Blog

Watch Haley and Levi Walker—aged 13 and 10—as they embrace the daily challenges of life, school, play, projects and partnerships—and you’ll see a couple of typical tree-climbing, beach-combing, dinosaur-digging, rock-climbing, snake-charming, adventure-loving kids. But for these busy siblings, their adventure includes a subliminal pioneering aspect, as well: they were born with an extremely rare neurological condition known as Hereditary Sensory and Autonomic Neuropathy, Type 6, and they’re blazing trails into this new territory every day, aided by colorful ankle-foot orthoses (AFOs) that keep them happily on the move.

Discover the inspiring story of Sophia Acosta, a young girl with spina bifida who defies the odds, living life to the fullest and spreading her bright smile to those around her.

Katie Verdi’s contagious smile began charming the world before she could walk—and it has seldom dimmed since, despite her ongoing battle with a relatively rare genetic condition known as neurofibromatosis Type 1 (NF1). Type 1, the version of neurofibromatosis that usually appears in childhood, has caused abnormal bone growth in her lower legs, requiring the support of a colorful pair of intentionally mismatched braces which keep her moving, dancing—and smiling.

Read the inspiring story of Callen Walck, a Lawall patient who overcame significant mobility challenges with the help of our experienced team of certified prosthetists. Discover how our personalized care and support helped Callen achieve his goals and improve his quality of life. Visit our website to read Callen’s story and learn more about Lawall’s prosthetics and orthotics services.

Sudan has a congenital deformity that left him with a shorter right leg, but that never slowed him down; instead, it has given him the drive to attempt everything.