Multiple Sclerosis -- Flare up with Vision loss
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11:55
Matt's Multiple Sclerosis: Vision Flare Upby mattalleng1990531 views- 9:57
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Clay Walker Talking About Diagnosis of Multiple Sclerosis - National MS Societyby NationalMSSociety21,553 views
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CNIB PSA May 2010 - Seeing Beyond Vision Loss - Tamara (English)by cnibnatcomm2,958 views
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What it's like having MS ( Multiple Sclerosis)by kwazykelli340,519 views
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Living with Multiple Sclerosis - Jewelry and Staying Positive.mpgby laurenvparrott2,168 views
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Vanda04 2 weeks ago
LOL! good vid. sound like my neurologist he likes to do nothing so I did it all and got cured!
gekiryudojo 1 month ago
ibroprofen, dont over heat, sleep, its all that helps my optic neuritis and if I were u Id ask for iv steroids x
nicolahawkinsyoutful 2 months ago
God Bless you, yes STAY STRONG!! I had to treat myself, I have those same Doctors the DO NOTHING DOCTORS they all suck and I have fired them all!!
presouz 4 months ago in playlist More videos from ToilBox
Stay strong dude!!! i know where you re coming from
doctors really DO NOTHING..as long as they keep their patients and get their money day in day out... and treat them with conventional medicine which basically doesnt CURE ANY DISEASE....makes you lose in humanity in general
stay strong and hope things get better for you
wreyoG 6 months ago
I had optic neuritis, and my MD, who has MS himself, takes Tysabri, and he told me to take it and I haven't had an exacerbation in 3 years. Seriously, check into biogen and Tysabri. It's a miracle drug
kylewitherspoon 7 months ago
I had optic neuritis, and my MD, who has MS himself, takes Tysabri, and I haven't had an exacerbation in 3 years. Seriously, check into biogen and Tysabri. It's a miracle drug
kylewitherspoon 7 months ago
Dr. Richard Serano treats this with anti virals.He treats me for CIDP. He told me of SM eye sight loss and success with anti virals.
richrocketlll 1 year ago
I feel your frustration - at 19 i had optic neuritis... and again 3more times before i was 25. It's the craps. Although - the last time i had it - i was put on solumedrol iv steroids. Within 5 days of that out patient treatment... my vision began to return. Currently i take copaxone - and ten years ago that seemed like a good idea...
anyway just wanted to say that i feel your frustration... the do nothing plan seriously does suck.
novanovagirl 1 year ago
"Let's upgrade from doing nothing, to doing something with the emphasiz on doing anything". That's epic! I feel your pain, been there done that, MDs carry a big title, but are for the most part pretty damn useless. Hang in there man, from a person in similar shoes.
kjelltp 1 year ago