Want to talk about how NxGen MDxβs carrier screening or pathogen testing helped improve health outcomes for you or your family? Visit https://t.co/2w5ULnKJx1 and let us know how we made an impact on you!
The NxGen MDx team wishes you a happy holiday! We hope you have a safe and healthy holiday. Please note that our lab and office will both be closed on December 25 and 26.
Equitable care for all people is a priority at NxGen MDx. We screen for genetic conditions that are common across all ethnicities to offer every patient actionable information that makes a difference. Click here to learn more about our carrier screening https://t.co/qiI1QYP5T3
This week is National Influenza Vaccination Week. The flu vaccine helps reduce both the symptoms and length of illness. Protect yourself and those around you by getting vaccinated!
Today we recognize Genetic Counselor Awareness Day! We are grateful for all the help you so graciously extend to patients everyday! Your hard work and dedication in the medical field does not go unnoticed!
With positive feedback from providers like Leslie Biggs, NP, we know that our tests give providers confidence and help provide better patient outcomes. Learn more at https://t.co/oJKWe9TYOJ
Ever wondered about recessive genetic conditions? Without having any symptoms, you may be a carrier of a genetic condition that you could pass on to your child. Learn more at https://t.co/eB0ShLfZTV
With the NxGen MDx Vaginosis Test, we are able to identify coinfections that might change how you treat your patient. Providers can be more confident in their diagnosis and treatment plans when testing with NxGen MDx. Learn more at https://t.co/CanTXqussF
According to the National Breast Cancer Foundation, in the US, someone is diagnosed with breast cancer every 2 minutes. Here at NxGen MDx, we stand to support the fight against breast cancer. This week we're wearing pink in honor of National Breast Cancer Awareness Month!
The NxGen MDx Hereditary Cancer Panel is a crucial step to keep you and your family healthy. With the benefits of detection, prevention, and education, you can get ahead of many possible cancer risks. Learn more at https://t.co/mw8nWwblaC https://t.co/0DB2pGl83E
Knowing if a baby could inherit a genetic condition before birth can lead to a timely diagnosis and early treatment. Learn more about NxGen MDx's Early Advantage Panel at https://t.co/sUzfyoM1aP
NxGen MDx can help determine your risk for inherited uterine and ovarian cancers, allowing you to take action based upon that risk level to stay healthy. Learn more about our Hereditary Cancer Panel at https://t.co/Qf0dV5uB1y
In September, we recognize Muscular Dystrophy Awareness Month. In this video, we hear from Genetic Counselor, Millie Anderson, who tells us about the condition.
Did you have screening or testing done with NxGen MDx? We would love to hear about your experience. Use this link to answer a few questions https://t.co/Dv9XdW8ocX
September is Tay Sachs Awareness Month. Check out this article on the Jewish communities' diligent efforts to combat this condition through carrier screening and activism. Their efforts have caused Tay Sachs rates to fall almost 90% since the 1970s. https://t.co/GiaP1W4xLX
NxGen MDxβs Early Advantage Panel screens for 68 of the most common genetic conditions that could be passed from a parent to their child. Learn more about carrier screening at https://t.co/eB0ShLfs4n