Before Help a Sickler found me, I did not know there were others like me nearby. The support group changed my life — I no longer feel ashamed of my condition.
Living with Sickle Cell Disease (SS Type)
Help a Sickler is a Uganda-based NGO dedicated to educating communities, sensitizing families, and providing care and medicine to sickle cell patients — especially those underprivileged in Uganda's rural areas.
✓ 100% Non-Profit · ✓ Uganda-Registered NGO · ✓ Internationally Supported
Our Impact to Date
Since our founding, every effort has been measurable. Here is what Help a Sickler has achieved — and we are just getting started.
Our Work
We run community workshops, school programmes, and digital campaigns teaching Ugandans about sickle cell disease — what it is, how it is inherited, and how to live well with it.
Learn more →We partner with local leaders, healthcare workers, and faith communities to break the stigma that surrounds sickle cell. Because silence costs lives.
Learn more →We facilitate access to early diagnostic screening, medication support, and specialist referrals for patients who cannot afford private healthcare.
Learn more →We connect sickle cell warriors and their affected families to counselling, support groups, nutritional guidance, and emergency care assistance.
Learn more →Why Us
Help a Sickler was not founded in a boardroom. It was born at a family bedside — from watching sickle cell take hold of someone we loved. That origin is our compass.
Rural-First Focus: We specifically target underprivileged patients in rural Uganda — the most underserved communities.
Family Origin: Born from the personal experience of sickle cell in our founder's own family.
Affected Families Network: Our network of affected families is the heart of our community — not just beneficiaries, but partners.
Transparent & Accountable: Every donation, every patient registered, every action — tracked and publicly reported.
Globally Supported: Backed by international well-wishers and partners, delivering local impact.
We promise to be a shoulder for every sickler who is underprivileged from the rural areas of the country.
Real Stories
These are real voices from sickle cell patients and their families across Uganda. Their stories are the reason Help a Sickler exists.
Before Help a Sickler found me, I did not know there were others like me nearby. The support group changed my life — I no longer feel ashamed of my condition.
Living with Sickle Cell Disease (SS Type)
My family could not afford the medication. Through Help a Sickler's programme, I received three months of medication free of charge. I am now back in school.
Living with Sickle Cell Disease (SS Type)
The awareness workshop in our village was the first time my mother-in-law understood why her grandchild suffers. That understanding was the beginning of healing.
Caregiver, family affected by SCD
I registered my daughter through the programme. Within two weeks, she had a specialist appointment that we had been trying to get for over a year.
Parent of a child living with SCD
Our Network
Help a Sickler works with organisations, medical institutions, and community groups who share our vision of a Uganda free from sickle cell stigma.
Want to partner with us? Get in Touch →
Get Involved
You don't need a medical degree to help a sickler. Whether you volunteer your time, your skills, or your resources — every act of well-wishing is felt by real people in real pain.
Join 120+ well-wishers from 18 countries already making a difference.