Looking for DNA reports? Those live at Genetics for the People →
Consulting for individuals

Working with me

For people who want to decode their genetics, find the root cause of symptoms that have gone unresolved for too long, or simply understand their bodies more deeply.

Begin the intake form See packages & pricing

Who this is for

I work with two kinds of people: those with ongoing symptoms despite "normal" labs, and generally healthy people who want to understand what their DNA means for the long run.

Either way, the method is the same. I take your genes (if you have them), your symptoms, your labs, and your history, and read them together as one biochemical picture. What you get back is a practical plan with a timeline, not a generic handout.

I hold a PhD in nutritional science and focus on the pathways that are most often overlooked: methylation, transsulfuration, neurotransmitter metabolism, histamine regulation, mitochondrial energy, and nutrient absorption.

Common reasons people reach out Chronic fatigue with no clear cause · histamine intolerance or MCAS · POTS nutritional support · anxiety or low mood tied to nutrient status · MTHFR, COMT, or folate pathway questions · interpreting raw 23andMe, AncestryDNA, or whole genome data · joint hypermobility and connective tissue questions · medication and supplement reactions · a second opinion on an existing plan

How it works

  1. Complete the intake form. About 8 to 10 minutes: symptoms, health history, DNA data, lab work, goals, and budget. There is an "anything else" box where you can ask about sliding scale pricing.
  2. We confirm the right package. My assistant reaches out within 1 to 2 business days to confirm a package and explain next steps. No payment is taken until this conversation.
  3. I review everything before we meet. Genetic data, labs, and your intake get analyzed in advance, including full pathway analysis for whole genome sequencing cases.
  4. We meet by video. I share your genetic maps and pathway diagrams on screen, connect your genetics and symptoms to the pathways involved, and we build a phased plan: supplements, diet, botanicals, medication considerations, and contraindications.
  5. You get a written summary. A referenced PDF you can share with your doctor. Follow-up calls are included in most packages.
Already booked? Before your consultation, complete the symptom screeners that match your concerns. Your answers come straight to me and feed your report.

Consultation packages

Prices reflect the pre-consultation analysis, written materials, and included follow-up. Payment plans are available on every package.

Genetics Foundations

Healthy, curious, and already have DNA data

$400+

  • Review of the major genetic pathways from 23andMe, AncestryDNA, or whole genome data
  • Your choice from 20+ topic reports
  • Diet, supplement, and lifestyle recommendations
  • Written PDF summary
  • Does not include a symptom recovery plan

Symptoms Foundations

Symptoms, but no DNA data

$400+

  • Detailed symptom and pathway assessment
  • Video consultation on your health history
  • Root-cause hypothesis map
  • Diet, supplement, botanical, and lifestyle recommendations
  • Phased protocol timeline and PDF summary

Genetics + Symptoms Deep-Dive

Chronic or unexplained symptoms, with DNA data

$600+

  • Full genetic pathway analysis
  • Symptom-to-pathway mapping
  • Lab and medication review when available
  • Root-cause map and recommendations
  • Phased timeline and PDF summary

Full Transformation

All-in, 12 weeks of support

$1,200+

  • Everything in the Deep-Dive
  • Comprehensive nutrition assessment and custom nutrition plan
  • One follow-up session plus messaging support
  • Updated plan at week 8

Single services and add-ons

  • Lab interpretationPer panel, organized by pathway$85
  • Single medication or supplement reviewHow a specific product interacts with your genetics and current plan$50
  • PharmacogenomicsHow your variants affect medication and supplement responsesQuote
  • Full genomic readEvery pathway, every report, one sitting$600
  • Youth and teen nutrition consultGrowth, mood, focus, and eating patterns in young people$250
  • Second-opinion reviewAn existing diagnosis or treatment plan, read against your biochemistryQuote
  • Whole genome sequencing alignmentSurcharge for raw WGS data that needs alignment before analysis+$175
A note on pricing A limited number of sliding-scale spots open each month. Ask in the intake form or when my assistant reaches out. No application required.

Common questions

Is DNA data required?

No. I can work from symptoms, labs, and history alone, though genetic data adds precision. If testing would help, I'll point you to the most cost-effective options.

Is this the same as seeing a doctor?

No. I'm a PhD scientist, not a licensed physician, and I don't diagnose or treat disease. The goal is a referenced, actionable framework you can bring to your doctor.

What does a consultation look like?

Sessions are by video call. I share your genetic maps and pathway diagrams on screen as we go, and you receive a PDF summary afterward.

How long until the first consultation?

Typically 1 to 2 weeks after intake, longer for whole genome sequencing cases that need alignment first.

What if I'm not sure which package fits?

Choose "not sure" on the intake form. My assistant reviews every submission and adjusts the recommendation before anything is booked or paid.

Do you work with international clients?

Yes. Consultations are virtual. DNA export and lab testing options vary by country, and my assistant can help you sort that out.

Ready to get started?

Fill out the intake form. It takes about 8 to 10 minutes and is the first step toward a plan that's actually built for you.

Begin the intake form