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Inspire Hope and Empower Dreams with “The Girl with Special Shoes”

 

We are thrilled to introduce The Girl with Special Shoes, an inspiring autobiography by Hilda Bih Muluh. Born with Muscular Dystrophy, Hilda’s journey is a remarkable story of courage, resilience, and unwavering faith. From battling depression to becoming a celebrated news anchor on Cameroon Radio Television (CRTV), known as the “Microphone Queen,” Hilda’s life is a shining testament to the power of perseverance and belief in one’s purpose.

Now, you can help share Hilda’s incredible message of hope with disabled individuals in South Africa.

Through her candid storytelling, humor, and deep faith, Hilda reminds us all that no challenge is insurmountable. As she beautifully states, “You may feel weakness is blocking your path. But often, it’s the route God has planned.” Her book is a powerful tool to inspire those facing their own struggles—encouraging them to pursue their dreams and live a fulfilling life despite any obstacles.

You can Make a Difference

We are offering an opportunity for generous supporters and well-wishers like you to purchase The Girl with Special Shoes at a special discounted price of just $9.99. Each copy will be gifted to the Muscular Dystrophy Foundation of South Africa (MDFSA) allowing them to share this uplifting story with children, teens, and adults in their care. By purchasing a book, you are giving the gift of encouragement, helping others see that they, too, can overcome adversity and achieve their dreams.

Together, we can empower individuals with disabilities to believe in their own potential and pursue lives filled with hope, faith, and purpose.

How You Can Help

Your support can bring this life-changing story to those who need it most. For just $9.99, you can purchase a copy of The Girl with Special Shoes to the MDFSA. Each book will be distributed to individuals who will benefit from Hilda’s empowering journey.

Purchase your gifted copy today from Oasis International Publishing, and let’s
spread the message of resilience, faith, and hope.

Miracles Don’t Always Look Like You’d Expect

Muscular Dystrophy Foundation of South Africa

History of the Foundation

The Muscular Dystrophy Research Foundation of South Africa was founded in 1974 by Mr and Mrs Newton Walker  who had a son affected with Duchenne Muscular Dystrophy. They, together with Wally Gough of the Rotary Club of Potchefstroom and representatives of Cripple Care Association formed the Foundation.

Today the Muscular Dystrophy Foundation of South Africa  is a registered non-profit organisation consisting of a national office and three branches which operate in the nine provinces of South Africa.

What they do

The Muscular Dystrophy Foundation of South Africa assists affected persons and their families by:

  • Providing access to international information regarding specific dystrophies.
  • Hosting informative workshops about muscular dystrophy.
  • Providing referrals to health facilities and professional counsellors.
  • Assisting with specialised disability equipment, if funding is available.
  • Providing access to social service professionals for emotional support.
  • Facilitating support groups.
  • Create public awareness on muscular dystrophy issues and disability.
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