The Government has clarified the blue badge criteria. Many of our members who previously received automatic entitlement to a blue badge (because they were awarded DLA mobility under the SMI criteria), no longer qualified for it once they moved to PIP because there is no criteria for behavioural issues. The requirement (for automatic blue badge) […]
Emily Buck has been announced as the overall winner of the Down’s Syndrome Association’s (DSA) international photographic competition, My Perspective 2018. Emily said of her winning image, Seven Sisters: “I like the contrast between the blue sky and the white cliffs and the different shapes of the beach and sea.” Emily also won the competition […]
We believe it is imperative that the official information provided to pregnant women/couples about pre-natal screening is up-to-date, accurate and balanced.
Welsh people with Down’s syndrome and their families share their experiences of what life with Down’s syndrome is like.
In the run up to the roll out of NIPT in England, the DSA and other organisations and parent focus groups, including Down’s Syndrome Research Foundation and SOFT-UK, who support families of children with Edwards or Patau’s syndromes, have been working, within limits, with the Public Health England (PHE) Fetal Anomaly Screening Programme. In addition, Public […]
From 30 April 2018 Wales will be the first of the UK nations to offer women non-invasive prenatal testing (NIPT) as a supplementary test. All antenatal screening tests are elective. Currently pregnant women can choose whether they wish to have a test or not. NIPT is considered more reliable than the test that is currently […]
We understand the concern that surrounds the proposed introduction of NIPT in NHS settings. The impact of the new test will be monitored, as recommended by the Nuffield Council on Bioethics last year, but at the moment we don’t yet know what effect offering NIPT more widely will have. The need for up-to-date, accurate, information […]
Our work to ensure publicly available information on Down’s syndrome is balanced and up-to-date continues in 2018
During the second half of 2017 we have been working with Public Health England, The Fetal Anomaly Screening Programme (FASP) and Antenatal Screening Wales to improve the quality of information that is provided to women at all stages of their pregnancy – from the beginning of their contact with their midwife (when options for antenatal […]
Three speakers from our Tell It Right® Start It Right training days tell us why they want to be involved
