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More handpicked essays just for you.
Multiple sclerosis quizlet
Multiple sclerosis quizlet
Multiple sclerosis quizlet
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In “Am I MS?” Miriamne Ara Krummel talks about her personal journey she endured dealing with multiple sclerosis. Krummel further explains at the end how she was finally able to accept her diagnosis and to embrace it. She finds that it’s important to be open about the disease. She believes that, “it might be helpful if more people would talk about death and dying as an intrinsic part of life” (76-77).When she was first diagnosed, she had a difficult time coping with MS.
Multiple Sclerosis is when the immune system attacks the nervous system. Higgins has multiple lesions on her brain and spine and she relapses and remits which means she gets sick and then better but she never restores complete function of her brain and body. To her children, MS means “Many Scars” because she has scars on her brain and spine. Harper and Hudson are too little to understand Multiple Sclerosis but they understand that sometimes Higgins is sick and in pain.
This article can turn out to be an inspiring article for people who are suffering from multiple sclerosis or other disabilities. Mairs begins her introduction with a hilarious event which is an attention grabbing for a reader. Then she
Even though she was diagnosed with Multiple Sclerosis, she is still able to have the strength to achieve anything that is possible to her. Because of having MS, the unpredictable course of the disease were terrifying to her. Each night she would get into bed wondering whether she will ever get out again the next morning. Whether she be able to see, speak, to hold a pen between, knowing that one day might come. With the horrible situation in Nancy's life she had the strength to overcome any obstacle.
She had an average life before being diagnosed. She “climbed trees, played hopscotch, jumped rope, skated, swam rode my bicycle,”…. and “walked down the aisle. I pushed baby carriages, changed tired in the rain, and marched for peace” (Mairs, 1993, p.40). Then at the age of twenty-eight she found out that she had multiple
As mother said the disease had passed and their troubles
After reading the book The Other Wes Moore many themes seem to nudge at you to realize many things that happen that you might not notice in everyday life. One of the life lessons that really plays a role in my life is loss, faith, and redemption. Loss. This word can mean different things depending on the person and their experiences. Loss might mean an event that causes immoderate feelings of despondency.
When Blair was finally diagnosed with MS in her 40s, she was told to keep it quiet so it wouldn't affect her career prospects. This made me think about the ways in which a diagnosis can change how others see us, and how we see ourselves. It can be hard to reconcile our past experiences with our new identity as someone with a diagnosis. Blair's decision to share her diagnosis with the world was a brave one, and it was heartening to read about the support she received from her coworkers, friends, and even the paparazzi. It made me realize that we all need support and validation, no matter what our struggles are.
Nancy describes her experience with multiple sclerosis, indicating how hard it is to lose your own body slowly. Mairs hated her disease and conforms to many harsh realities of
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.
Growing up with mental illness they called me crazy, annoying, and angry. They looked at me differently. They’d even talk about it amongst themselves, but never offered guidance. That’s the problem with society these days. Everyone loves a party, but no one wants to clean up the mess.
Through the course of his treatments and convalescence I have learned that listening and the understanding of the condition, greater outweighs the physical act of recovery. This has provided me with the skills to become a more confident, care-provider and teacher to make any child succeed. Currently I am undergoing training to become a Friendship Volunteer for Independent Age. Again, this I hope underlines qualities that I have. I also possess excellent communication skills, I am a good listener and I can understand and share the feelings of others.
Her disease was my disease. I would walk down the hallways and see people whispering and blatantly looking or pointing in my direction. Maybe they were talking about my mother being arrested last night, the number of times she had been thrown in jail and went to rehabilitation centers, or even how often she had been caught drunk driving. Fortunately, they did not know about the time I painfully watched my mother get tasered by the police. Watching her drop to the ground in my backyard like a shot deer, fracturing her wrist as she fell, was an event that will forever be ingrained in my memory.
No one wants to think about life altering events in which they have not controlled; I am no exception. The untimely and devastating death of my mother occurred without warning or preparation. Looking back, there was nothing to prepare for; she was only 51 years old. Could I have been more prepared for the loss of my mother?
I watched my mother fade away slowly as she was battling pancreatic cancer. I looked after her everyday as best as I could; however, the feeling of my eventual solitude was unbearable. The thought of my mother’s imminent demise made me feel like my heart was being continuously stabbed. Watching my mother suffer was one of the hardest things I have ever had to go through. After her passing; something changed in me, darkness filled where love once was.