Hope. Care. Empower.

We're here for you.

We support everyone affected by lupus and other autoimmune diseases in Uganda. Wherever you are living with lupus or you are a parent, spouse or loved one, we are your partner in this journey.
LUPUS IS NOT CONTAGIOUS
LUPUS AT A GLANCE

3.41 M

people living with diagnosed lupus worldwide

9 in 10

are women

38%

develop lupus nephritis

2

practising rheumatologists for 48 million Ugandans
Find your community

You are not alone

Find understanding, encouragement and care, with people who understand your journey.
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Living with lupus

Share questions and stories in our moderated WhatsApp community.

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Parents, spouses and carers

Practical guidance for supporting a loved one, and space for yourself too.

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Health workers and partners

Work with us on earlier diagnosis, affordable care and research.

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Lupus stories

Every story makes lupus visible

A life is more than a diagnosis. This space will hold a patient’s own words, experiences and hopes.
Know the signs

Could it be lupus?

If these signs keep coming back, see a health worker and ask about lupus.
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Painful or swollen joints
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Rash across cheeks and nose
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Extreme tiredness
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Fevers with no clear cause
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Mouth ulcers
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Hair loss
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Sensitivity to sunlight
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Swollen feet or ankles
Make hope possible

Small actions. Meaningful care.

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Help fund treatment

Help close the gap in access to consultations, tests and medicines.

Make a difference
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Wear purple with pride

Start a conversation with a piece from our merchandise collection.

Explore the collection
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World Lupus Day

Wear purple on 10 May. Share the facts and help make lupus visible.

Get involved
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