One4Another International

One4Another International One4Another International is a Canadian organization that helps children in Uganda access life altering surgeries
www.one4anotherintl.ca

Many children in Uganda grow up with debilitating conditions which lead to lifelong hardship and exclusion from their communities. A one time surgical intervention that costs on average around $500 can significantly shift the path of a child’s life from one of perpetual poverty to a life with the hope of education and eventually the ability to provide for one’s family. The surgeries and rehabilita

tions are being coordinated by our Ugandan staff in the greater Jinja area. The surgeries are usually performed at local clinics or hospitals by Ugandan surgeons. Some conditions are more complex and may require multiple interventions or specializations. Below is a list of some of the medical conditions that we can treat:

Clubfeet
Osteomyelitis
A**l malformations
Growths
Orthopedics
Organ repair
Urological problems
Traumatic injuries
Hernias

Children in Uganda are prone to bone infections, also known as osteomyelitis. They can start from a minor injury that fe...
09/02/2026

Children in Uganda are prone to bone infections, also known as osteomyelitis. They can start from a minor injury that festers over time, and if left untreated can lead to swelling, pus discharge, foul smell, bone erosion, and potential amputation. A child with a weakened immune system and poor diet is the perfect breeding ground for such infections, as was the case for Lukaiya.

We've been working with Lukaiya since 2021, when she arrived at our center with a severely infected and exposed right tibia bone. She has endured bone debridement, sequestrectomy surgery, corrective osteotomy surgery, ex-fixator placement, along with hundreds of wound dressings, many antibiotics, and physiotherapy. Her infection has been very difficult to eradicate, and though her leg is still not 100%, it is much better.

Lukaiya's home life is challenging, and between living 3 hours away, having no one to bring her to appointments at times, and just the overall lack of supplies for maintaining a clean wound, it is not hard to understand why the infection persists.

At the moment we are managing her condition with wound dressings and antibiotics, and she now has a strong enough tibia bone to be on full weight bearing, which is great progress. She has come a long way, and we are here to ensure she achieves her full health potential, no matter how long it takes. To be continued...

Pastor Thomas is the chairperson of our Village Resource Network (VRN). This is a group of volunteers who are active in ...
08/31/2026

Pastor Thomas is the chairperson of our Village Resource Network (VRN). This is a group of volunteers who are active in the villages of southeastern Uganda referring and following up on our patients. These Resource People (RP) not only help our parents access our services but help us work through any number of challenges that arise during the treatment process. They are truly on the front lines of our work.

Pastor Thomas, what are the challenges you face in this work?

"One of the challenges we face as RP in the villages is the difficulty in getting out to the villages. The roads are very poor and become slippery during rainy seasons. So, reaching some homes is very difficult. We are also challenged when we get parents who do not believe in the medical treatment. Some parents believe that disabilities are caused by the clan spirits or the spirits of their ancestors. It takes time for them to change their views. Some completely refuse treatment for their child. They believe that disabilities are inherited from the great ancestors and if we operate on them, the child may die or something bad will happen to the clan members. I try to engage the beliefs of the parent and show them cases where a child has been treated successfully so they can challenge their own beliefs."

What do you enjoy most about your role as a resource person?

"I enjoy seeing the smiles that I always see after the child's condition has been corrected. This makes me so happy, and I feel that I am being significant to the community. We are respected and honored as people who add great value to our communities through the service we provide to these children. On that note, we are so grateful that the organization has given us this opportunity to serve children in the communities because most of them reach out to us when they have failed to find any help and we have seen so many transformations. May God bless all involved with this work and the generosity of all those who support us. We are the ones who see the difference it makes in the lives of these children."

To learn more about this amazing group of people, check out: https://one4anotherintl.ca/about-us/

Small ➡ BigNewborn ➡ ToddlerCrying ➡ PeacefulClubfeet ➡ Flat feetWe never get tired of seeing these little ones go throu...
08/27/2026

Small ➡ Big
Newborn ➡ Toddler
Crying ➡ Peaceful
Clubfeet ➡ Flat feet

We never get tired of seeing these little ones go through BIG transformations!

Doreen came to us at the age of 15 with a large skin tag on her shoulder and chest. It was causing her pain and discomfo...
08/24/2026

Doreen came to us at the age of 15 with a large skin tag on her shoulder and chest. It was causing her pain and discomfort and often had a foul smell.

She underwent 2 surgeries to have it removed and is now healing and on regular wound dressings.

As a young woman, this skin tag brought her much shame and embarrassment. We love seeing her bright smile and renewed self confidence as she finishes off her treatments.

Kevin spent the first 6 years of his life in pain and awkwardness, unable to participate in activities around him and ma...
08/18/2026

Kevin spent the first 6 years of his life in pain and awkwardness, unable to participate in activities around him and made fun of for his clubfeet.

Kevin will now spend the rest of his life walking, running, playing, working, living, and thriving thanks to your support!!!

Scovia's mother was travelling for a funeral when she unexpected­ly went into labour and gave birth to a baby girl at a ...
08/12/2026

Scovia's mother was travelling for a funeral when she unexpected­ly went into labour and gave birth to a baby girl at a local health center. Her daughter Scovia was born with a congenital abnormali­ty: a parasitic twin that stopped developing early on yet remained attached was threatening Scovia's own life.

"When my daughter was born with a rare and complex deformity, my world fell apart. Instead of the joy I had imagined, I was overwhelmed with fear, confusion, and heartbreak. My husband and I believed she might not survive beyond her first few days.

With no access to specialized treatment and very little hope, all we could do was hold her close, pray, and cherish every moment. Despite our fears, our daughter kept fighting. I continued breastfeeding her every day, believing it was the best way I could care for her while we searched for help. As the days passed, we refused to give up on her.

Then hope arrived. Thanks to the kindness and generosity of 04A, who believed in our daughter's future, she was able to receive the life-changing surgery she desperately needed. The operation was successful and today she is growing, smiling, and living a normal, healthy life.

Our family will forever be grateful to everyone who supported us through this journey. You gave our daughter a second chance at life and restored hope to our family. May God richly bless you for making what once seemed impossible become a beautiful reality."

| Scovia's Mom

Mary's leg first became infected when she was 5 years old. Her mom never took her to the hospital because she was told t...
08/05/2026

Mary's leg first became infected when she was 5 years old. Her mom never took her to the hospital because she was told the infection was from witchcraft and that they would not be able to help. Her mother was worried and wanted to do something for her daughter so instead she tried treating her with herbal remedies.

Years later, when Mary was 14 and her leg was significantly worse and causing her pain, one of our Village Network Volunteers noticed the leg and proceeded to spend a long time encouraging, educating, and finally convincing Mary's mom to bring her to our center for osteomyelitis treatment.

Mary came for a sequestrectomy followed by many months with an ex-fixator and pins, antibiotics and pain meds, wound dressings, x-rays, and physiotherapy. Her leg is now free of infection and her bone is strong!

One of our most recent projects was creating booklets on treatable conditions for parents like Mary's mom. It has become a very useful tool for our volunteers with photos of real patients, medical information, and counselling tips.

Mercy's mom first noticed a lump in her leg at around the age of 12. Not knowing what it could be, she thought she would...
07/24/2026

Mercy's mom first noticed a lump in her leg at around the age of 12. Not knowing what it could be, she thought she would just observe it in the hopes that it would go away on its own. But the lump did not go away. Instead, it grew in size and started to affect Mercy's walking and kept her from being able to stand for long periods of time.

Her parents were able to have x-rays taken that confirmed Mercy had tumoral calcinosis. Tumoral calcinosis is a rare metabolic disorder characterized by the development of large, benign/noncancerous, calcium-phosphate mineral deposits (calcified masses) within soft tissues, typically around major joints.

They sought treatment for her but could not find any they could afford. It grieved them to watch their daughter suffer with pain. Thankfully they met a former patient of O4A who referred them our way, and Mercy had a complete excision of the mass.

Today Mercy is a healthy 16 year old young lady who is able to go to school and work and engage in her community! She, along with her mom and dad, are so thankful for the subsidized care they received at O4A.

John is 4 years old and has never been able to walk on his own. He suffers from mild CP and had severe equinus feet wher...
07/21/2026

John is 4 years old and has never been able to walk on his own. He suffers from mild CP and had severe equinus feet where his heels were pulled up tightly leaving him on his tippy toes. His father, a widower, has carried John every day since his birth.

But all that is about to change because John just graduated from our clubfoot treatment program with 2 straight feet and a big smile!! His feet are very stiff and sensitive at this early stage, with such a drastic transformation, but the hope is that he will be walking independently soon! This will allow him to start school and have a much better future in spite of his challenges. Amazing!!

Little Janet was wondering if you knew that 89%* of the money O4A receives goes directly to children like her?! At O4A t...
07/15/2026

Little Janet was wondering if you knew that 89%* of the money O4A receives goes directly to children like her?! At O4A there is no big overhead, so you can be sure that your donation is being used to helping kids in need of medical treatment.

If you've sponsored through O4A, comment below and share the name of the child whose life you changed forever!!

*remaining 10% - admin, 1% - fundraising

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374 Dunvegan Drive
Waterloo, ON
N2K2C4

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