Rare Diseases Lesotho Association is a Non-profit Organization registered in October 2017 in accordance with the Societies Act of 1966 of Lesotho. The Organization assists all patients affected by rare diseases to access treatment and support care for improved health and quality of life. The intention is to facilitate and support advocacy and engagement between those with the ability to prevent, inter, treat and provide support care for patients and families affected by chronic and rare diseases in Lesotho.
Co founder and mother to a baby girl with a rare kidney condition.
Founder of Rare Diseases Lesotho Association . After being diagnosed with Ehlers Danlos syndrome a rare genetic tissue disorder, she decided to start an Association that helps patients with rare diseases like her self.
Genetics Researcher on behavioral/human genetics for honours and interaction between selected gene variants in depression & anxiety.
Researcher on combating these microorganisms and how vaccines and antibiotics can be made, as well as identifying them for diagnoses bacteria and viruses.
The amount of time spent in the office, six days a week.
Number of t-shirts sold since our launch back in 2011.
Number of coffees consumed per hour on any given day.
There are 6 different languages spoken in our office.
Tel : +266 57796134
Cell : +266 53885912