DSSA is a proud member of Down Syndrome International www.ds-int.org.
20 October is National Down Syndrome Awareness Day, come celebrate with us
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Read our National Down Syndrome Awareness Month Statment Here
#ENDTHESTEREOTYPES
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Who we are
Down Syndrome South Africa (DSSA)is a non-profit organisation (NPO 009-415) and was formed in 1986 as the national umbrella body and parent advocacy organisation for the constitutional rights of persons with Down syndrome and other intellectual disabilities. DSSA currently has 12 regional associations and support groups throughout the country that provides services to persons with Down syndrome, developmental delays and their families.
Our Mission
Down Syndrome South Africa (DSSA) is committed to finding ways to improve the quality of life of all persons with Down syndrome and other Intellectual disabilities, promoting the idea that they have the right to live with independence, dignity and security as valued adults and full citizens in our society. It endeavours to empower families through dissemination of information, encourages research in the fields of early intervention, education, medical aspects and employment. Its ongoing mission is to bring South Africa in line with world trends in the field of Down syndrome and to see to it that the UN Convention on the Rights of Persons with Disabilities (UNRPD) is recognised and honoured in all spheres.
Each year on World Down Syndrome Day 21st March annually and National Down Syndrome Awareness Day 20 October DSSA raises awareness on key issues affecting persons with Down syndrome and DSSA is able to convey new information on Down syndrome to the South African public. It is hoped that this will create new opportunities for the thousands of children in our country who have up to now been greatly underestimated and stigmatised.
Reading Webinar
A replay of the reading webinar can me made available for a R100 fee. Feel free to leave a comment/feedback on the webinar so we can improve future webinars thanks.
Some comments on the webinar
- The webinar as a unit was informative.
- Valuable information on how DS kids learn. How to keep it interesting for them.
- How to teach literacy and different tools we can use for non- speaking learners.
- It was a good overview and addressed the parents’ questions well. It also confirmed much of what I tell parents, which was affirming for me personally.
- As always, one wants to hear more, but I think it was well paced for the content. Extended time may have allowed for more examples but I liked that it was short and sharp.
- Maybe talk a little slower. English is not my first language.
What we do
Advocate at national government on the rights of persons with Down syndrome and other intellectual disabilities.
To encourage the development of support groups, programmes and services that may be appropriate and beneficial for persons with Down syndrome and other intellectual disabilities.
To promote public awareness and improve attitudes towards persons with Down syndrome and other intellectual disabilities.
Capacity building of our members.
Programme Focus Areas
Capacity building
Of our members in all nine provinces
Rights Based Advocacy
On policy at national and international platforms on the right to education, universal healthcare for all, access to employment, political and social rights
Awareness on Down syndrome
Thereby reducing the stigma, myths and discrimination that surround the condition
