Special Needs Living Feb 2021 Issue

Page 25

non-profit spotlight

mom as I spend weeks at a time at the hospital with Hannah. The monthly adventures mean something positive for them to look forward to as well. We get to attend events that we otherwise would not have the means or opportunity to experience apart from A Kid Again. – AKA mom of Hannah

By Katie Pappas

A Kid Again allowed our family to form great friendships with other A Kid Again families, and the opportunity to have fun-filled days, even when financially we weren’t able to do these things on our own. – AKA Mom of Carter A Kid Again is like a life-line. Something we can point to each month and look forward to as a family. We make sure to put those events in big red letters on the calendar and it seems to make the yucky medical stuff pale in comparison. — AKA Mom Cheryl Katie Pappas 8275 Allison Pointe Trl., Suite 220 Indianapolis, IN 46250 317-295-3178 | kpappas@akidagain.org

Being a kid means waking up to endless possibilities and the anticipation of all the adventures that await outside your door. But when a child gets sick, childhood itself just stops. This is the very reason A Kid Again was created! Tell us more about your organization:

A Kid Again provides consistent, cost-free, year-round adventures for children with life-threatening conditions and their families, to remember what it was to live care-free. We also provide family support, peer-to-peer connections, and other resources to help families cope with the extended effects of life-threatening conditions. How does your organization support those in the special needs community?

We provide year-round fun-filled adventures that allow children with life-threatening conditions to feel like A Kid Again. A Kid Again works to create a communal and interactive environment. Our program establishes ongoing, nurturing experiences that complement but do not

overtake their day-today living. How can others get involved or support your organization?

Do you run a non-profit? Would you like to be a part of the non-profit spotlight or nominate someone else to be in an upcoming issue of Special Needs Living? Email us at SpecialNeedsLivingIndy@n2pub.com.

As a donor, sponsor, or volunteer you are an important part of the A Kid Again family. We encourage you to not only support our mission financially but also join us for adventures and other events to fully understand the impact of your generosity and meet the families you are supporting. Seeing the smiles and laughs of the children will have you asking, “why didn’t I get involved sooner?” What difficulties and/or challenges do you help families and/or individuals with special needs overcome?

We provide family support, peer-topeer connections, and other resources to help families cope with the extended effects of life-threatening conditions. Testimonials

As much as A Kid Again has been a blessing to Hannah, it has also been a blessing to her brothers. Being a sibling of a special needs child is difficult. Her brothers get dragged to appointments and therapies. They miss their February 2021 • Special Needs Living

25


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Articles inside

LOVE NEVER FAILS - a moment of inspiration – by a special needs mom

4min
page 36

Pioneer Parents in Indiana- Meet Beth DeHoff

5min
pages 34-35

Indianapolis Flames Alternative Baseball

6min
pages 32-33

Helping your child deal with the feels

1min
page 38

Be Your Own Valentine Sweetheart:

3min
page 30

A Mother’s Promise Promise

5min
pages 26-27

Non Profit Spotlight - A Kid Again - Giving Illness a Time out

2min
page 25

Pastor's Corner

3min
page 24

Siblings Perspective - Meet Tyler Ashby & His Brother, Caleb

3min
pages 22-23

Upcoming Events

1min
page 21

HEART SOS

3min
page 19

THE ABC’S OF IEP’S

3min
page 18

Meet Law office of Elizabeth A. Homes LLC. - Supporter of Special Needs Living

4min
pages 16-17

WHAT IS Sesame/East Syndrome?

2min
page 15

Ashley Caveda - No Legs Needed - A New Athlete's Intro to Adaptive Hockey

6min
pages 12-13

MEET NORA –Service Dog for Zoe

2min
page 11

4 Reasons Why Writing Composition May Be Hard for Your Child

3min
page 10

Meet the CEO of the Angelman Syndrome Foundation - Amanda Moore & her Family – Adam, Jackson & Baden

3min
pages 8-9

A UNIQUE KIND OF ART - Art by Olivia

4min
pages 1, 28-29
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