The South African Bone Marrow Registry (SABMR) has received the nod from its Clinical Governance Committee and board members, as well as the National Health Department, to allow 16- and 17-year-olds to become bone marrow stem cell donors.
This means that young South Africans aged 16 and 17 years can stand alongside their peers in the United Kingdom as the world’s youngest bone marrow donors.
Recent changes in legislation and advances in stem cell donation have allowed registries to reduce the age limit of donors. South Africa now joins the UK, which was one of the first countries to do this.
Dr Charlotte Ingram, Medical Director of the SA Bone Marrow Registry – the largest registry in the country – says it’s a landmark moment as the change in joining policy will contribute to saving more lives.
“In general, young people make better donors. Research shows that younger donors are associated with better survival rates for patients following a stem cell transplant. It’s a step towards further enhancing the registry towards a younger and more ethnically diverse pool for blood cancer patients and others in need of a bone marrow transplant.”
Previously, teenagers had to wait until they were 18 to join the SA Bone Marrow Registry. Now they can join by following the exact same procedure as others would. While it is not required, it is important for the SABMR to involve parents and address any questions or concerns they may have re the procedure and what it entails.
Once youth have applied online: https://sabmr.co.za/become-a-donor/, they will be contacted to discuss the easiest way of dispatching and collecting swab kits. The only initial sample that is required is a cheek swab.
Currently, 18- to 25-year olds only account for 6.8% of the SABMR registry but with increased awareness of bone marrow donation among young people the figure should increase substantially.
“Studies tell us that generation WE (aged 14-20) and generation Z (21-25) are a lot more self-aware, socially-responsible and globally-minded than previous generations. They are more concerned about tackling social issues and want to roll up their sleeves and make a difference. Young people today are often drivers of social change movements and we look forward to engaging them.”
She says there is no greater way to help another than to potentially save a life.
“So many lives are lost if there is a delay in finding a donor match. While we have 74 000 donors on our registry, we often discover that many older donors can no longer donate stem cells as they have developed hypertension, heart disease or diabetes. When this happens, we have to start the search process all over again, which prolongs the agonising wait for a patient, who doesn’t have time to waste. By opening up the donor pool to a younger audience, means doctors and donors can choose the healthiest matches that substantially increases a patient’s chance of survival.”
For now, social media will serve as the primary channel to create awareness among youth, but physical donor drives at schools and other initiatives, which encourage collaboration between learners, peers and patients are in the pipeline for 2021.
If you are between the ages of 16 and 45 and want to become a donor, contact the SABMR on 021 447 8638 or email: donors@sabmr.co.za. Financial donations can also be made via www.sabmr.co.za/donate.
About the SABMR
The SABMR was established in 1991, motivated by the concern that although bone marrow transplants were a life-saving treatment option, they were only available to patients with a matching donor in their family. Today, the SABMR searches both locally and internationally for donors, thereby making collaboration with international registries and observing universal standards of practice essential.
An internationally recognised registry, the SABMR is a member of the World Marrow Donor Association (WMDA) and was founded in Cape Town in 1991. It is also the only WMDA accredited registry in Africa.
Its mission is to save lives and provide hope for all patients in need of bone marrow stem cell transplantation and future therapies, by creating awareness, expanding the registry, embracing evolving technology and enhancing stakeholder relationships to the benefit of the community.