After 11 yrs of MS, and countless therapies (including not taking anything for the past 2-3 years) I am going back on 20 mg daily Copaxone.
My first DMD was Copaxone. After a severe Relapse, I choose to switch to Tysabri (& was on it 36 months). Since 2011 I have not been on anything other than a couple oral drugs each giving me such bad side-effects I had to stop quickly halt them.
I have not been on ANYTHING for over a year now. At my recent Neuro visit she was adamant about me being on something. She showed me my most recent MRI and kept saying "your MS is very aggressive you need to be on SOMETHING". So here I am...sigh, I hate this disease.
My first DMD was Copaxone. After a severe Relapse, I choose to switch to Tysabri (& was on it 36 months). Since 2011 I have not been on anything other than a couple oral drugs each giving me such bad side-effects I had to stop quickly halt them.
I have not been on ANYTHING for over a year now. At my recent Neuro visit she was adamant about me being on something. She showed me my most recent MRI and kept saying "your MS is very aggressive you need to be on SOMETHING". So here I am...sigh, I hate this disease.
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