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The Consortium at a glance

19+
participating clinicians and organizations
Across three tiers and a national advisory council, in 15+ states, with international educational collaboration.
5
target conditions under one root-cause standard
PMOS (formerly PCOS), endometriosis, infertility, recurrent miscarriage, reproductive-age endocrine disorders
4
charting systems represented
Chart Neo, Creighton, FEMM, Sympto-Thermal

Telehealth reach into all 50 states

plus DC and the US Virgin Islands, through a national telehealth practice, alongside multi-state member practices

Reproductive endocrinology at the table

The Advisory Council seats a reproductive endocrinologist who has practiced both conventional and restorative medicine.

100 percent clinic-owned data

Members keep control of their records; the Consortium sees only de-identified, agreement-governed extracts.

Member sites deliver multidisciplinary team-based care from one shared standard rather than one method. The Clinical Care Pathways define what must be assessed and treated; clinicians chart with whichever validated fertility-awareness system fits their training and their patient: Chart Neo, Creighton, FEMM, Sympto-Thermal, and others. Medical care and surgery sit inside the same pathway, and member sites include restorative surgeons trained at the field's founding institutions, performing excision of endometriosis, ovarian wedge resection, and microsurgical tubal repair, so conditions are treated at their root rather than managed indefinitely.

Here is what the Consortium builds, in order.

  1. Root-cause Clinical Care Pathways

    Standardized diagnostic and treatment pathways for the target conditions, written with the pilot sites and published openly, so a woman receives the same rigorous root-cause workup at any member site.

  2. Cycle-timed EMR/EHR Templates

    The Clinical Care Pathways encoded into the medical record itself: the prompts, the orders, and the observations that make up the workup, timed to the patient's own cycle and carried into each pilot site's own system, so the standard shows up where care is actually documented.

  3. Shared outcomes through the Data Commons

    Because the templates are structured, outcomes are captured once as part of ordinary care, standardized without anyone re-keying them, and pooled into a shared registry that member surgeons publish from. The NAVIGATE Data Commons below describes that layer and the terms it runs on.

  4. The Restorative Care Curriculum

    Competency-based training that gives a whole care team one shared clinical language: physicians and surgeons, nurses, dietitians, midwives, cycle-charting educators, and patient navigators. Curriculum and education standards are strengthened by international research and education expertise; RRM Academy operates delivery, from production and enrollment to continuing education, open to clinicians nationwide.

  5. Patient navigation

    Every patient who enters the network is offered a trained human navigator, drawn from the Consortium's cycle-charting educators and certified cycle coaches. Navigators teach a woman to read her own cycle, coordinate her care across the disciplines the model requires, and stay with her between visits and across pathway transitions, so the coordination work does not fall on the patient.

  6. A quarterly improvement cycle

    Every quarter the Advisory Council reviews the Clinical Care Pathways against what member sites are seeing. The pathways are versioned living documents: member clinicians propose evidence-backed revisions, and accepted contributions carry the contributor's name into the next version. Each year the Consortium recognizes member sites, in tiers, for faithful implementation, complete data, and ideas that move the field forward.

  7. Independent evaluation

    An evaluator from outside the Consortium studies results across every site: time to a root-cause diagnosis, symptoms and function, and what patients say about their own care. The people delivering the model do not grade it.

  8. An open toolkit

    A free implementation guide and the EMR/EHR templates themselves, published for any health system that wants to run the Clinical Care Pathways, membership or no membership.

  9. Getting it into the field

    Webinars, conference talks, and peer-reviewed publication, so the results reach both the literature and the clinicians who can use them.

A Center of Excellence stands on its evidence infrastructure. The Consortium runs on the NAVIGATE Data Commons: national data infrastructure purpose-built for restorative reproductive medicine, its core platform donated to the project, with the registry layer built and openly released by the program, and designed to feed the field's international outcomes registry.

Cycle-timed by design

Generic registries cannot represent the data that defines restorative care. This one is built for it: observations, laboratory results, and treatments indexed to the patient's own cycle, alongside validated patient-reported outcome instruments at intake and follow-up.

Clinic-owned, always

Each clinic keeps full ownership and control of its records. The Commons receives only de-identified, agreement-governed extracts under HIPAA-compliant data use agreements, and research activities proceed under IRB oversight.

Open standards, one evidence base

Built on open healthcare interoperability standards, so Consortium outcomes port cleanly into the field's international outcomes registry and strengthen a single shared evidence base instead of fragmenting it.

Turnkey for member clinics

Cycle-timed EMR templates and hands-on integration support come with membership, at no cost to the clinic. Sites start reporting structured outcomes without building anything themselves.

The Consortium spans 19+ participating clinicians and organizations across three tiers and a national advisory council, in 15+ states, with international educational collaboration, and reaches all 50 states by telehealth. The regions and anchors below map the member sites: six clinical pilot sites, two clinical network partners, and a research and education anchor.

Blank map of the United States, territories not includedAlabamaAlaskaArizonaArkansasCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaOhioOklahomaOregonPennsylvaniaRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahVermontVirginiaWest VirginiaWisconsinWyomingDistrict of ColumbiaDistrict of Columbia
Central Midwest
Ohio Valley
South
Southeast
West
Consortium reach: in-person care at member sites across five service regions, over nationwide member telehealth licensure covering all 50 states, DC and the US Virgin Islands. Sized dots count the clinicians serving each state through a member network's telehealth roster, from its public provider directory (July 2026).

Central Midwest

  • Clinical pilot site
  • Network partner
  • Multi-state telehealth

Ohio Valley

  • Network partner

South

  • Clinical pilot sites
  • Restorative surgery

Southeast

  • Clinical pilot site
  • Multi-state telehealth

West

  • Clinical pilot site

Research and education

  • Curriculum and standards strengthened by international research and education expertise
  • Research and education anchor
  • Clinician education

The regions above carry the member sites that deliver in-person care. Participants with no single regional catchment, including one national telehealth practice and the Advisory Council, are counted in the totals above and carry no region card.

Fields of expertise

The Consortium spans three tiers of membership plus an external Advisory Council. These are the fields of expertise those seats carry.

Tier 1

Clinical pilot sites

Six pilot sites

  • restorative reproductive medicine
  • restorative gynecology
  • endometriosis and advanced gynecologic surgery
  • male-fertility care
  • national and multi-state telehealth delivery
  • cycle-charting instruction

Tier 2

Allied network partners

Unfunded, in-kind

  • cycle charting education
  • nutrition and dietetics
  • nutritional therapy
  • midwifery
  • pelvic visceral manipulation and manual fertility therapy
  • gynecologic surgery
  • advanced gynecologic surgery
  • restorative clinical practice
  • allied restorative practice

Tier 3

Research and education collaborators

Open to researchers and educators

  • international restorative-medicine research expertise

Advisory Council

External expert seats

Seven seats, chaired by the Consortium's clinical director

  • research methodology and outcomes
  • reproductive endocrinology
  • international research
  • advanced gynecologic surgery
  • nutrition and allied health
  • restorative clinical practice
  • patient advocacy (seat held open)

Patients

Member clinics across the regions above welcome new patients, in person and by telehealth. Patient referral routes open here as member participation is finalized.

For Patients: See the member network

Clinicians and practices

Clinicians and practices that deliver root-cause reproductive care and want to adopt the Clinical Care Pathways, contribute outcomes, or join the training network.

Membership costs nothing. Members commit to the pathways, to outcome reporting appropriate to their tier, and to the Consortium's data-governance standards. Members who improve the pathways receive named credit in the revision their contribution ships in.

For Clinicians: Join the Consortium