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Reward Me Before I Die. Ogidi Brown Pens Down Emotional Letter To President Akufo-Addo

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Reward Me Before I Die. Ogidi Brown Pens Down Emotional Letter To President Akufo-Addo 

Ogidi Brown – Musician & CEO of OGB Music

Renowned Disabled Ghanaian Highlife/Hiplife Musician and CEO of OGB Music, Ogidi Brown earlier today shared a sad photo of himself and an emotional writeup urging Ghanaians to celebrate and reward him before he dies. 

In the letter which was addressed to his excellency the president of the Republic of Ghana, Nana Akufo-Addo, Ogidi Brown stated that he is the only disabled musician in Ghana in a wheelchair trying to give hope to other people with disabilities. 

The Boss of OGB Music also revealed that, he has invested a lot into music since 2016 but hasn’t been nominated in any category for an award before. He pleaded with president Akufo-Addo to reward him before he dies. 

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Below is the emotional letter from Ogidi Brown to President Akufo-Addo. 

“…Celebrate me today, talk about me today, post my picture on social media today and wish me well, pray for me everywhere, Tv and Radio, i want to see this live, Dont let me die before my family will see you were a big fan, I’ve been admitted at hospital for 8days in serious condition, Mr President, Nana Akufo Addo @nakufoaddo this is Ogidibrown, a Ghanaian hiplife/highlife musician. Am the only physically challenged artiste in a wheelchair trying to build the hope of others to know disability is not an excuse, Mr President my problem is Ghana music authorities are cheating me too much, i started doing music commercially from 2016 and I’ve invested alot in music, but i haven’t been nominated before, please i want you to reward me before i die, thank you Mr President thank you Ghana….”

Source: Sintim Media 

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Health

The Sickle Cell Helping Hand Foundation Extends Support with Health Outreach, Education, and Hospital Donation

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The Sickle Cell Helping Hand Foundation is once again making a meaningful impact in the fight against sickle cell disease as it prepares for its two-day programme slated for August 28–29, 2025. With a strong focus on community health, education, and direct support to patients, the Foundation is strengthening its commitment to awareness creation, early detection, and care for individuals affected by sickle cell disease.

Central to the initiative is the health talk and education session on sickle cell disease, which will provide valuable knowledge on prevention, management, and coping strategies for patients and their families. By equipping participants with accurate information, the Foundation seeks to dispel myths surrounding the condition while promoting healthier lifestyles and encouraging routine check-ups for early intervention.
Another key highlight of the programme is the health screenings and counselling sessions, which will give community members access to general medical check-ups and malaria testing. These services not only provide immediate healthcare benefits but also help participants better understand their health status and the importance of regular medical care.

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Counselling will further support families by addressing the emotional and psychological impact of living with or caring for someone with sickle cell disease.
The Foundation’s work extends beyond just outreach and screening. Through its Teen’s Educational Health Talk Tour at Bolgatanga Regional Hospital, the organisation continues to engage young people in meaningful conversations about health, wellness, and the realities of sickle cell disease. This tour empowers teenagers with knowledge, encouraging them to make informed health choices while serving as ambassadors of awareness in their communities.

As part of its commitment to practical support, the Foundation will also lead a donation exercise at the Bolgatanga Regional Hospital’s Sickle Cell Unit. This gesture is designed to ease the burdens faced by patients and caregivers, while also reminding the sickle cell community that they are not alone. The donation will be accompanied by words of encouragement, solidarity, and interaction with patients to uplift their spirits and inspire hope.

The programme is also expected to emphasize the importance of blood donation in the treatment of sickle cell disease. Blood transfusions remain a critical aspect of care for many patients, and the Foundation continues to advocate for regular voluntary blood donation as a lifesaving act of kindness.
Through these initiatives, The Sickle Cell Helping Hand Foundation is not only offering medical and material support but also spreading hope, compassion, and education. Its consistent efforts reflect a deep commitment to ensuring that individuals living with sickle cell disease receive the care, attention, and encouragement they deserve.

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We are calling on everyone to support our course by donating to our organisation through momo number 0552723595.

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