Most eleven year girls’ primary concern is whether or not her crush has a similar interest in her. I, on the other hand, had much more than boys on my mind during middle school. At that age, I was diagnosed with severe scoliosis. Throughout this entire experience, I faced various trials and heartaches, but I acquired a multitude of irreplaceable life lessons. For the first year after my diagnosis, I wore a back brace. Attending school with a suffocating piece of plastic wrapped around my waist was horribly embarrassing. Being the self-conscious eleven-year-old I was, I concealed it with every piece of clothing possible. Puberty was tough enough to deal with at that age, let alone adding a bizarre spine disease to my list of body changes. Plenty of time passed before I realized that my friends actually thought my brace was interesting. This came as a shock since I was completely sure that no one would want to be friends with a girl that had back issues. …show more content…
Up front, I knew of the 2 percent chance that spinal fusion wouldn’t be mandatory, but I held onto that possibility. It was agonizing to hear that I would never be able to bend my spine again. Had there been some reason to place the blame on me for this obstacle, this journey would have been much more manageable. Instead, I had no one to blame but God. I couldn’t believe that He would let my own body fail me. To make problems worse, I was an avid gymnast, and two titanium rods and twenty screws were about to take my passion away from me. After countless shed tears, I convinced myself that the surgery was going to help rather than hurt me. In the weeks leading up to my operation, it took every ounce of courage in my hundred pound body to be strong. And because of my bravery during this particular time-span, every obstacle I’ve faced since has appeared as a gust of wind rather than a
In my head I was scared I was paralyzed and that I would never walk again. Scoliosis scarred me for life because the pain subsides in my forever now. It hasn’t gone away since the surgery it is only tolerable now. My memories from the hospital stay consist of lying on the striker frame in pain, staring at the floor or the ceiling depending upon the way I was positioned. Every fiber in my body wanted to move, but the process of moving was unbearable. Only two days after my surgery they started having me try to walk to the bathroom on my own, I needed assistance the first couple of tries but after a while I could walk on my own. Sitting up or in a chair was another thing, I was only relearning the muscle movements for my back, but I couldn’t stand the pain and my stomach couldn’t keep the food down. I cried every day because I couldn’t do things for myself, I was mad at the world for putting me through pain. After about a week in recovery I was sent home, but there were problems there too. After 3 months I was able to finally sit in a chair for a long period of time, lay in my bed, run, and do every day things on my own again. I learning an important lesson through this; you don’t become successful without working for and the occasional obstacle. Spine surgery changes a person. It can fix
I walk into the cold, white hospital, my hands are sweating and my knees are shaking. Even though I have done this every six months since I was twelve years old, it never gets easier. I find a seat in the corner of the waiting room, embarrassed by the large, plastic, butterfly printed scoliosis brace I hold tightly against my side. The door opens, a nurse dressed in plain navy blue scrubs calls out “Emma for Dr. Meyers”. She leads my mom and me down a long hallway, and into a small, brightly lit room. The curse that is scoliosis is hereditary, which means my mom has it, and each of my sisters has been touched by this cruel disease that bends the spine as well. Scoliosis is a curvature of the spine that occurs during the growth period just before and through puberty.
Margaret has spina bifida, a condition in which one or more of her vertebrae did not form properly, leaving her spinal cord—the most vital component of the central nervous system—unprotected. She has had eight operations and wears braces on her legs to keep them in the proper positions. Throughout all of these ordeals, she has retained her outgoing personality and positive view of
Homophobia present in the black community has decreased over the years. Black culture is becoming more tolerant and accepting of the LGBTQA community. Churches are becoming more tolerant towards the LGBTQA community. A few decades ago, homosexuality could not be talked about in public without being shamed, however many Black celebrities are making their sexuality public, inspiring the change of mentality in the younger generations. Some of these artist include Frank Ocean, Azealia Banks, and Jason Collins. Also, the portrayal of LGBTQA persons of color in the media is becoming less stereotypical, they were portrayed as flamboyant gossipy men with feminine tendencies, however now they are represented as people that you can identify with. For
In, “Heterosexism and homophobia among college students,” Larry M. Lance starts off by explaining the difference between heterosexism and homophobia. Heterosexism is thinking that everyone should be attracted to the opposite sex and homophobia is having an irrational fear of gay men and lesbians. He mentions that efforts have been made to reduce heterosexism on campuses by encouraging homosexuals to be proud of who they are and not hide. However, with homophobia, he states that these negative attitudes are seen more in heterosexual males than heterosexual females. Heterosexual males could have more homophobic views on lesbians and gay men because of their exotic value even though they seem to be less homophobic towards lesbians. Lance
What if a disability happened to you? Or a close person to you? Like a sister or a daughter? How will you deal with it?.The book Wonder by R.J. Palacio, we read about a kid named August who was delivered with an uncommon face distortion. This disability.
The procedure always spoke to me as an embodiment of the human spirit. ‘ If we cannot fix it one way, we will do it another; If we cannot mend the brain, we will correct the feet.’ Ever since my operation, I have used this same outlook to overcome all the handicaps. When I came home from the procedure, I had both legs in soft-wrapped splints. I was to be non-weight bearing and to keep still. The recovery period was frustrating for me and absolutely maddening for my mother. I had no interest in being immobile. So within days of coming home in the splints, I had to be brought back to the hospital. I had snapped the splints in to by trying to crawl. Afterwards, I was put into hard castings and I was more cautious. Once out of my castings, I had to endure a year or more of physical therapy, because I had to learn how to walk again. To this day, I refuse to let my disability stunt my potential. I have tried at every available opportunity to challenge myself, to keep on fighting, and to invent ways around my
Adolescence is a difficult stage in life because it is a time for many when social status is seen as very important and self-esteem can be fragile. One’s social status can directly affect one’s self esteem and overall happiness. Unfortunately, many of those who possess a higher social status in middle and high school use it against those who are deemed socially inferior to them, whether that is due to race, attractiveness, intelligence or sexuality. In other words, the adolescents at the bottom of the social pyramid are often subjected to bullying and harassment from their socially “superior” classmates. Bullying
I ask myself, did it really get better? In many ways, yes. But when I read things like 'masc only' or 'no fems' I can't help but wonder why? I don't blame the individuals for having their own preference. 'Gay bros' are now becoming more predominant and
Australia is a rapidly evolving country branching off from the British monarchy. In this day and age, it seems almost petty to have the need to argue and fight for or against such obviously necessary things such as marriage and adoption rights for LGBT+ persons. In 1994, the Commonwealth passed the Human Rights (Sexual Conduct) Act 1994 - Section 4, decriminalising private sexual activity between same-sex, consenting males. Since then, there have been no major political advances for gay rights in Australia, especially after the rein of the Howard government, which made it more difficult for same-sex attracted and transgender people to associate with the country.
This article talks about both the pervasiveness of homophobia, characterized as "a bias that prompts scorn and segregation toward lesbian and gay individuals" (Croteau and Kusek, 1992, p. 396), and a particular approach to diminish homophobia—gay and lesbian speaker boards. Gay and lesbian speaker boards are board presentations by gay and lesbian individuals, whereby they share their own encounters, stories, and take part in a dialog with the gathering of people. Croteau and Kusek (1992) talk about six past studies that looked into techniques to abatement homophobia, with some using different sorts of speaker boards. Albeit methodological shortcomings are recognized in the exploration, 5 out of the 6 ponders presumed that homophobia can be
There’s things in life that everyone takes pride in, things that they won't ever be ashamed of. I have so much to be proud of especially in myself. After having Spinal Fusion surgery, i’ve done things I never thought I would be able to do, and one of them is learning to find my balance and walk again.
It continues to amaze me that even in the 21st century the church continues to be major focus in the discrimination homophobia. The church seems not to learn from our history. During the years and post years of the slavery of African Americans, the mistreatment, abuse and murder of black people was supported by the Bible and even condoned as acceptable behaviors. But as we now know, that neither God nor the Bible supports hatred or mistreatment of another human being as we are all children of Christ and we are to love one another and treat each other as we ourselves want to be treated.
Homophobia and transphobia have been the reason for many deaths within the LGBT community throughout the world. It seems that is the same ignorance that acts behind the fear of the unknown; to believe that heterosexuality is "normal" because so said our ancestors, culture, society and religion. Bobby’s mother upon learning of the death of her son begins to question her religion and the interpretations of the Bible. This leads her to find answers and support in the community Parents, Families and Friends of Lesbians and Gays (PFLAG). There she discovers that Bobby had always been different from conception and that there was nothing really wrong with it. Because of that, she becomes an advocate for gay rights, prompting people to think before
Parents of children diagnosed with AIS (Adolescent Idiopathic Scoliosis) face difficult decisions when determining a course of treatment. The information received from the child’s doctor or orthopedist may be the only reference parents have to base decisions on. This may leave many unanswered questions regarding the child’s treatment, effects of treatment and long term quality of life after treatment. Like most parents, upon hearing my daughter’s diagnosis, a million questions came to mind including what does this mean for her health, can she still play sports, will she have pain, and mostly, will she live a normal life?