Bad Spells, etc. (Pt. 2/?): How

Alright then, the “How”. Kind of.

First,  you drink a lot of tea. From your favorite mug. Herbal stuff, because of that caffeinatedanxiety thing. Or cocoa I suppose, if you’re one of those non-tea drinkers.

I say kind of because coping with shitty circumstances is never going to feel good: there is nothing that I know of that will take something that is a) hard and b) necessary and c) uncomfortable, and make you love doing it. And if you find it pretty please let me know?

I love to write–putting down my thoughts so that I can see them, read them and process them linearizes my thinking. Things aren’t this vast tangled web, and I can figure out what I’m actually thinking about and what I actually want, need, and feel. In fact when I’m manic there is almost nothing other than knitting and writing that actually helps me stay calm, or in one place. But writing this thesis: the first long writing piece I’ve had to write about the technical/mathematical craziness I love that is physics, has been hellish.

The other aspect to this that has taken a little while to understand and move past is that it truly knocked my confidence in my recovery. I thought I was a bad ass, honest, leave everything on the table, speak my feelings, recovery oriented ninja and then suddenly I was skipping meds, missing class, missing meetings with my advisor, neglecting myself, and my pets, and generally avoiding anyone who cared enough about me to question the mess that things were obviously becoming.

It turns out that the way I got things to start to come back around was the same way I’ve done so in nearly every other aspect of recovery: find people who I trusted to help me figure it out, spill my guts…

…(be incredibly grateful when they don’t judge me for avoiding everything and everyone and also for helping me come out of the panic attack that inevitably comes up)…

…make a plan, and execute with much communication and help.

For someone who tells those who honor me with their trust, and ask for my advice, that mental illness is physical illness: that it’s physical illness of the brain, and that they don’t need to feel ashamed for needing help, it was a bitter pill to swallow when I had to give the same talk to myself.

In my case this time, I was lucky enough to be at a small, liberal arts college where all the professors in the department know me, and know each other. My advisor reported concern, and I had to face up to the mess I’d been shoving under the rug all term. Since that happened, I’ve started making progress on my thesis again. It isn’t going to be what I wanted, or what it could have been, but that’s something for radical acceptance: I’m hanging onto what one of the lovely people told me when I asked for advice (they work for the college): “The best thesis is the thesis that is done.”

In the spirit of getting all the shit done, when everything is shit, please find below my attempt to distill my experiences here into some general to-do’s for the next time this happens.

And yes, if you know me in the real world please feel free to smack me upside the head with this if I pull a vanishing act on you.

  1. Find someone who you trust loves you enough to call you on your bullshit. Talk to them, tell them what is in your head, and then ask them to help you make a plan to get back above water.
  2. Spread your plan out, and make sure you’re not overloading yourself. It’s not going to do any good if you panic about your plan, and then feel shitty for not doing it “right”.
  3. Drink a cup of tea. Breath. 
  4. Ask your someone if you can check in with them, and if they don’t hear from you if they can check in with you. Feel that other people around you care, and that you aren’t alone in this.
  5. Get shit done. 

Treat yourself as kindly as you would treat anyone else who is feeling like you are. We’re all human here.

My thesis is due on the thirteenth, for better or for worse. A thesis that is the best I can do under the circumstances is better than a thesis that never appears. People are here for me. I’m not alone in my shit. You also, are not alone in whatever shit is going on in your life.

When mental illness rears back up it can really feel like it’s life interfering with the mental illness rather than the other way around. Remember in the midst of that, that you are a person with a mental illness and not reducible to it. We’re all here, dealing with our own shit, and rooting for you.

Until next time,

Kerry

Breaking Radio Silence and on Medication and Setbacks

Hello all, remember me?

If you’re new, welcome. If you’ve read before, welcome back!

I’ve befriended a few people on Facebook who may be reading for the first time, and learning a lot about me that they didn’t know, and so for their benefit I’ll do a quick recap. I’m Kerry, as you hopefully know, and I’m a lot of things including a sophomore in college, a barista at Starbucks, and an owner of many cute animals (including pet rats). I’m also in recovery from an eating disorder, and pretty severe depression. I hope this doesn’t change your view of me too much, as I’m obviously still the same person, but I’ve accepted that it might. I’m writing this blog to hopefully increase awareness of mental illness, and acceptance of mental illness, and I want that to start, or continue with me.

So anyway…

As Amy Poehler puts in her book that I got for Christmas, Yes, Please!, “There’s a lot of, ‘I dressed for writing and went to my writing spot,’ and it’s like ‘What the fuck are you talking about? This is a nightmare!’ Writing is a nightmare.”

Writing about your innermost fee-fees (feelings) is easier said than done. Especially when you’re being open with all the internet. This became obvious in the last month, when instead of writing about when I fell off the ‘recovery wagon’ I kept my mouth shut and tried not to feel like a hypocrite for all the advice I’ve been giving people.

But enough with me whining about how hard it is to write (something I truly love to do) and lets get on with it: yes, I fell off the recovery wagon.

You see, a very important part of the recovery process (for me, not everyone) has been finding the right medications. I’m including the name of my medication here, so that people who are taking it or considering taking it have a view of what it might be like to go off of it. That medication for me is Effexor XR, used alongside Abilify and Trazodone with the occasional Ativan.

Sounds like a mouthful right? (ha, ha–get it?) But seriously, if you’re on medication let me give you a small piece of advice:

Do NOT go off of them without your doctors help.

Yes, this sounds self-explanatory and you’re probably thinking, “Why Kerry, why ever would I do such a thing?” But if you are taking the right medications, you end up feeling better. For me, this automatically translated to ‘I don’t need these anymore, and they’re awkward to take in front of people, and so I’ll just stop.’

Of course, skipping them once led to skipping again and by the time I noticed that I was regularly skipping my medication it had been five days and nights. Luckily, I was in group when this happened and was able to tell my therapist, “Hey A, I think I know why I’m feeling so dizzy, nauseous, lightheaded, depressed, sleeping a lot and crying a lot.” Because that’s what was happening. By the time I got home I withdrawal had really kicked in, and I couldn’t watch a small section of a military-based TV show without becoming overwhelmed, anxious and bursting into tears.

You see a lot about withdrawal in the world: when people stop smoking, or drinking caffeine, or when people who use drugs try to stop. What its impossible to convey though, is how much it sucks when its actually happening to you. I’m just going to whine for a little bit here, because the people in my life got tired of hearing about how much it sucked pretty quickly–way before I was done complaining about it.

Effexor withdrawal is the most awful thing I’ve experienced (and I’ve gone through gallstone pancreatitis–more on that later). Not only do you feel the feelings that the drug has been keeping away, getting sadder, more tired, and yes–suicidal, but you also get the physical symptoms of your body adjusting to being without this drug (and so not performing the chemical reactions that it has been helping with the same way). These physical symptoms include: brain shocks (which essentially feel like a small current of electricity is going through your brain, or like its being shaken), nausea, migraines, lack of the ability to regulate your emotions, and more. Fun stuff!

Personally, I (as a neuroscience major) was morbidly fascinated, as what was happening chemically in my brain was pretty interesting. Effexor is (I’m pretty sure) an SNRI, which means selective serotonin-neuroepinephrine reuptake inhibitor. Basically, it causes the neurons (brain cells) to take back in less of the chemicals that they use to communicate (serotonin and neuroepinephrine in this case) than they normally do. This means more happy chemicals (they actually affect mood and energy levels generally speaking, respectively) swimming around in your brain. This means that your brain gets used to these new levels.

Now imagine taking that extra juice away.

So logically, I knew it was no wonder that I felt like shit.

After a couple weeks, including a really hard weekend that I may go into detail on later, and a lot of lectures from many medical professionals on stopping your medication without assistance (again, the upshot is: don’t do it) I was mostly back mentally, and physically. So why didn’t I post then?

This experience scared the hell out of me.

One week, I was doing well, visiting my friend in NYC, eating as I was supposed to, and the next I was contemplating putting myself back into the hospital. Thankfully, a lot of good things that I had set up in my life kept me from doing that.

First, there was work. I love being a barista, and the people I work with, and though I have no problem with them knowing that I’m in recovery (as a few people do know) I didn’t want this setback to affect my ability to do my job, or people’s confidence in me. I’m proud of having a job, and I love Starbucks as a partner and as a customer. Going inpatient would have meant taking a lot of time off of work, and it also would have meant the possibility of reduced hours (with increased care) for a while after I got out of the hospital. I didn’t want to go backwards.

Second, there was my team. If you’re going through any sort of anxiety, depression, eating disorder, or any other sort of mental illness, I hope you have a good treatment team–and I’ve got to say, mine’s fucking awesome. They made sure that: A) I was safe and B) I didn’t forget that this was temporary, and that I had shit to do other than being a patient.

I truly am thankful for their helping me stay out of the hospital, because although the hospital is “great” when you absolutely need it, its obviously something to be avoided if you can. You know that you have a good treatment team when they do what they have to do to keep you safe and on a good path, regardless of how you feel about the matter initially.

Thirdly, there was my family. Although my parents didn’t do the ideal thing, what the treatment team advised, they helped me to figure out a solution that worked for everyone at the time. If you’re going through a tough time, it pays to have family on your side, because you’re pretty much stuck with them loving you no matter what you do. My extended family ended up chipping in and helping me out where I needed it, and it was the perfect distraction.

And lastly, as cheesy as it sounds, there was me. You can set up the environment all you want when you’re feeling crappy, and try to prepare for everything your sad self might throw at you, but in the end there’s you and your thoughts. One of the main things that stood in my way from doing something stupid that really hard weekend was the memory of how exquisitely good life can be when you’re really in it, and trying.

So now I’m back. In school for the Winter term, with a full course load, stepping down on treatment and stepping up with that whole life thing (more on that later).

Let me know if you want to hear more about anything I mentioned here, or if you have any questions you want me to answer. I’m happy to help with pretty much anything and everything, and I don’t care if we’ve never talked, or if you used to hate me, or if you think I’m weird, or think that I think that you’re weird, or any of that. If you need to talk, message me–period.

This has been a rambling message, with a lot of odd details and I hope you’re still with me. My new goal, to hopefully not fall off of the radar, will be to post something daily, likely when I’m procrastinating (like now). So expect to hear from me tomorrow.

Love you lovelies, thanks for reading!

My Filofax Planning and Recovery

So I can’t stop writing. Seriously, thank you all for being interested in what I have to say!

Thank you to those who voted in the poll–the results were a tie (at least so far) between how my Filofax has helped with my anxiety, and my depression turnaround, and as I’m upgrading to a new Filofax system soon I really wanted to write this one so that I can chronicle the current setup. If you’re interested there’s also an accompanying video, which is my first venture into Youtubing.

I’m excited because this is my first post that will have pictures. And they’re pictures of one of my favorite things, the nerd that I am, my Filofax!

So, I got into planning one really awful night when I was home alone for the weekend. I was coming off of a pretty horrific binge, and I remember just thinking, “What should I be doing right now? Because it isn’t this.”

I started researching journals, and planners, and I came across the amazing Filofax community! Soon I was sucked into the videos, and the decorations, and the different ways of customizing your pages, and your setup, and I just had to get one. I ordered my black Domino that night, rush order (yes–next day delivery) because I had this feeling that it could help me for that weekend, and she’s been with me ever since!
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(Also you get to see my face–exciting I know)

So this is my baby now, and it helps me in so many ways. So when you open it up:

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This is what you see!! I have my dashboard, which has the occasional post it on it with reminders, but is more to protect the pages, sticky notes and quotes behind it. Silly as it may seem, opening my Filofax up to a big ol’ bright pink “Hello” makes me smile, so I keep it. On the back of the cover is five card holders, which I use for appointment cards and to hold sticky notes, in the pocket behind I have some labels right now– it’s super handy.

Oh and just a close up of one of my favorite quotes. I don’t remember where I got these printables but If someone knows please tell me!

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After that…

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Is a pretty piece of paper that I washi taped and had to show off, and then…

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Comes the meat of the planner–my week on two pages. This is one section that really helps my anxiety. I use it to make to-do lists for every day, and I make all the lists on the Sunday before the week starts, using my syllabi and notes I make as needed about appointments. This way, I know what I have to get done, and how I’m going to spread up the work so that I have some free time but everything gets done. After I finish the to do lists, if there’s any doubt about how I’ll get through a day I used the calendar on my phone and block out every single minute, starting with the time-sensitive things, like appointments and classes, and then fitting in the rest of what I have to do. If it doesn’t work out, I rework the spread of the to do lists.

I also keep here a positive things sticky note, which I’ll talk about later, and a goals sticky note, where I have my goals for the week.

This might seem like a lot to do just to make a to-do list, but it cuts way down on my time later because I never have to worry about how I’m going to get something done: it’s already figured out.

The time consuming thing I did not like was the entering things into my phone. So I’m moving to an almost entirely paper based system and making…

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Day per page pages! I’m not actually making them for long–I ordered a set for 2015–but for now they’re working out fine! So on these, as you can see I have my calendar, which is only ever completely scheduled out if I have a day that seems impossible. I kept a section for to-dos, and added a section that I was keeping on sticky notes before–positive things about the day. It really is nice to fill this out throughout the day, and just keep note of the nice things that happen. Also I love turning to a past week and being able to say, “Oh cool, this was when I started
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My goals are now incorporated into my to-dos, and calendar, and I keep the ones for the week on my dashboard at the front of the binder.

So then after the bulk of the binder are the rest of the sections: contacts, which are hidden because Internet, quotes, which I have a few pictures of! Notes, which is mostly Starbucks stuff to remember, Projects, which is stuff I’m planning to make for Etsy, and for other people, and last but for sure not least my Recovery section.

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The quotes help if I need a boost, but the recovery section is super important and I will forever keep it in my carry-along binder. It has all of the notes from my treatment groups–CBT, DBT, Nutrition, the works. This way if I ever find myself really stuck I can look and see what I can do in that situation. This is also where I make the lists I talked about in my last post, of things to do, and where I keep a running CBT log, because I’m a dork and find that they work.

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Basically, in here is everything that I could possibly need when I’m out and around. It keeps me on track, and helps me worry less, because it lets me both figure out how to handle a situation that’s come up, and plan to handle ones that may come up in the future.

If anyone wants a post about setting up their own Filofax let me know–I’m planning on doing one around Christmas but definitely can sooner!

Until next time, with lots of love.