Live data · Updated Feb 2026

OpenWillMy biology, open-sourced.

Genome. Bloodwork. Protocols. Published openly with the reasoning behind every decision.

Explore the DataSee Protocols

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blood markers — what your annual physical checks

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to assess your entire biology

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of healthcare spending goes to chronic disease

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genetic variants checked at your last physical

The Problem

“Half the population carries a genetic variant that changes how they process basic vitamins and common medications. Almost none of them know.”

A $200 DNA test told me more about my biology than 30 years of doctor visits. Not because my doctors were bad — because the system isn't built to look.

The system

You get 15 minutes. Your doctor guesses based on population averages. The supplement aisle treats everyone the same. Meanwhile your genome — the actual instruction manual — sits in a database nobody checks.

The fix

The tests exist. The research is published. The tools are here. Nobody connects them for you — so I did it myself and I'm sharing everything. No gatekeeping. Just data.

Results

The data so far.

3 months on protocol. Nothing cherry-picked. Every biomarker downloadable.

-71%

hs-CRP

Inflammation marker. 3 months on protocol.

+78%

Vitamin D

Deficiency identified by bloodwork. Corrected.

+17%

Testosterone

No TRT. Genetically informed protocol.

What's Different

Guessing vs. knowing.

Guessing
Knowing

Trust me bro

Here’s my genome

Paid course ($997)

Free download (JSON/CSV)

Cherry-picked results

131 biomarkers, unfiltered

No genetic context

Every protocol gene-matched

Anecdotes

Published research linked

Timeline

Still collecting.

Sep 2024

23andMe raw data export

Discovered compound heterozygous MTHFR: C677T + A1298C

Oct 2024

First comprehensive bloodwork

131 biomarkers. Baseline established.

Nov 2025

Protocol begins

Methylfolate, B12 injections, targeted supplementation

Feb 2026

Second bloodwork

hs-CRP down 71%. Vitamin D up 78%. Published here.

May 2026

Third comprehensive bloodwork

6 months on protocol. Full panel. Results published live.

This dataset grows every quarter.

Open Data

Public Health Dashboard

Genetics

178 variants

178 variants from 23andMe raw data. Interpreted against ClinVar, PharmGKB, and published literature.

Explore

Bloodwork

131 markers

131 biomarkers tracked over time. Filterable by blood draw date. Exportable as JSON or CSV.

Explore

Protocols

Open source

Every compound, dose, route, schedule, and genetic reasoning. All prescribed and supervised.

Explore

Stop guessing. Read the manual.

One person's full dataset. Published openly. Not because you should copy it — because you deserve better information.

Approach

Four rules. No shortcuts.

01

Test everything

If you can’t measure it, you’re guessing. 131 biomarkers, not 20.

02

Read the papers

Every protocol decision traced to published research. Not influencer bro-science.

03

Show the receipts

Full transparency. Every compound, dose, and genetic reasoning — published openly.

04

Work with a team

Licensed physicians, DEA-certified pharmacy, genetic counseling. Not DIY.

No gatekeeping. Just data.

Start Here

What are you looking for?

Whether you're just curious or deep into your own data, there's a path in.

01

“What should I actually be taking?”

Start with genetics. See how DNA variants change which supplements, medications, and protocols actually work for a specific body.

View genetics

02

“How do I know if it's working?”

Start with bloodwork. 131 biomarkers tracked across two draws. Filter by date. Download everything. See the before and after.

View bloodwork

03

“Show me exactly what you're doing.”

Start with protocols. Every compound, dose, route, and schedule. Each one mapped to a genetic variant or biomarker target.

View protocols

Newsletter

The Manual

One email per week. One deep dive into genetics, bloodwork, or protocols. No fluff. No selling.

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