FRONT PAGE AMPYRA AUBAGIO AVONEX BETASERON COPAXONE EXTAVIA
Stan's Angels MS News Channel on YouTube GILENYA NOVANTRONE REBIF RITUXAN TECFIDERA TYSABRI
 Daily News for Neuros, Nurses & Savvy MSers: 208,152 Viewers, 8,368 Stories & Studies
Click Here For My Videos, Advice, Tips, Studies and Trials.
Timothy L. Vollmer, MD
Department of Neurology
University of Colorado Health Sciences Center Professor

Co-Director of the RMMSC at Anschutz Medical Center

Medical Director-Rocky Mountain MS Center
Click here to read my columns
Brian R. Apatoff, MD, PhD
Multiple Sclerosis Institute
Center for Neurological Disorders

Associate Professor Neurology and Neuroscience,

Weill Medical College of Cornell University

Clinical Attending in Neurology,
New York-Presbyterian Hospital
CLICK ON THE RED BUTTON BELOW
You'll get FREE Breaking News Alerts on new MS treatments as they are approved
MS NEWS ARCHIVES: by week

HERE'S A FEW OF OUR 6000+ Facebook & MySpace FRIENDS
Timothy L. Vollmer M.D.
Department of Neurology
University of Colorado Health Sciences Center
Co-Director of the RMMSC at Anschutz Medical Center
and
Medical Director-Rocky Mountain MS Center


Click to view 1280 MS Walk photos!

"MS Can Not
Rob You of Joy"
"I'm an M.D....my Mom has MS and we have a message for everyone."
- Jennifer Hartmark-Hill MD
Beverly Dean

"I've had MS for 2 years...this is the most important advice you'll ever hear."
"This is how I give myself a painless injection."
Heather Johnson

"A helpful tip for newly diagnosed MS patients."
"Important advice on choosing MS medication "
Joyce Moore


This page is powered by Blogger. Isn't yours?

Monday

 

Correlation Between MS and Harry Potter Characters is Pure Magic




















Perhaps the most famous MS advocate today isn’t a patient, but the daughter of one. Author J.K. Rowling lost her mother to multiple sclerosis in 1990, something she describes as “an enormous shock.” In order to help fight and defeat this disease, she donated £10m to found the Anne Rowling Clinic in Edinburgh, Scotland, and since 2010, doctors and researchers there have been hard at work trying to cure MS and other neurological diseases like Parkinson’s and Alzheimer’s.

I am a long-time admirer of Ms. Rowling, and not just because of her philanthropic gestures. As a writer, I am amazed by a woman who, with only her words and imagination, created an entire literary universe and used it to become wealthier than the Queen of the U.K. Her wizarding world is populated by hundreds of characters of all shapes and sizes — everything from Aragog the Acromantula to a wizard named Blaise Zabini. And whether they’re in the Order of the Phoenix, Dumbledore’s Army, or the Death Eaters, all of them have a role to play.

Knowing that Ms. Rowling has a bone to pick with MS, which took her mother much too soon, I can’t help but think many of the characters in her works are shaped by this disease. And, while I can’t choose a favorite, there are three that inspire me as an MS patient.

Hermione Granger
Hermione Granger was played by Emma Watson.
Bookish, brilliant, brave, and bold—Hermione Granger is an idol for many young women who read and enjoyed Rowling’s books. There is no class too difficult and no tome too thick for this feisty muggle-born witch. If there’s a problem that needs solving, her first stop is always the library. When Harry Potter asks why, his best friend Ron Weasley responds, “Because that’s what Hermione does. When in doubt, go to the library.”

I admire Hermione for her cool head and her mad research skills. This is a girl who, unlike many of her classmates, didn’t grow up knowing there were such things as witches and wizards. Rather, she was born to a pair of dentists in London. She’s not afraid of a challenge, and she never gives up — even when a situation seems impossible. Hermione helps me remember that there’s hope in research and that I should never stop trying to find answers.

Remus Lupin
Actor David Thewlis played Remus Lupin.One of Hogwart’s many Defense Against the Dark Arts professors, Remus Lupin has a pretty tough row to hoe. When he was five, he was attacked by a werewolf and infected with lycanthropy, turning him into a werewolf as well. His condition can never be cured, so whenever there’s a full moon, he hides himself away from the world. “It is very painful to turn into a werewolf,” he says. “I was separated from humans to bite, so I bit and scratched myself.”

Remus wasn’t born with his condition; it was thrust upon him by an evil and vindictive creature. As an MS patient, I can definitely identify with that. I know what it feels like to have your body betray you, to feel intense pain, and to know that no treatment — no matter how powerful — can ever completely cure the illness inside you. But Remus doesn’t let this make him wicked. Instead, he works to stamp wickedness out. A fantastic teacher, a good friend, and a nurturer at heart, there’s much about him to admire. Remus Lupin helps me remember that though MS may impact my body, it doesn’t have to warp or cripple my mind or heart.

Nearly-Headless Nick
Comic genius John Cleese played Nearly-Headless Nick.
The house ghost of Gryffindor, Nearly-Headless Nick is one of the most underrated characters in the Harry Potter universe. He is the ghost of Sir Nicholas de Mimsy Porpington, a wizard who perished in a botched execution on Oct. 31, 1492. But he’s also a loyal friend and ally.

Beloved by students and faculty alike, Nick is fairly upbeat for someone who died a grizzly death and now roams the drafty hallways of a castle. But that doesn’t mean he’s without his share of sadness. When he was executed, his head didn’t quite come off cleanly. A half an inch of skin and sinew remained. Hence, the moniker nearly-headless. “I mean, nobody wishes more than I do that it had been quick and clean, and my head had come off properly,” he tells Harry. “I mean, it would have saved me a great deal of pain and ridicule.”

Like Remus, something terrible happened to Nick — something that altered him for eternity — and because of his quasi-headless status, he is barred from competing in something called the Headless Hunt. His handicap keeps him from doing something he enjoys. Sounds familiar, doesn’t it? However, Nick finds new things to do and people to befriend, and if he can do it, so can we.

Story Source: The above story is based on materials provided by MULTIPLESCLEROSISNEWSTODAY
Note: Materials may be edited for content and length


Go to Newer News Go to Older News