Kansas Council on Developmental Disabilities

Kansas Council on Developmental Disabilities Welcome to the Kansas Council on Developmental Disabilities (KCDD or Council).

The Council supports people with developmental disabilities so they have the opportunity to make choices regarding participation in society and quality of life.

Just a week and a half away đź“…đź“… Children's Mercy will be hosting a Bilingual Resource Fair on September 9 and we're excit...
08/28/2026

Just a week and a half away đź“…đź“…

Children's Mercy will be hosting a Bilingual Resource Fair on September 9 and we're excited to participate!

Registration is encouraged. Register at https://cmkc.link/bilingual-resource-fair

[Image descriptions: Blue and white flyer with details about resource fair Bilingual Resource Fair: Please join us for our Bilingual Resource Fair focused on mental health and developmental disabilities. Organizations that provide mental health services and support to children with disabilities as well as Spanish speaking families will be at the
fair.
• We will have Spanish-speaking providers who can speak with families • Spanish interpreters will be available to help groups that do not have Spanish-speaking providers
• Snacks will be provided
When:Wednesday Sept. 9, 2026
Time: 2 - 6 p.m.
Where: Kauffman Foundation
Conference Center,
4801 Rockhill Rd,
Kansas City, MO 64110
Registration is encouraged to help us plan for snacks, but it is not required. Walk-ins are welcome. Please scan the QR code or visit https://lnkd.in/gqzKXmVJ register.]

Kansans with intellectual and developmental disabilities are people—not numbers. KCDD has a clear, six-part plan to elim...
08/26/2026

Kansans with intellectual and developmental disabilities are people—not numbers.

KCDD has a clear, six-part plan to eliminate the I/DD waitlist through stronger leadership, smarter technology, seamless services, real accountability and protected funding.

Kansas can—and must—end the wait. Share our plan and help us make it happen.

You can also join our movement here: https://www.kcdd.org/kcdd-day-at-the-capitol



[Image description: Text flyer - white space at top contains large dark blue left aligned text "KCDD has a plan to eliminate the IDD waitlist." next to the KCDD logo and boxes containing six recommendations below:
1 Put One Leader—and One Number—in Charge
Appoint a statewide KDADS Secretary with the mission of eliminating the IDD waitlist and establish one accurate, publicly reported count.
2 Use Waiting Time to Get People Ready
Complete paperwork and service planning early between KDADS and CDDOs so support can begin as soon as funding is available.
3 Replace Spreadsheets with a Smart, Shared System
Give families one portal to update information, track their status, and know exactly what happens next.
4 Make CSW a Bridge to Comprehensive Services
Let people receive Community Supports Waiver services without losing their place on the I/DD waiting list—and define a clear process for Kansans to move seamlessly from CSW to the comprehensive I/DD Waiver as their needs change.
5 Set Deadlines—and Measure Services Actually Delivered
Hold every agency and contractor accountable until a person receives their first authorized service.
6 Protect the Funding and Enforce a Five-Year Plan
Dedicate waitlist dollars to waitlist services and require KDADS to present the Governor and Legislature with a transparent, fully funded five-year plan to eliminate the wait.]

Over the past several months, KCDD has worked alongside our Council members, self-advocates, families, partners, and com...
08/25/2026

Over the past several months, KCDD has worked alongside our Council members, self-advocates, families, partners, and community members to develop our Draft Five-Year State Plan (2027–2031).

Together, we identified the goals and priorities that we believe will create meaningful systems change for Kansans with intellectual and developmental disabilities.

Now, we need YOUR voice.

View the plan and give feedback at https://www.kcdd.org/five-year-state-plan

[Image description: a path through a field of wheat behind uppercase centered butter yellow text: YOUR IDEAS CAN INFLUENCE THE PATH WE TAKE. Below that is white sentence case centered text: Share your feedback on KCDD's draft 5-year plan. + the KCDD logo centered near the bottom]

What happens to your loved one's care plan when you're no longer able to provide it?Join us for Planning for the Future:...
08/21/2026

What happens to your loved one's care plan when you're no longer able to provide it?

Join us for Planning for the Future: Supporting Aging Caregivers of Individuals with Intellectual and Developmental Disabilities, a webinar offering practical guidance on building a comprehensive future planning roadmap through a 4Ms lens (what matters, medication, mentation, and mobility).

đź“… Friday, August 28, 2026
🕛 12:00–1:00 PM Central

You'll leave with:
✔️ Key components of a future planning process for individuals with IDD and their aging caregivers
✔️ Legal and financial tools — decision-makers, powers of attorney, guardianship, ABLE accounts, and special needs trusts
✔️ Strategies for organizing essential documents and communicating future support preferences
✔️ A 4M approach to planning future caregiving, housing, and decision-making

If you support aging caregivers or individuals with IDD, this webinar is for you.

Register at https://eeds.com/live/320677

[Image description: Blue flyer with a photo of a middle-aged woman embracing her younger daughter with down syndrome at the top right. At the left are text details about the event: Planning for the Future:
Supporting Aging Caregivers of
Individuals with Intellectual
and Developmental Disabilities
Friday, August 28, 2026
12:00 PM - 1:00 PM (Central)
Planning for the future is one of the most
important steps caregivers can take to ensure
continued support for a loved one with intellectual
and developmental disabilities (IDD). This webinar
will provide practical guidance on creating a
comprehensive future planning roadmap through
a 4Ms (what matters, medication, mentation, and
mobility) lens, including identifying future
caregivers and decision-makers, organizing
essential legal and personal documents, exploring
financial planning tools such as ABLE accounts
and special needs trusts, and preparing for future
housing and long-term support needs.
Participants will gain strategies and resources to
help ensure continuity, stability, and peace of
mind for individuals with IDD and their families.
Learning Objectives
Identify the key components of a comprehensive future planning
process for individuals with IDD and their aging caregivers through a 4Ms lens.
Describe legal and financial planning tools that support long-term stability,
including designated decision-makers, powers of attorney,
guardianship, ABLE accounts, and special needs trusts.
Develop a plan for organizing essential documents and
communicating future support preferences to family members and
other trusted individuals.
Recognize strategies aligned with 4M for planning future caregiving,
housing, and decision-making arrangements to
promote continuity of support and quality of life. ]

Our draft plan is open for public comment, and we invite you to read it and tell us what you think. Does it reflect what...
08/20/2026

Our draft plan is open for public comment, and we invite you to read it and tell us what you think.

Does it reflect what's most important to you?
Did we miss something?
What would make this plan even stronger?

We can't wait to hear from you.

View the plan and give feedback at https://www.kcdd.org/five-year-state-plan

[Image description: a path through a field of sunflowers behind uppercase centered butter yellow text: YOUR IDEAS CAN INFLUENCE THE PATH WE TAKE. Below that is white sentence case centered text: Share your feedback on KCDD's draft 5-year plan. + the KCDD logo centered near the bottom]

08/19/2026

Lola here - 🏆 I had the blessing of receiving the Youth Advocate of the Year (20–30) award at the Kansas Disability Caucus Conference!! ❤️

Receiving this award means so much to me—not just because I am being recognized, but because it reminds me how far my advocacy journey has come.

I am a self-advocate with Down syndrome, a professional with three paid jobs, and a college student! I work full-time for the Kansas Council on Developmental Disabilities (KCDD) as the Advocacy Coordinator, but my advocacy journey did not start there.

My advocacy journey started when I first learned that my voice matters in sixth grade. It started with the impact of Down Syndrome Innovations on my life and employment journey. It grew through getting involved in my community, and it continued when I landed my dream job in public speaking and advocacy. Along the way, I have made so many friends and connections! đź’™

I want to thank my wonderful team at KCDD and all my bosses and colleagues for believing in me, encouraging me, and motivating me to get things done. I am also grateful to Down Syndrome Innovations for helping me navigate the world as a self-advocate and for providing employment opportunities. And, of course, thank you to my family and friends for always supporting me and cheering me on! ❤️

This award is a reminder that our voices matter, our stories matter, and our advocacy can make a difference. We all have a role to play in creating a more inclusive community where people with disabilities are heard, included, and valued. 🗣️✨

Thank you for believing in me and in the power of self-advocacy!

Nothing About Us Without Us! ✊



Self Advocate Coalition of Kansas

[Video description: The Kansas Disability Caucus stage where Lola accepts her award]

Our roundtables are about people, possibility, and knowledge.Earlier this week, KCDD participated in our second roundtab...
08/19/2026

Our roundtables are about people, possibility, and knowledge.

Earlier this week, KCDD participated in our second roundtable discussion focused on financial empowerment and financial security for all Kansans. We were joined by Treasurer Steven Johnson and members of the Kansas State Treasurer Steven Johnson’s Office, Congressman Ron Estes, Senate President Ty Masterson, Ronn McMahon of the Greater Wichita YMCA, KCDD Council Chairwoman Karey Padding, KCDD Executive Director Sara Hart Weir, KCDD staff, families, and other leaders.

We continued the conversation around the implementation of Senate Bill 304, the Born to Invest Act, and how we can get the word out on how ABLE Accounts, Trump Accounts, and 529 savings plans can work for Kansans.

Financial literacy is a life skill. It matters to young people, adults, older Kansans, families, and absolutely to people with intellectual and developmental disabilities.

Good public policy is about more than passing a law or creating a program- people have to KNOW the opportunity exists.

KCDD is helping ensure families receive information about ABLE Accounts, 529 plans, and Trump Accounts when their child is born because we know that early knowledge can change so much.

For a family raising a child with IDD, it can mean understanding that disability and financial independence are not opposites. It can mean knowing that saving, planning, working, and building assets are possible.

People can disagree on politics and still agree that people with disabilities deserve opportunities, and families deserve information.

When we put the right information into people's hands, we give them opportunity, independence, choice, security, and hope.

KCDD is proud to keep bringing people to the table and keep pushing this conversation forward.

Knowledge IS power. Let's make sure everyone has access to it.

[Photo descriptions: 1 - Group photo with KCDD staff Lola, Sara, and Whit, KCDD Council Member Karey Padding, Congressman Ron Estes, Kansas State Treasurer Steven Johnson, Ronn McMahon of the Greater Wichita YMCA, and Senate President Ty Masterson
2 - Whit talks to the other attendees of the meeting. They are all sitting around tables in a square
3 - Closeup of Lola seated at the table speaking at the meeting. She is sitting next to Karey Padding]

What happens when a community that has spent nearly two years connecting through a screen finally gets to gather in the ...
08/17/2026

What happens when a community that has spent nearly two years connecting through a screen finally gets to gather in the same room?

Something really special…

Recently, We All Matter (WAM) held its FIRST ever in-person gathering, bringing together people with IDD from the WAM community and beyond for an afternoon centered around connection, belonging, mental health, and disability pride!!

We shared stories. We listened to one another. We talked honestly about mental health and what it means to belong. We participated in a World Cafe discussion that gave people with lived experience the opportunity to shape the future of WAM and help us better understand what people with IDD need from mental health supports.

We laughed. We ate ice cream from The Golden Scoop. We learned from an incredible keynote from Julia Connellis about authenticity, disability pride, and self-care. Most importantly, though, we got to be together!

We started WAM because we believe that people with intellectual and developmental disabilities deserve a place where they can talk about mental health, connect with peers, and belong without having to explain or apologize for who they are.

Watching that idea come to life at our very first in-person event was truly special!
We also want to extend our appreciation to Kelly Jones (our mental health professional co-facilitator), Dr. Jessica Schuttler, and every person who is a part of the WAM Research Team! We All Matter wouldn’t be the same without each of their dedication, expertise, guidance, and support.

To those of us who are a part of WAM, it feels like more than just a support group. We have created a community and a movement toward ensuring that the mental health system includes individuals with IDD.

[Photo descriptions:
1 - 11 people smiling and standing up for a picture in front of a screen that has the following text: We All Matter In-Person, a mental health support group for people with IDD
2 - A group of people spread out around three different tables. They’re all looking ahead as Julia, the keynote speaker does her presentation
3 - Three women sitting at a table. On the table is paper, markers, and a fidget toy
4 - A woman smiling and wearing a purple t-shirt that says disabled and proud
5 - Three people sitting at a table. One lady is speaking while the two others look at her intently
6 - Two people are seen sitting at a table that is covered with white paper
7 - Four people having a discussion around a table
8 - A young adult man lying on the ground while a woman sits on the ground next to him
9 - A dry erase board that has “how do you hope to feel today?” written on it. Stick notes are on the board. A few of the sticky notes read: patient, calm, happy, appreciated, secure, relaxed, rested, accomplished
A woman, Jess, standing in front of a room. People are seen looking at her as she speaks.
A table with four people seated around it. The four people all seem to be looking in the same direction.
A table with four women sitting around it.]

08/14/2026

Hello everyone- this is Whit, Vice President of Policy and Programming!

You know, I have provided testimony before the Bob Bethell Oversight Committee almost every single time they’ve allowed public testimony for the last three years. Giving testimony this week, though, felt the most personal, the most meaningful, and unfortunately, the one that hit a little too close to home.

I have shared my story many times with Kansas Legislators. I’ve shared about being on the IDD Waiver waitlist for 8 years. I have shared about how, in year four of my wait, I tried to end my own life. The issues that we advocate for at KCDD - these very important issues - are extremely urgent.

Kansas cannot afford to spend any more time taking backward steps. In 2024, 500 waiver slots were funded. In 2025, 200 waiver slots were funded. This year, however, 2026, there were NO slots funded for the IDD waiver.

This is an injustice to the 5,348 people currently waiting.

That is why, this week, I shared that the Bob Bethell Committee members act with urgency on this matter. This goes far beyond Legislative Members, though. As a community - especially as a disability community, we MUST tell anyone and everyone about the following reality:

All of the thousands of Kansans waiting on their IDD Waiver spot are all human beings with real dreams, real goals, and real hopes for their futures. Additionally, they all have real struggles and real barriers to community living. THAT is why they qualify for the IDD Waiver.

And that, my friends, is where my testimony hit a little too close to home…

As many of you know, our KCDD Council recently lost one of our own. Perri Spencer, 22, took his life. He was reaching year four of waiting for his waiver spot. Perri carried an immeasurable amount of emotional turmoil. And living his life without the proper support and services he could’ve received from the comprehensive IDD Waiver, his life was left to be a series of crises.

I shared that truth with the Bob Bethell Committee.

I wasn’t alone while giving testimony. Perri, our friend, was with us all in spirit. I even brought a bluetooth speaker and played part of Perri’s SPEAK Up! Video for all in the room to hear. His message to the legislature was simple: please fund the developmental disability waiver.

At KCDD, we are full of hope for the future! We know that this reality will one day be part of history - that one day, the waitlist will be eliminated. Until that day, we are committed, day in and day out, to join with fellow advocates, community members, legislators, and professionals to fight for every single Kansan who is waiting.

The wait will be eliminated. In doing so, Kansas will become better. People with IDD have a LOT to offer. We need to be supported so that we can be our best selves and live our best lives!

[Video description: Whit, a black woman with short, curly black hair wearing a red shirt jacket over a blue top, stands at a podium with many people seated behind her]

Mark your calendars for The ADA, the ABLE Act, and the Future of Disability Policy in America, a free webinar happening ...
08/12/2026

Mark your calendars for The ADA, the ABLE Act, and the Future of Disability Policy in America, a free webinar happening on September 9, 2026 at 12–1 pm ET/11-12 pm CT!

KCDD team members Sara Hart Weir, Whit Downing, and Lola Kernell will combine policy insight with powerful lived experience perspectives to examine both the progress achieved and the challenges that remain.

Find out more and register at https://www.cds.udel.edu/poweringfutures

University of Delaware Center for Disabilities Studies

Address

900 SW Jackson, Suite 569
Topeka, KS
66612

Opening Hours

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Tuesday 8am - 5pm
Wednesday 8am - 5pm
Thursday 8am - 5pm
Friday 8am - 5pm
Saturday 9am - 5pm
Sunday 9am - 5pm

Telephone

+17852962608

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