FAQs

Your journey starts with an initial complementary consultation to evaluate if BHIPM is the right fit for you.
Should you want to move forward, the initial assessment includes: a thorough medical history, family history, lifestyle history, personal goals, obtaining previous medical records including previous laboratory reports, submission of a whole genome sequence test that you can do at home or in our office, and enrollment in the patient portal for results and tracking.
Once all results have been received and reviewed by Dr Stanford, an extensive analysis report (The GetDNAbled Report) is generated, which contains: a detailed risk assessment using the genomic, medical, family and lifestyle history, recommendations for targeted interventions to furher evaluate and mitigate these risks and achieve your personal goals. These recommendations may include medication changes, supplements, laboratory and imaging tests, procedures, specific lifestyle and diet interventions.

We do not have a set of recommended labs and supplements that we prescribe for everyone; one size DOES NOT fit all!

We then advise you to take the report to your primary care physician (PCP) so they can continue being the primary manager of your health if so desired; we can assist in obtaining referrals to specialists and labs as recommended in the consultation report.
We will then closely monitor the outcome of the recommended further evaluations and interventions and meet with you weekly/biweekly to ensure ongoing optimal personalized health management. We periodically re-analyze your genomic profile as new literature is published that may be relevant to you and adjust recommendations and specifc interventions to always stay on top of the most recent science.

Individuals who would like to take charge of their own health and not rely on standardized guidelines for the masses. If you are someone who has specific goals or questions and feels there is not enough space in primary care to address those, you came to the right place!

The program is currently limited to persons in California, eighteen and over.
We also provide consult services to other physicians across state lines.

Whole genome sequencing (WGS) is a comprehensive, FDA approved genetic test that reads nearly all of a person’s DNA to identify genetic variants that may influence health, disease risk, medication response, and overall longevity. The benefits include the ability to detect rare or unexpected genetic conditions, personalize prevention and treatment strategies, and uncover actionable insights long before symptoms appear. However, WGS also has limitations—not all genetic variants are fully understood, some findings may be uncertain or have no clear medical guidance, and the test may not detect every type of genetic change (such as certain structural or mitochondrial variants). Risks include the possibility of learning unexpected or sensitive information, uncovering findings that may affect family members, and potential emotional or insurance implications. For most clients, WGS is a powerful tool for precision medicine when paired with expert interpretation and ongoing guidance

No. The entire GET DNAbled process can be done in the privacy of your own home. A whole genome sequence saliva kit will be shipped directly to you. The final report delivery is done via telehealth video, call or in person at our office if preferred. If blood draws are required, they can be done in the comfort of your chosen location, including your own home. If you prefer an in-person experience, you can make an appointment to come to our offices in the Los Angeles area.

Your whole genome testing and GET DNAbled reports are currently not covered by insurance — although some of the additional laboratory and screeing tests may be, depending on your personal medical and family history. We are happy to provide you with medical superbills that you can submit to your insurance company for reimbursement.

No one is allowed access to your whole genome sequence file or GET DNAbled reports without your permission. Your genetic rights under US law are protected by GINA (Genetic Information Nondiscrimination Act). Genetic information cannot be used for purposes of limiting access to health insurance or employment. It can be used to limit access to life insurance and long-term care insurance. We do not advise sharing or selling your genetic information unless it is de-identified and anonymized. Your actual name is not used at all in the sequencing of your DNA.
We do not communicate with your health insurance directly that you had genetic testing done; there may be instances where they may ask you about previous genetic testing or you may need or want to disclose your test results to your health insurance in order to obtain follow on treatment for any conditions we may uncover.

Your individualized results are securely uploaded to your BHIPM patient portal. Dr. Stanford will walk you through all the information compiled into your personalized blueprint. All of your GET DNAbled reports, raw Whole Genome Sequence (WGS) data file, as well as any other actionable results will all be summarized on your GET DNAbled Consultation Report which will remain saved in your HIPAA compliant patient portal for you to securely access and/or download and share with your family or doctor.
Our patient portal also allows you to track other health metrics such as lab values and wearable device data to monitor your progress towards your goals.
You may request deletion of all of this information at any time.

We act as a supplemental consultant service for your primary care physician (PCP) to help tailor your primary care management to your genomic risk profile.
We issue a consultation report (The GetDNAbled Report) that includes the genomic findings and recommendations as to how to tailor the current primary care guidelines to you as an individual. We may recommend additional laboratory or imaging evaluation to further investigate potential risks.

Your primary care management then continues witih your PCP, who can order the necessary follow on workup for you; however we are happy to make referrals and assist in obtaining the necessary follow on care if needed.

We welcome you to invite your primary care physician (PCP) to the walkthrough with Dr. Stanford. Thereafter, your PCP can help you manage the medical recommendations that are given. You will also be able to share your reports with your PCP who can download them and keep them in your chart for future reference (if you direct the PCP to do so).
We do not automatically share your information with any other physicians unless directed by you to do so.

From beginning to end, the full GET DNAbled process takes 6-8 weeks. Your whole genome sequencing takes approximately 4 weeks of that timeline. From there we are able to create your GET DNAbled Report and set up your final appointment with the doctor to discuss your results.

BHIPM puts the patient back into the driver’s seat: you are in charge of your own health and we are here to support you and your specific goals.
We operate with full transparency: at each step we discuss what we are doing, why we are doing it, what the results are, what they mean, what the options are going forward, and then you decide what you would like to do next.

BHIPM provides a healthcare strategy - just like a tax strategy, we first analyze your complete background and current situation and find out about your goals in the short term and long term. We then use this information to develop a personalized plan to help you achieve these goals using the risks and assets you have, with periodic check ins and re-evaluations to accommodate and mitigate anything that life throws at you.