I also made it to my final home infusion. I now have had four infusions for myasthenia. I haven’t had any real changes but I’m glad it hasn’t been a detriment to me.
I do not see my neurologist until October so I won’t have an update on tapering the prednisone or continuing these infusions for another month, but at least I’m on the right track with a treatment plan going forward, especially when six months ago I was so lost and full of doubt. I’m in a much better place, thank God.
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