From the Battlefield, to the Hallow Ground… to Space – Just a Typical Week at NDSS – #WeirsWeek

“(Almost) four score (divided by two) years ago, our National Down Syndrome Society co-founders brought forth on this continent, a new nonprofit organization, conceived that people with Down syndrome deserved more, and dedicated to the proposition that all individuals with Down syndromIMG_3223e are created equal and are entitled to the same human rights as all other Americans.

It is for us, this great team, to be dedicated here to the unfinished work which needs to be done on behalf of all people with Down syndrome and their families. It is for us to be here dedicated to the great task remaining before us – that we highly resolve and recommit each year to our mission, our self-advocates, our families, our advocates, our athletes, our supporters, our future employers and so many others —that this NDSS shall continue to grow, evolve, advocate and be an organization for people with Down syndrome, by the people with Down syndrome.”

I hope everyone had a great Memorial Day! For me, Memorial Day is always a great day to reflect on the past. I couldn’t think of a better way to spend this Memorial Day – finishing the book Killer Angels to prepare for our 2017 NDSS Staff Retreat at Gettysburg with the Lincoln Leadership Institute this week.

2017 NDSS Staff Retreat 

Our dedicated team spent the first day with the President of the Lincoln Leadership Institute studying the leadership and the Battle of Gettysburg and Civil War on the same grounds where the most influential battle of the civil war was fought. On the second day, we assessed our organization and put in place new strategies and initiatives to support our mission, as the leading human rights organization for all individuals with Down syndrome, to ensure we keep reaching for that “higher ground” and channel great transformational leadership and change – just like Col. Chamberlain accomplished in the Battle of Gettysburg. I am incredibly proud of our amazing NDSS tribe, who all even participated in our #TeamNDSS work-out at 6 am, for their dedication, vision, passion and leadership they put into serving all individuals with Down syndrome and their families. Stay tuned for some big updates this summer from NDSS!

One-Year Anniversary of ABLE Accounts

While our team was retreat-ing, we also marked a significant milestone for the disability community. June 1st, 2017 – much like the epic battle of Gettysburg in 186313331149_10208380145237823_8868320026358975276_n – represents a turning point in the disability community’s battle for economic self-sufficiency. We celebrated the one-year anniversary of National ABLE Accounts. Ohio’s STABLE Program opened for business one year ago today and we have a lot to celebrate. According to my friend, Paul Curley from 529 Dash, since March 30, 2017, there have been 7,286 ABLE Accounts opened with over $25.5 million invested – that is simply amazing and I can’t wait for our Q2 2017 updates! You can find more information about ABLE Programs that are
available here.

Please join NDSS and our ABLE Alliance for Financial Empowerment in celebrating the anniversary of National ABLE Accounts being a reality, but remember that this war is not totally won with legislation in the Halls of Congress or by the stroke of a President’s pen. Rather, it is won in the hearts and minds of all our advocates —and who fight on this new battlefield – by making phone calls, meeting with Members of Congress, State Legislators, sent tweets and most importantly – those self-advocates, our best soldiers, who told their personal stories and truly made ABLE a reality!

Houston: We “Don’t” Have a Problem – Building Bridges in Houston This Weekend

I am honored to spend the weekend with so many leaders from the medical and clinical community that work day in and day out to serve patients with intellectual and developmental disabilities for the “Building Bridges Conference” hosted by the American Academy of Developmental Medicine and Dentistry (AADMD) at the Cooley Center, part of the University of Texas Health Science Center at Houston and the National Task Group on Intellectual Disabilities and Dementia Practices. This was a unique conference on health and healthcare for people with intellectual and developmental disabilities – and I had the esteemed privilege to moderate the “Building Bridges Panel” this morning with experts from across the country.

Working with, collaborating with and forging partnerships with these individuals, leaders and organizations, I can tell you the future is bright for individuals with Down syndrome and other disabilities – there are no problems in Houston (other than the humidity) today!

–Onward & Upward – SHW

We’re Partnering With The Mighty!


We’re thrilled to announce a new partnership that will bring our National Down Syndrome Society’s (NDSS) resources in front of The Mighty‘s wide-reaching readership. We will now have a growing home page on The Mighty and appear on many stories on the site, allowing us to get many more people involved with our organization.

The Mighty is a story-based health community focused on improving the lives of people with disabilities and other conditions. Over 54 million people with the United States have a disability, and there’s always a need for more than information. People want to be inspired and know how they can make a difference. The Mighty publishes real stories about real people, including people with Down syndrome.

We’re dedicated to helping people with Down syndrome in their lives. With this partnership, we’ll be able to help reach more people!

We encourage you to submit a story to The Mighty and make your voice heard.

NDSS Makes a Mark on Kiev!

IMG_1221I just wrapped up my beautiful stay in Kiev where I had an amazing couple of days in Ukraine’s capital city helping to spread awareness about Down syndrome!

We are honored to take part in this incredible program through our U.S. State Department and American Councils that brings leaders from around the world together to make a difference in the world. Last fall, our team at the National Down Syndrome Society (NDSS) hosted an American Councils fellow from L’viv, Ukraine – Mariana Matys in Washington, DC. Mariana is also a mother to a beautiful daughter with Down syndrome and a phenomenal advocate. Earlier this year, Mariana applied to reciprocate the partnership, and we were accepted to take part in a week long visit to Ukraine to raise awareness about Down syndrome, provide our NDSS resources to the Down syndrome community throughout the country and help support the leadership of UDSO, led by the inspiring Sergey Kuryanov, to expand their existing efforts and mission.


Yesterday, we met with Commissioner of the President of Ukraine for Children’s Rights KULEBA Mykola Mykolayovych (a huge advocate for early intervention services in Ukraine), I also conducted a lecture for students, teachers and faculty from Borys Grinchenko Kyiv University about NDSS and Down syndrome in the US and wrapped up the day speaking with parents from ВБО «Даун Синдром» at their Down syndrome clinic.


This morning, I had the chance to see UDSO in action during a social therapy class, discuss opportunities for collaboration between NDSS and UDSO, toured two schools for students with Down syndrome and other disabilities, appeared on a local TV station -Соціальна країна – Social Country with Mariana and met with the dedicated team at the American Councils – those who helped make this important partnership all possible!

I am off to Zhytomyr now… but wanted to share an image from a historical Ukraine WWII Monument in Kiev- Mother Motherland – a great reminder, we’re all in this together and #advocacymatters!



Happy Father’s Day to our #DSDADS!

Days before World Down Syndrome Day in March 2018, Mark Johnson did the seemingly impossible by completing a double Ironman. A double ironman involves 4.8 miles of swimming, a 224-mile bike ride and culminates in a 52.4-mile run. What inspired him to undertake such a feat in rural Texas? His inspiration was his sister, Wendy, who has Down syndrome.


Although Wendy is 50, the Johnson family remembers her birth and subsequent diagnosis clearly. Doctors suggested to the family that they should leave Wendy at the hospital because of her diagnosis.  Richard Johnson, Wendy’s father, said, “I did not know a lot about Down syndrome, but I knew Wendy was special and her diagnosis did not bother me.”

As Wendy grew, her father treated his daughter just like his other children. The Johnson family made sure Wendy was included in school, community and church. “Wendy has been a blessing to us,” Richard said. “We have learned more than we need to about human nature by watching Wendy grow and develop into a fine young lady.”

Mr. Johnson is proud because he believes having a daughter with Down syndrome has made him a better father. “Wendy has taught me acceptance,” Richard said.

Mark observed his parents raise Wendy over the years and applied their parenting style to his own family. “My dad provided a lot of fatherly love, compassion and patience,” Mark said. “Just by watching how my dad surrounded Wendy with love put something on my heart to ensure I was always fighting and advocating for my kids.”

Screen Shot 2018-06-15 at 10.33.06 PM

The Johnson family never allowed Wendy’s diagnosis to impact or determine what she could or couldn’t do. They have been changed for the better because of Wendy.

The story of the Johnson family and their love for Wendy made an impact on the Down syndrome community across the United States. Mark’s double ironman feat raised almost $30,000 for the National Down Syndrome Society, the leading human rights organization for all individuals with Down syndrome.

This Father’s Day, the National Down Syndrome Society (NDSS) is proud to honor all fathers of individuals with Down syndrome. We are grateful for the love and support offered by every #DSDAD to the Down syndrome community. Consider making a charitable donation to NDSS this Father’s Day in honor of that superhero dad in your life. #DSDAD

Fathers Day Graphic


Share your #DSDAD story with us on social media!

Facebook: @NDSS1979

Twitter: @NDSS

Instagram: @ndssorg

United We Stand For All People with Down Syndrome — We Wish United Airlines Would Too

During my tenure as the President and CEO of the National Down Syndrome Society (NDSS), the leading human rights organization for all individuals with Down syndrome, NDSS has spearheaded campaigns pertaining to a multitude of issues ranging from employment, housing, civil rights and healthcare. At NDSS, we have firsthand experience of the ugly discrimination that continues to exist around the world and regularly address tragic situations such as Iceland’s more recent efforts to eradicate Down syndrome to the widespread practice of declining medical care to people with Down syndrome.

To everyone’s delight (and, considering 2017’s political climate, surprise), our United States Congress has excelled in advancing the interests of individuals with Down syndrome, who are now living longer, more productive lives than ever before. We have collaborated to create avenues for financial security and economic empowerment through the passage of the Achieving a Better Life Experience (ABLE) Act. In fact, a few weeks ago, NDSS joined by leading members of Congress from both sides of the aisle to announce the formation of a new nonpartisan Congressional Work Group on Disability Employment, which aims to end antiquated 1960’s laws, that hold individuals with Down syndrome and other disabilities back from seeking full independence and employment.

Our NDSS mantra is that if you are not at the table, you are on the menu; In 2017, we have brought more individuals with Down syndrome to that figurative table than ever before through our national grassroots advocacy efforts on Capitol Hill and in state capitals across the country, through our National Buddy Walk® Program and a litany of campaigns aimed at shifting the disability landscape.

Thus, you can imagine our surprise when NDSS learned of the blatant and disgusting discrimination against an adult with Down syndrome, Sean Cross, aboard United Flight 783 on October 15th flying from Los Angeles (LAX) home to Washington-Dulles Airport (IAD). Sean, a 25-year-old Eagle Scout, and an employee of a local coffee and chocolate shop, was asked upon boarding this United flight if he was willing to assist in an emergency situation as he was seated in an exit row. Sean answered “yes” and proceeded as we all do to board the plane. Unfortunately, when seated on the plane, without the second “exit row” mandatory question, a flight attendant approached Sean and his family, to move them to alternative seats on the plane — they simply told his family that they would not be allowed to remain in their seats and if they did not move they would be forcefully removed from plane. During this discussion, three flight attendants refused to look at, or even speak, directly to Sean.

According to the U.S. Department of Transportation, “FAA’s rule on exit row seating says that airlines may place in exit rows only persons who can perform a series of functions necessary in an emergency evacuation.” Sean’s rights under the Americans with Disabilities Act (ADA) were 100% violated — as he was ready, willing and able to assist if a situation would to arise. Sean, without even the opportunity to speak or advocate for himself in this tragic situation, was discriminated against for no other reason than he has Down syndrome.

Of course, this is not the first time the airline industry has been exposed for their culture of discriminating against individuals with disabilities. In 2012, American Airlines humiliated Bede Vanderhorst, who happens to have Down syndrome, by blocking his entry to the plane because the airline “did not want an individual with Down syndrome sitting in first class” (an ironic choice of words, indeed, considering the airline’s low-class exhibition of authority). And who could forget that this is hardly United Airlines’ first trip down discrimination lane?

These first-class cases of discrimination against individuals with Down syndrome or other individuals with intellectual and developmental disabilities are not condoned by NDSS in any setting, be it recreational, professional, educational, airborne, idling or otherwise.

At a moment when the disability movement is gaining wider social justice and inclusion in the U.S., it is clear that United Airlines, and, more generally, the airline industry, is stuck in a feedback loop of discrimination, putting short-term profits over the long-term goals of the community they claim to serve. The truth is that people with Down syndrome make meaningful contributions to their communities every day, yet they continue to face injustice, as evidenced by yet another egregious act on behalf of the airline industry.

To be sure, to advocate a boycott against the airline industry would be remiss: after all, the mission of our organization is to work with all people, not againstthem, in order to make the world a better place for all individuals with Down syndrome. NDSS has reached out to United Airlines multiple times on behalf of the Cross family in order to explore ways we can work together, be it through a training video including individuals with Down syndrome, the hiring of an airline attendant with Down syndrome or even a working group across the airline industry dedicated to learning about how best to serve customers with disabilities.

Each attempt has been stymied with silence and secrecy.

United Airlines, during another flight last week, offered a form letter apology to Sean. In this blatantly cookie-cutter correspondence, they provided no indication they plan to take our concerns seriously, even after our offer to collaborate to bring widespread change to the limping airline industry which, as demonstrated, could desperately use a PR boost before it is dragged ever further toward oblivion.

We hope the United Airlines leadership, especially Mr. Oscar Munoz, takes our concerns seriously and takes NDSS up on our offer to sit across the “table” with our leadership and the amazing Cross family. It is time to roll up our sleeves and discuss how we can incorporate disability awareness, sensitivity curriculum and training tools on how to interact with an individual with Down syndrome or any other intellectual disability. It is not just the culture of United Airlines, that needs an overhaul, but the entire airline industry as well.

Activism – Advocacy – Action


Our National Down Syndrome Society (NDSS) Philosophy on Advocacy & Advocate Empowerment

The mission of the National Down Syndrome Society is to be the leading human rights organization for all individuals with Down syndrome. To that end, as an organization, we are immensely proud of the fact our policy of aggressive, nonpartisan engagement has helped our organization become a highly effective voice for promoting economic empowerment and social change for all people with Down syndrome across all levels of government.

For nearly 40 years, NDSS has worked to educate policymakers — of all political stripes — to advocate and advance an agenda that spans the entire life experience of individuals with Down syndrome; these priorities cut across inclusive education, economic self-sufficiency, community integration, employment, healthcare and research.

Our NDSS National Advocacy & Policy Center supports our non-partisan mission in a number of important ways, including:

  • Working with the U.S. Congress, the Administration, state governors and legislatures — regardless of political party affiliation — to develop legislative and regulatory initiatives that improve outcomes
  • Training and educating parents, self-advocates and others to advocate on the local, state and national levels through our cutting-edge grassroots NDSS DS-AMBASSDOR® Program
  • Organizing and participating in national stakeholder coalitions
  • Developing public- and private-sector partnerships to advance common objectives

Screen Shot 2017-07-10 at 11.43.07 AM

As part of our 2017 efforts, the NDSS Board of Directors — working with our network of over 380 Down syndrome affiliate organizations, self-advocates, families and other members of the Down syndrome community — has established several key legislative priorities, including:

  • Opposing health care reform legislation that makes draconian cuts to Medicaid and other changes that undermine the health care and supportive services that individuals with Down syndrome need
  • Expanding the Stephen Beck Jr., Achieving a Better Life Experience (ABLE) Act, an effort originally spearheaded by NDSS where 49 states enacted state ABLE laws, and 23 state ABLE programs are now available to our families
  • Increasing inclusive education across all educational environments, advocating for full funding of the Individuals with Disabilities Education Act (IDEA) so that all students with Down syndrome are able to receive a free appropriate public education in the least restrictive environment (last month, we launched our new NDSS National Inclusive Education Task Force to create more inclusive educational environments for all students with Down syndrome all while ensuring our students are graduating with employment opportunities in a more inclusive workforce and world)
  • Supporting legislation to increase research on congenital heart disease, which affects approximately half of all people with Down syndrome, in an effort to improve long-term health outcomes and allow individuals with Down syndrome to live long, healthy lives
  • Promoting nondiscrimination in organ transplantation by increasing enforcement of federal nondiscrimination laws and enacting state laws to address continued barriers to receiving this lifesaving care
  • Increasing National Institutes for Health (NIH) biomedical research funding for Down syndrome research across all Institutes and Centers

The work of NDSS is designed to help meet our societal obligation to protect the vulnerable. As we continue to move forward, we are confident that through engaging with policymakers from all political parties equally and respectfully — and more importantly, telling our stories — we will continue to advance our values and the priorities of our community.

Join Our NDSS Army!


Subscribe to our NDSS Action Alerts: Whether you are not sure who your local elected representatives are or you are a seasoned advocate, everyone can get involved by signing up for NDSS Advocacy Alerts. Our NDSS team wants to keep you in the know on what you can do to help support and advance our Down syndrome legislative priorities. A quick phone call or submitting a letter by email both help affect positive changes for people with Down syndrome!

 Join Our NDSS DS-AMBASSADOR® Program: Participants are volunteer advocates committed to serving as liaisons between NDSS and their Congressional delegations. The backbone of NDSS Advocacy programs, our ambassadors are volunteers who build long-lasting relationships with their U.S. Senators and U.S. Representatives.

Join Us in Washington, D.C.: We host our annual NDSS Buddy Walk® on Washington Advocacy Conference each year, and it is the perfect opportunity to join hundreds of Down syndrome advocates from across the U.S. to make a difference for people with Down syndrome. This annual two-day advocacy conference includes a day of training and our NDSS “Capitol Hill Day.” Our 2017 dates are April 10-11, 2018. Stay tuned – our 2018 registration will open in September!

For more information, please visit

Follow NDSS on Facebook

Follow NDSS on Twitter

Follow NDSS on Instagram

At the table: The importance of advocating for ABLE

Individuals with Down syndrome need to be able to speak up and be heard. That’s why, as the leading human rights organization for all individuals with Down syndrome, the National Down Syndrome Society, works to be at every table. Today, NDSS will have a 400 person army of advocates on Capitol Hill with self-advocates from around the country telling their own stories to advance critical legislation for all people with Down syndrome.

Advocacy is at the heart of everything we do at NDSS – we advocate at the federal, state and local levels of government to advance policies that make the world a better place for people with Down syndrome. We believe “if you’re not at the table, you’re on the MENU.” At NDSS, we are at every table – advocating in all 50 state capitals, we are at the White House, the United Nations and today, we walk the halls of the U.S. Congress. We will storm the hill today for legislation that spans the life of an individual with Down syndrome – health, education, financial independence, community integration and employment.

We are excited to speak up in support of three bills being introduced today in the Senate and House to enhance the Stephen Beck Jr. Achieving a Better Life Experience (ABLE) Act of 2014. These measures, known as the ABLE to Work Act, The ABLE Financial Planning Act and The ABLE Age Adjustment Act, are the result of the tenacious leadership of a bicameral and bipartisan group that includes Sens. Bob Casey (D-Pa.), Richard Burr (R-N.C.), Jerry Moran (R-Kan.) and Chris Van Hollen (D-Md.) along with Reps. Pete Sessions (R-Texas),  Cathy McMorris Rodgers(R-Wash.), Tony Cardenas (D–Calif.) and Mike Doyle (D-Pa.).

Aimed at making ABLE accounts more effective in promoting financial independence and more accessible to a wider population of the disability community, NDSS is advocating for the passage of all of these bills in particular, the ABLE to Work Act, which is part of NDSS’ broader #DSWORKS® employment initiative to create meaningful employment opportunities for all individuals with Down syndrome.

NDSS always work to build bridges and advocate in front of any decision maker who can make an impact on the life of one person with Down syndrome. We speak with one, unified voice and advocating for the human rights of all individuals with Down syndrome. This is exactly how we passed the ABLE Act in 2014, when 85 percent of the entire U.S. Congress supported this effort.

Our Down syndrome community is a global army with seats at every table, sharing our own stories of advocacy in their own words – demonstrating that #advocacymatters.

#BeAtTheTable unspecified



NDSS is NOW “The Leading Human Rights Organization for All Individuals With Down Syndrome!”


U.S. Capitol Hill, Washington, DC on January 12, 2017

“Hello to our fellow advocates from across the country and around the world! I am Sara Hart Weir – the President of the National Down Syndrome Society. I am joined by some very special guests, advocates and colleagues today, as we are coming to you LIVE from the US Capitol in Washington, DC! We, at NDSS, are thrilled to share some very exciting news about the future of NDSS and the Down syndrome community with you today!

For almost four decades, NDSS has been an organization that has provided state-of-the-art, comprehensive programming to all individuals with Down syndrome and their families. Today, we couldn’t be more proud of the programs and services we offer our incredible community:

  • Our one of a kind National Advocacy & Policy Center that advocates right here in our nation’s capital and in state capitals across the country on legislative issues than span the life of an individual with Down syndrome!
  • Our National Buddy Walk® Program – the most recognized public awareness event in the world for people with Down syndrome!
  • Our Community Outreach and Resources efforts – which provide the very best information on Down syndrome in the world in over 140 different languages!
  • And, our Public Awareness initiatives, which are showing the world that people with Down syndrome not only deserve to be treated with dignity and respect but also through new campaigns like our #DSWORKS®  Campaign – the first-ever employment campaign for people with Down syndrome that is successfully showing everyone, including those on Main Street and Wall Street, that people with Down syndrome are ready, willing and ABLE to WORK!

Lili pic.jpg

Our core NDSS programs, under our new NDSS strategic plan, won’t change, they are only poised to grow stronger and more impactful. As a 4-Star Charity, one of the highest rankings a nonprofit can receive, we have made the strategic decision to capitalize on our current organizational strengthens, building on the ground work that has been set with three long-term goals in mind:

  1. Increase our capacity and grow revenue to provide our state-of-the-art, comprehensive and critical NDSS programs to the Down syndrome community by investing more resources into our programs
  2. Ensure NDSS, as an organization, has long-term sustainability for decades to come
  3. And expand our “footprint across the entire Down syndrome community” to encourage more individuals, supporters and advocates to join forces with us, “speak up, speak out” to help us make the world a better place for people with Down syndrome

We are reminded the very best ideas, big or small, come from the people, real people with life-changing ideas. Betsy Goodwin, our dedicated founder and board member, started NDSS in 1979 with Arden Moulton around her kitchen table.

The Stephen Beck Jr. Achieving a Better Life Experience (ABLE) Act – the most significant disability law since the Americans with Disabilities Act (ADA) is one of our proudest achievements of NDSS – it was also an “idea” born around a kitchen table, just a few miles from where we are standing by five dedicated parents from the Down syndrome community who realized – over a decade ago – the inequities that exist in our system – these advocates rolled up their sleeves and fought, not just for their own sons and daughters – but for all people with disabilities.

Mission Statement_Facebook[1].png

As the President of NDSS, under our new strategic plan, I am very proud and deeply humbled to unveil our new mission statement to you today. NDSS is now:

“the leading human rights organization for all individuals with Down syndrome.”

After all, a human right is “a right that is believed to belong justifiably to every person” – we know that people with Down syndrome still face a complex system that holds them back, we still phase discriminatory practices in education, employment and in the community, we still have outdated stereotypes that perpetuate low expectations.

The time is now. And on behalf of our NDSS Board of Directors and staff with the passionate members of our NDSS DS-AMBASSADOR® program, our dedicated Buddy Walk Organizers, our new NDSS Athlete Ambassadors and along side our strong network of affiliates, we invite you to help make our “army” stronger, and join forces with us on this journey of change focused on “activism, advocacy and action” to create a society full of high expectations, meaningful jobs, inclusive educational and community opportunities for all people with Down syndrome.

Our team, more than ever, is prepared to remain on the front lines to advance proactive policies and legislation that ensures all people with Down syndrome have the same RIGHTS as every other American – 

advocacy matters.jpgthe right to earn a fair wage and meaningful job

the right to be educated alongside peers

the right to save money

the right to live independently

the right to get married

And the right to just live your own life! 

The truth is, we’ve been a human rights organization for a long, long time, we are redefining our presence to make our community bigger and stronger, paving a clear path forward so that people understand that individuals with Down syndrome have their own hopes, dreams and aspirations – and what’s truly needed is a systemic change to allow this to happen.

I hope – whether you’re tuning in from your office computer, your iPhone in the elevator, your Samsung on your coffee break, between meetings on your iPad or from any device at YOUR OWN kitchen table, you join NDSS – we invite you to be part of this movement – a movement which will redefine what having Down syndrome means for decades to come.

Together, we will create a world in which all people with Down syndrome deserve the same the opportunity to enhance their quality of life, realize their life aspirations and become valued members of welcoming communities.

From our NDSS family to your family, we are deeply grateful to advocate for and along-side you each and every day!”

-Sara Hart Weir, MS, President, NDSS

NDSS Celebrates the 2nd Anniversary of the ABLE Act and the Launch of #ABLEnow!



Two years ago today, on December 19, 2014, President Obama signed the Stephen Beck. Jr. Achieving a Better Life Experience (ABLE) Act (PL 113-295) into law, creating a revolutionary opportunity for people with disabilities to save for their future without jeopardizing critical government supports. The National Down Syndrome Society (NDSS) and Autism Speaks led the advocacy effort behind the passage of ABLE Act, and ever since, we have been working with state ABLE programs to make ABLE Accounts available.

Check out our NDSS 2nd Anniversary Report!

Today, as the Co-Founder of the ABLE Alliance for Financial Empowerment and President of NDSS, I was honored to take part in the official launch of ABLEnow – the Virginia ABLE program – with the Beck Family, Congressman Beyer, Delegate Filler-Corn and Mary Morris, Chief Executive Officer of Virginia529 College Savings Plan! 

In this long, exciting and historic decade-long ABLE journey, it was a moment to see Natalie Beck, Steve’s daughter, now have her own ABLE Account – #ABLEnow! You can watch the press conference from our NDSS Facebook Live feed hereimg_0731-2

Or you can also read our NDSS remarks below:

It is beyond a pleasure and honor to provide remarks at today’s monumental launch of the Virginia ABLEnow Program. As the co-founder of the ABLE Alliance for Financial Empowerment and the President of the National Down Syndrome Society, today is a very historic day – As someone who  worked on the ABLE Act for nearly a decade, I can’t think of anywhere else I would rather be – celebrating the 2nd Anniversary of the passage of the ABLE, making even more history!

The ABLE Alliance was formed earlier this year to support individuals with disabilities in their efforts to achieve financial empowerment and economic independence. The ABLE Alliance is working to:

  • Promote and market the widespread availability and diverse utilization of ABLE accounts to eligible individuals and their families
  • Advocate for legislative and regulatory policies, at both the federal and state levels, to ensure effective ABLE Act implementation and full participation
  • Create and support initiatives that advance financial literacy tools for all persons with disabilities
  • Educate eligible beneficiaries and their family members and caretakers on ABLE accounts, their use as a savings vehicle, how they interact with public assistance programs, and ways to protect beneficiaries from financial abuse
  • Engage stakeholders in advocating for a federal and state public policies that will break down barriers to financial empowerment and economic independence, such as policies that creating meaningful employment opportunities for individuals with disabilities throughout their lifespan


It’s only fitting that two years to this exact day – President Obama signed the ABLE Act into law, and we are standing here in Virginia launching the 9th state ABLE program in the US. This state has been the place of so many ABLE firsts – the first state ABLE bill signed into law (by Governor McAuliffe) after the federal passage of the ABLE Act, one of the first states to have the entire Congressional delegation cosponsor the ABLE Act and most notably – the birth of ABLE itself.


While many people understand the importance of the ABLE Act and now, ABLE programs like ABLEnow – most folks don’t understand the blood, sweat and tears that went into making the ABLE Act a reality. The idea stemmed from a kitchen table – here in Northern VA by five parents who have children, and in some cases, (now) adults with Down syndrome. These parents came up with the idea for what ultimately became the ABLE Act, and set in motion the most significant disability civil rights legislation to date.

The ABLE Act was ultimately named after our late NDSS Vice Chair, one of those five parents around that kitchen table and my dear friend – the quarterback of the ABLE Act – Steve Beck. Steve was one of the most incredible individuals that I ever met – he was a dedicated father, husband and tireless advocate. He and I pounded the pavement (or marble) on Capitol Hill with Stuart from Autism Speaks for years – we experienced many trials and tribulations, many years (eight, in fact), many Congresses (four of them to be exact), many nay-sayers, small victories, set-backs, some House of Cards moments – but we never gave up. Never once.

Steve taught me so much – And he would probably kill me for quoting a Democrat, “one person can make a difference, and everyone should try.” So many people made the ABLE Act a reality – so many people told their own stories, so many people made phone calls, sent emails, tweets, made trips to Washington, so many advocates made this possible.

And while the ABLE Act took almost eight years and four Congresses to enact, when we did it, it was the most bipartisan legislation of all time – we had 85% of the entire US Congress cosponsor this bill, 381 of 435 in the House, and 78 of 100 US Senators! Steve left a legacy like no other, and now today, his daughter, Natalie can open up her own ABLE account. I would say that witnessing the ABLE Act pass the House, just two years ago with Steve sitting in the House Gallery would have been his proudest moment – but I would say today is!

I sincerely want to thank (and congratulate) Mary Morris and Chris McGee for their dedication, commitment and passion for the ABLE Act – they have been leading this effort for over two years. Mary and Chris have become friends and fellow disability advocates.

For ABLE, this is just the beginning, ABLEnow is a life-changing financial tool – that families all across the country will utilize day in and day out for necessary life expenses. Once again, congratulations to the ABLEnow team!

“Get to Know Me” – How NDSS is Teaching Inclusion in our Elementary Schools

A special thank you to NDSS DS-AMBASSADOR™ Indrani Solomon from Tucson, Arizona for authoring today’s guest blog. Indrani is an amazing and tireless advocate for her son, Pranoy, and all people with Down syndrome! 

screen-shot-2016-12-02-at-9-37-11-amThey say a classroom is only as good as the child it does least for. So many of you would agree.

From what we understand as parents of a child with Down syndrome, students with I/DD need a solid education in life just like their neuro-typical peers, learning alongside their peers and contributing to society one day, just like their peers.

My son, Pranoy, was recognized by the Mayor and the Council-member of Oro Valley this year for promoting inclusion in the community, owing his recognition to NDSS for selecting his photo for the video at Times Square. I remember those meetings at the Town Hall where I would get to see individuals with Down syndrome in janitorial roles representing an agency through which they would get hired and I would walk in to talk about inclusion in the community. I was constantly reminded how lucky our children were to have parents like us believing in our children’s potential and helping build a brighter future for them. Even though it was all new to the Town officials, they still listened and are in the process of collaborating with NDSS to bring in inclusive programs that benefit residents with all abilities. 

The resistance and the ignorance that I get to shatter one educator at a time takes up my day (and night) in many ways. But my husband and I are firm believers of collaboration and peace – doing this in steps, treading softly but surely while we win over hearts and minds.

This year, I asked Sara Weir to help me build this foundation at my son’s school by presenting to 4th and 5th graders. Her knowledge combined with her creativity in finding the most appropriate answers to so many hands raised (young and old) was such an amazing experience for each of us.ndss-poster_ds

A lot of parents came forward to thank me for the presentation – proving these 4th and 5th grade students did share their experience at the dinner table. A couple of them wanted to know the type of Down syndrome Pranoy had. Some of them got to learn their own friends did not like science as much as they did. Some of them wanted to sit at lunch with Pranoy. The questions they asked and the answers Sara came up with made the school library a promising ground for future thinkers, teachers, doctors, lawyers, scientists, artists, activists, legislators, police officers – the list goes on.

What stuck with me was why the math teacher suddenly asked about the Alzheimer’s connection – primarily to think no matter what you do, Alzheimer’s kills this population sooner or later. While Tucson really has a lot of catching up to do, I wish I could change their perception somehow, after all, it is all about keeping the brain active and the heart happy from the get go – and that is what inclusion really is in a nutshell: acceptance and opportunities.

Pranoy’s basketball league coach wanted all eight kids back on his team next season so when I jokingly said that he was being brave by wanting someone kicking water bottles, back on his team again, his thoughtful response was, “that keeps me alert.” This speaks volumes especially when I am surrounded mostly by decision makers in the education field who want change but don’t want to change.

I count my blessings every day. Pranoy’s current reading teacher did not want him in his class a few years ago when she was teaching 2nd grade because she didn’t have the right support system to offer. Fast forward, she has become his favorite teacher, he’s now wanting us to invite her to a beach vacation. At collaboration meetings, she thinks out of the box paving the way for the other subject matter experts to think creatively and believe in Pranoy’s ability to learn as any other. 

Thank you, Sara, for the awareness you have created here in Copper Creek Elementary. Even though weNDSS Poster_DS.png were faced with resistance and ignorance, please know that you emerged as a true leader in spreading love for all children with Down syndrome and helping peers understand how important it is to save for one’s future, embrace diversity and learn firsthand how all of us deserve the same chances in life amidst our differences. 

Thank YOU South Texas… A Few Days Down by the Border!

img_6284_2It’s quite true what they say “everything’s bigger in Texas”! This is especially true for the southern hospitality I experienced over the last few days in the Rio Grande Valley!

I was very honored to be invited to attend a series of events last weekend in Brownsville, Texas by NDSS DS-AMBASSADOR™ Sergio Zarate, one of our original ambassadors, and his family – a weekend that I’ve had saved on my calendar for over a year, since Sergio invited NDSS to participate.

img_3769We kicked off Friday with an inspiring event hosted by Driscoll Heath Plan led, by Lizbeth Shanholtzer, where I talked about NDSS and our advocacy and programming efforts for individuals with Down syndrome. I was so humbled that so many advocates and affiliate leaders from around the state of Texas attended, including: Down by the Border, Rio Grande Valley Down Syndrome Association and Down Syndrome Association of Laredo (who drove over three hours!)

img_6329That afternoon, Sergio and Dolores Zarate, Dr. Manuel and Olga Mendoza and the families of Down by the Border and leaders of the Order of Alhambra, Brownsville rolled out the red, I mean, “yellow”, carpet for me!
State Senator Eddie Lucio and Representative Eddie Lucio III, two dedicated champions for people with disabilities in the state of Texas, honored me with the Texas Yellow Rose and a flag flown from the Texas State Capital in my honor. Wow, this was some incredible southern hospitality! It was such a treat to meet Dr. Esperanza Zendejas, the Superintendent of Brownsville Independent School District, who serves over 500 students with disabilities across the Rio Grande Valley.

On Saturday morning, it was an honor to attend and speak at the 4th Annual Rio Grande Valley Down Syndrome Association Step Up for Down Syndrome Walk – a special thank you to Deborah Tomai for her leadership in the Rio Grande Valley!

I ended the day by having a “BALL” at the 2016 Children’s Festival in Brownsville – an inclusive festival for all individuals with disabilities and their peers! It was a phenomenal celebration and way to celebrate all abilities!IMG_3891.JPG

I can’t wait to return to the Rio Grande Valley! A very special thank you to the Zarate and Mendoza families for being such wonderful hosts! Thank you for showing Rio Grande Valley that #advocacymatters!