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Multiple Sclerosis without NEEDLES? A NEW ORAL DRUG IS COMING!!!!

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Uploaded by on Jul 12, 2009

Talking about laquinimod. A new treatment for multiple sclerosis that is in PILL FORM!!!!

Teva Pharmaceuticals out of Israel has bought the patent for this oral disease-modifying MS drug.

The drug has shown unprecedented efficacy and safety in clinical trials.
The medication is now in the second round of Phase III trials and has been given the most elusive
FAST TRACK status by the FDA.

GOOGLE LAQUINIMOD FOR DETAILS.

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Uploader Comments (irishbear76)

  • Maybe you can get on Tysabri. A infusion for it is once a month where you where you get one little needle prick. Oral does sound better but does it compare to Tysabri? I dont know, do you? Thanks

  • @2digitsoff

    I had the Liberation Procedure a year ago and my MS is gone.

    A good friend of mine almost died from Tysabri.

    I would rather eat a bowl of dung than put that in my body.

    I did not mind the Rebif injections every other day. IF I ever need to go back on meds, that will be the one.

    (I hated it too, though :)

    Blessings to you and thank you for thinking of others.

    Read up on PML and make sure you are informed.

    Keep truckin'

    Mark

  • I'm 16 and I was just diagnosed with MS and I literally got told today what injections i could take and its Rebith that I'm goin on, when i got home I looked on the ITV news and seen this pill and didn't know if it was true or not so hopefully it'll pass all the tests and stuff

  • I have taken Rebif and it is a wonderful drug. It stopped my MS from progressing for quite a long time.

    It causes some nasty flu-like symptoms but they become tolerable stay with it.

    Yes the oral drugs are coming and they will be very nice.

    i am yet to hear a date that they will be made available.

    You always will have a support system here on YouTube. There are a lot of good people with MS here.

    God bless.

    Mark

  • cared of needles man really scared and they're coming in couple of weeks

    thanks alot man i aint got a clue how am dealing with it though people look at me differently now but i dunno i'll just carry on with ma guitar ya know

    thanks mark

  • @Nonightmaresmusic

    It will be fine.

    GIving yourself a shot is so UNNATURAL but somehow it is easier than you can ever imagine.

    Just be strong and tell yourself it will give you years of function.

    I suggest ibuprofen an hour ahead of time and putting ice where you are going to shoot yourself to cut down on injection site pain.

    U will be fine.

    Mark

Top Comments

  • wish it was got now! love your paddy hat. keeping this short as the last one didnt go. best wishes louise

  • ooh ahh - does sound good! Thanks for sharing the discovery. Hope you are doing well :-) Love to you to, Kerri

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All Comments (27)

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  • Thats interesting, I have never herd of the Liberation Procedure. Does it work for everyone and how do you go upon getting the procedure done? I now all about the JC virus (PML). Yeah it is scary and yes the risks suck. Thanks for the response, much appreciated.

  • Maybe you can get on Tysabri. A infusion for it is once a month where you where you get one little needle prick. Oral does sound better but does it compare to Tysabri? I dont know, do you? Thanks

  • @abyroj yeah i've been on rebith for a year and it doesnt seem to be effecting me i went to see a man 3 days ago and started LDN and i have felt the effects i should of started it ages ago -> it's a liquid form and a 1ml dose thats how amazed i am i've litterally only had 3ml and 30 sesions of the hyperbaric chamber aswell as rebif - but i'd have to say the hyperbaric and the LDN deffinetly work

  • @Nonightmaresmusic hahaha same thing here i had it at 14 but i found out at now at 16 to xD If this pill comes out I wouldn't give a !@#$ about MS that much

  • Hi My Friend.. Thanks for the update... Rebiff did not work for me at all! I had one flair up at least per month on it.. so Tysabri has been my God send.. Miss you! huggss Violet

  • does tyrsabri really work im on betaseron now its pretty cool they're thinking about changing me to tysabri

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