, a pressing concern for many individuals who have suffered health issues due to prolonged exposure to talcum powder. Our mission is to provide you with accurate, up-to-date information on the legal aspects of talcum powder-related cases, potential health risks, and how our extremely skilled legal team can help you seek the compensation and justice you deserve. We are here to empower you to make informed decisions and protect your rights.

Taking the First Step:

If you or a loved one has experienced health issues linked to talcum powder use, it’s essential to act promptly. Time limits, known as statutes of limitations, apply to talcum powder injury lawsuits, so it’s crucial to seek legal advice as soon as possible. Contact our knowledgeable attorneys today for a free, no-obligation consultation to discuss your case and learn more about your legal options.

Don’t let the opportunity for justice slip away – reach out to our experienced legal team today and take the first step toward securing the compensation you deserve in your talcum powder injury lawsuit. Complete the 2-minute Talcum Powder Survey on the right and one of our highly trained legal representatives will call you back immediately.

Countless victims of corporate negligence and greed have started their journey right here at Tort Advisor to secure justice and compensation for themselves and, by extension, help ensure this doesn’t happen to others in the future. Add your voice to the many who stood up and demanded to hold Johnson & Johnson and other manufacturers accountable for their negligence exposing millions of babies and mothers to toxic Talcum Powder. 

Talcum Powder

Talcum Baby Powder Cancer
Lawsuit Claims

Welcome to our comprehensive resource on Talcum Powder lawsuits, a pressing concern for many individuals who have suffered health issues due to prolonged exposure to talcum powder. Our mission is to provide you with accurate, up-to-date information on the legal aspects of talcum powder-related cases, potential health risks, and how our extremely skilled legal team can help you seek the compensation and justice you deserve. We are here to empower you to make informed decisions and protect your rights.

Taking the First Step:

If you or a loved one has experienced health issues linked to talcum powder use, it’s essential to act promptly. Time limits, known as statutes of limitations, apply to talcum powder injury lawsuits, so it’s crucial to seek legal advice as soon as possible. Contact our knowledgeable attorneys today for a free, no-obligation consultation to discuss your case and learn more about your legal options.

Don’t let the opportunity for justice slip away – reach out to our experienced legal team today and take the first step toward securing the compensation you deserve in your talcum powder injury lawsuit. Complete the 2-minute Talcum Powder Survey on the right and one of our highly trained legal representatives will call you back immediately.

Countless victims of corporate negligence and greed have started their journey right here at Tort Advisor to secure justice and compensation for themselves and, by extension, help ensure this doesn’t happen to others in the future. Add your voice to the many who stood up and demanded to hold Johnson & Johnson and other manufacturers accountable for their negligence exposing millions of babies and mothers to toxic Talcum Powder. 

Tylenol Autism

Tylenol, a well-known brand of acetaminophen, is a widely used over-the-counter pain reliever and fever reducer. While generally considered safe when taken as directed, Tylenol has been linked to severe liver damage and other health issues when consumed in excessive amounts or combined with other medications containing acetaminophen. As a result, numerous Tylenol Autism Lawsuits have been fled against the manufacturer, alleging failure to provide adequate warnings about potential risks and proper usage.

Taking Tylenol While Pregnant and Autism

There has been a surge in new studies that suggest a link between the use of acetaminophen (the active ingredient in Tylenol) during pregnancy and an increased risk of neurodevelopmental disorders, including autism, in children.
Some of these studies have proposed that acetaminophen use during pregnancy could interfere with the normal development of the fetal brain by disrupting the balance of oxidative stress and antioxidant defense mechanisms. This imbalance might lead to inflammation and, consequently, increase the risk of neurodevelopmental disorders.
Millions of people regularly use Tylenol or generic-brand acetaminophen to relieve mild to moderate pain and reduce fever. Acetaminophen has also long been considered the safest over the counter (OTC) pain reliever medication for pregnant women, which makes this even more important that potentially affected people come forward and join this effort to hold Tylenol manufacturers accountable for such a mistake.

Taking the First Step:

If you or a loved one has experienced health issues linked to talcum powder use, it’s essential to act promptly. Time limits, known as statutes of limitations, apply to talcum powder injury lawsuits, so it’s crucial to seek legal advice as soon as possible. Contact our knowledgeable attorneys today for a free, no-obligation consultation to discuss your case and learn more about your legal options.

Don’t let the opportunity for justice slip away – reach out to our experienced legal team today and take the first step toward securing the compensation you deserve in your talcum powder injury lawsuit. Complete the 2-minute Talcum Powder Survey on the right and one of our highly trained legal representatives will call you back immediately.

Your case may qualify if
– If you regularly used Tylenol or acetaminophen (also called paracetamol) during pregnancy and your child developed autism, you may be eligible for compensation from the party responsible.

Hair Relaxer / Straightener

Hair relaxers are chemical products designed to straighten curly or coiled hair. While these products can deliver desired results, there have been many recent studies that link hair relaxers and an increased risk of certain types of cancer, such as Breast Cancer, Uterine Cancer, and Ovarian Cancer. As a result, numerous hair relaxer lawsuits have been filed against manufacturers, alleging failure to provide adequate warnings about potential risks and the need for proper safety precautions.

Hair Relaxer Lawsuits & Cancer Explained

Millions of women in the U.S. use hair relaxer products regularly. New scientific research has found that the chemicals in hair relaxers can cause uterine cancer. Women who have used hair relaxer products for long periods and subsequently been diagnosed with Uterine Cancer, Breast Cancer, or Ovarian Cancer are filing product liability lawsuits against the manufacturers and seeking compensation

If you or a loved one has been diagnosed with cancer that has been linked to hair relaxer use, it’s crucial to act promptly. Time limits, known as statutes of limitations, apply to hair relaxer cancer injury lawsuits, making it essential to seek legal counsel as soon as possible. This is a relatively new lawsuit, but our attorneys and our staff have been working with affected clients since the first day the courts allowed cases to be tried.

Don’t let your opportunity for justice slip away – reach out to our experienced legal team today and take the frst step toward securing the compensation you deserve in your hair relaxer cancer injury lawsuit. Please complete our 2-minute Hair Relaxer Survey on the right and one of our highly trained legal representatives will call you back immediately.

Requirements to file a successful Hair Relaxer Claim:

To file a successful hair relaxer cancer personal injury claim, you must meet specific requirements that demonstrate the legal elements of negligence or product liability. While the precise requirements may vary depending on the jurisdiction and the specifics of the case, the following general elements are typically necessary:

1

Product usage: You must provide evidence that you or the affected individual used the hai elmer product as intended or as directed by the manufacturer or seller.

2

Diagnosis: You must have a confirmed diagnosis of cancer, supported by medical records and documentation from healthcare professionals.

3

Causation: You must establish a causal link between the use of the hair relaxer product and the development of cancer. This may require expert testimony from medical professionals, toxicologists, or other relevant experts who can explain how the ingredients or chemicals in the hair relaxer product contributed to the development of cancer.

4

Manufacturer or seller negligence: You must demonstrate that the manufacturer or seller of the hair relaxer product was negligent in their actions, such as by failing to provide adequate warnings, failing to test the product for safety, or by selling a defective product.

5

Damages: You must provide evidence of the damage you have suffered because of the cancer diagnosis, such as medical expenses, lost income, pain and suffering, and other related costs.

6

Timeliness: You must file your claim within the statute of limitations, which is the legally prescribed time limit for filing a personal injury lawsuit. The statute of limitations varies depending on the jurisdiction and the specific circumstances of the case.

Boy Scouts

The Boy Scouts of America (BSA) is one of the largest youth organizations in the United States, with 2.3 million youth members and approximately 889,000 adult volunteers in 2017. In 1979 there were over 5 million youths in BSA.

The high risk of sex abuse in volunteer youth organizations has been recognized, and, in 1988, the BSA created a sex abuse education and prevention program called the Youth Protection program to help address the problem. There were around 2,000 reported abuse cases within the Boy Scouts of America before 1994 In 2010, a jury ordered that the Boy Scouts of America pay US$18.5 million (equivalent to $25.8 million in 2023) to a scout who was abused in the 1980s — the largest punitive damages award to a single plaintiff in a child abuse case in the US.

Legal actions

A number of lawsuits have resulted from Boy Scouts of America sex abuse cases. A study of 50 lawsuits against the BSA showed that from 1986 to 1991 BSA and local councils agreed to pay more than $15 million in damages. According to federal tax returns, BSA payments to one law firm in Miami working on abuse cases were more than one-half million dollars; the BSA insurance reserve, from which the damages are paid, stood at $619 million.

The actual payment total, said The Washington Times in 1991, is probably far higher because the Scouts sometimes agree to pay damages only if the payments are kept secret. Keeping damage awards confidential is. commonly required by insurers.

In August 2007, the Washington state Supreme Court ordered BSA to hand over documents concerning sexual abuse by Scout leaders. These documents showed that the organization removed about 180 of its leaders each year, although most of these removals are related to other issues besides child abuse.

NEC Baby Formula

What is Necrotizing Enterocolitis (NEC)

Necrotizing enterocolitis (NEC) is a severe disease affecting the intestines of premature infants, usually occurring within the first two weeks of life in formula-fed babies. Bacteria infect and inflame the intestinal wall, leading to weakened walls that can crack and leak germs into the abdomen, potentially causing serious infection or death if untreated.

Infections from NEC often require surgery, which can result in further gastrointestinal issues like Short Bowel Syndrome (SBS). SBS involves the surgical removal of parts of the intestine, reducing nutrient absorption and increasing health risks for the infant.

The Connection Between NEC and Infant Formula

Research links NEC to certain cow milk-based infant formulas. A 1990 study found NEC was 6-10 times more common than in those fed breast milk alone.

In 2011, Johns Hopkins Medical Institution discovered that extremely premature babies fed human donor milk were less likely to develop NEC than those fed standard premature infant formula derived from cow’s milk.

Infant formula manufacturers face numerous lawsuits for failing to warn about the NEC risk. They must inform parents about the potential dangers of cow mil.

Risks of Necrotizing Enterocolitis Injuries Associated with NEC

  • Intestinal perforation
  • Scarring or strictures in the intestines
  • Sepsis
  • Potential Neurological damage
  • Abdominal pain and swelling
  • Irregular heart rate, breathing, blood pressure, or body temperature
  • Diarrhea with bloody stool
  • Lethargy
  • Refusing to eat
  • Lack of weight

How Can We Help?

Providing the Legal Help You Need Manufacturers of infant formula have knowingly used dangerous ingredients in their products for decades without notifying parents of the potential dangers. Decades of research across multiple studies have produced probable connections between cows’ milk-based formula and Necrotizing Enterocolitis. Now is the time to hold the manufacturers accountable.

The Victims Help Now Network can connect qualified claimants to attorneys ready and willing to represent their cases. Call or complete our no-cost claim review today. Don’t wait to pursue the justice you deserve.

Zantac

What is Zantac?

Zantac was a popular antacid drug since the 1980’s. Ranitidine hydrochloride, better known under the commercial name Zantac, was an antacid medication available as an over-the-counter drug and by prescription from a physician. Millions of people used the drug to treat acid reflux, heartburn, Barrett’s esophagus, gastric and duodenal ulcers, gastroesophageal reflux disease (or GERD), and other gastrointestinal issues

It belongs to the class of drugs known as H2 (or histamine02) blockers, OTC ranitidine was commonly used to relieve and prevent heartburn, Prescription strengths were also used to treat and prevent more severe ulcers in the stomach and intestines.

Based upon the FDA’s ongoing investigation, levels of a carcinogen called nitrosamine (N-nitrosodimethylamine or NDMA) in the heartburn medication increase over time and posed a risk of cancer when stored at higher than room temperatures.

Testing and Research

Testing by the USS. Food and Drug Administration (FDA) showed that Zantac, the household heartburn medication, contained a cancer causing chemical NDMA. It was found in both the drug and generic versions at excessively more significant amounts than the daily intake limit when tested under the FDA recommended protocols

Testing and research from public and private groups found that NDMA resulted from the “inherent instability” of the ranitidine molecule. All manufacturers, brand or generic, and lots of ranitidine containing medications were affected and could generate very high levels of NDMA in the human body.

Associated Cancer Risks of Zantac Usage

Cancer risks associated with brand-name Zantac and generic ranitidine include:

-Bladder
-Liver
-Pancreatic
-Stomach/Gastric
-Esophageal

Has There Been a Zantac Settlement?

There have been no Zantac settlements or jury verdicts yet. Typically, bellwether trials help plaintiffs and defendants understand how much a case may be worth. The first bellwether trial is scheduled for October 2022.

GlaxoSmithKline, Boehringer Ingelheim, Pfizer, Sanofi, and various other manufacturers, distributors, and retailers involved in selling brand name Zantac or generic ranitidine pills now face lawsuits by consumers who allege Zantac caused cancer as NDMA moved through the body, following years of exposure.

Status of Zantac Lawsuits

Victims want to know when the Zantac suits will settle. Litigation involves class action lawsuits and a mass tort or MDL (multidistrict litigation).

The class-action suit against Zantac manufacturers in California is the first to schedule a trial date officially. Superior Court of Alameda Judge Evelio Grillo has set the start date for California Ranitidine Product Cases JCCP 5150 for October 10, 2022.

The first trial before Judge Grillo is the first in a series of bellwether tests, beginning with a case the plaintiffs selected. Next up will be the chosen defendants case scheduled to begin February 6, 2023. The following two are scheduled for May 1, 2023 (plaintiff selected) and August 7, 2023 (defendant selected).

Additionally, in October 2021, efforts to stop the Multidistrict Litigation (MDL) before the court in West Palm Beach, Florida, were rejected, U.S, District Judge Robin Rosenberg ruled that cases can proceed. More than 800 cases are pending before Judge Rosenberg.

While the California trial is the first to be scheduled, trials in the MDL in Florida, and an array of other cases in states such as Illinois, Minnesota, New Jersey, New York, Oregon, Pennsylvania, Tennessee, Texas and Washington could be scheduled to begin before the trial in Alameda.

Do You Qualify for A Zantac Lawsuit?

Our law firm is accepting new personal injury and wrongful death claims against the maker of Zantac for anyone who meets the following basic criteria:

You took Zantac (or another ranitidine product) daily or regularly for at least 6 months. After taking Zantac you were diagnosed with any of the following cancers:

-Bladder
-Liver
-Pancreatic
-Stomach/Gastric
-Esophageal

Ozempic

Ozempic Lawsuit

Ozempic lawsuits claim the drug can cause severe gastroparesis, ileus and intestinal blockage. Lawyers are also pursuing cases of Ozempic vision loss. Plaintiffs claim they weren’t properly warned of these risks. The first Ozempic stomach paralysis lawsuit was filed on Aug, 2, 2023

As of August 2024, there are 8 personal injury lawsuits for gastroparesis, ileus and intestinal blockage or obstruction in MDL 3094 in the Eastern District of Pennsylvania.

In July 2024, lawyers began investigating Ozempic vision loss lawsuits. People who took any semaglutide drug, such as Ozempic and Wegovy, and suffered vision loss may qualify to file a lawsuit for potential compensation.

Why Are People Filing Ozempic Lawsuits?

Currently, the bulk of people have filed Ozempic lawsuits because they took the drug and later suffered from gastroparesis, ileus or intestinal blockage. Ozempic, also known as semaglutide, belongs to a class of drugs called GLP-1 agonists, and lawyers are also investigating other drugs in this class. Gastroparesis is a severe disorder that causes food to move too slowly through the stomach to the small intestine. In some cases, food may stop moving through the intestine altogether.

Gastroparesis may cause nausea, vomiting, abdominal bloating, abdominal pain, severe dehydration, acid reflux, malnutrition and weight loss. Undigested food may remain in the stomach and harden.

“During this frightening obsession with semaglutide usage, particularly its off-label, higher dosage used for weight loss, I’ve been extremely concerned about the fallout of use of this class of drugs.” said J) a former Certified Pharmacy Technician who is using initials to protect her privacy.

“They have black box warning labels, yet all my friends are using them without a thought,” J told Drugwatch. “[They] have reported bouts of nausea, vomiting, diarrhea and constipation, which sound to me like evidence of gastroparesis — which can kill you.”

Who Qualifies To File an Ozempic Lawsuit?

You may qualify to file an Ozempic lawsuit if you took Ozempic for weight loss or any other indication and experienced gastroparesis. Currently, lawyers are accepting cases from people who suffered severe gastroparesis resulting in vomiting for four weeks or more. Currently, you may not qualify if you had gastric bypass surgery, gastric banding or gastric sleeve surgery before taking Ozempic. Additionally, lawyers are not taking Ozempic cases for those being treated for cancer. These criteria are guidelines, and only an Ozempic lawyer can tell you if you qualify to file a lawsuit. Make sure you contact a lawyer right away for a free case review and preserve your right to file a lawsuit for potential compensation. Depending on the state you live in, you may only have a limited time to file.

Ride Share

Were you sexually assaulted in an UBER?

You may be entitled to a financial settlement.

If you were abused in an UBER you may qualify to join the case, but there may be a limited time to file a claim. Enter your details and get the justice you deserve!

Confidentiality

Claims of inappropriate behavior require care and confidentiality. We always keep personal details private, sharing only necessary information to help you file your claim, so that you can maintain your privacy and confidentiality.


Compensation

Rideshare companies have either dismissed or have not taken victims’ claims seriously for too long. We are committed to assisting survivors in reporting their claims, seeking help, and pursuing lawsuits to obtain compensation for various losses, including:

⦁ Counseling
⦁ Pain and suffering
⦁ Medical treatment
⦁ Lost earnings
⦁ Damages


Types of Sexual Abuse

If you or a loved one experienced any of the following types of inappropriate behavior, you may be eligible to compensation:

⦁ Sexual Abuse
⦁ Attempted Sexual Abuse
⦁ Forced Kissing
⦁ Inappropriate Touching
⦁ Other Abuse
Rideshare Law Suit 1

Drivers and Passengers Affected

According to the latest rideshare sexual assault data, there were 4,158 incidents, including 360 rape reports over a three-year period.

Settlements

2019: LYFT agrees to a $25 Million settlement on claims including safety-related incidents.
2021: UBER agrees to pay a $9 Million settlement that will also go toward safety-related initiatives.

Background Check Issues

Uber has conducted background checks on its drivers since 2018. Despite these measures, Uber’s background check policy faced criticism due to past incidents. In 2018, an investigation revealed thousands of convicted felons driving for Uber. One driver, Talal Chammout, with firearm offenses on his record, was hired in 2015. Just three months later, he sexually assaulted a female passenger in her home, resulting in a 25-year prison sentence.

Personal Support

Our experienced support team is here for you throughout this process. We understand the sensitivity of these cases and will work diligently to get you the services you deserve.

Rideshare Law Suit 2