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When it comes to living with Muscular Dystrophy at one time
or another we meet those who make the mistake of believing that we have
Multiple Sclerosis when we don’t. What we have is called Muscular Dystrophy. It
was just a few years ago when I learned that other people with Muscular
Dystrophy are facing this very same issue. So what can we do about this? Well
the best thing we can try and do is raise more awareness about Muscular
Dystrophy in the hopes that one day people know exactly what it is. After all
Muscular Dystrophy and Multiple Sclerosis are two completely different medical
conditions.
So first let’s take a look at Multiple Sclerosis, according
to the Multiple Sclerosis Society of Canada, MS is a disease that is
unpredictable, and it affects vision, hearing, memory, balance and mobility.
Now, when it comes to Muscular Dystrophy the issues we face
are very different from those living with Multiple Sclerosis. So what is
Muscular Dystrophy? Well according to Muscular Dystrophy Canada it is a
condition that comes in many forms such as Duchenne, Becker’s, and Limb Girdle
just to name a few. Now the effects of Muscular Dystrophy range from Joint and
Muscle Pain, Leg and Foot Swelling, Muscle Cramping, Changes to Posture,
Difficulty Walking, Difficulty Gripping and Holding, Fatigue and can even lead
to issue’s with Breathing.
So what is Becker Muscular Dystrophy?
Now when it comes to Becker’s Muscular Dystrophy people with
this disorder typically experience progressive muscle weakness of the leg and
pelvis muscles, which is associated with a loss of muscle mass. Muscle weakness
also occurs in the arms, neck, and other areas, as well as in the lower half of
the body. It must be known that Becker's Muscular Dystrophy gets progressively
worse and it’s tough to say but over time some of us will eventually end up
using a cane or wheelchair. But the truth is most of us with Becker’s are fully
capable of living life like any other person, and that includes enjoying a
nearly normal lifespan. Sadly though when it comes to other forms of Muscular
Dystrophy for some the outlook is very different.
In the end I hope everyone takes the time to learn more
about Muscular Dystrophy and also joins in by helping to support organizations
such as Muscular Dystrophy Canada and other organizations around the world that
raise awareness and support and fund research into finding a cure for each and
every form of Muscular Dystrophy.
Eventually I hope that one day when we tell people we have
Muscular Dystrophy that they fully understand exactly what it is.
Related posts:
My personal story growing up with Becker's Muscular Dystrophy ,
My Childhood with Becker's Muscular Dystrophy ,
My Childhood with Muscular Dystrophy: School & Gym Class ,
Growing up with Muscular Dystrophy: The High School years ,
Living with Muscular Dystrophy: The joys of the winter season ,
Life after being diagnosed with Becker's Muscular Dystrophy &
Growing up with Becker’s Muscular Dystrophy as a teenager
My Childhood with Becker's Muscular Dystrophy ,
My Childhood with Muscular Dystrophy: School & Gym Class ,
Growing up with Muscular Dystrophy: The High School years ,
Living with Muscular Dystrophy: The joys of the winter season ,
Life after being diagnosed with Becker's Muscular Dystrophy &
Growing up with Becker’s Muscular Dystrophy as a teenager