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More handpicked essays just for you.
Pathophysicology for lyme disease
Pathophysicology for lyme disease
Pathophysicology for lyme disease
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Question 1 Patient : Samantha Gelly (F) D.O.B : 14/11/1993 Date : 08/09/2017 Samantha is a 23-year-old young woman. She had an injury on her right-sided head. During her soccer practice, she got hit in the right-sided head by a soccer ball. She stopped the practice after the injury and was conscious at the time.
The clue thus accidentally obtained has been followed up by months of patient investigation, and has been thoroughly sifted. Today we lay before the world a story
ever let a diagnosis win (majority of the time) and effect you from doing anything that 's your passion. Her story is
This caused many people to lose their lives, once you know you had this disease it wasn’t very much you could possibly
When a patient is told they have a disease, they are shocked. Some patients worry that they may die, and others feel numb or confused about it. They may have a hard time realizing that their disease could be fatal. “When he asked if she was okay, her eyes welled with tears and she said, “Like I’m always telling my brothers, if you gonna go into history, you can’t do it with a hate attitude. You got to remember, times was different” (Skloot 276).
Ehlers-Danlos Syndrome is known as an invisible illness. It is invisible because a person can physically appear fine, but they suffer chronic pain and frequent dislocations due to a defect in collagen production. Without knee braces and other assistive devices, I look normal. Quickly after my diagnosis, I was confined to a wheelchair for a period.
Day two clinicals. This day went so much smoother. I had the same two patient as the day before and one got discharged and I got a new patient. I feel like my second day I had an amazing relationship with my one patient. I got her to eat a little more that day because I knew what to talk to her about.
It was the middle of summer when it happened. I was about 9 years old and my mom and dad had just called me into my mom’s room. I had had a medical procedure about a couple of weeks before hand so I wasn’t surprised when they said it was about the results. They started talking to me about the results when they finally told me the main thing that had showed up.
One night, I woke up to my sister screaming; her body was drenched in sweat, and she repeatedly said, “I can’t move my legs”. I was young then and didn’t understand what she meant. I slowly lifted the covers off of her legs. They looked perfectly normal to me, so I asked her to wiggle her toes. Thirty seconds went by, and no movement occurred; she says, “I really can’t move my legs”.
As a child, I often spent my time constantly in and out of my pediatrician’s office and at hospitals getting my blood drawn, checking for jaundice, and making sure that my Hepatitis B remain dormant in my liver. But all of the appointments spent with these people made me view them second to my parents: if my parents couldn’t fix my Hep B, then they would call their “handy-dandy friends” to fix me up. And I always thought it was so amazing that these unbelievable heroes could assuage human pain and disease with their bare hands, whether it was performing a breast biopsy to scribbling a prescription down on paper—I wanted to be just like them. But it was when my little sister Kristine and I were racing for the keys on top of a shelf above the
A horrific killer is loose across the land of England. There is nothing to fight it as it continues to rapidly create chaos in a terrible nightmare called life. The killer is a sickening disease in the air that is impossible to contain. 1) It is 1352, in Northern Europe five years since the first symptoms of this illness had been exhibited. It was dormant in my body until when I recently contracted the wildly contagious illness by attempting to take care of my brother.
The decision was made that I would not go to the doctor again until the summer. So when June 2015 rolled around, I expected that I would go to the doctor. Well, I did not. I did not go back to the doctor until July. I found myself listing off symptoms to someone who actually seemed to be listening.
A few months after the diagnosis, the disease was manageable and I was able to live my riveting 14-year-old life. Two years later, I had relapsed for the fourth time and stuck in a brightly-colored hospital room once again. The three weeks I spent there proved to be even more difficult than the initial struggle. Through my anxiety-ridden thoughts and the never-ending tubes and needles, I felt powerless and was unable to imagine myself seamlessly entering my junior year of high school.
and I don’t see remission in my future. I worry what the future holds and where I will be in 10 years. How will I take care of myself. Who will I have when my parents are no longer around? Taking life one day at a time is all I can do and that is scary in and of itself.
My passion for healthcare lies with patient care. I enjoy taking care of patients and their family. I have chosen to become a family nurse practitioner because I can combine nursing and medicine to provide a higher level of care to my patients. As a nurse practitioner will be able to make an impact on my patient’s health through, health promotion, disease prevention, managing acute and chronic conditions and improving patient’s health (Wynne,