Jennifer Little-Fleck explaining a client's genomic results during a private session
You've Built a Life You Want to Keep

Now make sure your body can keep up with it.

Everyone should understand how their own body works. It is the key to optimizing your health and longevity. A comprehensive genomic test, read and explained to you personally.

You, explained.

Take the Biological Patterns Quiz → See What's Included

Ready now? See your options. Prefer to talk first? Book a consultation.

✓ ~1,000 genes + core pharmacogenomics ✓ At-home saliva collection ✓ One test, a lifetime of answers
Why Now

No one has had the time to really look. Until now.

More than ever, physicians have less time with each patient than they want. A twelve-minute appointment cannot investigate how your body is built; that is not their fault, and it is not their job. It is mine. I do the deep reading, and your physician gets a clear document instead of guesswork.

"Everything came back normal."

Normal is a population range, and it is wide. You can sit at the bottom of it, feel exactly as you feel, and still be told there's nothing to discuss.

"It used to work."

The training, the diet, the sleep routine: the things that carried you through your forties stopped delivering, and nobody has told you what changed.

"It runs in my family."

You think about it more than you say out loud. What you don't know is which parts you actually inherited, and which ones skipped you entirely.

Nobody has ever looked properly. Not at all of it, at once, with time to think about it. That's the thing money has never reliably bought you. It's what this is.

The Questions You Already Ask

You've been asking these your whole life.

Most of them have an answer written in your biology. Here are a few your results can speak to.

"Why do I wake at 3am even when I go to bed exhausted?"

Sleep & Recovery

"Why does one coffee keep me up all night when my friend sleeps after espresso?"

Metabolism & Food Response

"Why did that medication do nothing for me when it works for everyone else?"

Pharmacogenomics

"Why do I gain weight on the exact diet that works for my sister?"

Metabolism & Food Response

"Why does stress hit me physically when others seem to shrug it off?"

Brain, Mood & Stress

"Why do perfumes and cleaning products bother me so much?"

Cellular Defense & Clearance

"Why do I feel worse after taking B vitamins?"

Nutrient Processing & Methylation

"Am I actually getting anything from these supplements?"

Across Every System

These aren't hypothetical. Each one maps to a specific section of your report, and the program walks you through reading it yourself. See the full list of questions →

Just As Important

Where the line is.

Every company in this space implies the test answers everything. It doesn't, and you deserve to know exactly what you're getting before you spend a dollar.

  • Your reports do include predisposition results: inherited tendencies across many areas, some of them health conditions. You'll see them, and you'll see them explained.
  • A predisposition is not a prediction. "Increased" means your inherited baseline sits above average for that pattern. It does not mean you will develop anything. Most outcomes are shaped far more by environment, behavior, age, and chance than by any single variant.
  • This cannot diagnose you, but it can absolutely show tendencies and sensitivities that contribute to how you feel. If you carry slow histamine genes and aged cheese or chocolate reliably makes you unwell, that connection is real and it will be in your results. Diagnosis is still your physician's; explanation is often mine.
  • This is not clinical genetic testing. If you have a significant personal or family history of an inherited condition, the right first step is a genetics professional, not this panel.
  • What medication to take, or at what dose, is your prescriber's decision. Your pharmacogenomic results are information to bring to that conversation; never a reason to change or stop anything on your own.

Some results land heavier than others. When one of yours does, I'll say so plainly, and I'll tell you when it's worth taking to your physician, entirely at your own pace.

What You Actually Get

A test, and someone to walk you through it.

The test is the easy part. You understanding it is the product.

The test kit laid out: box, start-here instruction card, saliva collection tube, biohazard bag, and prepaid return mailer
What arrives at your door
Hands sealing the prepaid return mailer at a kitchen table, with the opened kit and collection tube nearby
Collected at home, returned by mail
01

The Test

A comprehensive panel of roughly 1,000 genes, including core pharmacogenomics. At-home saliva collection, returned by mail.

02

Your Reports

A private portal organizing your results into body systems you can actually navigate, plus your written summary and system cheat sheets.

03

The Program

A guided walkthrough of your own results, section by section, live with me each week. Bring your questions and your report; we work through them together. Prefer privacy? The whole thing can be walked through one to one instead of in a group.

04

The Community

Three months included with the group program, six months with the private. Live teaching, lab-result literacy, and open Q&A so you keep going after the reports make sense.

How the teaching works

Live now. Your choice soon.

Right now, all teaching happens live: we meet each week and work through your systems and your actual results together. The recorded version is being built now; soon you will choose to learn from the recordings on your own schedule or keep it live. Either way, live time with me stays focused on your questions and your results.

Where it gets interesting

Your genes are half the story. Your labs are the other half.

I don't stop at your DNA. Where you have bloodwork, I read it next to your genetics; that's where the useful answers live. Genes that say you'd respond well to a change, sitting beside labs that say the change is worth making, tell you something neither one could tell you alone.

Inside the Reports

See exactly what arrives.

One system, start to finish: the gene, the explanation, the recommendation, the cheat sheet. You get both: a portal that never closes, and a summary I write and discuss with you personally. Every other system goes equally deep.

In your portal, always on
The portal's nutrition grid: cards for Vitamin D, Vitamin C, Protein, Fats and more, with the B Vitamins report open listing seven results from optimal to moderate
Close-up of the portal's B Vitamins card: 16 variants, 83 percent enzyme activity
Written and walked through with you
A page of Jennifer's own methylation and detox summary: a plain-language big-picture paragraph, then a gene table showing each gene, her variant, its tier, what it means for her, and her action steps
"Why do I feel worse after taking B vitamins?" B Vitamins · Folic acid tolerance: Low 16 variants assessed
"Why doesn't my sister's diet work for me?" Low Fat Diets · Great Fit Matched against your metabolism
"Why am I hungry an hour after eating?" Hunger & Fullness · 9 variants Your appetite signaling, mapped

Real result labels from the portal. Yours will be your own.

Your portal holds 39 report sections and 830 individual results: everything the lab can tell you. The part I write is what tells you which of it matters: your Personal Overview with every program, or the complete gene-by-gene reading with the You, In Full Program.

What Gets Covered

Your portal, in plain English.

These are the actual sections you'll open when your results arrive, named the way you'd ask the question, not the way a lab would file it.

How My Brain Is Wired

Focus, mood, drive, stress chemistry, and resilience. 11 report panels.

How My Body Sleeps

Your circadian window, sleep depth, and how you actually recover. 4 report panels.

How My Body Cleans My Cells

Clearance and repair: the real biochemistry behind "detox." 15 report panels.

How My Hormones Are Wired

How you make, convert, and clear your hormones. 8 report panels.

How Food Affects My Body

Caffeine, alcohol, carbohydrates, fats, and the nutrients you use well. 11 report panels.

How My Immune System Works

How you defend, inflame, and recover, and what sets your reactions off.

How My Heart and Blood Vessels Perform

Lipids, pressure, and the long game of vascular health. 5 report panels.

New in this panel

How I Respond to Medication

How you personally metabolize common medications: the one thing a consumer DNA kit genuinely cannot tell you. Information to bring to your prescriber.

In the You, In Full Program

Other Genomics

30 further reports and 183 additional markers, included with You, In Full. Immersion members can unlock this section separately whenever they want it.

Where it all lands

Your Supplement Summary

Every recommendation across every system, gathered in one place, so you're not cross-referencing eight reports at your kitchen table.

Behind those sections sits a Lifestyle library of 33 further reports (sleep, micronutrients, fitness, weight, longevity, emotional health, and more) and 830 individual results in total.

Which is exactly the problem. Nobody can read 830 results and know what to do on Monday. That's what the report I write for you is for.

The Part Your Doctor Will Actually Use

You'll carry a card that tells any prescriber how you metabolize medication.

Pharmacogenomics, in plain English: how your genes shape the way your body handles medication. How quickly you clear it, how strongly it hits, and why the same dose can act so differently from one person to the next.

Most of what genomics tells you is interesting. This part is immediately useful, and it's the one thing a consumer DNA kit genuinely cannot produce: real pharmacogenomic testing needs true genotyping and curated star-allele calling, not an array.

You get a wallet card and a document written for your physician. Next time someone reaches for a prescription pad, you have something to hand them that speaks their language.

Information to bring to your prescriber; never a reason to change or stop a medication on your own.

Optional · Coming Soon

And then you can stop buying bottles.

Once you know what your body actually needs, we can compound exactly that, and nothing else.

The usual version of this is thirteen bottles on a shelf, a handful of capsules every morning, and a nagging suspicion that half of it is doing nothing. You researched it yourself, you're paying retail for each one, and most of what you swallow is filler.

We can make one formula instead. Your recommendations, compounded to your doses, by hand in a clean room. No fillers, no machines, no guessing at what to buy. When your labs change or your life changes, the formula changes with them.

  • No research. Your results already decided what belongs in it.
  • No filler. Only the actives, in the forms your genetics call for.
  • Not a handful. Seven ingredients can come out as roughly one capsule.
  • Not fixed. Adjust the formula whenever your picture changes.

Entirely optional, and never a condition of any program. The point of the test is understanding how you're built. This is just what becomes possible afterward.

How This Compares

Testing is everywhere now. Understanding is not.

That more companies now offer genetic testing is good news: the science is real, and the world is catching up. The difference is everything that happens after the sample.

A consumer DNA kit A clinical risk panel The Genomics Company
What it reads A few hundred thousand array positions, built for ancestry One to two hundred genes, focused on inherited disease risk Roughly 1,000 functional genes across every body system
Pharmacogenomics Not reliably possible from array data Sometimes, as an add-on Core pharmacogenomics, with a wallet card and a physician document
What you receive Raw data and generic reports A results PDF, and a referral if something is found A portal with 100+ reports, your written summary, and a program
Who explains it to you Nobody A counselor, if you call Jennifer, personally. At least one private session in every program
What happens after You search the internet You are referred out You are taught until you can read it yourself, and future reports unlock from the same sample

A test should never be the end. It's only ever the beginning.

Ways to Begin

Two ways to have it explained to you.

Both include the full ~1,000-gene panel, your pharmacogenomic card, the portal with all 100+ reports, and private time with me. What changes is how much of it I read for you, and how deep we go.

The Genomics Immersion

A group program, private if you prefer. Understand your results as deeply as you like.

$2,950

One-time · payment plans available

  • Comprehensive ~1,000-gene panel + core pharmacogenomics, with your prescriber card
  • Private portal with 100+ reports, recommendations built in
  • You never test again. New reports (preconception, peptides, muscle and bone) unlock from the same sample later for a small fee
  • Your Personal Overview: your priority findings by system, written for you
  • One private 90-minute session with Jennifer walking you through what matters and what to do
  • Morning and evening supplement formulas built from your results, plus a list of what you can stop taking
  • Systems teaching, live each week for now; recordings are coming soon so you can learn on your own schedule
  • The Other Genomics section (30 further reports and 183 extra markers) available to unlock separately
  • Weekly live sessions and three months in The Genomics Lounge; $47/month afterward
Get Started · $2,950 →

Klarna and installment options available at checkout.

The Complete Reading

You, In Full

The private program

Every gene, every system, read and explained personally.

$6,500

One-time · payment plans available · limited each month

  • Everything in the Immersion
  • Your complete gene-by-gene reading: all ~80 curated genes, what each one means for you, and what to do about it
  • Up to three years of your bloodwork read alongside your genes; trends over time say more than any single panel
  • Three private 90-minute sessions with Jennifer, one per area of your biology
  • A written document for your physician: what to ask, what to check, and why, in language built for the appointment
  • Your first supplement formula built by Jennifer, and your current shelf checked against how you metabolize your medications
  • The Other Genomics section included: 30 further reports and 183 additional markers, which Immersion members pay separately to unlock
  • A follow-up session once you've lived with it
  • Six months in The Genomics Lounge; $47/month afterward
Begin the You, In Full Program → Speak With Jennifer First

Klarna and installment options available at checkout.

More Than One Of You

Families & couples

Test one person and you learn what they carry. Test two or three and you can see where it came from, which changes what everyone does about it.

Couples, parents and children, adult siblings, or three generations.

From People Who've Done It

What actually changed for them.

★★★★★
I'd Tell My Past Self to Start Sooner

I was surprised by how much my genetics could explain about my body's needs and how everything connects. The Methylation and Detox class was my biggest aha moment: it helped me connect how genetics affect detox, inflammation, nutrients, and supplement needs. Some of it is naturally technical, but Jennifer made it understandable and practical. I feel informed, confident, and empowered instead of guessing what my body needs.

K
Kelly Smith
Genomics Immersion Graduate
A Huge Unlock

It was extremely confirming. I understood my body, but confirming it was rooted in my genetic code being expressed was a huge unlock. I'm more consistent with my supplements now and back to running again. I had a blast with it, and it's something high-level clients would love.

A
Andrew
Genomic Report Client
★★★★★
I Finally Understand Myself

What surprised me most was finally being able to understand everything. I always thought something was "wrong" with me: too sensitive, too reactive, too intense. My genomic results reframed it all: this is my design, not a defect. Jennifer helped me see what those genes are built for, and how to adapt to today's world without losing myself in it. I don't just feel healthier. I feel free to be me.

T
Tabitha H.
Director of National Accounts
Who Teaches This

I read the science for a living.
Now I read it for you.

Thirty years in research and medical writing. Over 2,000 people taught. I built this panel and the way it's explained because the reports everyone else hands you are technically correct and completely unusable. My job is to make your biology make sense to you.

More About Jennifer →
For the Professionals Who Look After Them

Your clients already ask you how they should feel.

Physicians, coaches, trainers, and advisors: your clients bring you their energy, their stress, and their sleep, because you are the one they trust. This gives you something genuinely new to put in front of them, it makes you the one who found it, and it sends them back to you better informed. Diagnosis stays with their physician; explanation is my job.

How Working Together Works →
Good to Know

Common questions.

How is this different from 23andMe?
Two ways. First, coverage: a consumer kit checks a few hundred thousand positions on a genotyping array; this panel covers roughly 1,000 genes chosen for how they function, plus core pharmacogenomics, which consumer raw data genuinely cannot do reliably. Second, and more importantly: 23andMe hands you data. This hands you an explanation, and a program that walks you through your own results until you can read them yourself.
Do I need any background in science?
None. The entire program assumes zero background. That's the whole point: explaining this clearly is what I do.
Is this medical care?
No. These are educational programs grounded in functional genomic interpretation. They are not a substitute for diagnosis or treatment by your physician, and they aren't meant to be. Many clients bring their results into conversations with their own providers.
Is the teaching live, or recorded?
Right now, it's live: a scheduled session with me each week where we work through your systems and your actual results together. Recorded versions of the teaching are being built now; once they're ready, you'll choose to learn from the recordings on your own schedule or keep it live. The goal never changes: you leave each week genuinely understanding that system or pathway, not just having heard something about it.
Do I have to book a sales call before I can buy?
No. Everything you'd learn on a call is on the What's Included page: the panel, the science, the limits, the privacy terms. If something still isn't clear, a consultation is there. If it is clear, just start.
What if I already have 23andMe or Ancestry data?
Start with the free Raw Data Course. It teaches you how to download your file, what it can honestly tell you, and, just as importantly, where it will mislead you. No purchase required.
How long does it take?
Your kit ships as soon as you order, the saliva collection takes about five minutes at home, and your results appear in your portal a few weeks after the lab receives your sample. The program is self-paced from there.
Will my genetic information stay private?
Yes. Your data lives in your private portal. It is not sold, not shared with insurers, and not used for research without your explicit consent. You can download it or request deletion.
Ready When You Are

Find out what you're actually working with.

One test, read and explained to you personally. Then you can stop guessing about the one system you can't afford to guess about.

Get Started → See What's Included

Still deciding? Book a consultation.