At Clubfoot Connect, we share stories, publish informative blog posts, and raise funds to support those with clubfoot and champion their journey towards a brighter future.
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Read our Stories
Emmy, late 20s, United States
Emmy, a young adult from the U.S., faced the challenges of bilateral clubbed feet from birth. Financial strains marked her early years as her parents funded her surgeries by depleting their retirement savings. Growing up, she dealt with the discomfort of orthotics and the embarrassment of visible foot supports. Persistent foot swelling led her to adapt her lifestyle, transitioning to online teaching for flexibility. Despite her struggles, including a recent bout with Achilles tendonitis and the necessity of a disability parking placard, Emmy continues to advocate for affordable healthcare as a crucial right.
Silvia, Dominican Republic
Silvia’s journey began when her son was born with bilateral complex clubfoot, a condition that required years of dedicated treatment to straighten his feet. Now at 12 years old, her son's left foot is fully corrected, although the right one's heel remains slightly elevated. Now, she runs her own organization in the Dominican Republic that works to raise awareness and funds for clubfoot, while facilitating treatment for patients. Silvia also currently has a social media following of over 10,000, where she uploads posts sharing common misconceptions and destigmatizing the condition.
Lindsey, 34, Arizona
"Lindsey, a 34-year-old mother and nursing professional, was born with clubfoot affecting her right foot. She underwent surgery as an infant, followed by serial casting until she was a year old, resulting in limited foot mobility. Balancing her career with long hours on her feet and an active lifestyle, including playing sports like tennis, Lindsey has navigated life's challenges with minimal long-term pain from her clubfoot. Her journey stands as a beacon of hope and resilience for parents of children facing similar conditions."
