Personalized Genetic Risk Assessment
Comprehensive review of your personal and family history to identify genetic risks early, guide testing decisions, and support timely care and prevention.
Whether you're looking to understand your risks for hereditary cancer syndromes, cardiovascular conditions, or other genetic conditions, we’ll discuss whether genetic testing is appropriate for you or family members and how it can guide your decisions moving forward.
Who This Is For:
This service is ideal for individuals who:
Have a family history of a genetic condition, such as a hereditary cancer syndrome or an inherited heart condition, and are interested in exploring whether genetic testing is appropriate for you or your family
Are concerned about a hereditary form of disease, such as cancer or heart conditions, and would like to explore the role of genetic testing in understanding your genetic risk
Are seeking a second opinion after receiving genetic testing or counseling, or want to explore further genetic testing options based on family history or previous results
Have genetic test results (including variants of uncertain significance) and want to discuss their implications or consider next steps
Have a diagnosis of autism and are interested in exploring potential genetic causes
What You Can Expect
A detailed review of your personal and family health history to assess genetic risks that may impact you or your family
A discussion of relevant genetic risks and an overview of available genetic testing options
Interpretation of any previous test results, if applicable
After your session, you’ll receive a written summary and relevant resources tailored to your goals and needs
If You Choose to Pursue Testing
We’ll discuss which test(s) are most appropriate based on your goals and clinical context
I’ll coordinate testing through CLIA-certified, state-licensed laboratories that meet clinical-grade standards
You’ll submit a blood or saliva sample (depending on the type of test ordered) using a test kit mailed to you
We’ll schedule a follow-up consultation via phone or video to review your results and provide recommendations
Timeline: From your initial consultation to results review, the process typically takes 2–4 weeks.
Pricing & Billing
Session Fees
All sessions are conducted via secure telehealth
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A 45–60 minute one-on-one session focused on your personal and/or family history, genetic risks, and testing options.
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A shorter session to review genetic test results, answer follow-up questions, or revisit decisions.
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This option is recommended if you move forward with genetic testing. It covers both your initial consultation and a dedicated session to review and discuss your results in detail.
Access & Affordability
If cost is a concern, please don’t hesitate to reach out. I offer flexible payment arrangements, and I believe financial barriers should never prevent someone from accessing supportive, personalized care.
FAQs
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I assess a broad range of genetic risks, including hereditary cancer syndromes, cardiovascular diseases, neurological disorders, and other inherited conditions. We’ll review your family history to identify the most relevant risks and discuss whether genetic testing could be beneficial for you or your family members.
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Even if your family history is unclear or you don't have a known genetic condition, genetic counseling can still be helpful. We can assess your personal and family health history and discuss potential risks that may not be obvious at first glance, as well as explore genetic testing options based on your unique situation.
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I do not make direct referrals, but I can provide recommendations for specialists who may be appropriate for further evaluation or care. I’ll work with you to navigate the next steps and ensure you have the information you need to make informed decisions.
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No referral is required. You can book an appointment directly. However, if a healthcare provider has recommended a genetic risk assessment, you can share that information with me to ensure we tailor the session appropriately.
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Genetic testing is billed separately by the laboratory. Genetic testing panels typically start at $250 for out-of-pocket costs, though the final price can vary depending on the type of test and your insurance coverage. Many labs also offer financial assistance programs to help reduce costs if insurance does not cover testing.
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I don’t bill insurance directly, but many clients with PPO plans are able to receive partial out-of-network reimbursement. I can provide a superbill with the necessary codes upon request. Be sure to check with your insurance company to ask about coverage for CPT code 96040 (genetic counseling via telehealth).

Ready to understand your genetic risks more clearly?
Reach out to begin your personalized assessment and take a proactive step toward your health.