A true hero. Thank you so much Dr. Ponseti ❤ My baby was born with clubfoot on her left foot and now on our 6th month in BNB. We are forever greatful to you. RIP From the Philippines
Thank you Dr. Ponseti. Your willingness to publish your procedure was in itself a miracle. My son was born with the condition in 2023 and your procedure is what is being adopted here in Nigeria. Thank you again.
Thank you so very much Dr. Ponseti. My son has bilateral clubbed feet and his methodology corrected my son's feet. If doctors would listen to each other and try methods that are working better than current methods, healthcare would grow exponentially. Its frustrating that it takes so long for things to get better. 😊
I was born in Iowa CIty with clubfoot in 2001 and was a patient of Dr Ponseti and this man truly is my hero without him my life could've been much different RIP Dr Ponseti
Thank you sir, having a kid with clubfoot, i know the miracle u have created for parents like us, the magic u have created, u r god to me,, thank you sir
right on my name is chris ,,, i myself was born with club feet ,, i went under the blade ,, dr. ponseti ,, is so right i'm 38 now and have a real hard time walk n now for some years now i would go to doctor's ,, the most of them would just look at my feet and say well it looks like they did a good job ,, disability even sent me to there dr,s they say there is nothing wrong , just got a foot dr. place called feet for life ,i can't work because of it ,, shriner's st. louis its cool to see this
Кто нибудь помогите мне пожалуйста !Моей дочке 11 лет .У нее косолапость левой стопы появилось с 3 лет .Она родилась с диагнозом детский центральный паралич,девочка не ходит .Три года назад оперировали но ей не помогло .Где мы живет ,нет лечения по методу доктора ИГНАСИО ПОНСЕТИ ..Скажите можно ли убрать сильную косолапость без операции в 11 лет .Спасибо ..
