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Creating a world where people with Down’s syndrome are equally valued and have an equal chance of being born.

United Kingdom
Joined January 2016
Photo by Don't Screen Us Out (@dontscreenusout)Photo by Don't Screen Us Out (@dontscreenusout)Photo by Don't Screen Us Out (@dontscreenusout)Photo by Don't Screen Us Out (@dontscreenusout)Photo by Don't Screen Us Out (@dontscreenusout)Photo by Don't Screen Us Out (@dontscreenusout)Photo by Don't Screen Us Out (@dontscreenusout)
Happy Halloween from Hector Monty 🎃🎃🎃
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📮 Ted from Cornwall Down’s Syndrome Support Group wrote to his MP — and got a reply! 👏 Thank you Ben Maguire MP for supporting the Down Syndrome Act guidance. Your voice matters. Write to your MP! 🔗 ndspg.org/october-campaign/ #FourYearsStillWaiting #ActIntoAction
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Don't Screen Us Out retweeted
Care does not always meet needs – why this happens. “…people with Down syndrome face wide-ranging barriers in accessing or receiving quality health care, including poor coordination of care, insufficient clinician knowledge of Down syndrome-specific health needs, and financial
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Well done to Angela - named ambassador for disability inclusion by catering company Thomas Franks 👏🏻
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👏 Down’s Syndrome Lancashire took action! Members used our Easy Read resources to write to their MPs about the delayed Down Syndrome Act guidance. 📮 Will your group be next? ndspg.org/october-campaign/ #FourYearsStillWaiting #ActIntoAction
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Super work Jonathan ⚽️ 🏆
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Day 20 Down Syndrome awareness Month. Enjoy be outside and listen to birds, and my favourite session is Autumn. #downsyndromeadvocate #disabilityadvocate
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💗 Our voices. Our rights. Our future. Our Advisory Group took their campaign to Downing Street. Four years on, we're still waiting for the Down Syndrome Act guidance. 📩 Write to your MP: ndspg.org/october-campaign/ #FourYearsStillWaiting #DownSyndromeAct
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Jenni was told baby had low chance of having Down's syndrome. Yet after birth, her concerns were dismissed & her request about receiving the diagnosis was ignored - illustrating urgent need to assess wider impacts of antenatal screening @YvetteCooperMP 🎧 youtube.com/watch?v=7yAtH93x…
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true story …. October is Down Syndrome awareness month …. ♥️#DownSyndromeAwareness♥️
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Just off to meet some inspiring people who really change lives @PrideOfBritain All will come clear @itv Thursday 8 pm
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This is what it m’s look like so far, I got through Christmas balls to do. I am enjoying it. They are for sale for £2.50 for one, they will be also be in a set to I will be doing. There will be a price list for all items to.
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Don't Screen Us Out retweeted
Day 15 Down Syndrome awareness Month. I am still celebrating Down syndrome awareness month, I am very proud who I am. #downsyndromeadvocate #downsyndromeawarness #downsyndrome #disabilityadvicate
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A packed @APPGDS AGM! Fair Shot CIC shared how they’re supporting people with #DownSyndrome into work, while the @NDSPolicyGroup Advisory Group raised concerns over delays to the #DownSyndromeAct2022 Guidance. Great discussions & importantly, hearing directly from people with DS.
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Four years ago, Cheshire families shared their views on the Down Syndrome Act. They did their bit. The guidance is STILL not published. 📮 Write to your MP and demand action. Get our Easy Read pack: ndspg.org/october-campaign/ #FourYearsStillWaiting
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Deeply moving account from Aaron John Huxter whose daughter Olivia-Grace died last year. Aaron says: “I’m sorry you never got to meet her” & “She was so incredible she deserves to be missed every day” Our hearts go out to all who knew & loved Olivia-Grace bit.ly/4hF5GO8
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Thank you Ben Ben, one of our Advisory Group members, met his Local Authority Social Worker team today to talk about the Down Syndrome Act and why the guidance matters. 📮 You can take action too get our Easy Read MP pack from our website. #FourYearsStillWaiting #ActIntoAction
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