Features
Jiyoma brings together peer support, symptom organization, and research participation for women managing fibroids. The platform is intentionally focused on fibroids, not general cycle tracking.
A moderated, anonymous-first space for women to ask questions, share stories, and find support without feeling exposed.
Surfaces stories, tips, resources, event reminders, and community conversations based on member interests and fibroid journey stage.
Focused spaces for newly diagnosed members, heavy bleeding, pelvic pain, fertility, post-surgery recovery, nutrition, menopause, and emotional wellness.
Q&A posts, polls, advice requests, bookmarks, replies, and topic tags make practical answers easier to find again.
Virtual and in-person events can include doctor Q&As, Fibroid 101 workshops, nutrition sessions, support circles, and surgery-prep conversations.
Plain-language articles, guides, videos, infographics, and peer tips help members understand fibroids without sorting through scattered information.
Anonymous posting, reporting, community guidelines, moderator review, and medical-content boundaries help keep the space supportive.
Tools for turning daily symptoms, cycle changes, treatment notes, and lifestyle patterns into organized information for self-advocacy.
Log the day quickly with wellness, pain, bleeding, medication, cycle, notes, and reminder prompts.
Capture overall well-being, bleeding and cycle updates, physical symptoms, emotional well-being, lifestyle factors, treatments, and notes.
Record medications, supplements, heat therapy, appointments, procedures, side effects, and recovery details in one place.
Summaries can highlight logged patterns across pain, bleeding, mood, sleep, hydration, cycle timing, and treatment use. Insights are observations, not diagnoses.
Premium reports are planned to summarize symptoms, cycle maps, pain patterns, treatments, lifestyle factors, notes, and flagged concerns for appointments.
A planned AI assistant that helps explain logged patterns, suggest relevant resources, and prepare questions for provider visits without replacing medical advice.
Consent-based research participation that lets members understand what they are sharing, why it matters, and how they can opt out.
Short 1-3 minute surveys and symptom snapshots can help researchers learn from real lived experience with less friction.
Members can see contribution counts, surveys completed, studies supported, consent status, and how shared data is being used.
Optional deeper studies can track symptoms, treatment outcomes, fertility experiences, hormonal patterns, and pain pathways over time.
Plain-language summaries, community briefs, partner studies, and findings help research come back to the people who contributed to it.
Every study should explain what is required, what data is shared, who receives it, how it is protected, and how a member can withdraw.
Jiyoma is designed to support universities, clinical researchers, public health organizations, and health systems with ethical aggregate insights.
Access Model
Basic community feed, select groups, select events, general educational resources, daily check-ins, and limited history.
Unlimited history, deeper analytics, reports for care visits, premium groups, expert-led sessions, and planned Jiyoma Guide access.
Expanded research library access, study reports, researcher-verified content, early findings, and optional biomarker-kit participation.
Aggregated, de-identified datasets, cohort analysis, survey deployment, dashboards, and research partner support.
Jiyoma supports tracking, education, community, and research participation. It does not diagnose conditions, prescribe treatment, or replace a licensed healthcare professional.