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However, the experiences encountered served to improve the quality of my life. Through medical treatment, I even visited the US a number of times, a luxury several individuals lacked.
‘You are a very lucky child’ my mother kept telling me. I did not know the meaning of that until I could dance and exercise with my friends at 18 years old. Among the triplets, I was the only one born with a disability. My right foot was completely disabled and found it as if all hell was on me when it came to walking. I later came to note that it was ‘club foot’ as referred to by doctors. Initially, it was a nightmare for me to understand because of two reasons: I was a child and was the only one with the disability. ‘Why me’ I wondered most of the times. However, most of the doctors in my city (Maracaibo as one of them) claimed that even with the surgery and therapy that I was to undergo, it was not a guarantee for a normal life like other human beings.
My parents’ resilience in searching for a competent doctor resulted in a contact with a Miami based doctor. He was a specialist and dealt with clubfoot in children. His name was Doctor Peter Romano. He was my ‘savior’ as he assured me that I would walk again and continue with my duties just as the other kids would do. As activists claim, the disabled have to go against all social, economic, political, and legal odds to make it in life. Davis identifies the historical struggles that the disabled underwent to secure the same privileges as guaranteed by the law (Davis, 16). However, I was lucky as the people around me supported me in all ways. Following intense research, I found out that clubfoot has no main cause and is caused by many syndromes (Adams 12). ‘Do your job as long as she will walk like me’ I recall my mother saying to the doctor.
At the time, stigma in relation to disability study was a major factor affecting the U.S. (Longmore 350). However, the breakthrough
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