National Down Syndrome Society: Protecting Civil Rights of Different Brains, w/ Sara Weir | EDB 88

Hi, I’m Dr. Hackie Reitman, welcome to another
episode of Exploring Different Brains, and we are so lucky today to have the president
of the NDSS, which is the National Down Syndrome Society, the very passionate and strong Sara
Weir, who I had the pleasure of meeting when we were both presenting at the AADMD, the
American Academy of Developmental Doctors and Dentists, in Houston, Texas, recently
and Sarah Weir, you do great work. Thank you so much for being here with us at
Different Brains. Thank you so much for having me, it’s an honor
to be here this afternoon. Sarah, you’ve done so much for so many through
the NDSS and why don’t you introduce yourself to our audience because you can do it better
than I can. I’d be honored, thank you so much again, I’m
so excited to be here with you this afternoon. I’m Sarah Hart Weir, I’m the president of
the National Down Syndrome Society. We’re actually headquartered in New York City. We were founded in 1979. We also have a large presence in Washington
D.C., our nation’s capital and we are an organization with a very powerful mission statement, in
fact, we just revitalized our mission statement earlier this year. We are the leading human rights organization
for all individuals with down syndrome, you know from an organizational perspective, we
felt that it was very important to put a stake in the ground that individuals with down syndrome
have all of the potential in the world to achieve their own hopes dreams and aspirations
but for the only thing that holds the back are archaic outdated laws and as an organization,
we want to change those laws to empower individuals with down syndrome to live long healthy lives,
speak out inclusive educational opportunities, seek out full and competitive employment and
when I say employment, I’m not just talking about a job, I’m talking about a career
and of course be a meaningful contributing part of society and be integrated into the
community in a very competitive way so we’re very proud of our mission and we have an amazing
team behind this organization that’s fighting for the rights of people with down syndrome
each and every day. I love the way your whole body language changes
when you start talking about human rights and all of these values that you have and
all that you aspire to accomplish. Tell us how you got into this Sara. How I got into this wonderful community. So I’m from Kansas originally growing up,
I’m actually the summer of my freshman year of college. I got a phone call from a really good family
friend that I’ve known the majority of my life. I had been recommended to one of her family
friends to work with her young daughter with Down syndrome. They were looking for a pyramid or somebody
to spend the summer with Casey working on life skills, job skills, voice of the library,
special Olympics and had the opportunity to meet Casey and her amazing mom and dad and
brothers and sisters and immediately it clicked, I was became a part of her family, she’s still
a part of my family and she was my inspiration for getting involved in this amazing community
that the summer after that I got to see you know how an advocacy organization can really
influence the lives of so many and I had the opportunity in college to go to Washington
dc and one summer work for a lobbying firm and the other summer I got to spend working
at the children’s defense fund and immediately that set my career path to graduate. I graduated from undergrad and then went on
to be my master’s in public policy from Carnegie Mellon and then moved to Washington and I
started working with NDSS almost immediately when I was working at a lobbying firm, we
became we as an BSS became one of my first clients that I worked for and brought into
the firm and then about six years ago, the organization called me and asked me to come
in house. so I started off by with our VP of advocacy
and affiliate relations for about four years and I’ve been the president for the last
two-and-a-half years. Educate us with your passion about those of
us who are ignorant about what the Able Act is. Tell us about the ABLE Act. It’ s one of my favorite things to talk about. So, the ABLE act stands for the achieving
a better life experience back to able act and what the able act does is the first time
that individuals with Down syndrome and other disabilities can actually save their own money. It’s a 529 account by 529 a or 529 Able account
and what it does is it allows the individual with a disability and their family and basically
any other source to contribute to that account about $14,000 a year for expenses related
to the disability and those expenses are very broad. Housing, transportation, health, and wellness. Community integration, the ability to save
for a job coach or pay your job coach, the ability to buy technology that helps you live
your life or helps you do your job better. ABLE really address the barrier that exists
in society for individuals with down syndrome and other disabilities because our folks can’t
have more than $2,000 without being met benefits like Medicaid and social security in jeopardy
and so what ABLE does or did when we passed it into law on December 19, 2014, when president
Obama made it a law of the land. It allows our folks to save and remain on
those benefits and since January of 2015, we were required to take our federal advocacy
and moving to the states, we’ve passed 49 state ABLE laws, 49 out of 50, well 51 if
you count a district in Columbia and as of yesterday, we have we now have 22 state ABLE
programs, actually states that are offering ABLE accounts to our family. Now what was the bill? When you and I were in down at the AADMD in
Houston recently, president George H. Bush, the senior, who I was lucky enough to get
to meet in person with his wife, Barbara to talk about children’s problems many years
ago. He couldn’t make he and Barbara couldn’t make
it cause health reasons but tell us about the act that he signed when he was in. Yeah, so he’s credited with signing the Americans
with disabilities act which was the first real landmark civil rights legislation or
the larger disability community and you know the able act follows you know right on the
heels of that. Unfortunately, almost you know 25 years later,
did we pass the second most civil rights legislation in the form of the ABLE act. I’m hoping we don’t have to wait another 25
years for us to sign that next code into law, so let’s hopefully we can do it in this administration. Tell us about the next bill. I’m so glad you asked, you know if you look
at the way our benefits our entitlement programs are structured for people with disabilities. It’s ad-sit access and its income. Well, ABLE really addresses the asset problem. You know, having more than two thousand dollars,
I mean they can tell you the countless stories that I’ve heard as parents that we have
on staff at the NDSS. Some of our incredible advocates from across
the country that will tell you. That doctor on day one you know will tell
you, don’t put any money in your child’s name and the low expectations that come from that. Well, ABLE now sets the expectation. You know, college is the possibility, employment
is a possibility, but what we have an address is income, you know there are still very low
income limitations on that other side of the coin. You know roughly about $1,400 a month in what
an individual with a disability can earn without jeopardizing benefits like Medicaid and social
security, we know how important those programs are and right now, unfortunately, we’re having
that debate in Washington about Medicaid and what’s going on with the affordable care act
repeal and replace and I think we could spend you know three other interview sessions talking
just on that topic but the next bill to get to your question. it’s employment, you know, we have to break
down those archaic outdated laws rooted in entitlement programs when it comes to allowing
an individual with a disability to actually earn a fair wage. You know earning below the poverty line, it’s
a vicious cycle of poverty and so the conversations that NDSS with what we’re having in Washington
right now is how do we decouple the poor from the disabled in these programs and allow the
benefit of health care and job supports and community living to remain intact, but how
do we empower our folks because I think that’s the biggest misconception when you actually
sit down to talk to a person with down syndrome. You know they’re not looking for a handout,
they’re looking for a hand up and they’re looking not only for a job, they’re looking
for a career and that’s what we need to get them. What is the biggest misunderstanding that
Public has about people with Down syndrome? That’s a good question. My first response right just right off the
bat would be that people with Down syndrome want to be a burden on system or on society. You know, I’ve had a lot of people with
Down syndrome over the last 20 years and a lot over the last six years in my positions
at NDSS that is just not the case. They really want to be taxpayers, they want
to earn a fair wage, they want to get benefits from their employer and they want to live
the American dream and you know I think as an organization and as a society, along with
members of congress and other elected officials, we need to empower them to do that. What is the #DSWorks campaign? Oh, I’m so glad you asked, so #DSWorks our
#DSWorks because it’s 2017 and you need a hash tag for everything these days, it really
is our first ever employment initiative focused on showing the world that people with down
syndrome are read, willing, and able to work and with #DSWorks, we launched it last spring
so we’re just over a year into this campaign and what we do, we have three components at
#DSWorks. The first is providing resources to everybody
involved in the employment process. Parents, most importantly the self-advocate,
educators, employers, job coaches, everyone that supports that individual with achieving
a lifelong career we’re providing webinars, brochures, resources on our website, we’re
pulling in experts across the sequel to process to provide the information to our families. We’re reaching out to organizations like Linked
in, we want to see people with down syndrome on you know utilizing technology to find employment
opportunities. I’ve never seen somebody with down syndrome
on linked in and so many of us utilize that platform to network and look for job opportunities
and resources to put us in a more successful position in the employment area we work for. The second component is what I talked about
when you asked me what’s the next ABLE or what’s the next ABLE act. Its legislation, we need to break down these
barriers to allow folks to earn a fair wage, we need to put an end to policies and laws
that allow for some minimum wage. I just think it’s discriminatory that individuals
with Down syndrome and other disabilities can make sense on the hour to do the same
job that you or I would do without having a disability. And the final piece, which has been really
exciting to experience the last year with our amazing staff at the national Down syndrome
society and that is working with employers. So we’ve developed a number of partnerships
with employers to create meaningful job opportunities for individuals with Down syndrome, we’ve
worked with the NHL and the new Jersey Devils, we had two interns who participate in a 10-week
fellowship with the devils, Freddie and Alexa. Freddie’s work with the kids zone and oversaw
that process on the game day operations and Alexa was a ticket taker and they got paid
above minimum wage, we gave them transportation stipends to get to and from their job coaches
on site and at the end of the season without us even pushing the devils hired Freddie and
Alexa on as full-time employees. We’re working with companies like Moya financial,
who are not just looking at hiring practices but they’re looking at their benefits and
their health care insurance and are they offering the very best opportunities and insurance
policies for families that have loved ones with disabilities and then we’re working with
small businesses like company out of finger Texas, lakes no shack, which leg is the youngest
business owner in his small town of Sanford, Texas, got his business license from the city
council and the mayor but he’s the only business owner with down syndrome in the state of Texas. So we’ve been working with lake and his family
to provide scholarship opportunities for other individuals with down syndrome that want to
start their own businesses so that’s #DSWorks, we are breaking down barriers to employment
and we’re showing everybody from main street to wall street that people with down syndrome
are ready, worried, and able to work. Well, you keep up the great work. Tell our audience here at Different Brains
how they can get in touch with you and learn more. Absolutely, the best thing you can do is go
onto our website, it’s, if you pop over there, you will see a wealth of information. We’re very easy to get into contact to. You’ll find that on NDSS and the staff that
we have are the best staff in the nonprofit industry and we’re very proud to serve our
constituents and all of the families that we represent. And we here at different brains are glad to
highlight all of your work and we look forward to helping you in forming a greater partnership. It’s been such a pleasure to talk to you. Sarah, we’re the president of the NDSS, the
National Down Syndrome Society. Thank you so much for being a guest here at
different brains. Thank you so much for having me.

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