Foundation offers support to those affected by muscular dystrophy

Muscular Dystrophy Foundation of SA’s Gauteng branch is adamant about giving its support to those affected by muscular dystrophy and endeavour to improve their quality of life.

The Gauteng branch is a registered non-profit organisation and operates in Gauteng, Limpopo, Northwest, Mpumalanga and the Free State.

There are also branches in KwaZulu-Natal and Cape Town.

Muscular dystrophy is a collective name given to a group of diseases that cause progressive weakness and loss of muscle.

It is caused by abnormal genes or “mutations” that interfere with the production of proteins that are crucial to form healthy muscles.

There are many kinds of muscular dystrophy.

Some occur in childhood while others can even occur in late adulthood.

While there is no cure for muscular dystrophy, there are medications and therapies available that can help manage symptoms and slow progression.

Robert Scott business development manager of the Gauteng branch said the foundation’s goals and objectives are to assist affected persons and their families by providing information, support and referrals to genetic counselling and health facilities.

“We also do our utmost to support affected people with specialised disability equipment if we have the funding available.

“In addition, we create public awareness, generate funds to support and sustain our work and assist individuals to form self-help and support groups,” he said.

Should you be affected by muscular dystrophy or know someone who is, contact Robert at mdfgauteng@mdsa.org.za or call 011 472 9824.