Duchenne MD
I have compiled a simple FAQ about the dreaded disease called Duchenne Muscular Dystrophy. Here’s the basic scoop on DMD, presented Scott Sands Alive-style:
What the heck is Duchenne Muscular Dystrophy?
DMD is a genetic progressive muscle disorder characterized by a gradual deterioration and loss of strength and bodily function.
Is DMD contagious?
OK, so what part of genetic do you not understand???
What causes DMD?
The lack of an essential muscle protein in the body called dystrophin, which holds muscles together. Basically, without dystrophin, muscles gradually degenerate – they break apart, wither and die.
Who commonly gets DMD?
Boys. Makes me wonder if God is actually a woman.
What bodily functions are affected by DMD?
Mobility, breathing, speech, chewing, swallowing, heart-beating, bowel moving…basically all functions involving, say, MUSCLE!!!
Does everyone with DMD follow the same rate of progression?
No. Some deteriorate more rapidly than others, and some die at a much younger age.
What happens when DMD gets to the most vital muscle, your heart? You’re basically screwed! You’re handed a death certificate with an empty space for you to fill in the date and time.
Is DMD a fatal disease?
OK, so what part of death certificate do you not understand???
What is the life expectancy for someone with DMD?
This is impossible to determine. Well, research scientists and physicians will tell you that survival is not expected beyond the age of 25. I have DMD, and I am now 44. You do the math.
Is there a cure for DMD?
Yes! And the tooth fairy really does exist!
Does it totally suck to have DMD?
Not really. DMD is like a big fluffy doggie that you just want to hug. Hey, don’t be a moron – of course it sucks!
Is having DMD the end of the world?
Absolutely not! Many of us lead very fulfilling lives despite this disease.
For more detailed information on Duchenne Muscular Dystrophy, simply visit these websites:
Parent Project Muscular Dystrophy
Muscular Dystrophy Association
What can I say Scott, and where do I even start my friend. You are so freakin amazing to me & I know you are for so many others as well! My son also has DMD, he is only 7 yrs. old & after reading your blog and several other of your blogs, you have totally shed a whole new light on the subjecy of DMD for me. What a breath of fresh air you are! Your personality shines through your words like a ray of sunshine. It is so precise and right to the damn point with a little humor, that makes me laugh hysterically! As we all know there isn’t much to laugh about when it comes to this shitty little disease called Duchenne…You should be an inspirational speaker! I love your FAQ Scott Sands style about DMD…
I am so proud of you and lucky to be a relative. Your mind and your heart are on the same plateau. You’re a wonderful young man, and it shows through your beautiful blog. You definitely know how to put the words together to bring us much happiness. I love you dearly, and I only wish that our family could be together so that we can enjoy your intelligence, humor and the fact that you are a positive person with a great personality.
I enjoy your uplifting blogs so very much. Keep them rolling!
May God bless you always. Kisses and love to all.
I am a 31 year-old who shares something in common with you, that is this lovely genetic disorder known as DMD. However, this has not stopped me from living my life to its fullest. I appreciate that somebody has the guts to openly inform and educate others who don’t know or understand what we go through. Your blog is very informative, mixed with a little sarcasm, which sometimes you need to get through this ordeal. Thank you so much for inspiring me not to give up or quit.
Great blog, man, I’m just getting started on it. I’m 35 and thought I was old in Duchenne years. How do you keep the dust off? LOL I feel fortunate to have crossed paths with you, Scott, and your pedal to the metal attitude. Burn up, don’t fade away, man!