Juvenile Dermatomyositis Statement of Purpose
My statement of purpose is to analyze the website of
curejm.org. It is an organization that is affiliated with Juvenile Dermatomyositis. Recently, my
cousin was diagnosed with this illness. I hope that my paper will let people
know about the illness and become more understanding of people. Also, I want
people to be aware of it and know all the signs and symptoms of it, in case
they or someone that they know gets it.
-I need to look at all the pictures on the website and how to
portray what it is like to have JDM. I will talk to my cousin and see if she
agrees that they correctly portray it.
-How they use words and colors to draw the person looking at
it and if it is an effective way to make people aware about the illness.
Audience: I need to
make my audience know that it is a serious illness and then maybe they will be
more interested in the topic. I also need to understand that not everyone is
interested in the same things that I am. Also I cannot use terminology that we
use in nursing school, because someone who is a business major may not
understand.
My Ethos: I need to
show my readers that I am passionate about the topic because someone very close
me to has it.
My Logos: I will use
it to discuss the facts and scientific research.
My pathos: I have a
personal connection with this illness and I can ask my cousin how she feels
about the website and it really shows what it is like to have JDM.
Choice of medium: I
will be writing a paper.
Ideas about
arrangement: I will start off with an overview of what the website looks like
and what my thesis statement is. I will then go into detail about all the
pictures and links on the website. I can also talk to my cousin and have her
review the website and give me her opinion.
Juvenile Dermatomyositis
What
if one day you thought everything was normal and then you realized that you may
never be able to do every day activities again? This describes the life of
someone who has just been diagnosed with Juvenile Dermatomyositis. JDM is an
autoimmune disease that can cause a skin rash and weak muscles, although there
is no known cure, there are many medications that can suppress the symptoms of
this illness. There are a few tests that doctors can run to diagnose someone
with JDM. If the illness is caught soon enough the patient may be able to
regain all strength back and live a healthy normal life. When someone becomes
diagnosed with Juvenile Dermatomyositis it can change the way they live in many
different ways because they have to adjust to taking medications. They also
have to be aware of the precautions they might have to take.
Juvenile
Idiopathic Inflammatory Myopathies (JIMM) are a group of rare, autoimmune
diseases that have symptoms of muscle weakness. The most common member of this
group is Juvenile Dermatomyositis, along with having symptoms of muscle
weakness a skin rash is also seen in a patient. Any form of a JIMM is so rare
that most doctors will never see a case while they are in the field of medicine,
this can cause early diagnosis, which is important, very difficult to
accomplish (Laxer 365).
For
any illness, a patient might not have every single sign and symptom, so some
patients might not have muscle weakness and only have a rash. Muscle strength
is the most important symptom that doctors assess. This is because if not
treated soon then the patient could lose their muscle coordination. Although
muscles weakness can happen with any muscles in the body the most common are
the shoulder, hip, paraspinal, and abdominal. One could also have weakness of
the throat muscles also known as dysphonia. This is detrimental because it
could cause one to not able to carry out the action of swallowing (Laxer 366).
Some other symptoms include fever, weight loss, and fatigue. Fatigue can cause
the patient to not carry out much activity like they normally would. Most
students can only go to school for a few classes causing them to potentially
fall behind in class work.
There
are a few tests that doctors can perform to test the strength of the muscles.
One is Manual Muscle Testing (MMT), which is used in everyday physical therapy testing.
Using dynamometry they test the muscle strength using strength measuring
devices. In order to assess the body it is divided into different group muscles.
Pressure is applied on each muscle and the doctors look for how the patient
reacts to the pressure that determines what “grade” they receive. If the
patient can hold the test position against strong or moderate pressure then
they pass the test. If they are able to hold the test position with slight
pressure or no added pressure, they receive a grade of fair. If no contractions
are felt in the muscles and no visible movement is seen then they receive a
zero (Laxer 366). Another test that can be performed is the Childhood Myositis
Assessment Scale (CMAS). It is a 14 step performance balance test that can test
the muscle strength, endurance, and physical function. The patients endurance
is tested using time and seeing how long the patient can keep a raised leg off
of the table for a certain period of time. Unfortunately, this test is
extensive and can cause the patient to become more fatigued that normal (Laxer
367).
Another
way that a patient can be diagnosed with through testing to blood to see if
there are high levels of muscle enzymes such as aldolase of phosphocreatine
kinase (Meneghini 155). Aldolase is an enzyme that helps to break down sugar
into energy and it is found in the muscle tissue. Phosphocreatine kinase is
found primarily in the heart, brain, and skeletal muscle. Through the blood
work doctors are able to see the levels and proceed testing the patient or
diagnosing them with JDM.
There
are other symptoms of JDM that are less common but can happen in any patient.
Calcinosis can affect up to one third of the children that have been diagnose
with JDM. It is when they develop small lumps of calcium under the skin or in
the muscle. It can feel like pebbles and can vary in size. In most cases the
body naturally absorbs the calcium eventually. If the body does not, then the
small bumps eventually make it to the surface of the skin and they can become
infected. Vasculitis Ulcers are holes in the skin or gastrointestinal tract,
when they occur in the skin they can look like open sores, and inside the body
they can harm the digestive tract. Contractures are muscles that are shortened
causing a joint to stay in a bent position. This can be from a calcinosis
crossing over a joint (What is JM). Lipodystrophy is a loss of body fat. The
fat cells become damaged in either specific parts of the body or all over the
body. If the face is affected it can cause one to look “bony” and have sunken
cheeks. Lipodystrophy is seen in approximately 10%-40% of patients who have JDM
(Laxer, 369).
One
prime example of a patient over coming JDM and leading a normal life is the
story of Caroline Farley. She thought that her Christmas of 2013 would be like
every other Christmas, but this was not the case. During Christmas break she
developed a rash on the back of her hands and on her face and ears. She was
visiting Chicago from North Carolina, and Caroline and her family thought that
the reason why she had a rash was just dry skin. Also, one day she realized
that her neck hurt her, but not thinking much about her pain, she just figured
she slept on her neck in a different way causing her to become sore. When she
went home to North Carolina and her rash persisted, Caroline’s parents decided
to take her to the doctor. After seeing just a regular pediatrician, the
doctors recommended that she go see a specialist for Juvenile Dermatomyositis
at Children’s Memorial Hospital in Chicago. Mrs. Farley and Caroline met with
Dr. Lauren Pachman. After running multiple tests, she was diagnosed with JDM. Caroline
started taking medications including Prednisone, Methotrexate, and an ointment
for her rash. Currently Caroline is coping with her illness in a positive way.
“Sometimes I get tired easily, and I only go to a few classes at school at day.
One time a boy at school asked me what happened to my hands and I told him that
I hurt them going sky diving, he totally believed me” (Farley).
When
someone is diagnosed with certain cancers it may have been because they smoked
and were diagnosed with lung cancer. While with most illnesses it is known why
people are diagnosed, unfortunately doctors and research do not what causes JDM.
Since JDM is an autoimmune disease it could possibly be related to other
autoimmune diseases. One reason why someone might get an illness is genetics,
so if someone in the family has an autoimmune disease it is more likely for
another person in the family to develop one. Caroline has a cousin who has an
illness called Ulcerative Colitis, which is an autoimmune disease that affects
the digestive system. Genetics is the only known reason why people get JDM or
any autoimmune diseases, but hopefully with research it will soon be found what
other causes there could be.
Dr.
Lauren Pachman is one of few doctors who treat JDM in the United States, she
works at Children’s Memorial Hospital, in Chicago, IL. Her and her team study
JDM and they have found that genetics and environmental factors can be causes
of why people are diagnosed with JDM and other autoimmune diseases. They are
interested in the TNF-a-308 protein associated with the A allele in genetics. When
someone is first being diagnosed they have found high levels of this. They
study muscle biopsies to look for changes in DNA. “This intensive research effort broadens the clinical, genetic
and immunological characterization of the child with JDM, which is a critical
aid in guiding current therapy and may lead to novel targeted interventions.” Along
with her research she continues to see patients who had JDM, including Caroline
Farley (Lauren M. Pachman’s Research Interests).
The
immune system is defined as part of the body that protects the body from
infection. When it attacks itself this causes inflammation. During any
autoimmune disease the immune system becomes overly active and it starts to
attack itself. This occurs to be a problem because it attacks healthy tissue
doing harm to the body instead of protecting it. The inflammation that is seen
is found in the blood vessels under the skin and in the muscles. When the blood
vessels in the skin become inflamed this causes a rash. It does not itch but it
looks like dry skin and the can cause the skin to crack and bleed. Inflammation
of the blood vessels in the muscles is more detrimental to the patients health.
This is because the patient could lose all muscle function if not treated and
in order to be treated one needs to be diagnosed with JDM first (What is JM).
JDM
will not go away on its own and the only way for someone’s symptoms to subside
is to take medications. One important medication is called Prednisone, it is a corticosteroid
that is used to treat people who have low levels of corticosteroid levels. This
means that their bodies do not produce enough steroids. Prednisone can be used
to treat various illnesses including arthritis, multiple sclerosis, lupus, and
other conditions affecting the lungs, eyes, skin, kidneys, and other organs. In
JDM prednisone reduces swelling and alters how the immune system works. This
medication can be taken as a tablet or a concentrated solution to take by mouth.
It is important to eat food right before the patient takes the medicine.
Patients should always take the medication everyday and they need to make sure not
miss doses. This is important because if someone just stops taking it the body
might not have enough natural steroids to properly function. This can cause
symptoms including fatigue, upset stomach, weight loss, changes in skin color
and mouth sores (Prednisone: MedlinePlus Drug Information).
A
patient has to be weaned off of prednisone meaning that they cannot just stop
taking it one day. Every day or every few days the amount of medication should
be lowered. In some cases as a patient is being weaned off, their symptoms may come
back and they doctor will raise the medication intake again. Although prednisone does help with the
symptoms of JDM, there can also be some severe side effects. These include
weight gain, mood swings, and if taken for a long period of time, growth
stunting (Prednisone:
MedlinePlus Drug Information). Caroline is currently taking
prednisone and her reactions to the medication are what most people have said
about it. “To be honest, I know the medicine is helping me, but it makes me so
hungry all the time, and as I eat I gain weight, and it is not very fun.
Although when I am hungry I try to eat healthy foods. I dance regularly so I
suppose that is my exercise” (Farley).
Another medication used to treat JDM is Methotrexate. It
can also be used to treat psoriasis, rheumatoid arthritis, and certain types of
cancer. It is in a class of medications called antimetabolites, which is a
chemical that inhibits the use of a metabolite. This plays a role in metabolism.
It works to treat JDM because it decreases the activity of the immune system.
This medication can be taken by mouth or as an injection. It is important for
the patient to take the medication as directed by their doctor. Some patients
have taken the medication daily instead of weekly and the results have been
fatal. Some side effects of Methotrexate include: dizziness, drowsiness,
headache, swollen, tender gums, decreased appetite, reddened of the eyes, and
hair loss. While those are not serious side effects, some serious side effects
include blurred vision or loss of vision, seizures, confusion and loss of
consciousness (Methotrexate: MedlinePlus Drug Information).
In another case study a girl of the age of three has
trouble walking and running and she had a fever. She was taken to multiple
doctors and received an ointment, which is another medication used to treat the
rash and she takes multi vitamins to help with her weakness. Unfortunately,
eleven years later her symptoms not only persisted but also progressively got
worse. Her rash spread to the back of her hands and on her fingers, the skin
over her knuckles had grown to be thick. She had difficulty standing up from a
sitting position and vice versa. After doing blood work, the doctors found that
she had high levels or kinase and aldolase in her blood. Because the doctors
did not diagnose her with JDM early, her symptoms worsened. If JDM is caught
early enough then the patient can lead a normal life on medications to help suppress
the symptoms (Ishaque).
Juvenile Dermatomyositis is an autoimmune disease that
can cause a skin rash and weakened muscles. The origin of the illness is
unknown but through research, it may be seen to come from genetics and
environmental factors. There are a few ways that doctors and researchers can
diagnose a patient, one being a strength test to see how much pressure the
muscles can withstand and they can also look at the patients levels of aldolase
and kinase in their blood. From the results the patient can then be put on
medication to help with the symptoms. Some medications include Prednisone and
Methotrexate. Although each drug does have its fair share of side effects, the
good that it does to help the patient is better than the negative outcome. Even
if a patient is on medication for JDM and their symptoms are gone, they will
always have the illness. Hopefully in the future doctors and researches can
find a cure for all autoimmune diseases!
Works
Cited
Farley, Caroline.
"Juvenile Dermatomyositis." Telephone interview. 7 Apr. 2014.
Ishaque, Sidra, et al.
"Juvenile Dermatomyositis." Journal Of The College Of Physicians And Surgeons--Pakistan: JCPSP 21.7 (2011): 434-436. MEDLINE Complete.
Web. 7 Apr. 2014.
Lauren M. Pachman’s Research Interests. Lurie
Children's Hospital of Chicago Research Center,
2014. Web. 07 Apr. 2014.
Laxer, Ronald. Pediatric Clinic Pediatric Rheumatology. Philadelphia:
Elsevier, 2012. 365-369. Print.
Meneghini Carlo. An Atlas of Pediatric Dermatology.
Chicago: Year Book Medical Publishers.
1986. 153-156. Print.
“Methotrexate:
MedlinePlus Drug Information." U.S National Library of Medicine.
U.S. National Library of Medicine, n.d.
Web. 07 Apr. 2014.
"Prednisone:
MedlinePlus Drug Information." U.S National Library of Medicine.
U.S. National Library of Medicine,
n.d. Web. 07 Apr. 2014.
What Is JM? Cure
JM Foundation, 2014. Web. 08 Apr. 2014.
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