Sign a petition
Add your name to current campaigns for better lupus diagnosis, coverage and care. Contact us to be notified when the next petition opens.
Notify meAdvocacy & policy
Lupus and other autoimmune rheumatic diseases must be recognised not simply as individual medical conditions, but as an African public health and health equity issue.
Why this matters
The impact of lupus reaches families, workplaces, communities and national health systems. Unequal access to diagnosis, treatment, social protection and specialist care continues to place a disproportionate burden on people living with chronic autoimmune diseases.
Most of these gaps are not medical mysteries. They are decisions: what a health insurance scheme covers, whether a medicine is on an essential medicines list, whether a district hospital can refer to a rheumatologist, whether a patient organisation is invited to the table.
That is why advocacy sits at the centre of our work rather than at the edge of it.
Systems should not simply be designed for patients but shaped with them.
LFA engages with national health bodies, including stakeholder meetings with the Social Health Authority, and works with clinical, media and civil society partners to keep lupus visible in health policy conversations.
You deserve care. Your circumstances should not silence your voice.
Take action
Advocacy works when it is not only staff doing it. Here are four things you can do, whether or not you live with lupus.
Add your name to current campaigns for better lupus diagnosis, coverage and care. Contact us to be notified when the next petition opens.
Notify meAsk your county or national representative what is being done to ensure lupus diagnosis and medicines are accessible and covered.
Get our templateBecome a member and take part in campaign actions, stakeholder meetings and awareness drives across our chapters.
Join LFAVisibility is advocacy. Sharing a story or a fact with your own network reaches people we never could.
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