OUR SERVICES
What We Offer SCD Warriors
Advocating for quality healthcare for Sickle Cell Disease
Access to Specialists and Personalized Treatments
Access to Partner and Nearby Hospitals
Virtual Consultations with On-Call Doctors
ABOUT US
Get To Know About Us
Our Story
MAHI was founded by Mr. Mo'sho Adeosun, an SCD warrior driven by a passion to effect change within the SCD community. Recognizing the urgent need for accessible medical attention tailored specifically for SCD warriors, he envisioned a platform that transcended traditional support groups. This vision materialized into a comprehensive initiative featuring a mobile application designed to offer hub-and-spoke consultation services, providing immediate access to specialized care. With aspirations to extend globally, MAHI seeks to foster international collaborations, ensuring that SCD warriors worldwide receive the support and care they deserve.
Target Audience
Our primary focus is on underprivileged and average-income SCD warriors. Additionally, we aim to engage the broader SCD community, healthcare providers, caregivers, governmental health institutions, and global health organizations.
Check Our Programs
Engage in our programs to raise awareness and empower carriers
Hub & Spoke Hospital System
A coordinated hospital care model designed specifically for sickle cell disease (SCD) patients. It connects a central hub--- hospital with several surrounding spoke clinics and centers
Who it Helps
SCD warriors in both urban and rural areas who need timely specialist care from hematologist and other SCD-focused health professionals
How it Works
Through our upcoming mobile app patients will be able to locate the nearest partner clinic or hospital (spoke), request transportation during crises and access virtual consultations with specialists at the hub. The model ensures consistency in care, faster referrals and wider outreach
Healthcare Access & Support
A person-centered initiative aimed at removing barriers to healthcare for SCD warriors, especially during emergency episodes.
Who it Helps
Underprivileged and underserved SCD patients who often lack the means to reach health facilities or afford consistent care.
How it Works
We facilitate access through emergency and non-emergency transport services, hospital referrals, subsidized treatment options, and a network of responsive healthcare providers. The mobile app will also feature emergency alert capabilities.
Education & Awareness Program
An ongoing public health initiative to increase awareness of SCD and educate people on prevention, management, and support strategies.
Who it Helps
SCD warriors, caregivers, school communities, healthcare providers, and the general public.
How it Works
We host virtual training sessions, create resource materials (videos, articles, infographics), and partner with schools, religious bodies, and healthcare institutions to run awareness drives. We also encourage lived-experience storytelling as a form of education.
Community Engagement & Support Kits
An outreach-focused program to build strong, responsive support systems around SCD warriors.
Who it Helps
Families, caregivers, and communities affected by or caring for someone with SCD
How it Works
We organize physical and virtual roundtables, conduct needs assessments, and distribute care toolkits containing guides, hydration bottles, pain tracking charts, and support hotlines. It’s all about empowering the community to walk the journey with warriors.
Research & Innovation Unit
A strategic pillar focused on scientific exploration, data collection, and innovation toward improving SCD treatment and outcomes. .
Who it Helps
Medical researchers, healthcare institutions, and ultimately, SCD patients globally.
How it Works
We collaborate with medical professionals to carry out research studies, pilot innovative treatment models, and advocate for affordable curative measures. Data from our mobile app will also guide research into real-time challenges faced by warriors.
Advocacy & Policy Development
A voice and bridge between patients and systems—aimed at influencing policies and promoting rights-based care for SCD warriors.
Who it Helps
SCD patients, caregivers, and the broader sickle cell community.
How it Works
We engage government bodies, health ministries, and global health institutions to raise awareness of policy gaps, suggest reforms, and push for better resource allocation. We also train patient advocates to speak for themselves in public and institutional spaces.
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