Thread: new Avonex pen
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Old 05-07-2012, 08:41 PM
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dmplaura dmplaura is offline
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dmplaura dmplaura is offline
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Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
15 yr Member
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Quote:
Originally Posted by doydie View Post
Anyone using it? If so is the cost any more? Just wondering. My leggs are heavy enough I don't mind the longer needle and I am an RN so the shot thing doesn't bother me either.
I've long been anti-DMD (well, not 'long' compared with some here, but since my Copaxone, dismissed DMDs). Since my O.N. attack and relapse, I've been holding onto a 'script' for the Avonex pen. My neurologist raved about how great it was.

I'm still debating if I really want to go back on a DMD, but as of today my MS symptoms that plagued me back in my limboland days (long before the IV steroids, prednisone etc were on the radar, or MS for that matter) are firing off here and there, and some are quite bad when they're active.

So I am really wondering if I should go ahead and fill the script, or not. I'll be sure to post back if I do decide to try, and my experience with it.

All aside, in Canada the pen's more expensive. I'm not sure if the cost is set at Federal or Provincial level here though, and if in the USA/abroad it's the same cost either way. I suspect the pen to always be more than the 'traditional' Avonex syringes.
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2004 to present - Trigeminal Neuralgia
2007 to present - Burning Mouth Syndrome
March 2008 - Multiple Sclerosis DX
05/2008 - Relapse
05/2008 to 02/2009 - Copaxone
10/2011 - Relapse - Optic Neuritis developed
9/2012 - Relapse - Balance issues 1 sided
8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax)
April 7/14 - Raynaud's Syndrome DX
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Dejibo (05-09-2012), doydie (05-07-2012)