Luke’s Posse: DIPG Ends Now

06/27/2026

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Save TODAY ONLY on beautiful blooms!!

05/04/2026

Go Grey in May!

05/03/2026

We made it through another dreaded April.

As the sun peeks out and seedlings emerge, we are reminded of the life Luke was cheated.

We are also reminded of how fragile life is and how quickly it can be taken away, so we savor each moment possible, especially when it comes to watching our Phebe grow up and experience the rites of passage Luke will never get to.

We continue to fund ground-breaking research and support for families facing through . Any donation is appreciated, as always.

Read more here:
https://morganadamsfoundation.org/lukes-posse-8-years/

05/05/2025

Friends! We are $400 away from reaching our $7000 goal to turn seven years of missing Luke into a "lucky seven"! Can you help?

was a happy, active, curious and loving five-year-old. He loved all things Hot wheels, colossal, squid, impromptu dance parties, The Beatles and his family. After symptoms that appeared suddenly, he was diagnosed with (Diffuse Intrinsic Pontine Glioma) and passed away in our arms just 17 days later.

This $7000 will move a groundbreaking discovery that has completely eliminated DIPG cells during testing closer to a clinical trial! To learn more about this study, please visit.

Thank you for your consideration!

Donate here: https:/morganadamsfoundation.org/lukes-posse-lucky-7/

04/25/2025

Today marks seven years since Luke Morin passed away from DIPG (Diffuse Intrinsic Pontine Glioma). Will you help make this a “lucky 7”?

Luke’s Posse (a tribute fund of The Morgan Adams Foundation) set a goal to raise $7,000 this month to move a groundbreaking treatment for children with DIPG brain tumors one step closer to a clinical trial!

Help Luke’s Posse reach their goal and donate here: https://morganadamsfoundation.org/lukes-posse-lucky-7/

About the Study:
Drs. Rajeev Vibhakar and Sujatha Venkataraman have developed immunotherapy treatments that safely and effectively target the protein that causes the DIPG tumors (a currently terminal diagnosis) – and leave normal cells unharmed. In fact, the team’s in vivo (animal study) testing has resulted in the tumors completely disappearing.

04/25/2025

Seven years ago today, the Earth lost a special little boy: our Lukie.

was a happy, active, curious and loving five-year-old. He loved all things Hot wheels, colossal, squid, impromptu dance parties, The Beatles and his family. After symptoms that appeared suddenly, he was diagnosed with (Diffuse Intrinsic Pontine Glioma) and passed away in our arms just 17 days later.

This year feels a tiny bit lighter than years past. I suppose time does heal in some ways? Regardless, we miss Lukie terribly every day and cherish the time we had together. I know he still shines brightly and is right by our side during the events of our lives, especially when his big sister Phebe is also shining brightly where she loves to be; performing on stage.

Would you help Luke's Posse reach our goal this month of raising $7000 to move a groundbreaking discovery that will closer to a clinical trial? Thank you for your consideration!

Donate here: https:/morganadamsfoundation.org/lukes-posse-lucky-7/

11/26/2023

Lukie would be 11 years old today. We miss you so much.

08/30/2023

Friends, we made it! We are now residents of Connecticut! There were times I thought this transition just might be the end of me, but then I remembered what bad ass warriors we are and all that my family has survived 💪🏽

Denver ➡️ Florida for a little beautiful break ➡️ B & B #1 in New Haven ➡️ B & B #2 in New Haven (love it, walking distance to everything!)

In November, we will move into our lovely home in !

Needless to say, pets and all, we are a little depleted..trying to grab some rest and reset time whenever possible 😴

Always missing our but I know he is still ever present with us whether we “feel” him or not.

On to new things! I’m ready!

08/03/2023

04/08/2023

Lukie didn’t get to go to kindergarten. He was so excited to start with Ms Julie and Ms Kristin…the same classroom as his big sister.

He wanted to sing this song for his Aunt Shannon because we had just left a family gathering at her house and forgot to share it with her. 🥹 this was one month before symptoms appeared and then….

Five years ago today, our life changed forever. Dx day. After sudden symptoms, Luke was diagnosed with and died 17 days later. 💔

It’s . It’s .

We miss you so much, Lukie. It hurts just to breathe some days.

Please say his name.