Our lawyers are actively reviewing hair relaxer cancer lawsuits across all 50 states. This page provides:
- Detailed news and updates on the chemical hair relaxer litigation,
- Insights from our hair relaxer attorneys on how these lawsuits may unfold,
Our lawyers are actively reviewing hair relaxer cancer lawsuits across all 50 states. This page provides:
We have also recently reopened the comments below to answer any questions you may have or simply give you a chance to share your thoughts.
This page is for victims considering filing a Depo-Provera lawsuit. Our lawyers provide the latest updates on these claims, explain the litigation process, and predict Depo Provera settlement amounts.
A new scientific study has provided stunning evidence that using Depo-Provera can cause brain tumors. Women who used Depo-Provera and subsequently developed a meningioma brain tumor can file a Depo-Provera lawsuit seeking financial compensation. This new evidence is leading to a wave of Depo-Provera lawsuits nationwide.
Our lawyers are speaking to over 100 women a week who used Depo-Provera and have been diagnosed with meningioma. Our law firm is committed to this litigation and handling Depo-Provera lawsuits for women who had at least two injections and were later diagnosed with a meningioma brain tumor. If you meet these criteria, we will make the process of signing up for this litigation easy for you. Contact our Depo-Provera lawyers today at 800-553-8082 or contact us online.
The Bard PowerPort (“BardPort”) is a port catheter device implanted just under the skin to allow for easy attachment to a catheter for the intravenous delivery of fluids or medication.
The Bard PowerPort has inherent design and manufacturing flaws that make the device prone to fracturing and migrating out of position. This can cause severe injuries, including internal vascular damage.
Individuals who suffered injuries due to a defective Bard PowerPort device are now bringing product liability lawsuits against the manufacturer of the PowerPort implants. Our firm is currently accepting new cases from anyone who had a Bard PowerPort port catheter device implanted and was injured due to a fracture, migration, or other implant failures.
This page is about social media addiction lawsuits and who is eligible to bring a claim. Our lawyers also provide the latest news on social media class action lawsuits (including the ongoing trial in California).
The problem that led to social media lawsuits is that millions of people, too many of whom are children, are addicted to social media platforms such as Facebook, Instagram, Snapchat, and others. For these vulnerable users, social media addiction can be very harmful and lead to things like eating disorders, depression, and, in some cases, suicide.
Now, these companies are facing a wave of new social media lawsuits alleging that they knowingly designed the algorithms of their platforms to lure young people into harmful addictions.
Anyone who was the victim of sexual abuse at school can file a civil lawsuit against the school and get compensation. You can sue the school for failing to prevent the sexual abuse, even for incidents that happened decades ago. Any form or level of unwanted sexual touching can form the basis for a sexual abuse lawsuit.
This post will look at sexual abuse lawsuits filed against schools. These school sex abuse lawsuits can be brought by current or former students who were the victims of sexual abuse committed by a teacher or another student at school. Successful plaintiffs can get significant financial compensation.
If you have a potential sexual abuse lawsuit against a school, contact attorneys today for a free consultation. Contact us online or call us at 800-553-8082.
On this page, our lawyers will discuss LDS sexual abuse lawsuits against the Mormon Church (Church of Jesus Christ of Latter-day Saints).
We will explain the legal requirements for bringing a Mormon Church sex abuse lawsuit, and our attorneys will also examine the expected average settlement payout value of remaining cases.
We expect more LDS Church sex abuse settlements in 2026. If you have a claim, contact us today at 800-553-8082 or get a free consultation.
Our lawyers are handling Similac and Enfamil infant formula lawsuits for families whose premature babies suffered or died from necrotizing enterocolitis (NEC) after taking one of these formulas. Our law firm is reviewing NEC lawsuits in all 50 states.
Medical research links cow milk-based infant formulas such as Similac and Enfamil to a dangerous neonatal medical condition known as necrotizing enterocolitis. These newborn NEC formula lawsuits make many allegations. But at their core, they allege that the makers of these formulas knew of the risk of NEC and did nothing to warn families and give them a choice.
If your premature baby was diagnosed with NEC after being given Similac or Enfamil formula, you may be able to participate in a class action lawsuit against the formula companies and receive financial compensation for the harm that was done to your child.
In this post, our Roundup lawyers will give you:
A spinal cord stimulator is an implantable medical device used to manage chronic pain, most often involving the back or spine. These systems are marketed as a way to reduce pain by interrupting nerve signals before they reach the brain. But for a growing number of patients, the device fails to help. It introduces new and sometimes permanent problems, including electrical shocks, burning pain, infections, lead migration, hardware failure, and repeat surgeries to reposition or remove equipment that was supposed to improve quality of life.
This page explains spinal cord stimulator lawsuits and why they are being filed nationwide. It focuses on what patients are alleging, how these devices have failed in real-world use, and why many of these cases go beyond ordinary medical malpractice claims. The most serious lawsuits do not center on a single surgical mistake. They examine how modern spinal cord stimulators were designed, tested, and approved, and whether patients were ever adequately warned about the risks that now recur repeatedly in medical records and FDA reports.
Many people arrive here with a practical question in mind: what do spinal cord stimulator settlement amounts look like, and how does compensation get calculated when a device causes lasting harm? That question cannot be answered in isolation. Settlement amounts and payouts are driven by the full medical timeline, including the cost of repeat surgeries, explantation, permanent loss of function, and the downstream consequences when a pain-management device leaves someone worse off than before it was implanted.