For over 35 years, Operation Smile has worked to provide safe surgeries in all parts of the world and educate hundreds of thousands of people worldwide. They partner with trained doctors, governments, hospitals and other organizations to give patients the quickest and most efficient surgeries. They have even visited over 60 countries, seeking support and volunteers from everywhere they encounter. Their work as an organization has impacted and is still impacting families all around the world.
Operation Smile mainly focuses on correcting cleft lips, cleft palettes, and other facial deformities. Children and adults with this condition face problems with speaking, eating, and drinking. In addition, they are constantly battling for social acceptance in a world that can’t stop judging.
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William P. Magee, Jr., his wife, Kathleen, and a few of their friends went on a medical mission to the Philippines to fix cleft lips and cleft palettes. When they arrived, they didn’t expect to find so many families in need, holding out their children in despair. Over 300 families came to meet them, seeking surgery for their loved ones, but William and his team only had the supplies to treat about 40 people. They felt compelled to come back, not only to help the poor population in the Philippines but all of the other desperate humans out there that lack health care. It was in that moment that the Magees realized how difficult it was for someone to grow up in a world where they are not socially welcomed. Because of their motivation and inspirational story, Operation Smile was created so that everyone can feel beautiful.
“Every child that has a facial deformity is our responsibility, If we don’t take care of that child, there’s no guarantee that anyone else will.” (Kathleen Magee, Co-founder of Operation Smile, United
The children were taught to always look at the glass half full that half empty. Throughout their struggle, their parents unique mindset set them apart from standard, but they never let their experiences turn into
Operation Smile' mission and vision parallel the mission Avi Weisfogel is on, to provide needed dental services to young children. He believes this organization should have expanded funding and has established a Go Fund Me campaign. The goal of the campaign is to raise
Additionally, his father wanted Lior to discuss Down syndrome in his bat mitzvah speech, but Lior did not want to talk about it. However, two years later, Lior seems more aware of his condition possibly because of increased cognitive abilities or conversations to assist in his processing of his disability. In the Jones et al study, studies found parents of children with disabilities postpone or waive these conversations with their children in order to protect their self-esteem, and may even contribute to false fictional identifies and hopes of the child. This is more likely to occur when parents view their child’s disability as something negative. Also, a large factor regarding the child’s processing of the disability is their
After reading this story, I also recognize that if I do not invest in my health now, I to could be faced with the same dilemmas as the Bane’s family in due time. I then, realized that it might have been destine for me to pursue a career and education in the field of social work due to the apparent need for advocacy and change in America’s healthcare system and in the educational system of those in poverty. In reading this story, I have truly realize the how the lack of proper education, jobs, and healthcare could have a damaging effect on the lives of its victims. I guess I never overlook how inadequate healthcare affects its subjects in the way the book descriptively expresses this reality.
Imagine being viewed by the world as different. Wouldn’t you want the people around you to understand? A 12-year-old boy diagnosed with autism was told he was not equal to his classmates. He had a hard time identifying social cues and a difficult time speaking, thus he was labeled “weird” and “an outsider”.
At the end of his presentation, we were all wondering what we could do to help this cause, to which he responded “tell 2 people about The Lost Boys”. The effect of ethos and pathos working together in Deng’s narrative made the audience care about the cause and want to know more about what we could do, therefore fulfilling the desire for awareness of the cause and of The Lost Boys nonprofit
In today's world there are many people with differences, but people may not always accept them. For example, I have a friend named Reece. Reece was in a car accident when he was 5 years old. This crash took away his ability to speak and he was paralyzed from the waist down. Since then he has had multiple surgeries to try to help, but sadly they have not been able to make him walk and talk again.
The onset of an unexpected illness my family brought upon a tough time in my family, and I was unsure of how to act, what to say, and what to tell others. After reading Unbroken, I felt that if Zamperini could survive years of torture, I could survive a seemingly small family emergency. The ability to relate Zamperini’s own story of resilience in a horrible situation inspired me to do the same in my own
In hopes of converting as many people to Christianity, Brace couldn’t ignore the thousands of vagrant children on the dangerous and filthy streets, the cause a rise in immigrants arriving there. With good intentions in his heart, Mr. Brace along with eight other men joined the organization that is still running today, The Children’s Aid Society (CAS). This organization raised a substantial amount of funds from the public and high members of society like the Roosevelt, and Astor families. With the funds the CAS
Company Name Company Address Date of Memo To: From: Subject: Recipient of Memo Title of Memo The Shouldice hospital is an excellent example of focused, well developed service delivery system.
Before all of this, Lizabeth didn’t know about the struggles of her family. She realized the struggle after hearing her dad cry for the first time. Her father who was a strong man, didn't seem like the kind of person who would cry. Her father was employed for 22 years, he feels like he has not been able to give anyone anything for years. Her mother, “small & soft, was now the strength of the family”.
Without this life saving transplant, Khalieghya would be dead; although, thanks to another grieving family, she is just like every other child. Instead of being locked away in a hospital her whole life, now she can play, run, jump, go anywhere she wants, and only has to take a small dose of anti-rejection medication twice a day (“A Chance to Be Just Like Other Children”). A little girl’s life was saved due to an inevitable accident, no single person can see the future; therefore, everybody should be prepared to give one last gift to another if their life is cut
Jaziah Shipp “Disabilities” I have experienced being under many labels. With all of these labels the excruciating painful times were harder when I was just finding out that I was adopted wondering “do my birth parents even love me”, “who is my real parent”, and “why didn’t she want me”. When I was in elementary school I was labeled with a speech disability. School became a big issue in my life. I was so hurt when I had to present in front of the class.
As I volunteered and continued to read, I began to see the kids I played with differently. I didn’t just see them for their disease or complications, but I saw their heart, and the joy they felt just by doing simple things. I started to imagine their families and wondered what they might be going through, having a child live in a hospital. I kept remembering how confused and misled the Lacks’ family was with the health care system, and even though, I’m not a doctor, I hoped the best for the patient’s well-being and their
I will tell how Make-A-Wish foundation has completely changed children’s