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Shaunmelbourne
I am a 38 year old male from Melbourne Australia. I was diagnosed with MS almost 10 years ago and getting over the shock of my diagnosis I began using Betaferon as recommended by my Nuerologist. I went from being a very active sportsman...
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Written on February 6th, 2013
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285 Views
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megbat
Feeling Fence-y:
I have had 7 doses of Tysabri, now. Two months ago, I started aspirating liquid when I tried to drink. After a few experiences, within a few days, of violently and abruptly (and oh! so gracelessly) choking on my...
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Written on December 16th, 2012
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376 Views
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Christine2686
I was diganosed with MS back in april 2012 while I was pregnant. My left side of my face went numb. I have had numerous of MRIs and numerous attacks. The past 7 months, I think I've had a week where I walked normally and felt normal...
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Written on November 17th, 2012
2 Rate Ups
266 Views
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Jstuly1
Unfotunately the worst possible side effect hit me using tysabri PML. Paralyzed lft side of my body
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Written on November 13th, 2012
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483 Views
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finnboy77
I have taken most of the D.M.D'S do very little avail. I am now 40 years old and this blooming fatigue is never ending and unpredictable. I have been injecting for 15 years now and am a little fed up always having to inject myself daily...
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Written on April 11th, 2012
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604 Views
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bunne2
My name is Charlene and I was dx last year with Ms and and is currently taking Avonex to treat it well i had a flair up and my doctor says beacause of this is is swithing me to tysabri says it a better treatment just need some other...
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Written on April 7th, 2012
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651 Views
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reelwood7
Hello, trip to her              My name is John and my wife has MS,diagnosed in 1997 with remitting / relapsing now has progressive??? On a recent trip to her neurologist they suggested that she may be interested in...
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Written on February 10th, 2012
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732 Views
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buckleybets
It has been my fourth time in early December taking Tysabri. I felt like I was hit by a Mack Truck. Normally, I walk pretty good a little bit wobbly. But each time after taking Tysabri the first week I can not walk at all and I...
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Written on December 15th, 2011
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1356 Views
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meganomalie
Don't be afraid of Tysabri if you neurologist suggests it. I would be bed-ridden, blind and probably vegetative if I didn't switch to Tysabri. Been on it since I was 22. Don't feel like writing my main experience of my whole MS...
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Written on April 11th, 2011
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1772 Views
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Rxpsycho1
I have had about 55 treatments on Tysabri. Although I am doing very well I don't know when enough is enough. I had been on Beta Seron before the Tysabri, the side effects were terrible. My only other choice would probably be Copaxone...
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Written on February 3rd, 2011
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2096 Views
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MSMom
Short version--Married in 1991, age 22...start of first symptom 3 days after return from honeymoon...new city, no friends or relatives...diagnosed after typical series of tests...Neurologist said no kids for 5 years, must have heard...
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Written on May 13th, 2010
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1245 Views
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Wiccad
I con't really even remember my first Dx date.
First I tried all the herbal remedies, but the MRIs showed that the disease was progressing anyway --- Alas --
So it was on to Avonex... That took a while to get used to, in fact...
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Written on July 24th, 2008
1 Rate Up
2010 Views
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gemini76
"I take Tysabri" I was dx at 27............in 2004 i was Married on an island at 25, : ) great times!!!having a great time parting my ass off with friends on my free time and just enjoying life with my hubby .My...
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Written on May 24th, 2008
3 Rate Ups
2516 Views
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