For ostomates and families
Get supplies and support.
If you or someone you care for is living with a stoma, contact us. Support does not depend on your income or where you live in Zimbabwe. You are not alone. We walk this journey with you.
What we will ask you
So that we send the right appliance, please have this ready. If you do not know an answer, contact us anyway and we will work it out together.
- Your name, and the name of the ostomate if you are asking for someone else
- The type of stoma: colostomy, ileostomy or urostomy
- When the surgery was done, and whether it is temporary or permanent
- The size of the stoma in millimetres, if you know it
- The pouch type currently used, one piece or two piece, and the size
- The town or district where you live, so we can plan delivery or collection
- A phone number we can reach you on
Other ways we can help
Learning to manage your stoma
Many people leave hospital without being shown how to change a pouch or protect their skin. We teach patients and families, and our guides cover the practical basics.
Counselling and peer support
A qualified volunteer counsellor supports ostomates who need it. We also bring ostomates together to share experience, which for many members is the moment they realise they are not alone.
Support for parents
We support families caring for babies and children with stomas, including supplies in paediatric sizes where available and contact with other parents.
Help for health workers
Nurses and clinics who encounter stoma patients rarely can contact us for guidance, and to connect patients to ongoing supply.
Contact us
Reach us by WhatsApp, phone or email. Our office is at 1 Headingley Drive, Ashdown Park, Harare, Zimbabwe.
- Joseph Muchesa, Executive Director: +263 775 494 015
- Rachel Muchesa, Trustee: +263 774 135 953
- Alexander Nyakunu, Trustee: +263 772 276 383
- Landline: +263 8644 087566
- Email: info@zost-zw.org
