You did the
DNA test.
Then what?
Most people never find out. The report arrives, it's overwhelming, and it goes in a drawer. We take that genetic data, verify it against your real-time metrics, and turn it into one thing you can actually use: a formula mapped to your genome and made for you.
in practice
London doctorates
question
A genetic report is a map. Nobody was giving people the route.
For a decade at the clinic, the same thing kept happening. People arrived having taken a genetic test — 23andMe, Ancestry, a private genomic panel — and they had no idea what to do with it.
It wasn't their fault. A raw genetic report is a hundred pages of variants and probabilities written for scientists, not for the person who paid for it. So it did what those reports almost always do: it went in a drawer. The single most information-rich thing about their biology, unused.
Your genome tells us what's possible. Your day-to-day data tells us what's actually happening.
That's the part nobody was joining up. A gene only matters if it's actually under stress and expressing itself — and you cannot see that from the DNA alone. But cross-reference the genome against someone's real-time metrics — their wearable trends, their glucose data, their bloods — and the picture sharpens immediately. The data shows you which genes are putting strain on this person's ageing right now, not just which ones theoretically could.
And underneath all of it, the same driver kept surfacing: inflammageing — the slow, systemic rise in the body's inflammatory baseline that sits upstream of almost everything we associate with biological decline.
The genetic test was the starting point. Everything else was how we'd verify it. What was missing was the thing at the end — a way to turn all of it into something you could actually take.
Paid for, delivered as a hundred-page PDF, never acted on. The richest data about your biology, doing nothing.
A variant only matters if it's actually expressing itself. DNA alone can't tell you that — it tells you what could happen, not what is.
Wearables, CGM, blood markers — these confirm which genes are genuinely under stress in your body, today. The genome becomes actionable only when it's read against them.
All that data should lead to one place: a formula made for you. That endpoint is what was missing — and it's what we built.
From the test in your drawer
to a formula in your hand.
Most of our members already hold piece one: a genetic test they've taken and never used. The richest map of their biology in existence, sitting unread.
What had never existed was a method to make that map actionable — to verify it against a person's real-time metrics so you could see which genes were genuinely under strain, then turn that into a single physical intervention calibrated to them specifically. Not to a population average. To one person, as they are right now.
AI-assisted analysis made that precision possible for the first time. So they built it.
Biokonstra® is the result. It begins with your genome, verifies it against your own data, and ends with one thing you can actually take — reviewed by a named practitioner and compounded individually in an ISO-7 cleanroom.
Your genome
The map. Your genetic test, parsed once and read across all thirteen inflammatory systems — the full picture of what's possible in your biology.
Your real-time data
Wearables, CGM, blood markers. These confirm which genes are actually under stress and expressing themselves right now — turning the map from theory into something specific to you, today.
One formula, made for you
Everything resolves into a single botanical formulation — mapped to your genome, verified by your data, dosed to you, signed by a clinician, compounded in an ISO-7 cleanroom. The destination the whole process exists to reach.
Dr Abigail El-Doueik — the clinician who discovered what medicine couldn't offer by running out of it herself
Dr Abigail El-Doueik has spent her career at the edges of what medicine can do — which is precisely how she learned where its limits are.
She started in emergency medicine at sixteen, working as a nursing assistant in A&E before most people have chosen what to study. She trained as a nurse at the University of Wales Cardiff, then moved to the Adult Intensive Care Unit at the Royal Brompton — one of the UK's foremost cardiac centres — caring for the most critically unwell patients on the ward. Working at that edge made her want to go further: she read medicine for six years at King's College London, took an intercalated BSc in Immunology, and kept working ICU shifts throughout.
Training through the Oxford Deanery and working acute and emergency medicine at the Royal Berkshire, her thinking began to shift. A single session of acupuncture produced an effect she couldn't explain away — and didn't dismiss. She trained in it formally, and when members started asking about herbal medicines and supplements, she filled the gap the way a serious clinician does: systematically, through the Institute for Functional Medicine.
Then in 2012, she burned out. Significantly. The system she had given everything to offered her what it offers most people in that situation: a prescription and a suggestion to slow down. She declined both.
She recovered fully — not with pharmacology, but with botanicals, movement and a complete nutritional overhaul. That outcome was not lost on her as a clinician. She had trained at one of the UK's best cardiac hospitals and qualified at King's, and what restored her had come from outside the prescription pad. Not by chance — by mechanism. She left the NHS to build something that understood why.
Outside the clinic she grows her own fruit, vegetables and herbs using organic methods, and is completing her RYT200 yoga teacher training — the same conviction running through everything she does: that what the natural world produces, used precisely, is rarely improved upon by replacing it.
Dr Abigail El-Doueik
Pharmakopoeia Laboratories Ltd
Haytham El-Doueik — the herbalist who watched it happen and spent twenty years finding out why
Haytham El-Doueik's relationship with plant medicine began in Lebanon in the early 1990s — long before he had any scientific language for it.
He trained under a medical herbalist, worked the land, and built a workshop where he learned to extract, distil and formulate compounds from raw plant material. It was an apprenticeship in a tradition that predates modern pharmacology by centuries, and it gave him something a laboratory education rarely does: an intuition for what plants actually do. Back in England, he formalised it with a diploma from the Tisserand Institute — then the most rigorous aromatic-medicine qualification in the UK.
Then came the moment that defined the next twenty years. Through that work he began collaborating with the Immune Development Trust, applying botanical compounds in a clinical setting with HIV-positive individuals at Charing Cross Hospital. He could see these compounds doing something meaningful in people whose immune systems were seriously compromised. He could not explain it — and that gap was intolerable. He needed the mechanism.
He took a foundation year in sciences at the University of East London to qualify for a science degree, then read Immunology at King's College London, then a PhD in Medicine focused on vaccine development and HIV immune response. He wasn't taking the conventional route into academic science — he was reverse-engineering his way to an explanation for something he had already seen.
Then Oxford. His postdoctoral research — first in Pharmacology on inflammatory burden in HIV, then in Oncology with plant-derived compounds — was where the question finally became an answer. He watched, in real time, what happened to live human immune cells when herbal extracts were introduced to them.
He watched them change. The cells that drive inflammation shifted. The cells that regulate and resolve it increased. A human immune system — in live blood, in a laboratory — responding to botanical compounds in a way that was measurable, repeatable, and real.
The herbalist had been right all along. He now had the science to explain exactly why.
Haytham El-Doueik
Pharmakopoeia Laboratories Ltd
Two paths. One conclusion. One thing to build.
They founded the Integrated Immunology Clinic London together. Over the following decade, one pattern kept repeating: people arrived holding a genetic test they'd never been able to use, and underneath it, a quietly rising inflammatory baseline driving the decline unaddressed.
Everyone else hands you a report — or worse, a to-do list. Nobody was building the one thing that actually helps: the formula at the end.
A genetic test that stops at a PDF is a map with no destination. A wellness app that turns your results into meal plans and workouts is just homework by another name. What was missing was the method to read the genome against a person's live data, find the real leverage points, and turn them into a single formulation calibrated to that one person — checked for safety against their own genetics and medications first.
AI-assisted analysis made that precision possible. They built Biokonstra to do it.
Every protocol starts with your data.
Every batch ends with a clinician's signature.
AQ — the analysis
AQ reads your genome, wearable data and biomarkers across all thirteen inflammatory systems simultaneously — not as thirteen separate reports, but as one connected picture. It finds the leverage points. It flags the safety stops. A practitioner then reviews everything and makes the call.
Konstra — the liaison
Konstra handles the admin so your practitioners can focus entirely on the science. Scheduling, updates, reorders — all through Konstra. Any health question goes directly to your practitioner, who responds in their own name. Every time.
Bio-Vault — your data
Your genomic profile, biometric exports, audio briefings and formulation records, held securely. Anonymised by design. Never used to train any public model. If you leave, your data leaves with you — or is deleted in full within 30 days.
This is not for everyone.
It might be for you.
We compound one formula for one person at a time. That caps how many members we take on — deliberately. If you're after a quick fix or a subscription you'll forget you're paying for, this isn't it. If you want precision, the waitlist is how you raise your hand.
By referral and waitlist only · Members, not patients