My Rare Dwarfism Makes Me 1 in 4 Million | BORN DIFFERENT

The video follows Landon, a 7-year-old with a rare form of primordial dwarfism. It details his diagnosis, the challenges of his condition, and the journey through a bone marrow transplant. Despite complications, Landon shows resilience and hope for a healthier future. His story highlights the rarity of his condition, the medical interventions required, and the emotional impact on his family.

What type of dwarfism does Landon have?

• Diastrophic dysplasia

• Primordial dwarfism

• Achondroplasia

• Spondyloepiphyseal dysplasia

What was a significant challenge Landon faced due to his condition?

• Difficulty in walking

• Frequent headaches

• Vision problems

• A failing immune system

Why did Landon need a bone marrow transplant?

• To improve his growth

• To strengthen his immune system

• To help with his breathing

• To enhance his vision

What is TMA, a complication Landon experienced post-transplant?

• A respiratory issue

• A digestive problem

• A blood clotting disorder

• A type of infection

How has Landon's lifestyle changed after the transplant?

• He no longer needs medication

• He can participate in sports

• He has to avoid public places

• He can now attend school regularly

What activity does Landon enjoy that showcases his imagination?

• Drawing and painting

• Playing video games

• Reading books

• Pretending and imaginative play

What is Landon's family's hope for his future?

• To become a professional athlete

• To live a productive adult life

• To become a famous artist

• To travel the world