WITH HEAVY HEARTS BUT UNWAVERING FAITH, WE ARE ASKING FOR SUPPORT...

Our family is facing a reality we never imagined. After nearly two years of unexplained symptoms, painful cramping, progressive weakness, and countless tests, my husband Gabriel (Gabe) is now facing the most devastating diagnosis of our lives: Amyotrophic Lateral Sclerosis (ALS) — a terminal, progressive neurodegenerative disease with no cure.

We believe deeply that God is with us in every step, every breath, every moment, and that He brings people together for a reason. Today, with humility and faith, we are asking for help.

✨ GABE’S WORDS OF HOPE

We want Gabe’s voice to be part of this story. Even in his hardest moments, he holds onto hope and faith. He said recently:

“I still have so much I want to live for. I’m not ready to stop fighting.”

And on another day:

“God isn’t done with me yet. I’m trusting Him one breath, one day, one step at a time.”

His mind is fully there. His faith is strong. His will to be a husband, a father, and a provider has not changed — even as his body fails him.

✨ OUR FAMILY’S JOURNEY SO FAR

Gabe’s symptoms began nearly two years ago, starting with subtle weakness and muscle twitching. Over time, everything progressed:

Today, Gabe can no longer dress himself, bathe himself, or drive. He faces each task — even holding a toothbrush — with unimaginable effort. His brain is 100% intact, trying to tell his body to move… but ALS does not allow the signals to reach the muscles.

Our children, Makaela (14) and Dominic (13), have watched their dad struggle with pain, fear, and limitations that challenge him every day. They’re incredibly strong, but their hearts are hurting.

In 2024, we moved across the country to Lewes, Delaware — thousands of miles from our families in California — hoping for a slower pace of life and new experiences together. Instead, we suddenly find ourselves fighting ALS far from the support of extended family.

I (Keri) am now Gabe’s full-time caregiver while raising our children and managing our home. It’s a role I take on with love, but it comes with emotional, physical, and financial strain that no family could prepare for.

✨ WHAT ALS REALLY MEANS

ALS is terminal.

Most people live 3–5 years after symptom onset. Gabe is already close to two years in.

The disease will continue to weaken his muscles, including those for eating, swallowing, speaking, breathing, and moving. Our goal is to give Gabe the highest quality of life, the most comfort, and the deepest love for however much time God gives us.

✨ WHY WE ARE ASKING FOR HELP

ALS is not only devastating — it is extremely expensive. Many needs are urgent, ongoing, and not covered by insurance.

Your support will help with:

✔ Medical Bills

Neurology visits, EMGs, MRIs, hospital care, medications, infusions, and constant testing.

✔ Mobility & Home Modifications

✔ Assistive Devices

✔ In-Home Caregiving

As Gabe’s needs progress, we will need help with:

✔ Travel to Penn Neurology & Specialists

✔ Loss of Income & Future Needs

Gabe can no longer work. And as his full-time caregiver, I cannot work outside the home. Your support gives us breathing room as we face one of the hardest battles a family can endure.

✔ Anything Unexpected

ALS brings many sudden expenses — medical, safety, and emergency needs that arise quickly.

✨ WHAT YOUR SUPPORT MEANS

Your donation will help us:

We are trusting that God will bring the right people into our lives in this season. If you feel called to give, share, or pray for us, it means more than words can express.

✨ FROM OUR FAMILY TO YOURS

Thank you for reading our story. Thank you for being here with us.

Thank you for surrounding our family with prayer, compassion, and love.

“The Lord is close to the brokenhearted…” – Psalm 34:18

We cling to Him. We cling to hope. And we cling to the belief that we are not walking this road alone.

With gratitude,

Keri, Gabe, Makaela & Dominic