The story of a little girl named Caitlin

Photo courtesy of Sherene Hustler of Inner Eye Photography

When you become a parent, you become even more aware of how precious a child is. And it touches you even more when you hear about children suffering, or hurting. This is the story of Caitlin, a 5-year old girl. She is also the daughter of Dries’s cousin, Michelle.

She was born prematurely with her twin sister at 30 weeks. There were complications such as stopping to breathe, struggling with reflux, and she contracted the Rotavirus at 7 months. At nine months Michelle’s niggling suspicions were confirmed that something was very wrong when she demanded answers. Up until then the paediatrician told her not to worry. Caitlin had undetected brain bleeding since birth which led to the fact that her entire motor section in her brain was gone.

The prognosis was very bad: acute cerebral palsy! Caitlin would only live until 15 years of age!

Michelle has not given up hope. To the contrary: she has been researching Caitlin’s condition and she has tried to get her the extra special care she needs. It is very difficult because she is single parent. Their hope is now focused on Neuro-endoscopic Autologous Stem Cell Implantation, which Caitlin has already been approved for at the X-Cell Centre in Germany. Michelle needs R300 000 for the trip and the medical procedures.

She is now bringing the plight of Catlin to everybody’s attention. The story of Caitlin has been published in People Magazine of this week.

Michelle has also started a Facebook fan page for Caitlin, called The Little Train who Can: Caitlin’s story so far. You can find more information about Caitlin and her condition on the page.

We are so blessed when we have healthy children. We believe that this little girl will also outlive her prognosis.

Miracles do happen every day, don’t they?