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Decisions, Decisions

So I have, finally, reached a decision about The Medication Question. Copaxone has come out ahead. Why, you ask?

Well, it all came down to depression.

After my doctor diagnosed the depression last month and bumped up my anti-depressant dose I started to feel a bit better. I still feel a bit better, but I also still feel a bit down, a bit uninterested in the day-to-day happenings of my life and a general lack of interest in anything I used to find interesting. My energy level is low and I'm happier, most of the time, to spend the entire weekend in bed than I am in meeting up with others of the human race.

Now, I could go see my shrink and bump up my anti-depressants again, or I could try a different disease-modifying medication, one that does not typically cause or worsen depression in patients.

Since my depression seemed very stable and manageable on the doses I was at before I started the Avonex, it seems to make a certain amount of sense that the Avonex might be the cause of the increased malaise. Additionally, my ever-increasing aversion to giving myself the weekly intra-muscular injection (which involves jamming a big, long needle into my thigh) seems to indicate the need for a change of some kind.

Yes, the Copaxone has injection site reactions but, as I understand it, those are mitigable. Yeah, it sucks that I have to give myself an injection every day, but the fact that this is a subcutaneous injection and has an auto-injector makes that little pain in the rump a bit more bearable. The kicker is that the Copaxone doesn't - in most cases - cause depression or flu-like symptoms. So I'm going to give it a try. If nothing else, I will have more information about my body and how it reacts to these lovely chemicals.

The call has been made to mi médico so updates will surely be forthcoming once I've heard back.

Comments

good luck with the copaxone!

can't wait for an oral medication so we don't have to deal with nasty needles.

"my ever-increasing aversion to giving myself the weekly intra-muscular injection (which involves jamming a big, long needle into my thigh) seems to indicate the need for a change of some kind."

Yeah, that was one of the biggest factors for me going off all drugs for MS. I hope the Copax works well for you.

Good luck with Copaxone. I've been taking it for about 4 years and I don't even bat an eye when I give myself a shot anymore. I don't have ANY side effects that I can tell. I hope that your experience is as good as mine has been.


"I could have me a million more friends, and all I'd have to lose is my point of view."

~John Prine

My Multiple Sclerosis Diagnosis

On June 23, 2006, I was diagnosed with Multiple Sclerosis. Among other topics, this blog is devoted to my ongoing experience with the disease.

Pharmaceuticals

Shortly after my MS diagnosis, I began taking Avonex. Although I managed to mitigate the "flu-like" side effects, for the most part, the drug unfortunately seemed to exacerbate my clinical depression.

So, on July 19, 2007 I switched to Copaxone.The Copaxone worked quite well for a couple months - except for some minor issues with injection-site reactions - and I felt much better.

Unfortunately, the Copaxone also exacerbated my depression. So I met with my psychiatrist to find a mix of anti-depressants that would counteract the debilitating depression I experienced. After spending most of December 2007 in a complete funk and - some days - being totally unable to leave the house, I finally stopped taking the Copaxone on my own. I immediately began to feel better and with some help from my primary care doc - who discovered I also had a mild case of hypothyroidism - I started to feel like myself again.

On May 16, 2008, I had my first infusion of Tysabri. With the exception of some anxiety issues, I've had no trouble with it so far. Still, it's early and the jury is still out... stay tuned for ongoing updates!

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