Wow...four miles a day huh?? Bravo u!!! I walk to our mailbox once a day and that seems like a lot! haha Have u talked to u'r doc about any of the other meds?? Maybe Avonex isn't the med for u? There are many here who are on Copaxone and love it! It's a once a day injection, but none of the chills or flu like symptoms. LDN is not a med that most here use. U may get some feedback, but it's typically not a med selected for treatment in ms. I DO suggest u choose one of the CRAB's meds and get on it soon. It's quite important to work to slow this disease even if u feel great. Feeling great only means u'r not feeling the disease...it doesn't mean it's not progressing. The meds don't stop progression either, but do attempt to slow things down and hopefully minimize u'r flares. Please do consider this and talk further with u'r doc.
CRAB's = Copaxone...Rebif...Avonex...Betaseron
Co-Moderator, MS Forum
*~*Sometimes the Lord calms the storm. Sometimes He lets the storm rage and calms His child.*~*
Things that make u go hummmm......
*I wonder how much deeper the ocean would be without sponges.*
*One day without sunshine is like...um..well...night?*