Peter Bruce has been a patient of NOPCO (now Boston O&P) since. Bruce was born in Philippines where he spent the initial five years of life in an orphanage for religious reasons managed by limb issues. He recalls being treated as children who lived there. He didn’t think of him as being different, since everyone else did.
Peter has been born with the use of both hands and one foot. He was diagnosed with a rare disorder known as Pierre Robin Syndrome. A Massachusetts family adopted Peter and he was first observed by NOPCO prosthetics near me when he was just six years old. He said that his parents viewed beyond the physical appearance and saw a thriving child. It’s this inner strength and determination that has enabled Peter to become an inspiration to everyone who he interacts with.
We requested Peter whether he would like to have a conversation with us about the experiences he had as an amputee to ensure that other families and patients who are in similar situations could know that they aren’t in isolation and maybe be able to learn from Peter.
Why did you stay at NOPCO since 17 years?
He appreciated the treatment he received, like a typical child: “I saw how medical specialists interacted with children and I liked the fact the fact that I was treated in exactly the same way at NOPCO”. Peter said that NOPCO staff members have become more like friends , and even at a limb issues young age, Peter was involved in the decision-making. The employees think outside the box and constantly look for fresh ideas. “NOPCO granted me to let me express my personal style.”
As a kid What was your most cherished prosthesis?
“The bigmouth bass” Peter stated without hesitation. He enjoyed fishing with his dad and was wearing a T-shirt that featured an enormous mouth bass that was coming out of the water , with hooks inside its mouth. “I realized my leg wasn’t real, why bother to make it appear like one? I’m not able cover my arms or hide my the face of my friends, why conceal the legs”? Peter’s Bass T-shirt was made to make his prosthesis. The following year limb issues, his second most favored prosthesis was the dog with three heads in Harry Potter. Laughed when he told the story of how he didn’t know that the drool of the dog was actually black and light sensitive. Peter was a target for his buddies when playing laser tag. Peter was awarded an award for the “most hit” award that day.
He was a user of task-specific upper limb prosthesis while an infant. He loved his numerous “hand” accessories that let him to throw and catch baseballs; dribble and shoot basketballs. Peter’s current Peter utilizes myoelectric hands and enjoys running on the “sprinter” foot.
What are things you aren’t able to do you’d like to be able to do?
Peter declared with great vigor that there’s nothing that he does not do. He is extremely involved in his activities orthotics near me and day-to everyday chores. Peter played football at high school. He also is a dancer and loves drawing and is a great escape for Peter. Peter insists that he is not limiting himself to any thing. He is determined to show others and himself that he is capable of doing whatever he sets his mind to. Peter declared, “You should always want more from yourself. You must push your fears away and push on until you reach your goal.” Peter also said that parents should not limit their children’s abilities to what they can accomplish or think they aren’t capable of doing things, and then take the loss. The parents of his never said they couldn’t do something however they encouraged him to be successful.