+254 142 851 978 info@lupusfa.org Nairobi, Kenya
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For health professionals

The patients you are looking for are already in your clinic

Lupus is called the Great Mimic for good reason. Across Africa, diagnostic delays of five to ten years are common, and most of those years are spent in front of clinicians. Earlier recognition changes outcomes.

Recognise lupus

Consider lupus when a patient, most often a woman aged 15 to 45, presents with a constellation rather than a single complaint: arthralgia or arthritis, unexplained fatigue, photosensitive rash, oral or nasal ulcers, serositis, lymphadenopathy, recurrent low-grade fever, cytopenias or proteinuria.

The pattern that matters is symptoms that come and go, recur over months, and cross organ systems, particularly when a patient has already been treated for several unrelated diagnoses.

Diagnosis & referral

No single test confirms or excludes lupus. Diagnosis combines clinical features with serology and evidence of organ involvement, interpreted together and over time.

Where rheumatology access is limited, early referral still matters: it establishes the pathway before organ damage accrues. Urinalysis is one of the highest-yield, lowest-cost checks you can do at first suspicion.

Patient management

Treatment aims to control disease activity at the lowest effective corticosteroid dose, with antimalarial therapy as a backbone and immunosuppression or biologics where indicated.

Adherence in this setting is frequently a cost problem rather than a belief problem. Asking directly about affordability, distance and out-of-pocket burden changes what you learn.

What patients tell us

What would have helped, earlier

Our members consistently describe the same turning points. These are the ones clinicians control.

  • Being believed. Many patients are told they look well on the days they feel worst.
  • Someone joining the dots. Symptoms treated separately over years rarely get named.
  • Naming the possibility out loud. Saying “this could be autoimmune” starts the right pathway.
  • Explaining the treatment. Patients who understand why they take a medicine keep taking it.
  • Asking about mood. Depression is a recognised part of the picture, not a side issue.
  • Referring to peer support. It is free, and it measurably changes how people cope.

Ten years is a long time to live without answers. There is a particular kind of exhaustion that comes with knowing something is wrong and not being believed.

Faith Mukoya, Medical Laboratory Technologist and LFA Operations Manager

Work with LFA

  • Training & webinars. Sessions for clinicians, nurses, laboratory staff and community health workers.
  • Patient resources. Plain-language materials you can share in clinic.
  • Referral to peer support. Connect your patients to a support group near them.
  • The LFA professional network. Join clinicians engaged in improving lupus care across Africa.
  • Research collaboration. Contribute to building African lupus evidence.

Clinical partners we work with

Aga Khan University Hospital, Mater Hospital, Kenyatta National Hospital and the Nairobi Arthritis Clinic support lupus awareness, specialist rheumatology care and access to quality care. See all partners.

This page is an awareness summary for context, not a clinical guideline. Please follow current national and international clinical guidance and your institution's protocols for diagnosis and management.

One earlier referral changes a life

If you see patients who might have lupus, we would like to work with you. Training, materials and a patient community are all available at no cost.

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