Photography series looks to shed light on children diagnosed with rare genetic conditions
This moving photography series looks to shed light on children with rare genetic conditions.
The children featured have been diagnosed with the likes of Marfan syndrome, megalencephaly-capillary malformation syndrome, and 22q11.2 deletion syndrome – titles unknown to most of the general public.
By shooting children in their natural environments – as cheerleaders, playing on trampoline, at home – photographer Karen Haberberg hopes to provoke thought, be it of daily struggles or uplifting hope.
The series, entitled “An Ordinary Day,” was a “labour of love,” Karen, 44, from New York City, New York, said.
There was an element of personal connection to the subject matter, too: Karen’s parents lost a child to Tay Sachs Disease before she was born, and, most recently, her best friend’s son was diagnosed with Angelman Syndrome.
Karen said: “She added: ” One in 10 families in America has a child with a rare condition and 95 percent of those conditions do not have one single FDA approved drug treatment.
“I knew I wanted to raise awareness for this community so I began to research the best way to find participants.
“I wanted the images to be authentic and representational of “an ordinary day” in these families lives.
“Choosing the images was very challenging because I wanted depict a sense of balance between struggles and victories while not being overly depressing or too saccharine.”
The first child Karen photographed, named Mackenzie, suffered from Tay Sachs Syndrome, like Karen’s brother, and after that shoot, she opted to turn one image into a series.
In order to identify subjects with rare genetic conditions, Karen reached out to Global Genes, a non-profit advocating for those with rare genetic conditions; took to social media; and simply relied on word of moth.
Earlier this year, in October 2017, Karen’s images were released as a book entitled “An Ordinary Day: Kids with Rare Genetic Conditions.”
The images for the book were taken between January 2016 and October 2016, Karen said.
Moving forward, she plans to seek funding for a documentary film on the same subject matter.
Karen said: “I am hoping to spread the word about this book in hopes to work with pharmaceutical companies or other organizations to create similar projects for other causes.
“The profits from this project are going to Global Genes to fund genetic research so that someday perhaps there is a cure for one of these devastating illnesses.”
Do you, or someone you know, have a similar story to tell? Get in touch today to earn £££ and raise awareness.