It’s interesting to see how people’s experience differs. I kind of understand the difference between Citalopram and Sertraline, which are SSRIs, versus Mirtazapine which is an SNRI, but even so, I can’t understand why Citalopram/Sertraline was very unhelpful, but Mirtazapine somehow does work for me. Maybe it’s a combination of individual metabolism and what (or who) created our problems in the first place.
From googling, I can see that some people experienced extreme tiredness in the middle of the day when taking Mirtazapine; I did have a bout of absolutely needing to sleep in the day, but I’m not sure if that was a side-effect of Mirtazapine, or the horrible cold I was suffering at the time. But that did wear off eventually. And I could easily give in and have a nap, as I’m retired, and only occasionally needed for day-time childcare for a grandchild.
It’s a lot more difficult for people who have young children or work responsibilities to deal with side-effects. I mean: how long do you give a medication to see if the side-effects diminish? And then maybe try another one to see if that one works? All at a time when we’re feeling just about as low as can be.
Some people think that it’s just a case of popping a pill (or, worse, just getting out for a walk in the fresh air). Well, good for them, but they really don’t understand how challenging it can be to find the right meds and therapy. It can feel like a long and lonely road to have to travel down.
I saw my GP this week and he was OK that I’d changed from as-and-when to daily, and said he was OK if I occasionally upped my dose from 15mg to 30mg by taking two tablets at night; or to go back to taking 15mg as-and-when. It’s good to feel that I’m supported in having that kind of control over my meds. He also gave me info on therapy. I think that’s good GP care.
All I can say is that Mirtazapine has made a difference for me in a good way.