thanks for the link! I saw my gp today after I noticed my site from yesterday acting up in the same way as the one on my leg that was positively confirmed as cellulitis.............and the result is MORE CELLULITIS!
He does not figure it to be an allergic reaction YET, but is basing it on the fact that I have been sick with a bad cough, body aches and chills for the few days before my cellulitis began. As well he thinks that it could have been assisted in developing from finishing my high dose prednisone the same day I began injections, which may have lowered my immunity a tad. I contacted Teva and Shared Solutions and they both said it has been known to happen...RARELY but it has happened and usually does not interfere with continuing the Copaxone. I was told by my gp that I can keep up with my injections as I am already on the Keflex antibiotic, but the MS Clinic said if it continues to cause this reaction they may want me to change drugs, so my fingers are crossed that I can continue on my adventure with copaxone....we'll see!
My husband thinks I'm nuts.....of course anyone I know without MS thinks the same. I'm sticking with it!