Tough2gether Fighting Childhood Cancer

Goal: $15,000.00

Specific Need

Your child has cancer.  It is aggressive. It is inoperable. It is terminal.  No one can prepare you for that.  Where would you turn?  As parents we faced that same question when our son Jace Ward was diagnosed with DIPG, the most deadly childhood cancer.  He was 20 and a KSU student.  Through his experience we decided that if we could not answer that question, it was time to make a path easy to find and wide enough to support childhood cancer families throughout our region.  This year we have provided over $150K in family support through the LiveBrave2gether network.  We wish to continue our grants for families in the Manhattan - Flint Hills region battling childhood cancer. 

This includes offering each family assistance navigating clinical trials, connections to childhood cancer resources, financial support to travel to trials, assistance with unexpected expenses, emotional support during the journey, and if needed bereaved parent and sibling support.  We are now able to walk with the family and share the knowledge acquired over five years of immersion in the national and regional childhood cancer community. Last year we helped over 121 families receive direction to clinical trials, individualized right to try protocols not otherwise offered to them, grants and support, and access to community resources.

Additionally, Tough2gether Foundation is a thought leader and funder nationally of the DIPG/DMG Brain Cancer research and clinical trials.  We are currently leading a groundbreaking project to provide navigation to individualized precision medicine opportunities for children with brain cancer, the number one cause of death by disease in children.

No one can prepare you for the day you find out your child has cancer.  Having someone help prepare you every day after is a privilege Tough2gether Foundation is willing to provide.

Mission

Tough2gether Foundation fights childhood cancer alongside families impacted with this devastating news. Our mantra is Connect . Question . Collaborate . Cure.  During the last full year of operations we have done just that delivering nearly $2M in family support and research through collaborations Tough2gether has established acrossed the country.

We place special emphasis on supporting regional Kansas families and families fighting childhood brain cancer, the most deadly childhood disease. Whether it is gas card or hotels to travel to trials, paying rent when a parent must become the caretaker, or purchasing a child size casket.  We know when we come together we're Tough2gether.  No child should fight alone.

Tough2gether funds research for pediatric brain cancer working very closely with researchers across the country.  We know this journey because our son Jace fought Diffuse Intrinsic Pontine Glioma (DIPG) courageously for 25 months.  The NIH cancer funding allocates only 6% to all childhood cancer.  Now, pediatric brain cancer is THE most deadly type of cancer.  In two years we've funded $2.4M in research by bringing foundations together, started a national brain tumor board, a national BrianStorm Summit for advocates and researchers, a DMG Data hub to study longitudinal data of the disease and helped 150 families. This does NOT mean we have enough funds do to everything necessary by any means.  We stretch your dollars fully and are actively involved with the research.

We're not finished.  We know this journey well.  Our son Jace Ward battled courageously for 25 months.  He inspired us to make sure the children who had not yet found their voice were never forgotten.  Join with us. 

Let's work together for the day that we are no longer afraid of what cancer can do to our children, but celebrate what was accomplished when generous caring individuals came together to help the smallest among us.  

Profile

There was one moment when we stood in silence as the doctor said "You have an inoperable, aggressive, terminal brain tumor.  I began to cry.  Jace asked "How long do I have.  I'm not afraid to die, I'm afraid I won't make an impact before I do."  The doctor replied you have 6-9 months.  Jace was 20 years old, otherwise perfectly healthy, ready for a weekend in the 'ville.

Tough2gether Foundation was founded by Jace Ward and his parents Roger and Lisa Ward of Wamego.  Jace Ward was a 20 year old KSU student headed for law school when he was diagnosed with the most deadly pediatric brain cancer called DIPG.  DIPG ravishes children and young adults stealing their voice, sight, walk, swallow, use of their limbs, hearing until the child is locked in their body.  Eventually stealing the child's last breath.  All the while, the child knows everything that is happening.  They never lose their cognitive ability.  No standard of treatment has changed for children with DIPG in 60 years.  At that time Neil Armstrong's daughter lost her life to the same tumor.  We can change this 2gether.

Jace entered clinical trials on the cutting edge in hopes of making a difference. He advocated, and we continue to advocate nationally speaking at the White House Cancer Moonshot Forum, the NIH on patient data and immunotherapy and leading an effort to end randomized trials for terminal pediatric conditions. 

We have helped over 500 families directly who feel absolutely lost.  We started parent chat feed, and now a platform for famlies with childhood cancer.  We host emotional support online, we provide family grants to pay expenses so the family can stay together, afford their health insurance and groceries while in treatment.  We listen and navigate the family to treatment, resources and sharing of brain tissue for research.  

It is humbling to see the reach of Tough2gether Foundation across the world in such a short time period within pediatric brain cancer.  However, the work is not done.  We know there are regionally families battling childhood cancer who are told, as we were, to go home and make memories.  They deserve the right to try innovative treatments and to also receive the best advice available across the country.  Tough2gether is opening regional support with navigation to treatment as centers of excellence.

Photos & Videos

2026 Family support provided in Q1 - now over $150K
2026 Family support provided in Q1 - now over $150K
Jace Ward explains DIPG
What We Do
What We Do
Advocating for increased research for brain cancer with Senator Marshall
Advocating for increased research for brain cancer with Senator Marshall
Lynch Family New Car for Treatment Travel
Lynch Family New Car for Treatment Travel
Jace with research/clinician Dr. Carl Koschmann of Michigan
Jace with research/clinician Dr. Carl Koschmann of Michigan
Elita never finished grade school - her life was cut short by DIPG. She inspires our work
Elita never finished grade school - her life was cut short by DIPG. She inspires our work
Jace was the 2nd pediatric brain tumor patient to receive Car T Cells for treatment.
Jace was the 2nd pediatric brain tumor patient to receive Car T Cells for treatment.
Kaia - a brave DIPG warrior in the car t cell trial with Jace lost her life too soon
Kaia - a brave DIPG warrior in the car t cell trial with Jace lost her life too soon
Jace and his sister Brooke leaning in for a pep talk
Jace and his sister Brooke leaning in for a pep talk
Chloe - beautiful girl with DIPG taken far too soon.
Chloe - beautiful girl with DIPG taken far too soon.
We fight for Levi, who never stopped smiling until DIPG locked him within his body & stole his smile
We fight for Levi, who never stopped smiling until DIPG locked him within his body & stole his smile
Noah, our friend take too soon and the KSU Baseball Team warrior 2021
Noah, our friend take too soon and the KSU Baseball Team warrior 2021
Jace and Lisa advocating in Washington DC at the request of the President
Jace and Lisa advocating in Washington DC at the request of the President
Brooke and Jace  from early life battled every single obstacle 2gether.
Brooke and Jace from early life battled every single obstacle 2gether.
Jace represented at the Childhood Cancer memorial. 2800 pairs of shoes = lives lost yearly.
Jace represented at the Childhood Cancer memorial. 2800 pairs of shoes = lives lost yearly.
Noah Halek, fought DIPG alongside Jace and inspired Jace to speak up for kids.
Noah Halek, fought DIPG alongside Jace and inspired Jace to speak up for kids.
DIPG is cruel as it disfigures the body, drooping the smile and turning the eye in
DIPG is cruel as it disfigures the body, drooping the smile and turning the eye in
Fighting together and grieving together. Tough2gether.
Fighting together and grieving together. Tough2gether.
The first dose of Car T Cells with the dream team at Stanford.
The first dose of Car T Cells with the dream team at Stanford.
Representing Tough2gether Foundation and One Voice Foundation speaking at the White House
Representing Tough2gether Foundation and One Voice Foundation speaking at the White House
In NYC speaking on Jace's behalf
In NYC speaking on Jace's behalf
The Childhood Cancer Shoe Memorial in DC every September - until we end kids cancer as we know it.
The Childhood Cancer Shoe Memorial in DC every September - until we end kids cancer as we know it.
Mary from Colorado continues to battle DIPG now 30 months after diagnosis, we support her family.
Mary from Colorado continues to battle DIPG now 30 months after diagnosis, we support her family.
Jace advocating in New York City fall 2020.
Jace advocating in New York City fall 2020.
standing with parents funding research in kids cancer.
standing with parents funding research in kids cancer.
Blake Ward at the Tough2gether Breakfast in DC advocating for childhood cancer
Blake Ward at the Tough2gether Breakfast in DC advocating for childhood cancer
Neev Kolte taught Jace to play a video game, and Jace taught is parents Neev had double vision.
Neev Kolte taught Jace to play a video game, and Jace taught is parents Neev had double vision.
Maria continues to battle DMG, we support her efforts to battle this monster.
Maria continues to battle DMG, we support her efforts to battle this monster.
Nicole continues to battle DIPG from NY.
Nicole continues to battle DIPG from NY.
DIPG families joining together in Washington DC to support the work of Tough2gether Foundation
DIPG families joining together in Washington DC to support the work of Tough2gether Foundation
Jace joined with ChadTough to begin the first of kind www.mydipgnavigator.org helping families
Jace joined with ChadTough to begin the first of kind www.mydipgnavigator.org helping families
The Ward family supporting Jace in his battle.
The Ward family supporting Jace in his battle.
Tough2gether spreads awareness by sharing the stories of children so we all look DIPG in the face.
Tough2gether spreads awareness by sharing the stories of children so we all look DIPG in the face.
Jace and Noah speaking to Congress.
Jace and Noah speaking to Congress.
Mitch Albom, author of Finding Chika's daughter Chika.  Our friend gone too soon.
Mitch Albom, author of Finding Chika's daughter Chika. Our friend gone too soon.
Jace and Noah speaking to Congress
Jace and Noah speaking to Congress
Jace speaking with Senator Moran about the Department of Defense cancer research funding
Jace speaking with Senator Moran about the Department of Defense cancer research funding
Jace was honored in NYC for moving the needle years ahead in DIPG
Jace was honored in NYC for moving the needle years ahead in DIPG
Carson fought DIPG from Hutchinson, KS.
Carson fought DIPG from Hutchinson, KS.
2000 children per year are diagnosed with terminal brainstem cancer called DMG
2000 children per year are diagnosed with terminal brainstem cancer called DMG
Join us annually the first Saturday in Wamego for Live Free 5K and community event.
Join us annually the first Saturday in Wamego for Live Free 5K and community event.
Cece is battling strong with help from Tough2gether
Cece is battling strong with help from Tough2gether
Charlie inspired Jace and many others. We continued to fund research for Charlie
Charlie inspired Jace and many others. We continued to fund research for Charlie
Londyn lost her battle last month, but her voice remains strong
Londyn lost her battle last month, but her voice remains strong
Moms helping other moms
Moms helping other moms
Jack’s family continues to fund research with Tough2gether
Jack’s family continues to fund research with Tough2gether
Alex fought DIPG along with Jace. Now 2gether we find research.
Alex fought DIPG along with Jace. Now 2gether we find research.
Nicole and Lilly with other children impacted by Brain Cancer
Nicole and Lilly with other children impacted by Brain Cancer
Londyn supporting Tough2gether, while we support Londyn’s family
Londyn supporting Tough2gether, while we support Londyn’s family
Emily Hood Car T Cell pioneer we proudly supported
Emily Hood Car T Cell pioneer we proudly supported
Elowyn and mom, we are proud to support
Elowyn and mom, we are proud to support
Jace speaking at the NIH on patient data.
Jace speaking at the NIH on patient data.
We were pleased to support Joe as he navigated to trials.
We were pleased to support Joe as he navigated to trials.
Jace and Brooke Ward shortly after diagnosis of DIPG.
Jace and Brooke Ward shortly after diagnosis of DIPG.
Rydder has new wheels, Tough2gether continues to fight alongside Rydder
Rydder has new wheels, Tough2gether continues to fight alongside Rydder
Jace and Mary learning to walk again 2gether.
Jace and Mary learning to walk again 2gether.
$10,265.00 received
in 45 gifts
68.43%  of  $15,000.00 Goal

Contact

2201 Columbian Rd
Wamego, KS 66547
Phone: (620) 669-7811

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