Mfantsipim Old Boy Who Has Been Standing For 5 Years Opens Up About Rare Disease

Mfantsipim Old Boy Who Has Been Standing For 5 Years Opens Up About Rare Disease

  • University of Cape Coast student, Enock Eshun, has opened up about a rare disease he has
  • The disease is known as fibrodysplasia ossificans, which leads to muscle and connective tissue gradually being replaced by bone
  • Eshun studied visual arts student of Mfantsipim School and said he has chosen to remain upright

A first-year University of Cape Coast student, Enock Eshun has been battling a rare disease that has left him standing stiff for 5 years.

The disease he suffers from is known as fibrodysplasia ossificans, which leads to muscle and connective tissue gradually being replaced by bone.

Zion Felix, Enock Eshun, Mfantsipim, University of Cape Coast, fibrodysplasia ossificans
Enock Eshun speaks to Zion Felix about his rare condition. Source: Zionfelix
Source: Twitter

Eshun, aged 19, shared his struggles with blogger Zion Felix, noting that his situation deteriorated due to his family’s reliance on herbal medicine.

He was diagnosed with the disease when he was two years old.

Eshun studied visual arts student at Mfantsipim School and said he has chosen to remain upright instead of being wheelchair-bound to keep his academic dreams alive.

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Eshun struggles with his daily activities, such as commuting to and from class.

Due to his condition, Eshun has to remain standing throughout the day, including during lectures, and only takes a rest at night when he goes to sleep, lying in the same position.

"With how the illness is, let's say if I fall and break my hand and leave it like that, let's say it would be like this forever, and I wanted to further my education too. I didn't want to be sitting in a wheelchair. Even walking around like this, look at how people stare at me; then imagine sitting in a wheelchair. So I had to take the risk to stand so that when it is forming, it will block me in standing, not sitting," Eshun explained.

Leukaemia patient supported Ibrahim Mahama dies

YEN.com.gh reported that Lisa Laryea, the 10-year-old leukaemia patient flown to South Africa for surgery passed away.

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This heartbreaking news came weeks after Ghanaian millionaire Ibrahim Mahama funded her care.

Laryea had reportedly been battling leukaemia for many years, and in November 2024 Mahama, offered to pay for her surgery in South Africa after news of her illness reached him.

The CEO of Engineers and Planners, reportedly paid $110,000, equivalent to GH¢1,623,221.39, to treat the 10-year-old’s stage 4 acute myeloid leukaemia. He offered similar support in the past.

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Source: YEN.com.gh

Authors:
Delali Adogla-Bessa avatar

Delali Adogla-Bessa (Head of Current Affairs and Politics Desk) Delali Adogla-Bessa is a Current Affairs Editor with YEN.com.gh. Delali previously worked as a freelance journalist in Ghana and has over seven years of experience in media, primarily with Citi FM, Equal Times, Ubuntu Times. Delali also volunteers with the Ghana Institute of Language Literacy and Bible Translation, where he documents efforts to preserve local languages. He graduated from the University of Ghana in 2014 with a BA in Information Studies. Email: delali.adogla-bessa@yen.com.gh.

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