Hello i have been injecting beta interferon injections for 8 years and now copaxone daily for three years. My needle sites hurt and i swell with hives and bleed it was driving me crazy and changing the way my body looks especially my legs. I now do the injection every second day but getting tingly sensations all over my body? What is this, any thoughts? Was my decision a bad choice? What are the alternative options if i stop copaxone here in New Zealand? Welcome advice?
Last reply 1 year ago
Copaxone user needlsites