Hey there, I'm Zanele People admire me because I am very humble, loving, kind hearted and a friendly individual. I have a condition named...

Hi everyone, Im Camilla. Having Rare Diseases isn't all that makes me different. As much as I've been through, I still fight the good...

I am Chané Botha and I am a Wegener Warrior I’ve had this disease for many years but what this journey has taught me is how to be brave,...

I am Tové and I am a qualified Biokineticist. Some people say that I am different due to my patience, kindness and always wanting to look...

We are the parents of a very special child Tumisho. He was born at Netcare Femina on the 27 October 2010 ( Born in the year when South...

I am Janine Sokwane a 39-year black female I was born with a motor neuron immune disease called Spinal Muscular, for short it’s a...

My name is Sumaya Gasnola. I am 62 years old. Just after my 50th birthday I started getting very bad knee pain and swelling in my knees...

Hello, I am a Rare Woman chosen by the Lord to be Nabeelah’s mom. I am a teacher by profession and in my classroom I always loved the boy...

My name is Matthew May, I am 7 years old and going to Grade 2 (in spite of having mum and dad home school me through this pandemic.) I...

Hi There This is our story… One November morning in 2019, my daughter woke up, screaming and crying that she has stomach pain, she is...

Hello, my name is Kerry Walsh. I was born on the 22/10/1997, I was born in a set of fraternal twins. I have SMA (spinal muscular atrophy)...

Hi there! My name is Tové and I am a qualified Biokineticist. Some people say that I am different due to my patience, kindness and always...

I stay positive. My motto is never give up. Mommy told me never to give up on a cure and to keep praying one will come.