Essay about Dwarfism

Educating people on their ignorance can be helpful. Although it is hard to change someone’s opinion if that is how they already think.

In the United States today, there are over fifty-one million disabled adults and children. Throughout our nation’s history, we have not allowed the best treatment and care for these numerous citizens. But, in the recent past, the government has passed laws, made exceptions, and thoroughly tried to provide accommodations to these people with special needs. While this is true, America, as a whole, still views this group as strange or different. Even though this is exceptionally normal, it is not correct. The United States needs to be opened up to the truth about their fellow American citizens. The people of America ought to understand that these disabilities affect not only those who are disabled, but that it affects the family and friends

For someone with a physical disability and for example wheelchair bound they have to plan outings carefully to ensure where they are going has wheelchair access. Wanting to go somewhere then realising they are unable to get in a building or have appropriate toileting facilities would be extremely frustrating and upsetting for the individual.

Achondroplasia is a genetic disorder in which there is a growth hormone deficiency, or there is a genetic mutation in either the father’s sperm or mother’s egg. (mayo clinic, March 20,2014.) Achondroplasia was the first discovered in ancient Egyptian records. People with achondroplasia were considered people with supernatural powers. Many people call dwarfs midgets but to them, it is very disrespectful because midget literally means little person. Some acceptable names that you can use that will not offend them would be little people, LP, person with short stature, or dwarf. Even though dwarfs feel as if they do not have disabilities, the Americans with Disabilities Act (ADA) will protect the rights of dwarfs. (who discovered it? March

     When a child doesn’t seem to be learning, some teachers and parents in his/her life might criticize the child and think of them as stupid, or maybe just too lazy to want to learn. What they don’t realize is that the child might have a learning disability. But how are these children being helped? There are many programs, special schools and facilities, home teaching methods and many other ways in which children with Learning Disabilities are being helped.

Elongated arms and legs I grew like a sprout into a tree. Running was always my favorite activity in gym; it was the only physical activity I was above average at. However, I never spent much time pursuing sports in my youthful years; I had rather wanted to sit alone and listen to “Pictures of You” for hours on end.

Some ways to detect Progeria are genetic tests of the patient’s blood and clinical exams. Furthermore, the major signs begin developing when the child is around eighteen to twenty-four months old and he will experience accelerated aging even though he was born looking normal. One major symptom is hair loss. Patients are born with hair texture and color, but around six months to two years, the hair begins to fall out. Then, from two to three years, they are usually bald, but might have some thin, light hair. Loss of eyelashes and eyebrows are also experienced. Along with hair loss, these children grow slowly resulting in a shrunken physique and minimal weight gain. For males, their approximate height and weight are 40 inches and 25 pounds; but females are about 32 inches and 20 pounds. In When Good Things Happen to Bad People, doctors have stated these kids will "grow to be very short," and "would never grow much beyond three feet."( Kusher 1-2) Moreover, there are distinctive physical traits in the face and body. "By the second year of life, there is also under development (hypoplasia) of the facial bones and the lower jaw." ("Hutchinson-Gilford Progeria") Also, "the face appears disproportionately small in comparison to the head, and bones of the front and the sides of the skull (cranium) are unusually prominent." ("Hutchinson-Gilford Progeria") Some other characteristics observed in the face are a thin

birth length, and with a small heads resulting from prenatal alcohol exposure. There are many

The provider is correct that short stature is not necessary for the diagnosis of growth hormone deficiency if the member is short for expected height; however, this member’s height has never clearly been outside the expected range for family. It also can be argued that delay in growth velocity can be masked by the pubertal growth spurt. However, review of the growth charts provided by the member’s primary care physician and endocrinologist does not clearly demonstrate abnormal growth velocity. While he did have one point that dipped down to the 10th percentile, overall his points are between the 10th and 25th percentiles and generally follow the same curve, indicating that one point is likely aberrant or perhaps consistent with normal prepubertal slowing in growth. After puberty started, the member grew at the upper end of the normal range, which is generally not seen in growth hormone

Noonan syndrome is a genetic birth defect that results in many physical deformities and possible developmental handicaps. Noonan Syndrome affects male children while Turner Syndrome affects females. This paper will focus solely on Noonan Syndrome, which affects 1 in approximately 2,000 people. Complications include but are not limited to: short stature, widely spaced eyes, some form of heart disease, and stunted puberty or infertility. Noonan syndrome is a biochemical disorder that occurs before a person is born and is formed through the genetic makeup of the parents that result in that of their offspring.

beginning with growth failure during the first year of life. Progeria is a rare condition but has come into

There was something strange that strongly stood out when Jeannie Peeper was born in 1958: her big toes were short and crooked. Two months after her birth, a round swelling surfaced on the back of the her head. Her parents didn’t know the cause of it, and after a few days, it disappeared. Then, the Peeper’s mother noticed that she couldn’t open her mouth as wide as her siblings. After taking her to many different doctors, Mayo Clinic discovered that she had a rare disorder. This diagnosis meant that over her lifetime, she would develop a second skeleton, and she would begin to grow new bones that would stretch across her body and some that would fuse to her original skeleton, causing her locked into immobility, within a few years. The Mayo doctors told Peeper’s parents that she would not live long. As she grew older, she realized that she could no longer fit her left hand through her sleeve, because it was locked in a backwards position due to a new bone that generated on her arm. Peeper was taken to the doctors to take a muscle biopsy from her left forearm and had to wear a cast for 6 weeks. Except, it made it worse, because the biopsy and the cast caused her elbow to grow a new bone that frozen the joint, making her unable to move it. Over the decade, as she grew more bones that stretched across her back, locked her right elbow, and froze her left hip, she became accustomed to the pain. Fortunately, she is still alive today with the disorder.

Limb-girdle affecting males and females start making your bones weak. Showing symptoms in your teens or in your twenties.

The most common type, called Achondroplasia is the cause of about 70 percent of all dwarfism. It makes your arms and legs shorter than that of your torso. Achondroplasia affects about 1 in 15,000 to 1 in 40,000 live births.

Living with disabilities on a daily basis can be more difficult then some realize. Many people who are born with developmental disabilities start their education and therapy at a very young age and there are also those people who have been diagnosed with a disability sometime during their lifetime. But what is there for them to do once they have graduated from high school or are told they are too old to continue in a regular school or they are simply told they aren’t accepted in the “normal” community? In all reality there really