Wednesday, December 5, 2012

Extra! Extra!

With what I hoped you learned here thus far I wanted to show various media clips showing different ways others and you yourself could get involved and help, theres something for everyone!!! Examples will follow....

*Celebs*




















http://www.youtube.com/watch?v=J-Mn8VRBfR4 



*Communities*















http://www.youtube.com/watch?v=flE7jiG9_94



*Kids*

http://www.youtube.com/watch?v=PbpBSY1ADc8


*PSA*

http://www.youtube.com/watch?v=jOCfnOp9AD4


NOTE: To view any of the clips, simply click or copy & paste link into your web browser. All images and video clips are from youtube and google searches.


Questions/Concerns?
Contact: Kayla Stewart
kaylstew@iusb.edu

Monday, December 3, 2012

Could my son or daughter have this?

(DMD)

Signs and Symptoms

boy with enlarged calf muscles
Boys with DMD often have enlarged calf muscles.
Children with Duchenne muscular dystrophy (DMD) are often late walkers.
In toddlers, parents may notice enlarged calf muscles (see image at right). This enlargement is known as pseudohypertrophy, or "false enlargement," because the muscle tissue is abnormal and may contain scar tissue.
A preschooler with DMD may seem clumsy and fall often. Parents also may note that children have trouble climbing stairs, getting up from the floor or running.
By school age, children may walk on their toes or the balls of their feet with a slightly waddling gait, and fall frequently. To try to keep their balance, they may stick out their bellies and pull back their shoulders. Children also have difficulty raising their arms.
Many children with DMD begin using a wheelchair sometime between ages 7 and 12. Transition to a wheelchair usually is a gradual process; at first, the chair may be required only to conserve the child's energy when covering long distances. (Children often experience renewed independence once they fully transition to a power wheelchair.)
In the teen years, activities involving the arms, legs or trunk may require assistance or mechanical support.
Boy performing Gowers maneuverBoy performing Gowers maneuverBoy performing Gowers maneuver
Boy performing Gowers maneuverBoy performing Gowers maneuverBecause of weakened leg muscles, boys with DMD have a distinctive way of rising from the floor, called a Gowers’ maneuver.
They first get on hands and knees, then elevate the posterior, then “walk” their hands up the legs to raise the upper body.

Pain and sensation

The muscle deterioration in Duchenne MD isn’t usually painful in itself. Some people report muscle cramps at times; these usually can be treated with over-the-counter pain relievers.
Because muscular dystrophy doesn’t affect nerves directly, touch and other senses are normal, as is control over the smooth, or involuntary, muscles of the bladder and bowel, and sexual functions.

The heart

Lack of dystrophin can weaken the muscle layer in the heart (myocardium), resulting in a condition called cardiomyopathy. Over time, sometimes as early as the teen years, the damage done by DMD to the heart can become life-threatening. The heart should be monitored closely, usually by a pediatric cardiologist. See Medical Management for more on cardiomyopathy in DMD.

Respiratory function

Beginning at about 10 years of age, the diaphragm and other muscles that operate the lungs may weaken, making the lungs less effective at moving air in and out. Although the child may not complain of shortness of breath, problems that indicate poor respiratory function include headaches, mental dullness, difficulty concentrating or staying awake, and nightmares.
Weakened respiratory muscles make it difficult to cough, leading to increased risk of serious respiratory infection. A simple cold can quickly progress to pneumonia. It's important to get flu shots, and when infections occur, to get prompt treatment. See Medical Management for more on respiratory care in DMD.

Learning

About a third of boys with DMD have some degree of learning disability, although few have serious mental retardation. Doctors believe that dystrophin abnormalities in the brain may have subtle effects on cognition and behavior. Learning problems in DMD occur in three general areas: attention focusing, verbal learning and memory, and emotional interaction.
Children suspected of having a learning disability can be evaluated by a developmental or pediatric neuropsychologist through the school system’s special education department or with a referral from the MDA clinic.
If a learning disability is diagnosed, educational and psychological interventions can begin right away. The specialist may prescribe exercises and techniques that can help improve these areas, and the school also can provide special help with learning. See Medical Management for more about learning disabilities in DMD.
Disease:
 
 
 
NOTE: This information is from the web address below. I simply wanted to show the signs & symptoms of this disorder and in effort of not simply writing the same thing over I pulled from the website its self. The link is below for more insight if needed.
 

 

 

Sunday, November 25, 2012

Background of DMD

Duchenne Muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy. It typically affects around 1 in 3,600 boys and in the end causes muscle degeneration and eventually death. It's caused by a mutation of the dystrophin gene which is a gene that is a key component that provides structure and stability for the muscles.

While both female & male can carry the mutation its rare that females exhibit the signs of it.


Stay tuned to here about symptoms & what to look out for...




Sources:

http://en.wikipedia.org/wiki/Duchenne_muscular_dystrophy

Thursday, November 15, 2012

MDA Muscle Walk 2013

Hope you all enjoyed the pictures I included in the last post and also hope you all are looking forward to more posts to come regarding several topics including what Duchenne Muscular Dystrophy (DMD) is and the MDA Muscle Walk 2013 which I will give you insight on now! :)

The MDA Muscle Walk started years ago and according to the website is the largest walk event funding research and services for people with any of more than 40 muscle-damaging diseases. The best thing to compare it to to understand what its like is very similar to how a breast cancer or March of Dimes walk would run. This coming year will be my 3rd year I've been involved in our local walk. I walk in honor of my brother and to me its just another way to celebrate him as well as support other families who are currently dealing with a related muscle disease. Ways to help out with this coming year's Muscle Walk is by; donating any amount your able to, register to walk with our Team Alex's Angels and raise donations, or even word of mouth is always appreciated to spread the word about a great cause. Details on this year's Muscle Walk;

What? - Muscular Dystrophy Assoc. (MDA) Muscle Walk 2013

When? - March 23, 2012 12-3pm

Where? - The Cove baseball stadium in Downtown South Bend, IN

Why? - In support of Muscular Dystrophy Awareness as well as raising money to help find a cure!

Donate/Register at walk.mda.org & search Team Alex's Angels

Questions/Concerns?
Contact: Kayla Stewart
kaylstew@iusb.edu

Saturday, November 3, 2012

Everyone loves pictures!!! :)

Below are the few photos I have left of my brother. Yes its only 2 pictures plus one of his gravestone but I treasure them that much more. Take a look...

 

 

Saturday, October 6, 2012

Why?

You ask why am I doing this blog? Yes it is for a required class project but I'm doing this because the topic of Duchenne Muscular Dystrophy (DMD) holds a special place in my heart. My brother Alex "Miles" Stewart passed away just days after his 16th birthday from DMD.

In short Duchenne Muscular Dystrophy is a muscle disorder that causes muscle weakness and lost of muscle  mass over time. For my brother this seemed to be something that in the beginning seemed to slowly progress but then as he grew and got older it got worse and progressed faster overtime. DMD as I personally witnessed it is especially dangerous for young men. I making this about DMD; 1) to tell my story on how I was personally affected, 2) most importantly to raise awareness for DMD, 3) With raising awareness I also want to show the symptoms, signs and even treatment if this is possibly something your family could be dealing with now! With the background knowledge I'll give you here I hope you take that and put the knowledge to work helping yourself and others if possible.

Even if this is something your personally not affected by I hope you take a look at the ways to help including making monetary donations, joining your local MDA Muscle Walk to help raise funds or just simply lending your time to others in hopes to make this easier for everyone :)

Make a Muscle. Make a Difference.!

Thanks everyone,
Kayla
kaylstew@iusb.edu