Genetic Risk Assessments for Cancer and Rare Diseases
Understand Your Risk and Take Control of Your Health
Most Health Insurance are accepted.
Comprehensive Risk Assessments
Personalized Genetic Testing for Cancer and Rare Diseases
Pregnancy Genetic Risk
Early Detection of Genetic Disorders: Understanding your genetic risk can help identify the possibility of passing on inherited conditions like cystic fibrosis, sickle cell anemia, or Down syndrome. This allows for early diagnosis and preparation for any medical challenges the baby may face.
Cancer Risk
These genetic test help identify inherited mutations that increase the risk of certain cancers. Which enables early detection, prevention, and personalized treatment. By knowing your genetic risk, you can take proactive steps such as, increased screening, lifestyle changes, or preventative surgeries. These simple genetic test helps reduce your cancer risk and improve health outcomes. It also helps inform family members who may share the same genetic risk.
Rare Genetic Disorders
Rare genetic disorder testing is important because it helps identify the presence of uncommon genetic conditions early, allowing for timely medical intervention, personalized care, and better management of symptoms. Early diagnosis can improve quality of life, guide treatment options, and inform family members of potential genetic risks. It also aids in understanding and managing inherited conditions for future family planning.
How Our Genetic Testing Works
Schedule a Telehealth Appointment
Speak with a specialist through our secure platform.
Discuss Your Health Concerns
We’ll guide you through the process based on your medical history.
Collect Your Sample
We’ll send a testing kit, or we may refer you to a local testing center.
Receive Your Results & Recommendations
Delivered confidentially with tailored health advice.
Schedule Your Consultation
Speak with a Specialist to Discuss Your Genetic Risk
During the consultation, you’ll meet with one of our healthcare specialists in a secure, virtual environment. In this session, we will:
- Review your personal and family health history.
- Discuss any concerns or symptoms you may have related to genetic conditions.
- Provide a thorough explanation of the genetic testing options available, tailored to your specific health needs.
- Offer guidance on the testing process and how the results can inform your medical decisions.
This telehealth consultation is a critical first step in assessing your risk for Cancer (such as breast, prostate, colon, or cervical cancer) and for Pregnancy Genetic Risk, especially for couples planning to have a baby. The information gathered during this appointment will ensure you receive personalized recommendations and insights based on your health profile.
After your consultation, we will arrange for any necessary genetic testing and provide follow-up support to review your results and next steps.
Note: A telehealth appointment is required for both Cancer Risk Assessments and Pregnancy Genetic Risk Testing to ensure proper guidance and personalized care.
Insurance Information: “We accept a variety of health insurance plans for your testing needs. Contact us to verify your coverage.”
Frequently Asked Questions
Genetic testing for cancer risk analyzes DNA to detect inherited mutations that may increase a person’s chance of developing certain cancers, such as breast, ovarian, or colorectal cancer. Identifying these mutations helps individuals understand their cancer risk, make informed decisions about prevention and screening, and guide personalized treatment. It also helps inform family members of potential hereditary cancer risks.
Breast cancer, colorectal, prostate, ovarian cancer, and many more.
If they have a family history of genetic disorders, belong to an ethnic group with higher risks of certain conditions, or if they or their partner are known carriers of genetic mutations. Genetic testing is also recommended if they’ve had previous pregnancies with genetic abnormalities or if there are concerns about passing on inherited conditions. A healthcare provider can help determine if testing is appropriate based on personal and family medical history.
From the time the lab receives the collected sample it takes 1-2 weeks. With DNA testing, extra time is needed to identify the complex amount of data the receives.
