COMING SOON
The Elora app brings personal symptom tracking, a flare diary, and your self-assessment results to one private, beautiful space.
No spam. We will only contact you about the app launch.
WHAT IS INSIDE
Everything the website cannot do. Because some things need to be personal, private, and longitudinal.
Track pain, swelling, fatigue, and mobility day by day. See patterns emerge over time. Bring real data to your next appointment.
Record what triggered it, how long it lasted, and what helped. Over time you will know your flares better than any clinician can.
The full Lipedema self-assessment, beyond the preview on the website. Your stage, your type, your personalised next steps. Private to you.
Track your measurements over time, with optional photo documentation. A private, chronological record that belongs to you.
WHY ELORA
Not a generic symptom tracker with Lipedema added as a tag. Every feature is built around how this condition actually behaves.
Your data is your data. Nothing is shared, nothing is sold, nothing is used to target you with anything. That is not a feature. It is the baseline.
The women who shaped what Elora built are women with Lipedema. Their experience is in every feature decision.
GET A TASTE
The website shows the first three questions of the self-assessment tool. The full assessment, your personalised stage result, and your next steps are in the app.
QUESTION 1
Do you have disproportionate fat distribution in your legs or arms that has not responded to diet or exercise?
QUESTION 2
Do you experience pain, tenderness, or heaviness in the affected areas?
QUESTION 3
Do you bruise easily in the affected areas, sometimes without an obvious cause?
Waitlist members get early access, help shape the features, and hear about the launch before anyone else.
No spam. Unsubscribe any time.