PS Advice--Almost Final Draft
Posted: Wed Sep 25, 2013 2:47 am
Hey guys. I have edited this around 4 times and I think I'm getting close to a final draft. Any advice would be very much appreciated. If there is anything as a reader you think does not need to be there please let me know. I need to cut 2 lines or so out so it is less than 2 pages I just don't know where! Thanks in advance guys!
It was Christmas morning and I was fast asleep in my bed just like a child despite the fact that I was nineteen years old. It is my favorite holiday and I look forward to it all year. The subtle knock I heard at my door that morning would change more than I could imagine. I rolled over, as it woke me from a deep sleep, to see my dad standing in the doorway, looking at me, waiting for me to be alert. All I seem to remember is, “mommy fell. I need you to go down and sit with her until I get out of the shower, she’s in her wheelchair.” I knew it was bad. She hates the wheelchair, and he called her mommy like I was five years old again.
For over 25 years my mom’s mobility and independence has slowly been taken by relapsing remitting multiple sclerosis. The older I grew the more I understood about her disease, and the harder it was to watch. There were good days where she almost seemed healthy, but there were bad days where just getting around the house was difficult. Even though it is a tough life, it is the life she has been given. She is a fighter, and my biggest inspiration.
As we sat in the bathroom that morning she kept saying it hurt, everything hurt, and she knew she really did it this time. I tried to reassure her everything was fine, that she was probably just sore like she was when she fell in the past. I was wrong. My dad took her to the hospital where we learned she had broken her hip. She went through surgery and a two-week hospital stay before finally coming home well after New Years. I only had three weeks left before I went back to school, but I never realized they would be so difficult.
With my brother at school and my dad at work I was left to tend to my mom who was confined to a wheelchair. While I was home the only time she was out of the wheelchair was for physical therapy. For weeks I followed her around the house making sure she didn’t fall, and when she did I was there to pick her up. Every time I picked her up the hope I had for a full recovery faded. Despite this, my mom never gave up on herself. She showed me what true courage and determination look like. I like to think from this experience some of that rubbed off on me. Watching her make strides in her recovery taught that me anything is possible if you never give up. It wasn’t easy for her, but she made nearly a complete recovery. I know that if she can overcome a broken hip with multiple sclerosis anything I have to do will pale in comparison.
Throughout this entire struggle, there was an assortment of problems stemming from the insurance company. Everyday it seemed like there was something else they weren’t going to pay for. One day it was the amount of nights in the hospital. The next it was physical therapy. Seeing my mom everyday I knew she needed these things, but the insurance company didn’t see what my family and I saw. It pained me to hear that, even with insurance, necessary treatments wouldn’t be given to my mother. The more I thought about it, the less I understood. It wasn’t right, and I couldn’t wrap my head around it. I have always heard of things like this happening, but it didn’t impact me until it was happening to someone I love. Luckily, my dad has an amazing job and could afford the majority of the things the insurance company refused to pay for. I know not everyone is this fortunate, and it upsets me to know people like my mother may not receive all of the necessary everyday treatments this disease requires.
The whole month seemed like a nightmare that I couldn’t wake up from. I was in a state of constant worry, something I wouldn’t wish on my worst enemy. There was only so much I could do to help, and I never felt like it was enough. Not being able to fix everything was very difficult for me. I’ve always had a strong desire to help others and an appreciation for equality and justice. Once everything calmed down and I had a chance to reflect, it hit me; health law. This is something I could do that would help people. At some point we all need a little help, and I want to be there to help others who need it. I hope that someday I can start a career in health law and aid people who received improper treatment or were wrongfully turned away from getting the necessary appropriate treatment. No matter what aspect of the law I find myself in, I want to make a difference in peoples’ lives.
It was Christmas morning and I was fast asleep in my bed just like a child despite the fact that I was nineteen years old. It is my favorite holiday and I look forward to it all year. The subtle knock I heard at my door that morning would change more than I could imagine. I rolled over, as it woke me from a deep sleep, to see my dad standing in the doorway, looking at me, waiting for me to be alert. All I seem to remember is, “mommy fell. I need you to go down and sit with her until I get out of the shower, she’s in her wheelchair.” I knew it was bad. She hates the wheelchair, and he called her mommy like I was five years old again.
For over 25 years my mom’s mobility and independence has slowly been taken by relapsing remitting multiple sclerosis. The older I grew the more I understood about her disease, and the harder it was to watch. There were good days where she almost seemed healthy, but there were bad days where just getting around the house was difficult. Even though it is a tough life, it is the life she has been given. She is a fighter, and my biggest inspiration.
As we sat in the bathroom that morning she kept saying it hurt, everything hurt, and she knew she really did it this time. I tried to reassure her everything was fine, that she was probably just sore like she was when she fell in the past. I was wrong. My dad took her to the hospital where we learned she had broken her hip. She went through surgery and a two-week hospital stay before finally coming home well after New Years. I only had three weeks left before I went back to school, but I never realized they would be so difficult.
With my brother at school and my dad at work I was left to tend to my mom who was confined to a wheelchair. While I was home the only time she was out of the wheelchair was for physical therapy. For weeks I followed her around the house making sure she didn’t fall, and when she did I was there to pick her up. Every time I picked her up the hope I had for a full recovery faded. Despite this, my mom never gave up on herself. She showed me what true courage and determination look like. I like to think from this experience some of that rubbed off on me. Watching her make strides in her recovery taught that me anything is possible if you never give up. It wasn’t easy for her, but she made nearly a complete recovery. I know that if she can overcome a broken hip with multiple sclerosis anything I have to do will pale in comparison.
Throughout this entire struggle, there was an assortment of problems stemming from the insurance company. Everyday it seemed like there was something else they weren’t going to pay for. One day it was the amount of nights in the hospital. The next it was physical therapy. Seeing my mom everyday I knew she needed these things, but the insurance company didn’t see what my family and I saw. It pained me to hear that, even with insurance, necessary treatments wouldn’t be given to my mother. The more I thought about it, the less I understood. It wasn’t right, and I couldn’t wrap my head around it. I have always heard of things like this happening, but it didn’t impact me until it was happening to someone I love. Luckily, my dad has an amazing job and could afford the majority of the things the insurance company refused to pay for. I know not everyone is this fortunate, and it upsets me to know people like my mother may not receive all of the necessary everyday treatments this disease requires.
The whole month seemed like a nightmare that I couldn’t wake up from. I was in a state of constant worry, something I wouldn’t wish on my worst enemy. There was only so much I could do to help, and I never felt like it was enough. Not being able to fix everything was very difficult for me. I’ve always had a strong desire to help others and an appreciation for equality and justice. Once everything calmed down and I had a chance to reflect, it hit me; health law. This is something I could do that would help people. At some point we all need a little help, and I want to be there to help others who need it. I hope that someday I can start a career in health law and aid people who received improper treatment or were wrongfully turned away from getting the necessary appropriate treatment. No matter what aspect of the law I find myself in, I want to make a difference in peoples’ lives.