Building toward early access  ·  2026  ·  Globally
Longitudinal health intelligence for women

The health record
Women's health
has never had.

And the evidence women's prevention has never had.

Most of what medicine knows about women's health was built on studies of men, with a small adjustment added on for sex. The rest treats a woman as an average, not as someone whose body changes over years. Ashwam is building two things at once — a longitudinal health record for each woman, and the evidence base that finally makes prediction models built on women's actual lives possible.

Across years, not snapshots
Built around her, not around averages
Midlife and after, not the reproductive years
Clinically defensible, not wellness-as-usual

The data asymmetry
at the heart of
women's health.

i.
Male physiology with a sex coefficient.
Framingham, QRISK, SCORE — every major cardiovascular risk model was validated on cohorts where women were under-represented, then adjusted for sex rather than rebuilt for women's biology.
ii.
Cross-sectional where trajectories matter.
Risk in women is a function of variability and drift from her own baseline, not her position against a population mean. The signal is longitudinal. The studies have not been.
iii.
Reproductive years only.
The 30-plus years across the perimenopausal transition and after — the longest and most biologically dynamic stretch of most women's lives — have been studied through a handful of single-snapshot research cohorts. For most of the questions that matter, there is no published evidence to find.
iv.
Population-homogeneous.
Risk models built on white European and North American cohorts systematically under-predict in South Asian, East Asian, African and diaspora populations where disease rates, onset ages and physiological baselines differ.
What Ashwam is building

One platform.
Two resolutions.

Ashwam is a longitudinal health intelligence platform for women. It operates at two resolutions on the same substrate. The same data infrastructure serves both — which is why building either alone would not work. The N-of-1 record is the training data women's health has never had. The evidence infrastructure is what turns it into prediction models women's prevention has never had.

Resolution I

The record built around her.

Five minutes a day builds an N-of-1 longitudinal health record that compounds across her whole life. Her own baseline. Her own drift. Her patterns, understood on her terms — not against a population average she was never represented in. The daily check-in connects to wearables, diagnostics, and clinical data she already has.

Live  ·  For every woman  ·  Available 2026
Resolution II

The evidence base for women's biology.

Millions of these individual records, with each woman's consent, become the evidence base women's biology has never had — covering the life stages, populations, and physiology that existing research has missed. From there: prediction models built on real women's lives, for cardiovascular risk, metabolic disease, cognitive decline, and the conditions that shape the post-reproductive years.

Under development  ·  Via consented research programmes  ·  Outcome-anchored

Each record is hers. The evidence is what it makes possible for every woman who comes after.

The questions a longitudinal record
of her biology would finally let us ask.

Midlife is where women's biology has been least well studied — and where the questions that matter most have been hardest to ask. Because the data that would answer them has never existed.

i.Observe
How do we observe the drift in insulin, cardiovascular, cognitive, and joint health over the years where the shift is actually happening?
ii.Intervene
Is there a way to surface these shifts early enough to intervene — and to identify the window where the right support would make the most difference?
iii.Enable
How can the new generation of wearables and biosensors help researchers better understand autoimmune disease and chronic inflammation in post-reproductive women?
These are the questions a longitudinal record of a woman's biology — built with her consent, governed for research — would let medicine finally begin to answer.
Platform maturity

A universal
Intelligence platform.

Ashwam is built to deepen over time. Each layer adds a new data slot to the same architecture; existing logic runs on richer inputs. No layer assumes data from the next. No layer requires code changes to the one before. A woman on the platform today benefits from every layer that follows, without interruption.

i.

Lived experience

Journaling  ·  QDG  ·  Symptom signal

Five-minute daily check-in across eight domains — body, mind, emotion, sleep, food, exercise, social, environment. The foundation the rest of the platform is built on.

Live
ii.

Wearable signal

HRV  ·  Resting HR  ·  Skin temperature  ·  Sleep architecture  ·  CGMs

Reads the actual signal from your device — sleep, heart rate, activity, skin temperature — measured against your own baseline, not a manufacturer's average score. Apple Watch first, then Oura, Ultrahuman, Garmin, Fitbit, Samsung.

Rolling out 2026
iii.

Blood & urine

Lipid  ·  Glucose  ·  Hormonal panel  ·  Inflammation

Lab results — when she chooses to add them — recalibrate her personal baseline. Raw values stay where they belong, in clinical and research systems; Ashwam sees only the derived signal.

In view
iv.

Genetic signal

Polygenic risk  ·  Pharmacogenomics  ·  Family history

Genetic risk context for each woman, integrated into the same architecture. Basic first, advanced later. Governed by distinct consent.

Building toward
v.

Emerging sensors

Smart jewellery  ·  Bio-textiles  ·  Therapeutic wearables  ·  Neuromodulation

Devices that capture or modulate signal in ways the mainstream wearable category does not yet. Ashwam reads their signal into the same longitudinal record.

Ecosystem-paced
vi.

Emerging diagnostics

Microbiome  ·  Saliva  ·  Breath  ·  Sweat  ·  Menstrual blood  ·  Joint markers

Diagnostics emerging across new substrates — body fluids, breath, structural imaging — at a pace the medical system has not yet adopted them. Ashwam folds their results into the woman's longitudinal record as they become available.

Ecosystem-paced

A deliberately
sequenced Evidence Engine.

The Ashwam platform is built for every woman — across every starting point, every population. The evidence programmes that will generate its prediction models are sequenced with intent.

The first programmes address women the founding cohorts left out — South Asian, African and African-diaspora, Latina, Middle Eastern, and Indigenous women — on the disease axes where every major risk model in medicine today systematically under-predicts. There are no large-scale longitudinal cohorts of perimenopausal cardiovascular and metabolic transition for these populations — no SWAN equivalent. Building this dataset is where the evidence sequencing starts, with South Asian women first.

Subsequent programmes extend — new populations, new disease axes, or both — as the platform, the evidence base, and the clinical partnerships mature together.

~3.16 billion women.

The evidence base does not have them.

Africa
770M
India
703M
China
690M
Southeast Asia
345M
Latin America & Caribbean
336M
Middle East & North Africa
225M
Global North — women understudied
~95M

Each bar shows the women whose biology and health trajectories are missing from the longitudinal cohorts that anchor women's health today. The Global North bar aggregates the women within the US, UK, Australia, and Europe who are similarly understudied — ~95M in total.

Most data is 2024 estimates from UN Population Division, World Bank, or national census authorities.

The cardiovascular gap  ·  South Asian women
5–10yrs
Earlier onset of cardiovascular disease in South Asians than in Europeans.
By the time existing risk models flag a South Asian woman as elevated risk, she has often already been at clinical risk for nearly a decade.
2–3×
Higher cardiovascular mortality risk than white European women, age-matched.
A South Asian woman of the same age and apparent health profile as her European peer carries materially higher risk that conventional clinical screening does not surface.
< 1%
Of the cohorts that built Framingham & WHI cardiovascular risk models.
South Asian women are statistically invisible in the foundational evidence base of modern cardiology — risk models that are still in everyday clinical use across Australia, the UK, and the US.
The metabolic gap  ·  South Asian women
23BMI
Type 2 diabetes risk threshold, where European-derived guidelines flag at 25–30.
Standard diabetes screening systematically misses metabolic risk in South Asian women because the risk thresholds were never calibrated for their physiology.
~3×
More visceral adiposity at the same BMI than European women.
South Asian women carry the "thin-fat" phenotype — more visceral fat (the kind that drives metabolic disease) at any given weight. BMI doesn't see it. The signal is in body composition and how it shifts over time.
2–4×
Higher gestational diabetes prevalence than white European women.
A predictor of long-term cardiovascular and metabolic disease that, in most of the world, is not tracked longitudinally beyond the postnatal six-week check.
Programme sequencing  ·  in view
Illustrative · detail follows
First programmes
Cardiovascular & metabolic health, South Asian women 35–55. Longitudinal cohort studies anchored to clinical outcome data, conducted with academic and clinical partners. Outputs include upstream risk-factor evidence and the first prediction models purpose-built for this population.
In motion
Adjacent axes
Bone, cognitive, and immune health across the perimenopausal transition, and cardiovascular and metabolic extension into other populations the founding cohorts left out. Building on the infrastructure laid by the first programmes.
Planned
Horizon
Healthspan prediction across the second fifty years. Integrated cardiovascular, metabolic, cognitive, bone, immune and reproductive risk across a diverse global cohort — the prediction infrastructure women's medicine has never had.
Building toward

Let's build the foundation
for women's health together.

Built around each woman — her biology, her baseline, her life. From a million such records — each held with consent, governed for research — comes the evidence base women's health has never had.

If you're building in women's health and your work belongs in this sensemaking layer,

Building toward early access  ·  2026  ·  Globally