Mum Takes Touching Photos of Children With Rare Genetic Diseases

Mother and child with a rare genetic disease resting together peacefully.

A photographer mum has decided to photograph children with rare genetic diseases to educate people about rare diseases.

For someone whose family have been living with pain since�her brother died of Tay-Sachs disease, a rare neurological genetic condition with no known cure,�Karen Haberberg�knows the challenges�rare diseases bring to a family so she decided to help�ease the pain of other families through photographs.

Young boy with a sandwich sitting on a wooden bench outdoors.

She then�realised that�families could use a place to share their stories and hear others�especially as she�has relived the hardship as she watched her best friend struggle to find a diagnosis for her son. Karen told Popsugar:

“Finding a proper diagnosis can be incredibly challenging and frustrating for families, and without a correct diagnosis, these children are not properly treated, which stifles their progress.”

“Families often feel incredibly isolated when they find out their child has a rare genetic disease and they want their children to experience life to the fullest every day “� even when death may be imminent.”

So, with her skills as a photographer,�she started a�photo campaign,�Project Believe, in order�to raise awareness for rare diseases while also hoping to change the lives of others suffering. In her�Kickstarter page, Karen describes her campaign�as “Life affirming photos of extraordinary children contending with rare genetic conditions and finding joy and beauty in daily life.”

Father and young child sharing a heartfelt hug outdoors.

She has been taking photos of children with chronic illnesses that also show the never-ending�support of their families.

“The chronic illness of a child requires a commitment that is with the family every moment of every day. It steals precious time as families battle insurance companies, search for solace, and struggle to manage everyday tasks,” Karen said.

Karen also aims�to create�a book of portraits that will serve as an educational resource, which would include�a brief medical explanation of each disease.

Child's feet with medical braces and supportive footwear for rare genetic condition.

At least 30 families were featured in the book. where they�share their stories in their own voice. Karen said that she is�privileged to know these families and to be allowed into their world for a short�time to photograph their situation. She was able to see how the families�cope with such an illness that can also provide moments of profound dignity, grace, transcendence, and joy.

“This project will provide a record of such moments, illuminating what it means to be a family . . . no matter how brief your time on earth,” she shared.

Source:�Popsugar.com

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Clare Whitfield Chief Editor
Clare Whitfield is the Editor of Stay at Home Mum and a recognised voice in practical home management for Australian families. Based in the northern suburbs of Sydney, she balances editorial leadership with life as a stay at home mum to two school age children. Her background in home economics and more than a decade of experience in recipe development, family budgeting, and household systems inform her work.

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