Podcast “Seriously!”: Aydah Abu Eliem on living with a rare disease
A conversation with ORDA’s president on her personal experience of a rare disease, stigma, and a national rare-disease registry.
Read more →ORDA helps people living with rare diseases and their families connect with those who understand what they face, links them with specialist doctors and supporters, and welcomes every partner who wants to help.

Join for free and ask to be connected with a specialist, a service or a supporter.
Ask for support →Join our network of partner specialists and help a patient looking for someone who understands their condition.
Join the network →Support or sponsor a patient: tests, treatment, devices or surgery — transparently followed up by ORDA.
Become a supporter →A rare disease affects a small number of people compared with the general population. Each is rare on its own, but together they touch millions of lives worldwide.
Learn about rare diseasesThree areas we work on every day to ensure a better life and comprehensive care.
Workshops with specialist partners, remote psychological support, and safe patient-to-patient channels supervised by professionals.
Lectures, workshops, booklets and videos featuring specialist doctors and patients sharing their experience.
Agreements with labs and centres for discounts, free physiotherapy and psychological sessions, and referral to specialists.
A patient reaches us with a request; we assess the need and connect them with the right doctor, lab or centre — or with a donor who funds treatment or sponsors the case — and we follow up until it is done.
The latest from ORDA and our upcoming events.
A conversation with ORDA’s president on her personal experience of a rare disease, stigma, and a national rare-disease registry.
Read more →An episode on the causes of rare diseases, consanguinity, genetic testing and the diagnostic odyssey, referring patients to ORDA.
Read more →An interview with ORDA’s president Aydah Abu Eliem and Dr. Eman Al-Massad on missing national data and the long road to diagnosis.
Read more →
Diagnosed with scleroderma in her mid-thirties, the disease reached her lungs. She found her way through treatment and a new way of living, then founded ORDA so that no one faces a rare disease alone. Her story appears in the Scleroderma International Organization’s 2025 book.

We are The Organization for Rare Disease Awareness (ORDA) in Jordan, the first organization of its kind in the Middle East and North Africa, established on September 29, 2024.
We work to support patients with rare diseases and their families, and to raise awareness among healthcare providers and in the community to ensure a better life and comprehensive care for them.
More about ORDA →Choose the membership that suits you.
We welcome questions from patients, families, doctors and organizations wishing to partner or support.
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Sponsor a patient, offer your expertise, or join our supporters network — every contribution shortens a family’s journey.