Our son came into this world fighting. During birth, he suffered a hypoxic brain injury, and those first six weeks in the NICU felt like a lifetime. When we finally brought him home, people assumed the hardest part was over. But for us, it was just the beginning of truly understanding the road ahead.
He’s our miracle, our fighter. But he can’t eat on his own. Not a single bite. Everything he needs to survive goes through a feeding tube. We’re waiting on tests to confirm whether he’s lost his hearing. The doctors tell us cerebral palsy is likely. Some days the weight of it all feels crushing, but then we look at him and we see possibility. We see hope. We see our son who deserves every chance to experience life fully.
We’ve found stem cell therapy. Real research, real doctors, real families who’ve watched their children improve in ways they were told weren’t possible. It’s not a miracle cure, but it’s hope backed by science. Insurance won’t cover it. Between the treatment costs and flying to the US every two months for his ongoing care, we’re stretched beyond what we ever imagined. We’re his parents. We’ll move mountains for him.
This is where you come in. We need a community around us. We need people who believe that every child deserves a fighting chance. Your donation, whatever you can spare, directly funds his treatment. Treatment that could help him become physically and cognitively independent. Treatment that could give him the ability to eat, to move, to learn, to live without limits we can’t yet imagine.
Can’t contribute financially? Your share is just as valuable. The more people who see this, the more support we can build.
Please help us give our son his best shot. Not someday. Now, while this treatment can make the biggest difference. Thank you for standing with our family.
