psalm
Recently, my sister’s best friend became momma to the most precious little boy, Psalm. Their family has experienced an unexpected start to Psalm’s life, and my sister felt very compelled to help them financially.
Out of that desire, we designed some products to benefit the Cooper family as they take on numerous expenses.
Would you please read Savanna’s, Matt’s, and specifically, Psalm’s story and consider buying an item to go toward their medical bills, extended stays, and travel?
Meet Psalm Matthew Cooper
Our names are Matthew and Savanna Cooper, and we are the proud parents of our sweet baby boy, Psalm Matthew Cooper.
Psalm was born on December 30 at 8:56 PM after what we believed was a completely healthy and normal pregnancy. We were overwhelmed with joy and gratitude as we welcomed him into the world. But by the next morning, everything changed.
Doctors began noticing that Psalm’s oxygen saturation levels were dropping—first into the low 90s, then into the mid-80s. It quickly became clear that something was seriously wrong. He was rushed to the NICU, placed on a ventilator, and doctors began running urgent tests.
They soon discovered the issue was his heart.
Because of the severity of his condition, Psalm was airlifted by helicopter to Children’s of Alabama in Birmingham, a hospital specializing in advanced cardiovascular care for infants. There, we received the diagnosis that no parent is ever prepared to hear:
Psalm has severe aortic valve stenosis with diminished left ventricular function.
His aortic valve—the valve responsible for allowing blood to flow from the left side of his heart to the rest of his body—was nearly closed. His heart was struggling to pump blood properly.
At just one day old, our newborn underwent a life-saving procedure. Doctors inserted a balloon catheter into his heart to stretch open the valve and improve blood flow. By God’s grace, the procedure helped, and we were given a glimpse of hope.
But Psalm’s journey is far from over.
This diagnosis is extremely rare—his doctors see approximately one case like his each year. Within just weeks of that first procedure, Psalm’s condition unexpectedly worsened. He had to be airlifted again for an emergency intervention that no one anticipated.
He now remains in the ICU in critical condition and has been referred to the heart failure/heart transplant team. We are praying and believing for his left ventricle to strengthen and recover. If it does not improve as hoped, he may need to be placed on the heart transplant list—an unimaginable reality for any family.
Alongside the emotional weight of these unknowns, we are facing an overwhelming financial burden. We are currently fighting for insurance approval for essential medications Psalm must have to survive once he is discharged. These medications are extremely expensive, and coverage has not yet been approved.
On top of that, there have been unexpected expenses including:
• Emergency air transport (multiple helicopter flights)
• Extended ICU stays and surgical procedures
• Specialized cardiac care
• Travel between Mobile and Birmingham
• Lodging near the hospital
• Time away from work
Like so many families, this sudden medical crisis has turned our world upside down—emotionally, physically, and financially.
There is still a long road ahead filled with unknowns. Every hour of stability, every small improvement, and every breath feels like a miracle to us.
We are standing firmly in our faith. We are Christian, Bible-believing followers of Jesus, and we believe with our whole hearts that God is able to heal our son. Even in fear and uncertainty, we trust in a mighty God who has a plan and purpose for Psalm’s life.
We are sharing our story not only to ask for help, but to invite others to stand with us—through prayer, love, and support—as we fight for our son.
If you feel led to give, please know that every donation will go directly toward covering the immense medical and travel expenses and allowing us to remain by Psalm’s side during this critical time. If you are unable to give, we ask just as sincerely for your prayers and for sharing his story.
Thank you for taking the time to read about our precious boy. We believe a miracle is coming.
With gratitude and unwavering faith,
Matthew & Savanna Cooper
