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november december 2018 connections

november december 2018 connections

Volume 23 Issue 98 November/December 2018


Building a network for individuals with Down syndrome, their families and the professionals who serve them.

KFC Coupon Books Pathways™ Program Launches Jan 2019
Benefit DSG
DSG hosted two informa on mee ngs for parents to come and learn more
Local KFC restaurants joined together for four about our Pathways™ program and we packed the house at each session. The
weeks in suppor ng the DSG! They provided program is designed for youth with Down syndrome who are 4‐20 years of age.
coupon books valued at $40 to any patrons
who made a dona on to the DSG. We are The Pathways ™ program is a transforma onal and comprehensive program
thrilled to share that $45,000 was raised to individualized to the needs of your child and your family. Across the year, your
support DSG’s vital programs and services. family can receive 50 hours of support from an interdisciplinary team con‐
sis ng of an Occupa onal Therapist, Speech‐Language Pathologist, and Board
Cer fied Behavior Analyst. Tis team can help you create a long‐term vision for
your child while achieving meaningful, func onal progress on short‐term goals
that ma er to you today.

HUGE THANK YOU to all the store managers and
team members who made this promo on a
priority. You raised awareness and much need‐
ed funds for the DSG.

Jo Ann Butaud On July 8th, 2017 my life changed forever. On that
Shawnee, KS day, I not only became the father of a sweet li le
boy, Evere , but it also was the beginning of a new
Bob Fagan perspec ve and the path for my life. When I
Prairie Village, KS thought about my son’s future, I never even
dreamed I would have a child with a heart defect,
Mike Frazier let alone, Down syndrome. When he was born and
Overland Park, KS a Down syndrome diagnosis was given, like most

John Melvin men, I didn’t know what to do. Should I cry? Should I be strong? Somewhere in between?
Overland Park, KS
Not only was I dealing with a diagnosis that would change my an cipated trajectory of my
Joe Roos son’s life, but also had to think about a heart issue that could possibly take him from us (as
Parkville, MO if the first was not already enough). Fortunately, Evere ’s heart issues did not include heart
failure and we were able to take him home a er a week of monitoring.
Chris Sorenson
Prairie Village, KS During the first 6 months of his life, I really didn’t know what my place was a father (at this
point I was already a father to a wonderful 2‐year‐old girl) or as a husband. I knew I needed
Tom Wagstaff to support my wife and love my kids, but I didn’t see that as that easy answer.
Mission Hills, KS
Along the way, I felt, I also needed to keep it together for the family (emo onally), make
Connec ons is a bi‐monthly publica on of sure Evere got the best care possible, work 60 hours a week, be an a en ve husband,
the Down Syndrome Guild of Greater Kan‐ donate my me to this, spend extra me doing that, the list goes on and on… All I was do‐
sas City. Please contact the office at (913) ing was pu ng unneeded ac on and pressure on myself.
384‐4848 if you have any ques ons about
the contents of this newsle er or would Every issue that came my way got added to my plate un l I finally broke then Evere un‐
like to contribute an ar cle. knowingly healed me. Like most kids with Down Syndrome, unless something truly is
wrong, Evere doesn’t let the world get to him. It was from this simple observa on of my
Disclaimer: The informa on provided is done so son that I had my epiphany… Don’t sweat the small stuff.
through a variety of sources including names pro‐
vided by members of DSG, networking, referrals by Almost 12 months to the date we met our li le man we had to go through the journey of
professionals, other agencies, mail adver sements, his open‐heart surgery. It was the mindset of “Don’t Sweat the Small Stuff” that got us
etc. DSG cannot a est to the quality or qualifica‐ though the whole situa on with very few tears (maybe more than I will let on) and a lot to
look forward too. I am so blessed to have my son in my life, with Down Syndrome, as he
ons of the individuals or organiza ons described. unknowingly has ins lled in me one of the keys to a happy life.
We encourage you to be a wise consumer and ask
ques ons in order to make your own independent To live is to struggle. The point of living is to make one’s struggles diminish or easier than
evalua on of u lizing the services described. We they were before. This is how we mature, grow, and ul mately be happier as humans. Life
share informa on about research projects but in isn’t always easy or fair, but if we acknowledge, learn from, and accept our experiences we
doing so, it is not reflec ve of endorsement. will be happy. Along the way, we must learn what is important and what is not.

Simply put, if focused on the BIG THINGS, a person will be able to more easily reflect on
their struggles, consider their best resolu ons, thus making their opportuni es endless …
and so are my son’s.

The proud father of an excep onal teacher, Rhys Gay

Help DSG Go Green! Download the DSG App Today to Stay Connected

DSG is taking the leap and going green! Because of the successful launch of our new app, you will see
fewer postal mailings from us moving forward. That means you will need to check in regularly on our
app to learn about upcoming events, programs and awareness ini a ves.
Visit your app store
Search “DSG”
Find our logo and download the app
Allow push no fica ons to receive reminders when deadlines are near for event registra on
First me users will need to register by clicking on the “Login” le.
The DSG app has the latest issue of Connec ons, all of our social media posts in one click and upcoming
events right at your finger ps. Download today and encourage your DSG friends to follow your lead!

Calling all
7-11 year olds

with DS!


The Eastland Friends will host a mom's night on Monday, De‐
cember 3, 2018 at Konrad's in downtown Lee's Summit at
7pm. Please rsvp to [email protected]. The DSG
will cover a por on of each mom's dinner.



Familias, tendremos junta el dia 21 de Sep embre de 6:00‐ Join us Saturday, November 17 at 1 pm at Pizza Ranch, 3007 N
8:00 pm en las oficinas del DSG. Tema sera sobre la caminata, Belt Hwy, St. Joseph. DSG will cover the cost of the meal for
se acerca la fecha y hay que prepararnos. Porfavor de confir‐ your immediate family.
mar a Yadira Murguia 913‐563‐8951 o a Brenda Quintana 816‐
278‐0219 RSVP to Stephanie Mefford, (816) 262‐2827 or email
[email protected]



FRIENDS Please join us for a Mom’s night out at The Mason Jar restau‐
rant, 941 N 74th Dr., KCK, on November 12th at 6:00. Rsvp to
Birth – three playgroup for babies with DS on the first Tues. of Do [email protected].
each month from 9:30‐10:30am at TARC in our Children’s Play‐
room. First date will be on 9‐4‐18. Families can come in Hope to see everyone at the DSG Family Holiday Party on De‐
through the main doors or through the playground doors cember 9th at the Overland Park Conven on Center! They
have a fun breakfast with santa planned.
Please RSVP for events to [email protected] or call (785)

Visual Cues and Consistency are Key to Curbing Behavior

Are you struggling with behaviors right now? Are behaviors Use visual schedules or First/Then visuals
ge ng in the way of life? We know that individuals with Down
syndrome struggle with communica ng their wants and needs
and o en use behaviors as a way to communicate. Here are
some strategies and informa on regarding behavior that can
make every day life easier:

 Behaviors come from a desire to avoid or seek an ac vity,
person, or event. Always look for the antecedent to the be‐
havior. What are they trying to avoid? What are they seek‐

 Most behaviors stem from a breakdown in communica on. Pair preferred with non‐preferred ac vi es
The behavior is a way to tell you something that is not easily  Wri ng prac ce with listening to music
communicated for our individuals with DS.  Walking in a crowded area with a preferred friend
 Singing with po y me

 Being proac ve is key in behavior management. If you know Using strategies and understanding the event causing the behav‐
your loved one with DS does not want to transi on from one ior are key to elimina ng behaviors.
room to another, plan ahead and find ways to make it more
appealing. Visit DSG’ behavior page on our
Some strategies that work for our children and adults:
We also highly recommend you
 Be inten onal with language used. purchase a copy of Dr. Stein’s book
 Give direc ons posi vely; “say Walk” instead of “Don’t run”. for more great behavior ps and
 Use consistent language and vocabulary strategies to reduce problem be‐
 Limit emo ons in your voice when redirec ng haviors. Purchase you copy here:
 Give processing me

SAVE THE DATE! Keys to Success Conference January 26, 2019

We look forward to welcoming parents, siblings, educators, therapists, service providers and other interested par es to our Keys
to Success Conference on Saturday, January 26th at the Overland Park Conven on Center. We have great breakout sessions cover‐
ing topics across the lifespan such as medical and research updates, behavior, paren ng, toilet training, fostering independence,
financial planning and preparing for adulthood. Registra on will open November 25th and more details coming soon.

Megan and Kris Bomgaars and Rachel and Laurie Osterbach from Born This Way will be joining us and doing keynotes as well as a
breakout session. You won’t want to miss these ladies sharing their wisdom on becoming self advocate super stars and their moth‐
ers will also share feedback on the roller coaster of being in the limelight.

DSG Celebrates Our Homecoming Royalty!

Homecoming season has come and gone and DSG is so proud of all of our kings and queens. We know these teenagers are making
a posi ve impact on their peers and en re school communi es. Congrats to all the winners and their proud parents!

Ma Santalauria Nolan Smith Jack Melvin Melanie Montes Libby Rall
Mill Valley High Lawrence High School Shawnee Mission East Olathe South High School Liberty High School

My Son’s Future Depends on Inclusive Educa on

As I walked through the lobby of my doctor's office in a dreamlike
state, my mind was hyperaware of the unfolding events, but eve‐
rything around me was blurry. "Benfield . . . Benfield . . . Ben‐
field?" I snapped out of it and walked to the front desk where I
found a recep onist whose eyes were heavy with pity. It was
clear everyone in the small‐town office knew, but what did they

I'd received a call an hour prior from my doctor saying that our
noninvasive prenatal screening results were back, the results
were not good, and we needed to come see him right away. My
20‐week pregnant body fell on the kitchen floor, the words, "Oh
no, oh no, oh no" poured out of my mouth, matched by rapid
tears that streamed down my face.

My husband and I walked into the doctor's office knowing the Speaking of typically developing students, Vanderbilt University
NIPT screening came back indica ng something was gene cally conducted a recent study that found students educated alongside
off with our 20‐week‐old baby growing inside me, but we didn't their disabled peers performed 15 percent higher in academic
know which gene or chromosome was affected. A nurse escorted achievements than students educated without their disabled
us to an exam room where we waited in silence. Sweat damp‐ peers. No study since the 1970s has shown an academic ad‐
ened the white crinkled paper beneath my legs. The doctor finally vantage for students with disabili es when segregated in special
walked in, ripping through the quiet that hung in the sterile air: needs classrooms, and yet only 17 percent of students with cog‐
"Your son has a 99 percent chance of having Down syndrome." ni ve disabili es are included in high school general educa on
I would recognize someone who had Down syndrome, but I knew
nothing about the condi on. I found two words that pulled me October is Na onal Disability Employment Awareness Month.
out of the fog: school inclusion. Realizing my son could one day People with disabili es are the largest minority group in the Unit‐
sit in the same classroom as all of his peers changed my percep‐ ed States, but recent studies found 78 percent of eligible adults
with intellectual disabili es are not working. How can we expect
on of what his future could hold. companies to hire individuals with disabili es if their leaders
don't know them? Our kids with disabili es have to grow up
The doctor laid out our op ons, concluding with, "Don't wor‐ alongside their typically developing peers if we want them to
ry, you don't have to be a hero. If you don't terminate, you can be included in the workplace. Inclusion starts at school.
have the baby here, and we can keep him comfortable, but we
don't have to do anything dras c to save his life." In plain speak,
we could choose to let him die.

The doctor believed our son didn't have a life worth living, so I That's not a nice ideal from a mom of a child with Down syn‐
grieved like a death had taken place. A er a few weeks passed, I drome — it's backed by research. Researchers from the Universi‐
gathered enough strength to start par cipa ng in life again. I ty of Wisconsin found inclusive school environments were a fac‐
dusted off my old journalism skills and started researching what tor in those with intellectual disabili es maintaining employ‐
life would look like with our child with Down syndrome. That's ment a er high school. Vanderbilt special educa on professor
when I found two words that pulled me out of the fog: school and researcher Erik Carter focuses on evidence‐based strategies
inclusion. Realizing my son could one day sit in the same class‐ for suppor ng those with intellectual disabili es to access the
room as all of his peers changed my percep on of what his future general curriculum, saying, "Early segrega on does not merely
could hold. predict later segrega on; it almost ensures it. The trajectory we
establish in school is quite likely to con nue a er gradua on. We
Over 20 years of research consistently demonstrates inclusion of must establish a trajectory of full and meaningful par cipa on.
students with disabili es in general educa on classrooms results When it comes to transi on prepara on, loca on ma ers."
in favorable outcomes. Gains are seen in reading and math, and a
two‐year longitudinal study found that students with disabili es Con nued on next page>>>>>
scored significantly higher on social assessment tests when inte‐
grated into classrooms with their typical peers.

My Son’s Future Con nued

Special educa on is not a loca on, it's a service. Under the Individuals With Disabili es Educa on
Act (IDEA), the Least Restric ve Environment (LRE) clause reads, "To the maximum extent appro‐
priate children with disabili es are educated with children who are not disabled. And that the re‐
moval of children with disabili es from the regular educa on environment occurs only when the
severity of the disability of a child is such that educa on in regular classes with the use of supple‐
mentary aids and services cannot be achieved sa sfactorily."

This is the law. The benefits of including children with disabili es in the general educa on classroom are backed by decades of research,
and yet parents o en have to fight, and at mes unreasonably hard, to make this happen; recent cases go as high as the supreme court.
This Na onal Disability Employment Awareness Month, let's not just call on our employers to include those with disabili es in their
companies, let's get to the cause of why they are not hiring them in the first place.

We need to have higher expecta ons for our children with disabili es at home and fight for educators to do the same. We cannot se le
for the majority of their days to be in self‐contained classrooms. We must advocate for what we know from research to be true: segre‐
gated classrooms lead to a segregated world.

Perhaps my doctor believed my son's life was not worth living because he grew up in a me where it was us and them. Sadly, despite
major advancements in laws and research, so much more work needs to be done to erase the divide.

Schools, including our kids, their futures, and the future of our society, depend on it.

This ar cle was originally published on You can follow more of Jillian’s wri ngs by following her in Face‐

DSG Back to School Resources

Mass Mutual Offers Whole Life Insurance to People with DS

MassMutual is now offering whole life insurance coverage to individuals with Down syndrome, Cerebral Palsy and Au sm. This is
made possible through the MassMutual Special Care Enhanced Underwri ng Program. The insurance plan is knows as the Whole
Life Legacy 10 Pay which ensures permanent life protec on that will be paid up a er 10 years. The coverage offers up to $25,000 for
the benefactor/owner of the life insurance policy. Eligible benefactors include parents, grandparents and anyone that has insurable
interest. The minimum age requirements for the insurance is one year old and must have one of the diagnoses listed above.

This is exci ng news for any individual with Down syndrome . It is
incredibly hard for people with pre‐exis ng condi ons to obtain
life insurance from most providers. MassMutual’s underwri ng
program made specifically to help find coverage for people with
these disabili es will make a huge difference in their life and that
of their families lives. To find out more informa on on this plan
contact the KC MassMutual representa ves below.

Twin Financial
Katheigh Degen
Raleigh Lang

Your Child’s Strengths: What Parents Need to Know

We talk about focusing on strengths, but what does this mean?

It’s not uncommon for parents, teachers, advocates, and provid‐

ers who support people with Down syndrome, to say— “Look for

the individual’s strengths…ask them about their strengths…play to

their strengths.” But what kind of “strengths” are they talking

about? O en, in the disability field the focus, when discussing

strengths, has been on “skills” (e.g., reading skills, communica on

skills, social skills, cooking skills, etc.) and “resources” (e.g., having

many friendships, living in a safe neighborhood, going to a good

school, etc.). And these are hugely important areas. But, another

incredibly important aspect of focusing on strengths is under‐

standing character strengths, those strengths that deal with who Since one’s highest strengths are viewed as “the real me” and

we are as human beings— the strengths that define us. “my best self,” it is by these strengths that people with Down syn‐

In 2004, a breakthrough occurred in the social sciences. A new drome can feel “known” and “seen” for who they really are. Iden‐
language for understanding what is best in human beings was fying, discussing, and working with character strengths helps us
conceived. This “language of strengths” is known as the VIA Clas‐
sifica on and consists of 24 character strengths that fall under 6 all move beyond the surface and around the stereotypes, and
virtue categories (see Table on p. 59). For example, bravery, per‐ truly do what all of us want to do: to see and know the person,
not the disability.

severance, and honesty are strengths of courage while curiosity, Strategies for parents These 24 character strengths are like seeds
crea vity, and perspec ve are strengths of wisdom. These charac‐ that are within each individual. When we give seeds proper nour‐
ter strengths are posi ve quali es all human beings have and can ishment they will grow into something beau ful. Seeds that grow
express, to live their best life and to posi vely impact others. into fruits, herbs, and vegetables enhance our health; seeds that
develop into trees, flowers, and plants inspire us and improve our
This breakthrough, the result of a 3‐year project involving 55 sci‐ environment. Similarly, when we give a en on, encouragement,
en sts, has impacted millions of people around the world. The and support to a child’s character strengths, this can help the
applica on of character strengths with people with Down syn‐ strengths grow.

drome is a new area of study. But we are finding that the VIA When the strengths grow, the child is able to express themselves
Classifica on provides a useful framework for iden fying each more fully as well as offer a posi ve impact on others. Some mes
person’s (with and without Down syndrome) highest strengths it is obvious that a child’s “humor” seed has grown significantly as
and ways to build posi ve outcomes based on an understanding he cap vates a room with laughter and funny stories while anoth‐
of those strengths. er child has developed her kindness strength as she goes out of
her way to hold doors for people, do favors for those in need, and
Parents and support providers resonate with the use of this show compassion for friends who are struggling. For parents, this
strengths “language” in describing what is best in individuals with classifica on represents a fresh, accurate, and helpful way of
Down syndrome. One parent exclaimed, “This gives me a whole looking at their children. With any new approach, we o en need a
new way for thinking about my daughter. It’s a recipe for seeing gentle “push” or at least some ini al ps or strategies.

and talking to her and it’s like a special tool that gets me to know Here are a few steps to get you started on the journey of iden -
her on the inside.” And, in a world that is dominated by our nega‐ fying and boos ng your child’s character strengths:

vity bias, stereotypes, and a focus upon what is wrong, addi on‐ 1. Make a list of your child’s top 5-7 character strengths.
al perspec ves are sorely needed. Working with character As you look at the Table lis ng the character strengths, which 5‐7
strengths offers a perspec ve shi from “what’s wrong to what’s quali es best describes who your child is? If age‐appropriate for
strong.” As you can see in the table, these character strengths are your child, ask your child which strengths they believe to be their
easy to understand and when given a chance, are easy to recog‐ best quali es. Compare your list with your child’s list.
nize in others.

Research tells us that working with our character strengths is con‐ 2. Spot your child’s strengths in ac on. When you no ce your
nected to many posi ve outcomes such as greater happiness, life child use a character strength, even a small amount (e.g., asking
meaning, be er rela onships, more achievement, and less de‐ one ques on shows curiosity; coming up with one new idea indi‐
pression. When people are encouraged to express their character cates crea vity), point this out to them. Explain to your child what
strengths – especially their strongest strengths – they tend to feel you observed. See the examples in the Table. Express apprecia‐
energized, more engaged, and happier with what they are doing.
on to your child. Make it clear to your child that you value who
they are and that you appreciate the strengths they express.

Your Child’s Strengths (con nued)

3. Reflect on stories. Think of something recently that your child did that made you marvel or laugh or
feel inspired. Replay that story in your mind. Go back through the story again and spot the character
strengths your child was using.

4. Be a character strengths “champion” for your child. Don’t forget about you! In addi on to no cing
and building the strengths of your child, an addi onal perspec ve is to consider that raising a child who
knows and uses his or her character strengths starts with the parents and what the parents (and teach‐
ers and other family members) are modeling day‐today in front of the child. If a parent does not bring
forth character strengths of fairness, love, curiosity, social intelligence, gra tude, and humility, how can
they expect their child to?

Parents can get a jump‐start on the study and prac ce of their own character strengths by taking the free, online VIA Survey
( that measures the 24 strengths. It takes 10 minutes and you’ll receive a rank‐order of your strengths of char‐
acter star ng with the highest. You can then make a conscious effort to model your highest strengths when you interact with your

Ar cle originally published in NDSC Down Syndrome News Volume 37 #4. Reprinted with permission. Visit h ps://
ndscstrengths and scroll to page 59 to see the two page strengths chart.

Ryan M. Niemiec is author of Mindfulness and Character Strengths (2014) and Posi ve Psychology at the Movies (2014). He is a
psychologist and educa on director of the global, nonprofit VIA Ins tute on Character, a posi ve psychology organiza on that
teaches and collaborates with people around the world with regard to the educa on, research, and prac ce of character

Karrie Shogren works in the area of self‐determina on and posi ve psychology, and focuses on using strengths‐based approaches
to support posi ve outcomes for all people, including those with disabili es. She is an associate professor of special educa on and
associate director of the Kansas University Center on Developmental Disabili es at the University of Kansas.


I am Rachel Mast. I am 19 years old. I really love my life. I have a great life, and I love
telling people how great my life is. I was born in Memphis. In third grade, my family
moved to Olathe, Kansas. I love lots of things about my life. I love my church. I love my
school. I love my family. I love dancing, ac ng, and singing. One of the best things about
my life is my friends. I graduated from Olathe South High School in May. Just like my
friends, I got a diploma. I loved my school. I was on student council, and was the volley‐
ball manager for four years. In ninth grade, I was on the Winter Court. I was the Prom
Princess. I was in Na onal Honor Society and on the honor roll.

I took general educa on classes with my friends. My favorite classes were my theatre classes. Even though it was hard, I learned
Shakespearean monologues. It is hard for me to memorize, but I worked very hard and did a great job. One of my best high school
memories was being Strato in “Julius Caesar.” I am a member of my school’s thespian troupe. I have my name on a brick at my

I liked all my classes, but I don’t like math very much. Math is hard for me. I really like English. My favorite book was “Romeo and
Juliet,” but I didn’t really like “Frankenstein.” I worked very hard in my classes, so I could make good grades and go to college.

I really liked my paren ng class. We pretended we were going to have a baby—that was funny. I had to bring a baby home and I
named her Sarah Nicole. She cried three mes during dinner. I decided I do not want children.

My senior year, I worked in the a endance office and the counseling office. It was so much fun. I took passes to people and greeted
people. They told me my smile made everyone happy. I just got a job as a hostess at the Olive Garden. It is kind of like what I did in
the school office. One of the best things I remember in high school was scoring a touchdown at the powder puff football game.
During homecoming weekend, the junior and senior girls always play a powder puff game. My friends helped me out and, when I
got the ball, I scored a touchdown. It made me have happy tears.

I love my friends very much. My volleyball friends called me the #bestmanagerever. I gave them pep talks. My theatre friends
helped me to know when to do things on stage. They helped me when I was on the crew for the “Addams Family.” I love them very
much. My friends from church are the best. We go to church camp together. We went on mission trips. We had fun. I miss them
very much. We s ll pray for each other.

Theatre is my life. I have been in 22 plays. My favorite was “Hairspray” because I love to dance and sing. I have the same dreams as
my friends. I want to go to college. In January, I am going to start as a student at Missouri State University. I will be in the first Bear
POWER class. I am so excited to live in the dorm, take theatre classes, and make friends. Some of my friends go there, too!

I also travel to Washington, D.C., and to the Kansas state capitol building in Topeka to talk about laws that will help people with
Down syndrome. I even got to tes fy in Topeka. I helped to pass the Achieving a Be er Life Experience (ABLE) Act. I was the first
person to open an ABLE account in Kansas. U.S. Senator for Kansas, Jerry Moran, says that I am “the best lobbyist in Washington,

When I started going to Washington, D.C., I told them to support the ABLE Act so I could live in a pink house. My dream is to move
to New York City, be on Broadway, get married, and live in a pink house. Did I men on I have Down syndrome? I have Down syn‐
drome, but I am not Down syndrome. I am Rachel. I have dreams. I REALLY love my life.

ELKS Lodge Partnership Brings Baby Baskets to Families in Need

The Northland Elks Lodge has been raising funds and suppor ng DSG for the last eight years.
They host a breakfast annually which draws a large crowd and raises thousands of dollars.
The Elks also submi ed a grant to their regional council for DSG to receive funding for our
new parent baskets. Members of the Elks delivered a $2,500 grant to purchase items for our
baskets and with the help of some teens with Down syndrome they packed up a few baskets
for delivery. We are so grateful for the past and con nued support from our wonderful
friends at the Elks Lodge. They have raised over $30,000 for DSG since our partnership began!

Thank You for Your Support!

The 1st Annual Central Missouri Step Save The Date
Up Walk was Awesome!! Private Cellar
Wine Tas ng
Wow! What a great day! Over $85,000 raised!
Food, games, and family fun. Smiles, dancing, & Auc on
laughter, energy, hope, and community ‐ an awe‐
some day in Columbia. The DSG is proud to be Join us for an evening of fun and great wine as we celebrate those
spreading our mission and expanding our impact. with Down syndrome at “The Gallery” on Thursday, April 25th
from 6pm‐9apm

Taste wines from around the world and have an opportunity to
bid on unique wines from Kansas City’s foremost private

For further details or to donate wine, please call 913‐348‐4848

Host a Dress Down for Down Syndrome Day

to Benefit the Down Syndrome Guild

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16th Annual Tee Up for Down Syndrome Golf Tournament : A Huge Success!

The Down Syndrome Guild held their 16th Annual Tee Up for Down Syndrome Golf Tournament, at Shadow Glen on Monday, Sep‐
tember 10 raising over $271,000, a record breaking amount. The tournament featured breakfast for all golfers, shopping in the
concept store, lunch on the course, specialty drink holes, hole contests with premium prizes, mee ng and playing against our self‐
advocates, and an a ernoon cocktail recep on.

"Thank you to our presen ng sponsor, The Mitchem Family and to all of our golf team sponsors for once again making our annual
charity golf tournament a huge success," said Amy Stoll, Execu ve Director of the Down Syndrome Guild. "Without our loyal spon‐
sors, vendors and volunteers, we would not be able to raise the money and that we do. Thank you for suppor ng our mission and
making a difference in the Kansas City Down syndrome community.”

Non‐Profit Org
U.S. Postage Paid

Olathe, KS
Permit No. 932

5960 Dearborn Street
Suite 100
Mission, Kansas 66202
[email protected]

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