Negative assumptions about people with Down syndrome can become self-fulfilling prophecies. Try positive assumptions and maybe we can create more opportunities at school, in the workforce, in sports, and in social life.
#AssumeICan
#EndTheStereotypes
#WDSD24
An extra chromosome hasn’t held Micah back from getting an education or a job (or being the best brother a girl could ask for)!
Happy World Down Syndrome Day 💙💛
Hey
@Eminem
and
@Beyonce
, we need you to be leaders! We are asking you to not use the "R" word from your newest song. This word is extremely hurtful to the Down syndrome community. Please remove the lyric immediately.
Happy 2nd Birthday to the one-and-only Stella Tremonti! 🎂 We loved getting to celebrate you at our gala last week where we honored your dad
@MarkTremonti
and the entire Tremonti family!
Happy
#WorldDownSyndromeDay
! 🎉
We’ll be celebrating and raising awareness all day with our virtual
#Racingfor321
event! If you’re joining us for 3.21 miles in honor of
#WDSD
, be sure to tag us to share your progress! 🏁 (1/2)
We are thrilled to share our 40th Anniversary Video 📽️! 💛💙 As the leading human rights organization for ALL individuals with Down syndrome,
@NDSS
knows we have come so far but have so far to go. Join us in the fight to end
#LawSyndrome
Have you heard? The 2023 NDSS Gala & Auction will honor musician
@MarkTremonti
& family! 🤩🥳 This amazing event will conclude with a live performance of songs from Mark’s Billboard
#1
jazz album, 𝑻𝒓𝒆𝒎𝒐𝒏𝒕𝒊 𝑺𝒊𝒏𝒈𝒔 𝑺𝒊𝒏𝒂𝒕𝒓𝒂, which benefits NDSS. (1/2)
ICYMI on
#WorldDownSyndromeDay
, our friend
@MarkTremonti
is putting out an album of
#FrankSinatra
covers! Mark is generously donating all proceeds from the album to NDSS in honor of his adorable daughter Stella. Pre-order your copy at the link below! 💙💛
🚨UPDATE🚨 NDSS has been working with Congressional leaders and the appropriate Federal authorities to find a solution to reunite the 10-year-old child with Down syndrome who was separated from her family. We are pleased to report that the girl will be reunited with family.
LEGISLATIVE WIN!💥 Employees with disabilities must be paid at least minimum wage in the State of Virginia! With the signing of HB 1924 yesterday by Governor Youngkin, VA became the 16th state to eliminate the practice of paying individuals with disabilities subminimum wage.(1/3)
“We hope that this will open conversations about Down syndrome and how wonderful this community is.”
Thank you for covering this huge step for inclusion,
@michael_roppolo
!
Our friend
@nyjets
Jamison Crowder is passionate about many things-including football🏈
and Down syndrome!
Support him as he raises money for NDSS in honor of his brother Jamaris!
Over 500 individuals with Down syndrome’s faces were shown celebrated in a video presentation in the heart of Times Square today, which is the official kickoff of our
#NYCBuddyWalk23
! 🌆✨This celebration means so much to us and our community— let’s keep it going all day long!
“This is a great win for everyone who has been fighting for our kids to get noticed and included […],” Bassey, whose daughter Anoushka has Down syndrome. “Everyone wants to see themselves reflected, and it’s just the beginning.”
Did you see Kayla's NowThis Her interview? She spoke about her life as the FIRST registered lobbyist with Down syndrome and how she is taking Washington D.C. by storm.
We are deeply saddened to learn of the passing of Zion Sarmiento, an infant with Down syndrome who was denied the heart transplant he needed to survive. Our team has been in touch with Zion’s family in Florida, and we are working to ensure equity in organ transplants nationwide.
Did you catch this great article on
@MarkTremonti
Sings Frank Sinatra in the
@washingtonpost
?! 🤩🎉 We’re so grateful to be the recipients of this amazing album and movement. Check out the article in case you missed it! 🥳⬇️
We are thrilled to have
@TODAYshow
's
@SavannahGuthrie
serving as emcee for A Night of Celebration on March 17 at 8pm ET! Join us as we celebrate the
#Downsyndrome
community and honor trailblazer David Egan at our virtual event.
Welcome to the NDSS Tribe Kayla! Kayla McKeon is making history today as she officially joins our staff and becomes the first registered lobbyist with Down syndrome! Join us in welcoming her to our team!
We are THRILLED to announce our 2023 Gala & Auction will honor musician
@MarkTremonti
& family! 🤩🥳 This amazing event will conclude with a live performance of songs from Mark’s Billboard
#1
jazz album, 𝑻𝒓𝒆𝒎𝒐𝒏𝒕𝒊 𝑺𝒊𝒏𝒈𝒔 𝑺𝒊𝒏𝒂𝒕𝒓𝒂, which benefits NDSS. (1/2)
@tomsegura
, we just watched your
@netflix
special and we find your repetitive use of the “R” word very disgraceful. We invite you to attend an NDSS event and meet individuals with Down syndrome. Individuals with the extra 21st chromosome will far exceed your expectations.
Yesterday, NDSS President & CEO Kandi Pickard spoke at the United Nations as part of the 12th World Down Syndrome Day Conference! 🎉 Kandi spoke on the importance of empowering individuals with Down syndrome to make their own choices through supported decision making. 👏 (1/2)
Did you see Kayla on
@CBSNews
with
@SteveHartmanCBS
? 📺 She spoke about her life as the FIRST registered lobbyist with Down syndrome! You can watch it right now while donating $7.25, the Federal Minimum Wage to NDSS! 💰
#TIMEforTIME
⌛️
Today is the 9th anniversary of the ABLE Act, a landmark legislation that allowed for the creation of ABLE accounts, offering a pathway to financial security & independence by allowing individuals with disabilities & their families to save money without (1/2)
“People with Down syndrome have value and worth because of who they are, not because of what they can or cannot do.” -Heather Avis,
@luckyfew
#DSAC2023
Calling all
@alterbridge
fans!🎸Did you see
@MarkTremonti
rocking his NDSS shirt this past weekend during their show? 🤩 Mark is spreading the word about our upcoming Gala & Auction coming up on 3/2 in NYC, where he's performing LIVE! Tickets at !
Have you seen all of the amazing scholarships and awards NDSS offers? We are currently accepting applications for five scholarships that support individuals with Down syndrome to pursue their dreams, expand their business, and follow their passions! 🌟 .
NDSS is proud to have partnered with
@coordown
to bring you, “RIDICULOUS EXCUSES NOT TO BE INCLUSIVE,” ahead of
#WorldDownSyndromeDay
.
This video features Charlotte Woodward, our Education Programs Associate, and a ridiculous excuse she’s been given. (1/2)
Happy Down Syndrome Awareness Month! 🎉 Each October, we raise awareness and celebrate the abilities of our loved ones with Down syndrome. Check out the link below to learn how you can get involved this year! 💙💛
Happy
#InternationalFriendshipDay
! These self-advocates from NZ initiated, co-designed, co-researched, and co-authored an academic article about the experiences of people with Down syndrome during the COVID-19 lockdowns in NZ! 👏 You can read it at .
Detrez Newsome, of the
@Chargers
, has revealed his
#MyCauseMyCleats
shoes!👟 Thank you Detrez for selecting NDSS and supporting the Down syndrome community! 💛💙
@NFL
🏈
We’re excited to share we have ANOTHER graduate to celebrate this weekend! 🎉🎓 Kayla McKeon, our Manager of Grassroots Advocacy, graduated with her associates degree yesterday from
@OnondagaCC
! As many of you know, Kayla is the first registered lobbyist with
#DownSyndrome
. (1/2)
“If I could sit with others with Down syndrome, I’d say, ‘Go to college.’ I want to show them how they can do it themselves.”✔️Congrats to Marina for graduating from the Destination Dawgs program at
@universityofga
!
Legislative update! 💥 This evening, NDSS team members Nick & Charlotte, & DS-Ambassador Bill Lawfield provided testimony on HB 1924 which would end the use of 14(c) certificates in the state of VA to ensure individuals with disabilities are no longer paid subminimum wages. (1/2)
𝗧𝗢𝗠𝗢𝗥𝗥𝗢𝗪 is October 1st, which means it will finally be
#DownSyndromeAwarenessMonth
! 🤩🥳 This year for
#DSAM
, NDSS has put together a set of fact cards to share a different fact each day throughout the month to help promote and celebrate Down syndrome awareness. (1/2)
It’s a little known fact that the majority of people with disabilities in our nation are paid below the federal minimum wage - sometimes as little as 30 cents an hour.
Help us change that.
Today is
#WorldAutismAwarenessDay
! 🎉 Many of our loved ones with
#DownSyndrome
experience dual-diagnoses and have
#Autism
as well. Today we celebrate all of the strengths, talents, and skills that people with Autism bring to our communities and to the world! 🤩 (1/2)
Lamar Stevens wrote a children’s book while he was at Penn State, which was illustrated by local kids with Down Syndrome with whom he built relationships through various events.
What a cool guy and a great addition to the
@celtics
and the Boston community
Attention
#SelfAdvocates
! 🚨 This Employment Tip of the Month is all about making your resume stand out to potential employers. Do you have other questions about resumes? Reply here or email us at employment
@ndss
.org!
The day has FINALLY arrived! 🎉
@MarkTremonti
Sings Frank Sinatra - out TODAY! All proceeds from this incredible album are being donated to NDSS 💛💙. We are so grateful to Mark and the entire Tremonti family! Order your copy today! ⬇️
🤩
There are over 260 college programs for individuals with Down syndrome! 📚 At NDSS we believe one of the best ways to prepare all students for college is by ensuring ALL have access to an inclusive education! ✏️⭐️ What do you wish your teacher knew?
It's World
#BirthDefects
Day
The most common severe birth defects are:
🔸Congenital heart defects
🔸Neural tube defects
🔸Down syndrome
🔸Hemoglobin disorders (thalassemia and sickle cell disease)
👉
NDSS is outraged to see video of
@RepMTG
using the R word & directly mentioning individuals with Down syndrome. People w/
#downsyndrome
deserve to be treated w/ respect. We urge everyone to use our preferred language guide & understand that
#wordsmatter
:
This afternoon, our Manager of Grassroots Advocacy Kayla McKeon met with
@RepJohnKatko
before he retires at the end of the year. Kayla interned in his Syracuse district office from 2015 to 2017, working on a variety of projects and attending important events. (1/2)
That’s a wrap on the
#NYCBuddyWalk23
! We had over 2,000 people in attendance 💥 and we are grateful for every single one of you! This event is such an impactful and 𝗙𝗨𝗡 celebration of our community and we couldn’t do it without you! 💙💛
“…thinking about this on the eve of Father’s Day, it may well be that Gabriel has taught me more about meeting challenges, overcoming hurdles, and living in the moment than anyone else.”
#HFD
to all of the dads & Father figures in our community! 💙
.
@Pink
shares the sweetest story about what she did after reading a message from a mom on social media who said she’d be in the wheelchair section at her concert with her son who just beat cancer
33 years ago today, the
#ADA
was signed into law. While we commemorate this day, it’s important to remember that there is still 𝐬𝐨 𝐦𝐮𝐜𝐡 𝐰𝐨𝐫𝐤 𝐭𝐨 𝐝𝐨! (1/2)
Today is Day 2 of
#DownSyndromeAwarenessMonth
! Here’s Fact
#2
of our 31 Facts for 31 Days series. Did you know that
#DownSyndrome
is the most common chromosomal condition? Follow along throughout the month for more facts & to celebrate
#DSAM
with us!
@NDSS
Sylvia Piper, mom of the late Dan Piper (the NDSS Dan Piper Self Advocacy Award is named for him and the 1st person with Down Syndrome to testify before Congress for the ADA) loves her new Barbie!
#Barbie
Did you know the GRAMMY Award-winning musician
@MarkTremonti
recorded his album 𝑇𝑟𝑒𝑚𝑜𝑛𝑡𝑖 𝑆𝑖𝑛𝑔𝑠 𝑆𝑖𝑛𝑎𝑡𝑟𝑎 in honor of his daughter, Stella, who has Down syndrome and is donating 100% of the proceeds to NDSS? 🎶 What’s YOUR favorite
#Tremonti
and/or
#Sinatra
song?
It’s October and our
#WouldntChangeAThing
ambassadors are here to open up
#DownSyndromeAwarenessMonth
with a bang.
We all have worth.
Whatever our abilities, whatever our strengths, whatever our talents, whatever our qualifications, whatever our differences. We are all worthy.
#ICYMI
, our staff member David will be starring in an upcoming
@hallmarkchannel
movie! We can't wait to see David & his co-star Lily shine. We are thrilled that Hallmark is showing that individuals with
#DownSyndrome
can play LEADING roles in film! 👏
Have you seen NDSS’ “I wish my teacher knew” campaign? What do YOU wish teachers knew about students with down syndrome? Email 📨 your “I wish my teacher knew” pictures to ssoldovieri
@ndss
.org for a chance to be featured on our social media!
NDSS is devastated to learn of the passing of disability rights advocate Judy Heumann. We send love to her family and friends during this time. May her memory be a blessing.
(1/2)
Congratulations to NDSS Board Member John Cronin of
@JohnsCrazySocks
who was recently awarded the 2022 Henry Viscardi Achievement Award! 🎉 This award was presented to John in honor of his advocacy for the disability community. We are so proud of you, John!💥
We are THRILLED to announce our 2023 Gala & Auction will honor musician
@MarkTremonti
& family! 🤩🥳 This amazing event will conclude with a live performance of songs from Mark’s Billboard
#1
jazz album, 𝑻𝒓𝒆𝒎𝒐𝒏𝒕𝒊 𝑺𝒊𝒏𝒈𝒔 𝑺𝒊𝒏𝒂𝒕𝒓𝒂, which benefits NDSS. (1/2)
Congratulations once again to Isla! Yesterday, Hazlet Township, New Jersey declared November 6th to be Isla Day because of her work with NDSS! We are so proud to work with Isla and her family to end
#LawSyndrome
!
2,500 Barbies, generously donated by
@mattel
, will be celebrating Down Syndrome with us at the
#NYCBuddyWalk23
. 🩷💛💙 A variety of
@barbie
dolls will be give out at t-shirt pick up on Friday, September 8th— first come, first serve. See you there! 🥳
Part of NDSS’ mission is to shift public perceptions of the Down syndrome community, and these actors have helped do just that through their roles in film and television. We are so excited to honor them at our annual Gala & Auction in New York City on March 7th! 🌟🎞️