Our Story

Muscular Dystrophy Society Kenya (MDSK) is a patient and family driven organization providing a support platform for people with muscular dystrophy and other neuromuscular conditions in Kenya. The main aim is to provide a support system and information hub for those with muscular dystrophy, neuromuscular conditions and their families in Kenya.

MDSK works closely with medical and para-medical practitioners, educational and welfare support persons towards improving the quality of life of those with muscular dystrophy in the country.
MDSK is a co-organiser of the annual Rare Disease Day which is celebrated on the last day of February each year.
MDSK also marks special days related to various types of muscular dystrophy.

One thought on “Our Story

  1. Hello, my brother’s boy iam worried he could be ailing from MD, he’s slowly losing the ability to walk but visited hospitals can’t find anything wrong with him.

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