After relapse and hospitalization, neuro wants me to switch to high-dose interferons. I chose Betaseron. Any hints, stories, tips, ideas - whatever would be greatly appreciated.
I was afraid of the Interferons, so I chose Copaxone when first diagnosed and have had no problems with it at all. Except - that I seem to be progressing - so I guess that counts as a problem!
Most concerned with health effects on liver, heart, etc., the blood test monitoring, flu symptoms, depression. Would love to hear others experiences on it and
ANY tips or hints on making it a better experience. Thanks.
Hi Maryanne, we call it betaferon downunder in Oz. I too am on copaxone now but tried betaferon for a couple of years and had flu-like symptoms the next day after every shot which was a real pain. Hope it works for you though. :-)
rickileeway 1 year ago
Sorry to hear about your relapse and hospital stay. I was thinking about you and that hot weather back east. Maybe you were in the hospital during that time at least and not suffering at home. I know it sucks playing around with medications and I hope you find the right one. Let's talk on Skype you feel up to it. Take care love Christine
christinedavi 1 year ago