Life Almost Unmedicated: How it is right now.
So, Aaron was asking me this morning when I was going to get the pictures from our trip to Torquay uploaded to Flickr. My response was “when I feel better.” He teased me a bit by saying “well I can’t wait until summer,” and then gave me a big hug.
I have been quiet here over the last year. It’s been a challenging one for a lot of reasons, most of which I am attempting to put into a thank you/2009 holiday letter…which probably won’t be done until summer. (Right. I know you’ll all be waiting with bated breath for 4th of July.) But I need to write some of it down for the record while I’m in the thick of it because it’s such a huge part of my life right now. I don’t want to forget.
The main reason it’s challenging right now is that I have been working (since we moved here basically) to get off of my antidepressant meds, which, even with increased dosages, weren’t making any difference.
I did a lot of preparation to help my brain get settled back into a baseline level before I really started cutting back. I didn’t exactly follow the directions of the program I chose to use (Potatoes Not Prozac) because my doctor was on my case to get off of one of the drugs that isn’t approved in the UK sooner rather than later, but I did follow the steps outlined in the book so that it would be easier in the long run. It took me a year to get through those steps and steady with support and then, last March, I started cutting back with the support of my friends at Radiant Recovery, whom I have lovingly dubbed, my Sugar Peeps.
I don’t know that I’ve ever done anything this difficult that requires such a strong commitment to getting better. Nothing comes to mind at the moment so if it’s not *the* hardest, it is *one of* the hardest things I have ever done. I suppose anyone struggling with an addiction feels this way. There is nothing that can prepare a brain to go from being spoon fed a pill every day for the last 12 years to having that taken away (even if slowly, bit by bit) and being asked in a not-so-polite way to please get off its ass and start doing its job. It’s a painful process at times – and brains don’t really like pain.
Before I talk about the hard times though, I should also mention that there are times it has not been hard – at least 1/2 of the time, actually. My brain seems to have a threshold. Sometimes I could do several cuts without being affected and move along in life quite nicely – and then something else would happen and suddenly, BOOM, I was on my ass and my brain was screaming.
These are the hard times.
For me, BOOM is exemplified by turning into a person that I am not. Since I started doing the Potatoes Not Prozac program, I have actually become pretty calm and patient, and a hell of a lot less of a drama queen. As a general rule, I do not cry over every little thing. Nor do I get burning hot, 0-100 angry in a millisecond and yell. But during a difficult time, those are things to be counted on if I don’t catch them before they come bubbling to the surface.
The BOOMs seem to happen after I have been taxed with prolonged or excessive stress. These are things like Aaron having major surgery, the gray winter here in London, PMS, travel, visitors, the kids on break from school, dealing with Liam’s SPD diagnosis, extended illnesses, etc. The day-to-day stuff I can handle, but anything that interrupts the basic routine of my life causes an overload in my brain. It just can’t work that hard right now.
I can feel it trying to slow me down when it gets overloaded. To cope sometimes it shuts down my body to the basic, “must-do” level. I get a “heavy, can’t move” feeling and it takes a lot of energy that I don’t really have to do the things that need to be done. It can last for several days. When this happens, we are lucky that there will be food in the house and that everyone has clean underwear. That is a good day in times of BOOM! Everything else stops. The basic activities of life are just too taxing because I can’t think. Phone calls are too difficult to make, the laundry feels like too much, being around people is hard (but helpful if they are understanding and it’s not stressful), there’s no cohesive thought process that allows me to write emails or make conversation, I don’t have the motivation to do the things that make me feel better, I’m tired, blah, blah, blah, yadda, yadda, yadda. I have to just sit and be still and kind of mindless, really. Sewing is good, television is ok as long as it’s not stressful. Reading something that doesn’t have to be digested is good. Solitaire will do. Staring at a wall and just letting thoughts drift in and out is perfect. Sleep is also really, really nice.
If I have to keep going despite the warning signals I’m getting from my brain (as happens often enough when one has two children), it typically ends up with me crying or get really, really angry – and *then* crying. (Always with the crying…it’s so annoying!) Fortunately I have learned (and I am completely serious) that Macey will let me know when I am about to lose it and yell, and I’ve started trying to pay attention to that and stop whatever it is and sneak away before it all comes bubbling out. Unfortunately, with kids, that’s not always possible, so I try let them know that I am angry or sad, but not upset with them in a way that warrants my behavior (Even though they do usually do the final thing that sends me over the edge, LOL). It’s the best I can do at the moment.
The good thing about it is that I know it WILL get better. I’ve been doing this for a year now and it always does.
Sometimes it just takes more time.
And I do have coping skills that really do help: food is first and foremost, but the light box, fun activities, friends I can call on to make me laugh, relaxing activities, music, making space for myself, my sugar peeps, gentle exercise, quiet time in the mornings during the week, rest, and trying (sometimes really, really hard) to be positive most of the time all help. And the sun. There’s nothing like the sun to give me a boost.
It also helps me to look back at the winters when I *was* on 450 mg of Wellbutrin and 150mg of Zoloft and I was worse than I am now. I couldn’t get out of bed…Aaron had to pull me out. And we didn’t have all of the additional stuff going on that we do now! I’m definitely better now on good food, 37.5 mg of Wellbutrin, and no Zoloft than I was then!
And another really great thing? Even when it really sucks, I can still laugh and smile through tears because I know it will get better. I think that’s progress.
So, maybe more in a few days. (Hopefully on a really good day? LOL!) I think this is important for me to keep track of. Maybe here is good, maybe not. We’ll just have to see.






