Duchenne Muscular Dystrophy Autobiography

They had told my parent that a few of my red blood cells had a malfunction they started to break down. They had told my parents that I had something called sickle cell which is a group of disorders that cause red blood cells to become misshapen and break down. I never really understood what that meant but I just knew that I had a weak heart and that I never really played gym in school because they said I had “Limitations.” I never really knew what it meant but I just went along with it. A year later on March 11, 2008 I was back in the hospital because I needed surgery on my heart. I remember waking up after surgery and seeing my mom crying and asking my dad if I was going to die. I never really thought that was a possibility but I just pushed it to the back of my mind so I wouldn’t think about it. But turned out dieing was a possibility but I didn’t die, but the doctor told me that I could never be on a sports team and I could never play gym. I never really took it to the heart because I was only five I told myself that it was not the end of the world. That all changed a few months later and I was 6 now and it was a nice day on October 23 2008 and I was at the park with my dad and my older brother and they started to play baseball while I watched. After watching them play for a while I wanted to play so my dad pulled out a softball and a glove and I started to play on my own. I sucked at first but after a while I was really good. I remember on the same day I asked my dad if I could play on a team but she said no because of my “limitations.” Later that day I asked my mom and she took to play on a rec center team even though I wasn’t allowed and that's how it all started. And know I have played softball ever since and my

Scientists have been struggling with the cause, treatment of, and cure for Muscular dystrophy since its discovery in 1886, by Dr. Guillaume Duchenne. Muscular dystrophy is a hereditary disease, affecting thousands of people every year, two-thirds being children between the age of birth through adolescents. Muscular dystrophy can also occur with no family history of the disease.

My niece Mikah Bradford was born October 13th, 1988. She was born prematurely. Mikah spent the first month of her life in a neonatal incubator. My second oldest sister Crystal sat by her side the whole time singing to her. I was born May 18th, 1990. Mikah and I grew up as if we were sisters. The year she turned thirteen she was diagnosed with Juvenile Diabetes. The doctors did not want to scare her too bad with the diagnosis, but looking back now they should have. Mikah kept eating what she wanted and gaining more weight. By the time Mikah turned twenty-one her doctors did not like the way her body was causing her pain. A few months after she turned twenty-one Mikah suffered a server diabetic attack.

When I was eleven, my oldest brother David, fell off a roof, and was injured very badly and his condition

Muscular dystrophy is an inherited disease that was discovered in 1861, by Guillaume B.A. Duchenne. Muscular dystrophy is a group of heredity disorders characterized by rapidly-worsening muscle weakness. The trait for muscular dystrophy may be transmitted as an autosomal dominant which means a disorder that has two copies of an abnormal gene that must be present in order for the disease or trait to develop. In this case, if some original carrier of the disease had children, the children would have a fifty-fifty chance of inheriting the disease. It is also carried as an autosomal recessive trait, in which case the offspring of the original carrier would have a very small chance of

Duchenne muscular Dystrophy (DMD) is the most common out of nine types of muscular dystrophy. This genetic disorder causes progressive muscular weakness, and deterioration due to the lack of a protein called Dystrophin. This protein keeps the muscles in tack, so when it's missing, the muscles slowly break down. (MDA, 2015)

Having a crippled brother can be hard. But if you keep your faith things might just work out. Doodle was a crippled boy from birth. He had many things wrong with him but he kept on living. Brother was nice and helped him learn things. The brother was guilty about having a crippled brother so he took pride on keeping their brotherhood and taught him a lot of things.

The affects of Duchenne muscular dystrophy as well as various solutions performed to provide accurate diagnoses and treatment of Duchenne muscular dystrophy.

Ben has Duchenne Muscular Dystrophy (DMD). DMD is a degenerative disease of the muscles. When someone has this disease their muscles do not produce enough dystrophin to stay together. This causes the muscles to deteriorate over time. With proper care, the rate of muscle degradation can be slowed down. Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle degeneration and weakness. Muscle weakness can start as early as age three. It first affects the hips, pelvic area, thighs, and shoulders. This disease is still fatal and will be until further studies and research are done to find ways to cure this disease.

Imagine how it would be like if you can’t run and have to be in a wheelchair at a young age. You would face lot’s of difficulties like having to get up and walking. A rare disease called Duchenne Muscular Dystrophy can do this to you. Duchenne is a disease with rapidly worsening muscle weakness. It is not very well know. Boys are more likely to have it them girls because boys don’t inherit a flawed dystrophin gene. This gene protects you from Duchenne.

Duchenne Muscular Dystrophy (also referred to as DMD) is a type of muscular dystrophy that weakens the muscles that we need to support our body, body weight, to stand, and to move around. It also can cause you to have scoliosis. Some of the main causes for DMD are genetic disorders, mutations, and DMD has to be passed down throughout everyone in that family for generations. The symptoms you can have if you have DMD are weak muscles, lack of strength, and difficulty walking. DMD is a negative mutation because it affects your muscles horribly bad that you can get a disability of walking and even moving. You need to tell your doctor immediately if you experience any symptoms. If you don't tell your doctor, you may find yourself in a very difficult situation where you can't get up or can't get something you need. When you do talk to your doctor, you will have an advantage of getting the help you need.

Duchenne Muscular Dystrophy is a sex-linked disease, which is inherited in a recessive fashion (National Human Genome Research Institute, 2013). Over thirty similar genetic disorders exist (Duchenne Foundation Australia, 2015). All types of muscular dystrophy are considered to be a rare disorder (Duchenne Foundation Australia, 2015). Duchenne Muscular Dystrophy is most common in children and causes muscle weakness and wasting, which commonly begins in the lower limbs (Duchenne Foundation Australia, 2015; National Human Genome Research Institute, 2013). The disease itself is caused by changes to the DMD gene, which is responsible for providing instructions regarding the creation of the dystrophin protein in one’s muscles (Duchenne Foundation Australia, 2015). This protein is responsible for protecting muscles from damage, and without it the cells of a person’s muscles deteriorate and symptoms of Duchenne Muscular Dystrophy are exhibited (Duchenne Foundation Australia, 2015). The disease results from changes in the DMD gene, or other genetic changes in a child (Duchenne Foundation Australia, 2015).

Duchenne Muscular Dystrophy is an X-linked genetic disorder caused by a genetic mutation in the dystrophin gene. The disorder is recessive, therefore males are more at risk for displaying the mutation than women. However, women can be carriers and have mild effects. Duchenne Muscular Dystrophy affects the neuromuscular systems, which can result in deterioration of muscles and eventually death.1 The disorder usually presents itself in early childhood, and can affect the respiratory and cardio systems. The disease can cause spinal problems, respiratory problems, intellectual disability, and cardiac disease which is the main cause of death.4

As a child, I thought my parents were invincible. I grew up believing they were superheroes who had the ability to whisk away all my problems. Unfortunately, when I was 15-years-old, my father was diagnosed with multiple sclerosis. The hardest part about his diagnosis was that his sister had been diagnosed with MS a couple years before and we had seen her health deteriorate so quickly that she was already wheelchair bound. During this time my family was scared. The little information we knew about MS did not seem hopefully and we were worried about what the future would hold for our family. Lucky, we were blessed with a great neurologist who eased the insecurity we felt and gave my father the strength to be optimistic about his diagnosis.

I was getting evaluated for Autism, and I came out with a report that I had Severe-Moderate Autism, and the language of an eighteen month old. In July or August 2006, I was throwing a HUGE tantrum, it was also the day my mom and my grandma brought me to the doctor. I was still screaming and crying at the doctor’s office, and the doctor said something that changed both my mom and my grandma’s life forever.