People who lived, worked or were in utero at Camp Lejeune, for a period of at least 30 cumulative days, sometime between August 1, 1953 and December 31, 1987, and have one or more of the qualifying diseases.
Loved ones who were sexually abused or assaulted by a priest, clergy or other church official. We have qualified intake staff who have been trained to handle the sensitive nature of their claims.
Claimants who used a recalled Philips CPAP, BiPAP or mechanical ventilator device for at least 12 months. First use prior to 4/25/2021 and did not smoke during the time they used recalled device, and were diagnosed with a qualifying condition.
We seek out claimants that used firefighting foam (AFFF) for at least 6 months or longer, and developed cancer associated with PFAS.
Our marketing targets people that have used any relaxer/straightener product containing Formaldehyde or Phthalates chemicals and were diagnosed with cancer. We require one or more year(s) latency between first full year of product use and diagnosis.
A claimant that had at least one Hernia Mesh surgery that required a revision due to mesh complications or failure. If no revision, must be suffering from injuries directly related to the hernia mesh implant that requires physician intervention to resolve.
There is a correlation between infants fed formula and subsequently being diagnosed with NEC (Necrotizing enterocolitis) as an infant. The main manufacturers being sued are the makers of Enfamil and Similac.
Paraquat is a toxic commercial chemical used as an herbicide in the agriculture industry. It has been linked to Parkinson’s disease for those that were exposed to it.
We target mothers who ingested a form of Acetaminophen or Paracetamol (APAP) during pregnancy. Their child is now under the age of 18 and has been diagnosed with Autism Spectrum Disorder (ASD).