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When children become caregivers, who cares for them?

When Sanyu Musoke thinks of her teen years, she remembers loneliness, particularly as she stepped into the role of caregiving for her mentally ill mother and, later, her disabled father. For a while, she left school to focus on helping her family.

“Not only am I dealing with all that, but teenagers are trying to figure out life and you think the whole world is against you,” says Ms. Musoke. 

Why We Wrote This

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When crisis hits, sometimes young people are thrust into taking on responsibility for their entire family. But with that extra obligation, who cares for the carers?

Ms. Musoke was in a position that has a legal definition in the United Kingdom: young carer. About a million young people under 18 years old there spend more than 50 hours a week caring for family members struggling with illness, disability, addiction, or other afflictions, according to Carers Trust. 

So now, Ms. Musoke is using her unique understanding to help young carers. Through a social enterprise charity she founded named Yucan, she aims to give young carers mental and emotional support, help educate school staffs about how to identify carers, and even train carers for the workforce later on. 

“We’re protecting them as well as supporting them to know that it’s OK to receive the help,” Ms. Musoke says.

Sanyu Musoke was barely out of her teen years when she found herself with responsibilities coming from all directions. 

Her mother already needed full-time cognitive care when, in 2015, her father was in a horrific car crash. It left him disabled and Ms. Musoke in a position that has a legal definition in the United Kingdom but felt anything but clear to her: young carer.

From negotiating with doctors and navigating medical equipment, to grocery shopping and ensuring siblings’ homework was completed, her new purview covered nearly everything. She remembers struggling to learn to fold her father’s wheelchair.

Why We Wrote This

A story focused on

When crisis hits, sometimes young people are thrust into taking on responsibility for their entire family. But with that extra obligation, who cares for the carers?

“I suddenly had to care for a physical disability as well as a mental disability,” says Ms. Musoke, who dropped out of college for a time. “It’s like, does my father have the equipment he needs, are the bathrooms OK, and what are these new medications, and has my mother taken her own medications?”

The obligations and responsibilities add up for young carers. Many find themselves falling behind in school or forgoing college. They have more frequent mental health issues. And they often feel they cannot ask for help, perhaps due to cultural expectations or social stigmas.

So now, Ms. Musoke is using her unique understanding to help young carers. 

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