Barbara Kwateng passed away in Brussels on 9th August 2005, briefly after being diagnosed with the Lupus disease at the age of 28. Due to a lack of general knowledge of the disease, Barbara was unaware of the symptoms associated with Lupus. It was for this reason that her family and friends have set up the BARBARA KWATENG LUPUS TRUST. This trust aims to raise awareness and support research into the causes and effects of Lupus. This is an illness The Barbara Kwateng Lupus trust aims to help all those affected by this disease.

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“Our mission is to raise awareness of Lupus and support research into the causes, treatment and cure of Lupus, with a view to providing solutions that effect change.”

Offer Support

To offer support and understanding to the emotional & physical wellbeing of people with Lupus.

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Lupus in Africa

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Preserve Privacy

To preserve the privacy, opinions and personal feelings of the persons suffering from Lupus and to safeguard their confidence.

We hope you do find this website a tremendous help whether you are searching for help for yourself or for a loved one. Lupus can be a frightening disease and its course rather uncertain.

It is natural for anyone who had just learnt about the diagnosis to feel rather scared but there is more to having this disease than these feelings. Support and understanding are very important to the emotional and physical wellbeing of those suffering or living with Lupus

There is a huge amount of information on Lupus on the web, in libraries and through your doctors. Don't be discouraged. Being well educated on Lupus is the best tool you can have to address lifes issues.

BKLT aims to provide and recommend the most proven, current and trusted information on new research, successful and experimental treatments, new and existing Lupus organizations, tools for leading a healthy lifestyle and more. This information is presented in a clear and simple way so you can easily locate what's most important to you.

Currently many people do not know what Lupus is. Please pass on this information to your family and network of friends so that they are also aware of Lupus. So much help and assistance is required and periodically, we organise events including sponsorship and other fundraising activities. You are welcome to take part in these activities which will be featured in our events webpage.

© 2020 Barbara Kwateng Lupus Trust

Proudly created by Kayla Byfield

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