Five Months Without Copaxone…

…and I feel great. I know there are people reading this who think I should be on my meds, but I have to say, I have felt so much better since stopping the injections. I still ignore the fact that I have MS, but I think that’s better than dwelling on it and letting the disease consume my life.

My ankle pain has gone away, and I’m not injecting myself daily with a chemical compound that lowers my immune system, making me prone to even worse illnesses than multiple sclerosis.

I believe that life is what you make it today. It’s always the mindset I have lived by – to live life in the moment – so why let this stupid diagnosis change that? I won’t.

I believe we can overcome anything with the right atitude. This is just one more of those examples in my life.

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About mssocial

I was diagnosed with Multiple Sclerosis on October 1, 2009. Never really being sick before in my life, besides the occasional cold or flu, I was devastated by the diagnosis. What I learned in the days and months after being told, "You have MS.", is that no matter where I searched, I could not find answers. I was lost with nowhere to turn. Now, I work to make sure the 200 people diagnosed with MS every week in the US have access to the answers they are looking for. MS Social helps them find those answers on their own terms.

Posted on April 14, 2012, in Uncategorized and tagged , , , , , . Bookmark the permalink. 2 Comments.

  1. Michelle, I am truly inspired by your approach and attitude toward MS. I don’t know anything about the meds you’re “supposed” to be on, according to the medical community – or whoever has this opinion. You know yourself better than anyone. If you feel better off the meds – it’s real, and good for you, for listening to your body.

    It is so true – life is what you make of it. And it sounds like you’re living your life to the fullest.

    Thank you for sharing.

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