Jace Ward - #Tough2Gether

Jace Ward - #Tough2Gether 2gether we’re fighting childhood cancer, providing family support and funding DIPG & DMG research.
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We believe 2gether we can bring real hope to all with this terminal brain cancer! We believe DIPG Won’t Wait so we work effectively to inspire real change.

This is your sign!! You SHOULD attend the Brainstorm Summit Sept 16-18 in McLean VA. (Just outside Washington DC) Www.br...
06/11/2026

This is your sign!! You SHOULD attend the Brainstorm Summit Sept 16-18 in McLean VA. (Just outside Washington DC)
Www.brainstormsummit.org

06/11/2026
May was bigger than awareness. It was action.Because of this community, Brain Cancer Awareness Month became a month of i...
06/09/2026

May was bigger than awareness. It was action.

Because of this community, Brain Cancer Awareness Month became a month of impact.

📖Powerful stories shared through our awareness campaigns, capturing the daily realities of families facing pediatric brain cancer
🔬Research conferences attended, bringing together families, researchers, clinicians, and industry partners to move progress forward
👕Awareness shirt orders fulfilled by our production team and shipped across the country with many more currently in production
💸Families supported through treatment, travel, living expenses, and critical needs
🧪Clinical trials championed, funded, connected to the families who need them most
🗣️New advocates, volunteers, donors, and partners joining the fight every day
✈️Families visited and listened to, strengthening relationships and improving how we communicate our families' needs
🎪Fundraising and advocacy events hostesd across the country, honoring our children and raising awareness and critical funds

And together, we raised over $550,000 to support pediatric brain tumor research, clinical trials, and family support.
Every shirt packed. Every mile traveled. Every story shared. Every dollar raised. Every conversation started.
To everyone who donated, volunteered, attended an event, shared a post, wore a shirt, sponsored a program, funded research, or simply helped spread awareness...

THANK YOU

Brain cancer awareness month may be over, but our fight continues.

Events: http://tough2gether.org/events

🏇Chasing Down Dreams: https://events.tough2gether.org/cdd26
🥎Jace Ward Memorial: https://events.tough2gether.org/jw5
⛳️Warrior Golf: https://events.tough2gether.org/warriorgolf2026
🔬ChadTough Research: https://events.tough2gether.org/chadtoughresearch2026
🏰Best Day Ever: https://events.tough2gether.org/bestdayever2026
🍦Ice Cream Day: https://events.tough2gether.org/icrecreamday2026

Awareness Campaigns: http://tough2gether.org/advocacy

🎗️Behind the Ribbon: https://awareness.tough2gether.org/behindtheribbon2026
👕Because of Them: https://awareness.tough2gether.org/becauseofthem2026

As we continue to streamline our family support services and build this network of foundations and funds driven to provi...
06/08/2026

As we continue to streamline our family support services and build this network of foundations and funds driven to provide financial support to families facing childhood cancer, we like to make a point of acknowledging those organizations and share the impact we're making each month. We are also excited to announce a milestone of surpassing $250K reported funds supporting families in the fight in 2026!

LiveBrave2gether allows families to fill out a single application, review available grants, and find support more easily, quickly, and efficiently so we can do the work of contacting the appropriate organizations and families can focus on their child.

NEW! Families can now request additional funds for new expenses without submitting a new application!
Families, contact Debbie to receive the link for your application to make new requests & updates!

We are determined to connect as many foundations & funds as possible to ensure these applications are fulfilled in the most efficient and sensitive ways possible.

THANK YOU to these foundations and many more that have supported families in need in May - we look forward to supporting families and fulfilling new and existing applications this month and continuing our consistent support numbers.
livebrave2gether.org

Foundations: Please contact us to join the LiveBrave2gether network! No membership or commitment needed, we simply notate your support specifications and share applications that match with your foundation as they come in!
Contact [email protected] to learn more!

To make the process even faster, complete the contact preference form so we can add you to the list and know when to share applications:
tinyurl.com/lb2g-contact-form

Family Support Coordinator: Debbie Carver
[email protected]

06/07/2026

On National Cancer Survivors Day we want to recognize every cancer survivor. Your courage and resilience inspire all of us. For our brainstem cancer survivors in particular we know survivor really means you’re a warrior extending your survival past the expected time period at diagnosis. You are living with symptoms, PTSD of treatments and diagnosis, afraid most of the time of what may happen should you see a change in symptoms or an unclear MRI. You have often gone on to school or started work or a family showing the courage to HOPE that your story will be different than the many friends you have lost along the way. Most importantly, you volunteer, you encourage, you share information on treatment and you make the world a much better place. We, at Tough2gether, want to thank you. We see you and we are cheering you on!

If you have crushed the timeline you were given, post a photo, the date you heard Cancer and everything changed and share as much about your diagnosis, life advice or fun facts about yourself (or your family member) as you wish. Let’s fight cancer 2gether!

06/07/2026

It’s June! Time to register for the Brainstorm Summit Sept 16-18 in McLean VA! You want to find your people? You want to get involved? You want to find answers to brain cancer? You want to help your kids, your partner or yourself heal from a brain cancer journey? You want your story to really matter and your voice to be heard? You want to spotlight your foundation or learn how to start something? It happens one time each year— don’t miss out! Come together!

Here’s your one stop sign up link:
https://brainstormsummit.org/

Don’t wait!!! SPECIAL OFFER: the first 20 families who register receive a $20 merchandise coupon to use on any BrainStorm Summit OR Tough2gether Awareness merchandise!!

06/07/2026

DIPG looked different for Myla, and it ultimately ended her life in the same way. I think it is important to share this side of how it looked for us because it was the complete opposite of everything I ever read and learned. And it left everyone in complete shock.

Myla suffered minimally with her disease. She lived as if she did not have it and never allowed it to hold her back. She had many days of inconveniences, and more days lived fully. We had the best 11 months of our life together, we loved, we laughed, we said everything we ever needed to say, we experienced as much as we could with her all while living with the worst possible diagnosis one could receive. But always knowing that the worst possible case scenario of it taking her life meant the best case scenario for her..that she would be with our Lord and Savior in complete peace, which is the whole entire goal of our short life on earth itself.

DIPG was so stealthy to the point we questioned if she really had this. The only indication of her cancer was her eye turn. She did not experience ANY of the usual symptoms until her last few days of life when she lost every single ability all at once. From having no symptoms to having every symptom, to death. It was not until her final few days where I was finally convinced: yes, she has this rare, brutal, reckless, ruthless, TERMINAL disease that is DIPG and had to watch it shut her body down. Function by function, until it took her last breath. It was not slow with weeks to months of suffering, it was rapid and instantaneous almost.

We find peace in knowing exactly where Myla went. While she is no longer here physically with us, we felt the exact moment her soul left to be with Him. As much as I wanted to keep her with me, I would never want to take eternal peace from her if He needed her and it was her time.

She was complete perfection, she was beyond this world. She was kind, smart, hilarious, creative, athletic, cool, witty, sassy, talented, fashionable, humble and most of all Faithful to the Lord to the very end. In her short 9 years on earth she impacted and changed the lives of so many.

We prayed daily for a miracle, but Myla WAS the miracle and she changed our life forever. One of the last things she told us days before she passed was that she was okay with having this brain tumor because it brought so many people back to Jesus and she loves Him.

And the very last thing she spoke to us,
after having no ability to speak was

“I’m going to go be with God”

and we heard it perfectly clear.

After she left us, the sun came out and a powerful wind hit my face as I was praying, I looked up and Jake and I counted at least 10 horses in the clouds, one with a small rider with angel wings. It was the most beautiful peace we have ever felt and I thank God for that immaculate confirmation that she was there.

We miss you so much angel.
Your mission is complete.
We are so proud of you.
I will be strong because you were.
🫶

06/07/2026

Myla Flock 🕊️ February 26, 2017 - June 5, 2026 ☦️

Address

Wamego, KS
66547

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