RESOURCES
Please watch the instructional video below BEFORE collecting your saliva sample. The video will guide you through the collection process using the NEST saliva collection kit, including how and when to add the solution provided in the kit.
Before returning your sample, please complete the following steps:
- Collect your saliva sample as demonstrated in the video and securely close the tube.
- Label your sample tube by applying one of the barcode stickers provided. Where possible, please also write your surname on the tube.
- Place the sample tube in the specimen bag provided and seal the bag securely.
- Please print and sign the laboratory request form, then place one of the barcode stickers in the dedicated space in the top right-hand corner of the form.
- Keep one barcode sticker for your records.
- Place the following items inside the white envelope provided:
- The sealed specimen bag containing your saliva sample
- Your completed and signed laboratory request form
- Any remaining barcode stickers
- Clearly label the white envelope with your surname, initial and date of birth.
- Returning your sample: Once your sample is ready, please contact your genetic counsellor to arrange its return. You may drop the sample off at our offices (by prior arrangement) or, if more convenient, we can arrange a courier to collect it from you.
Before sending your sample:
Please check that all required information is complete, accurate and clearly readable, and that the details on your sample and paperwork match.
Please follow the instructions in the video carefully. If you are unsure about any part of the collection process or what needs to be returned, please contact your healthcare team before sending your sample.
NCCN Guidelines for Patients®
The National Comprehensive Cancer Network (NCCN) provides patient-friendly guidelines covering a wide range of cancers and cancer-related topics. These resources offer information about diagnosis, treatment, screening, follow-up and supportive care, and can be a useful starting point for understanding your condition and the management options available.
The guidelines are regularly updated as new evidence becomes available. You can access the full collection of NCCN Guidelines for Patients® directly through the NCCN website.
RareChromo – Unique
Unique provides free, patient-friendly information guides on a wide range of rare chromosome and gene disorders. The guides can be a helpful resource for individuals and families looking to understand more about a specific genetic diagnosis, including what is known about the condition and related genetic findings.
Rare Diseases South Africa
A national organisation supporting individuals and families affected by rare diseases, with information, advocacy, support and connections to relevant resources and services.
Southern African Society for Human Genetics (SASHG)
SASHG provides information about human genetics and maintains a directory of genetics professionals and services across Southern Africa, which can be useful if you are looking for a genetic healthcare provider in your area.
From time to time, I have the opportunity to contribute to research and publications in the field of genetics and genetic counselling. I’ve included some of this work below for anyone who may be interested in learning more.
Articles:
- The Utilisation of Genetic Counselling Services Amongst Prenatal Healthcare Providers in Gauteng, South Africa
This study explored how prenatal healthcare providers in Gauteng use and understand genetic counselling services. The findings highlighted gaps in awareness of when genetic counselling may be helpful, and the importance of making referral pathways clearer for healthcare providers.
Case Studies:
- Article coming soon