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Aubagio

Has anybody here taken Aubagio? My neuro is thinking about a change to my meds, because I've had the infamous post-injection reaction to Copaxone too many times. Also because I haven't had an MS relapse for over 3 years, but I don't understand her logic there: if Copaxone has stopped my relapses, please don't take away my Copaxone!

Note to this comm's Mod: please can we have an 'Aubagio' tag?

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sammason
Jun. 26th, 2014 02:14 pm (UTC)
Thank you for commenting. As it happens, I don't think my neuro doubts my compliance. She's never doubted me at all, in fact, since reading my graphic description of my symptoms 12 years or so ago and diagnosing me before we'd even met! After examining me she confirmed her diagnosis. At my request, over the next few years, she wrote to

- the bank with whom I had an endowment policy with a Critical Illness clause. My neuro's letter got me £49K which paid off my mortgage.

- the University with whom I was studying for a PhD. My neuro's letter got me 14 months' extension on my thesis hand-in deadline which allowed me to become Dr Mason.

- the Office of Public Guardian. My neuro's letter verified my sanity which allowed me to update my Last Will and Testament.

More recently, when I had a PIR in one of the nurses' rooms at the MS clinic, my neuro (and my specialist nurse) heard my very loud swearing and came through. Between F bombs I remarked to my neuro that she needn't doubt me any more. She said that she's never doubted me and I said that it's mutual.

Edited at 2014-06-27 04:49 am (UTC)

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