Perpetual Smile

Pam wasn’t kidding when she said the Seroquel would make me drowsy. I took it at about 12 or 1am, and by 2am I could barely hold my own head up. Today I’ve been pretty lethargic; all I want to do is, well, nothing. She said it would pass after a few days. I’m pretty sure she said it would phase out once I hit the 150mg dosage, which is about five days from now.

I just downed a cup of coffee, though, and I feel a bit more lively now.

Speaking of lively, today’s been an interesting day. Remember how I told you about my living situation? You know: my parents, great-grandmother, and Apollo the cat on the first floor, my great-aunt on the second floor with her cat Charlie, and my sister, grandparents, Squirt the cat, and I on the third floor. My grandparents and parents ended up making the switch, so now Mom, Dad, Lauren, and I live on the third floor, and Noni, Popi, and Biz Noni live on the first.

We decided that we would eventually move Apollo up here, too, but knew that it would be rough because Squirt? Is Napoleon in disguise. She weighs maybe eight pounds soaking wet, but she’s got tons of attitude to make up for how teeny she is. Apollo, on the other hand, weighs probably two or three times as much as she does, but he is a big baby. Squirt originally belonged to my ex-boyfriend, and his family didn’t treat their cats very well. I found Apollo outside a few years after my ex gave me Squirt. He was a teeny, orphaned kitten, and you could tell that he had been dumped by his original owners.

So we knew that Squirt was pretty much going to push Apollo around. We decided to move him upstairs last night, and it’s been a Mexican standoff since. Right now, we have a door with a glass window standing between them, with him prowling most of her territory. Last night and most of today, she had him cowering in a corner. Even though she is my baby, I felt really bad for him, so I moved his litter and food into the corner with him and as soon as she left the living/dining rooms, we closed the door behind her. Now he is all badass, like, “What, bitch? You can’t touch me now!” Currently he is exploring under my desk and she is sulking in the window in the pantry, I think.

Squirt has always been my buddy, but I couldn’t stand seeing Apollo hiding under a table, not coming out to eat or drink; if he so much as raised his head, she would start to hiss at him, and if he tried to come out, she would charge. She is scary for such a tiny little thing; she has kicked my ass on more than one occasion.

But I love them both. I hope they at least learn to ignore each other.

I need your advice! Have you ever introduced a new pet to your current pets? How did you do it? Did they become friends? Is there hope? Please leave a comment with your pet advice!

I leave most doctor appointments feeling pretty frustrated, as if I’ve gotten nowhere and am starting over — all over again. Having an undiagnosed autoimmune disease means bouncing from doctor to doctor, telling my story over and over, and usually receiving a response something like, “Well, shucks, you’ve got a lot of symptoms, but fucked if I know what’s wrong! Also, all of your blood work is normal. You’re normal. Yay!” I try not to blame the doctors, but really — they’re doctors. They’re supposed to know, dammit!

I’m also always very hesitant to admit when I’m depressed. It’s easier to write about it here than it is to say the words out loud while looking someone directly in the eye.

But today — well, okay, technically it is now past 12am Saturday so this all happened yesterday — I shoved all of those fears aside and went to see Pam, my PA. And you know what? It wasn’t bad. At all.

Pam asked what I was there for, and I right away admitted that I’m having a hard time with my depression, and that things weren’t going too well with my rheumatologist. When I explained to her how I’ve been running through cycles — wanting to kill yourself one night and then being high on life the next two days is so not normal — she immediately agreed that I need to be tested for bipolar disorder and drew up a plan of action.

“I’d rather start you on medication used to treat bipolar disorder right away so that we can see if it works,” she said. We then discussed a few psychologists and a pain management specialist that she really likes, and narrowed it down to psychologist Dr. M and pain therapist Dr. P. We also decided that I would try Seroquel, a medication used to treat bipolar disorder. She explained that she has people start with 50mg for three days, then 100mg for three days, then 150mg for three days, then 200mg for three days, and so on, and that I would start to notice the effects within a couple of days. She also explained that people with bipolar disorder don’t normally respond to regular depression medication — or that it does odd things to them — which would explain why Zoloft basically made me a zombie and why Cymbalta made me hyper as a kangaroo on crack. She gave me samples of the Seroquel so that I wouldn’t have to pay for several different prescriptions, and said that she would see me back in two weeks to check on how the meds are working (and to call her in the meantime if anything comes up). I’m to call Dr. M before I contact Dr. P and am to start seeing Dr. M as soon as I can get in.

Then we moved on to my mystery autoimmune disease.

I told her that my aunt has Crohn’s, which I had apparently forgotten to tell her before. I also told her about the weird thing with my hands (I sometimes get little “spots” that are sensitive to the touch, as if I’ve been burnt or scraped, but there is nothing there). She confirmed my suspicions; this is another classic autoimmune symptom. She said that autoimmune diseases can attack the skin cells, so that is why I have that sensation. I’ve had this since childhood but never thought anything of it; I thought it was normal up until a week or so ago, when my hands were pretty much covered in these little invisible spots and I couldn’t let anything touch them because it fucking hurt.

We discussed me getting a colonoscopy to test for Crohn’s, and she said that she would contact my rheumatologist for his reports to see if he had any thoughts as to which autoimmune disease it could be before sending me to a gastroentologist. The last report he sent her was in September, and I continued to see him once a month through to November. I told her about how he didn’t really seem to remember me from visit to visit, and how each visit his ideas would change; one visit he would suggest that it was my birth control, the next he would send me for more blood work. From her face, I could tell she agreed with me that he is pretty out of it. (He’s a nice guy — don’t get me wrong! — but he’s pretty old. His brother was exactly the same way: nice, but very forgetful and a little cooky.)

Pam is going to get my reports from Dr. G (rheumatologist), and when I see her again in two weeks we’ll go from there.

I may not have gotten any solid answers this time, but I still feel like I got somewhere. I got the ball rolling on taking care of my mental health, which is ironically the easiest thing for me to fix (with counseling and medication, and with a diagnosis that will hopefully confirm my suspicions of bipolar disorder*), but it’s always hard for me to admit that I need to get help and to actually go get the help. I got the ball rolling on my physical health again, as well. I feel like I got a lot accomplished, because I took the steps I needed to take.

*Other people around me have also seriously suggested that I may be bipolar, including a social worker I used to see when in high school. Ms. Amenta, wherever you are, I miss you so much. You were the best.

PS: I should totally just make a “Depression” category.

“I havnt talked to you in a while and wanted to say hi and stuff,” reads the text message. Ever since opening it, all I can think of are his hands around my throat.

* * * * *

Things have been absolutely bonkers on planet elizawhat. Aside from people from my past popping up like germs on a little kid’s hands, life has been packed with huge projects for clients with looming deadlines, a new niece to snuggle and love and gaze at while she sleeps, anxiety about Popi’s angioplasty that he had done today, a renewed sense of connection and even deeper love for Mike (who has been amazing beyond words through all of the shit hitting the fan), a slew of phone calls to schedule appointments with various doctors, more worry while we wait to see what the doctors say is going on with Dad, depression cycling in and out of me faster than fucking bunnies (and “fucking” is a verb here, heh), and a deep, unquenchable urge to play Sims and write even though I barely have time to sleep.

Suddenly, “bonkers” doesn’t seem quite appropriate; things are absolutely batshit.

* * * * *

Popi has been having chest pains, that go all the way down to his elbow. They found two clogs in the arteries of his heart, and did an angioplasty this afternoon to open up the arteries. They’re not sure why the arteries were clogged; it could be the chemo, it could be something that was already there before the cancer came along. More than likely it is the chemo, because a few weeks ago they did a full slew of tests and no clogs were detected.

I’m angry and afraid, to be perfectly blunt. I’m angry at the chemo, and afraid that it’s going to destroy him, piece by piece, before the cancer does. And then I saw him last night, and seeing him looking well and being with him made me think more positively. I look at my great-great-aunt Nan, who is in her nineties and was diagnosed with stage 3 cancer more than six years ago. She’s fine today, still kickin’, feisty for such an old lady. She makes her own clothing. She drinks wine. She cracks jokes, sometimes dirty ones. She’s got an uncanny strength for someone who looks so fragile. I admire her, deeply.

She is proof that Popi can make it through. It pisses me off when everyone starts discussing hospice. It’s like they’ve already given up. I don’t want to give up. Call me selfish, but I want to keep my Popi. I like to think that he can kick this thing’s ass, even if it’s already taken its toll in so many places: hip, spine, liver, lung. Fuck you, cancer. My Popi is stubborn and won’t go down so easily. I won’t let him.

* * * * *

My niece is a doll. She has Jaysa’s nose, Robbie’s face. Her hair is black and her head is full of it. Her eyes are big and constantly open, aware. She may not be able to see much yet, but she looks like she’s perfectly aware of what’s going on. Ciana Olivia Pelletier already has all of us wrapped around her tiny, long fingers.

* * * * *

It’s hard to talk about everything that is swirling through my mind. I don’t really even know where to start. I’m bone tired, thanks to a week full of nights spent staying up until the ass crack of dawn to get pieces of projects complete. I keep reminding myself that if I work hard now, in five to ten years I’ll be able to enjoy things. Sometimes I wish I could be a “normal” twenty-one-year-old, spending my late nights partying instead of working, falling asleep with veins full of thin, beer- or vodka-chased blood, then waking up to do it all over again the next day. But my partying stages were years ago, when being fifteen meant that I didn’t care much about my future. Now, I want that future, whatever it may be.

* * * * *

I know things have been pretty serious around here. I promise to try to make this place fun again. Thank you for listening.

Wednesday, I hid.

I called out of work. I threw on some headphones. I buried myself under my comforter, afghan, and fleece blankie. I stayed like that for about an hour or so, falling in and out of sleep while listening to Lacuna Coil’s “Shallow Life” and Silversun Pickups’ “Swoon”, my current comfort albums.

I thought about going to the hospital. I thought that maybe I should talk to someone, someone who would get it and would be able to point me to a therapist who would get it even more. I imagined being handed a prescription to try, that might give me more energy and a little more sparkle inside.

I finally got up to go get dressed and eat so that I could go to the hospital, but I could barely eat and didn’t have the energy to get dressed. I crawled back into bed for another hour or so.

I know it was bad. I know that I need to get my ass into a therapist’s office. I know that I need to be tested for bipolar disorder, put on some medication, and need to go through pain management therapy. I know all of this, and still I shy away.

I make passing references to the people around me about how I’m feeling, but I don’t go all the way and say, “THIS IS BAD. IT’S REALLY BAD. I REALLY NEED HELP.” I don’t reach out. Instead, I keep it all to myself. I drop little hints, enough so that I can tell myself I said something, but not enough for anyone to get really concerned. Because, if I did truly say how bad it is, they might be very concerned.

It’s been a long time since I hid like I did on Wednesday.

In a way, it was just what I needed. I needed to regroup. And yet, on Thursday I felt the same as I did the day before. I felt drained, like I wasn’t really here, but at the same time it felt as if there were little teeny jumping beans inside of me and static fluff in my head. I barely sleep, I barely eat, and I feel like I’m barely making it through the days. Thoughts race through my head, about everything going on: about Popi, about Dad, about my stupid mystery autoimmune disease, about my relationship with Mike, about my new niece, about my clients, about my day job. On Thursday I felt like, at any moment, I was going to split into two. Or four. Or nineteen-thousand.

Today, I felt sort of normal — if normal means being on the verge of tears one minute and wanting to laugh like a maniac the next. At the moment, though, I feel okay.

It’s not just everything that’s going on; I go through these cycles all the time, for as long as I can remember. Last week, I thought about killing myself. For two or three days after, I felt high on life. And then I dropped again. I didn’t feel like dying, but I still dropped.

Part of me is ashamed. Part of me admonishes myself. “This was supposed to be over,” that part says. “We don’t want to go back to therapy. We were already there. Things should have been resolved then.” But the other part steps in and say, “That therapist didn’t do her job, and neither did the second therapist we saw about a year ago. We need to be tested for bipolar disorder. We need pain management skills. We need someone to talk to about everything.”

And the argument goes ’round and ’round, until I’m so tired of hearing these thoughts wrestling each other that I consider cracking open my head and throwing a grenade in there. (That’s a joke. You can laugh. I’m not actually going to grenade my brain.)

The truth is, my friends, that I NEED HELP. I am drowning, and with all of the external things going on as well as what is normally in my head, I’m having a really hard time staying afloat. I don’t want to die. I don’t want my mental illness to kill me. I don’t want to be the zombie I feel like. I’m tired of faking. I’m tired of being afraid to say anything to the people around me, partially because I’m afraid they have enough problems of their own and I don’t want to be yet another weight on their shoulders.

It’s also because I am partially ashamed of going back to therapy. I don’t want to. I tried it again, with Kitty Bhide, and she sucked. I know that if I just try a few different people, I’ll find the right person. But then I make the excuses of, “Well, I don’t have that kind of money,” and “It’s going to take forever to get in anywhere, and by the time I get in, I won’t feel this way anymore.” Even though that’s true — hi, that’s why I need to be tested for bipolar disorder — it’s still not a good enough excuse, because I still know that soon I will feel this way again.

I go through this, every time.

And it’s draining.

I’m typically what I like to call a “functioning depressive.” When I’m depressed, I can still perform everyday tasks. It just takes every ounce of energy I have. I can’t remember a time when I just completely shut down and couldn’t get out of bed.

Is it so wrong, then, that I want to do just that now? I feel like I’m running out of energy. I don’t want to function anymore, dammit. I just want to hole up and kick the world out for a little while. I want to call out of work. I want to sit in my own little bubble and numb everything out.

Honestly, I feel like I can’t take much today. I don’t feel very strong. I just feel like an open target. I want to hide. I’m tired of going through the motions, pretending that I don’t feel like shattering. For once, I just want to tell the motions to fuck off.

I have a favor to ask you all.

Some of you might know that I run a pen pal support group, Letters of Love, for people with depression, self-injury, etc. Some of you might know that I suffer from depression, that I used to self-harm, that I have on several occasions wanted to take my life. In the almost two years that I’ve been running Letters of Love (LOL), it has grown very large, helping many people.

I’d like to take it a step further.

I’ve long been wondering why there isn’t a directory of organizations who help people with mental illness, as well as a directory of bloggers who struggle with mental illness. I mean, we spend an awful lot of time feeling alone. I’ve been using LOL to try to connect us all, but I really think I need to do more. I’ve been wanting to put this directory together, but wasn’t sure how to tackle the job.

I’ve finally decided to do it, but I need your help. If there is an organization, such as LOL, Holding of Wrist, or To Write Love On Her Arms, that you know of that helps people with depression, or a blogger you know of who openly writes about his or her experiences, please comment with a link to their website. (I will, of course, ask any bloggers for permission before linking to them in this directory.) If you could also write a short description of who they are, what they do, and why you recommend them, that would be great.

Please pass this link along to anyone you think might want to help or who might benefit from the directory when it’s complete.

Thank you.

PS: If you’d like to share a link but don’t want to comment publicly with it, just shoot an email to me at elizawhat@gmail.com.

I want to tell you all about so many things, like Christmas Eve, my latest bout of depression, the Nintendo DS I bought myself as a treat, all of the pain I’ve been having lately, the insane workload I’ve been carrying, and a few other things. But when I sit down to write, all of my thoughts blow away like clouds on a clear summer day. I could tell you about how I lost my appointment card and have no idea when my next rheumatologist appointment is (or was). I could tell you that I feel like it does no good to go anyway. I could explain to you how amazing Mike is and that without him I would not have made it through the last few days.

I want to tell you how badly I want to reorganize my life right now, because it feels so messy and everything I want feels so out of reach. I want to tell you that not every moment in my life has been gloomy; I’ve had some good happy moments lately, too. I want to tell you all about how my family is doing, the love, the fights, the eggshells.

I just don’t know where to start, my friends.

I’ve been reading everyone’s blogs and it seems like we’ve all been having more than our share of ups and downs. I can barely get my thoughts together enough to leave a comment worth reading let alone encouraging. Everything feels so chaotic right now. My own head is a mess and my heart is lost. There is so much to fight right now, but I feel like every time I swing, I miss by a wide berth. (Can you tell I’ve been running around as Link in the latest Zelda game for the DS?)

I know that the end is in sight. I tell myself that, as soon as I finish my big client’s project, things will get a little better. But I know it isn’t just the project that is weighing me down. I spend so much of my time worrying and stressing that when it comes time to take action, I freeze. I think this is defined as ANXIETY. I know that I should probably grab a phone book and call a therapist. I know that I should call my rheumatologist’s office and find out when my next appointment is (or was), since I’m worrying myself sick that I might have to pay a fee if I missed it.

I worry, worry, worry.

I wish that someone would guide me through this, like some sort of magical creature that will say, “Okay, do X and Y will happen, so then do Z and it’ll be all set.” I wish someone would take care of me, even though I am old enough to take care of myself. I need a rope, friends. A thick, knotted rope that I can climb up to the top where I can see everything.

Or maybe I am already able to climb up and look. Maybe I only need to let myself SEE. Maybe I have become so comfortable with the bottom that I’ve allowed myself to stay there. To quote Silversun Pickups, “I don’t care, I’m still here, everything seems perfect from down here.” Except it’s not.

I wish that I only had to handle one thing at a time, but that’s not the way life goes. Maybe if I put everything out, examine everything that I’m dealing with, and SEE it for what it is, then maybe I can figure it out. So if you don’t mind, I’m going to do that. Let’s see:

• The big project. This project is HUGE and is making me a lot of money, which is awesome. The not awesome part is that I’m stuck on a couple of things with it, and being stuck makes me freeze instead of taking action. This needs to stop. I need to figure out how to fix the issues I’m having with the coding. I need to force myself to sit there and work through it. Standing still is not going to help. Letting the anxiety of the Impending Deadline stop me in my tracks is not going to help. If I don’t say “fuck you” to the anxiety, I’m going to be frozen until the Impending Deadline hits me right in the head. I need to remember that it is not only me that will take the hit if Impending Deadline comes and the project is not done. I need to also not let that scare me into frozen fear. I need to keep saying “fuck you” to the anxiety and work through the stubborn code.
• The pain. Whatever the hell is wrong with me has been pretty aggressive lately. A few days ago, both of my hips flared up, with the ache radiating back and forth, so that my whole front hip area was in agony. The next day or maybe the day after, my right hip flared up, then radiated to my back. The back side of my hips and my lower back were a big glow of RED pain for maybe an hour or two. I fell asleep some time after it started, and when I woke up it was gone. This morning, from the front of my hips all the way to my toes ached so badly, I could barely walk. All I wanted to do was lay down and go to sleep, but I had so much work to do and also had to go to work. It quit around the time I went into my day job, so I’d say it lasted at least three hours, maybe four.

  I’m so tired of bouncing from doctor to doctor, spending so much time and money when all I get are no answers. It all feels like a huge waste of time, and once again I feel like they are never going to figure out what is wrong. I think I’m going to spend the rest of my life bouncing between mind numbing flareups and a very thin time slot of remission. What I’m experiencing is the definition of rheumatoid arthritis or some other autoimmune disease, and yet all tests come back negative — except for that one double stranded DNA, which is supposed to mean I have some sort of autoimmune disease, but so far my rheumatologist has been unable to determine which one. I know this requires a lot of patience, but I am not the most patient, and I think after almost three years of pain, pain, pain and a slew of other symptoms, most other people would also have lost their patience.

  I’m also tired of A Certain Person scoffing at me when I complain, as if I am just making this all up. I want to be taken seriously by A Certain Person, but I get the feeling they don’t because they can’t physically see any of my symptoms. I’ve gotten to the point where I mostly say nothing when I’m around them and experiencing symptoms. And anyone who deals with chronic pain knows that it’s so hard not to say anything. Since I spend a lot of time around A Certain Person, I spend a lot of time not saying anything. (And no, it isn’t Mike.)

  I know what I need to do. I need to push the fears of never finding an answer aside once more and I need to call my rheumatologist to either reschedule my appointment or get the date so I can go. When I do call, I need to be adamant about getting in sooner, and I need to stress that my symptoms have once again gotten worse. I need to not let the fact that I feel okay right now get in my way. I need to remember that “okay” can quickly turn into agony and that by speaking up and being a little more vocal, I might be able to get closer to the answers and treatment I need. I need to remember that I do NOT deserve this.

• My wish to write. While I spend most of my time working, I yearn so badly to get back to the novel I started during November. I know that my client’s project has to be done before I can get back to the novel. I need to remember that the sooner I finish this huge project, I will have more free time and will be able to spend that time finishing my manuscript so that I can start editing it.
• Taking the time to relax. I absolutely NEED to do something nice for myself once this project is done. It’s time to use that spa gift certificate my uncle gave me for my birthday so that I can go get that massage. I have been treating myself with DS Zelda breaks, but I also need to remember that too many breaks kills productivity. I need to remind myself that I do deserve the breaks, but should try to get more work done first.
• Popi. This is the hardest of them all, because there is nothing I can DO. Instead, the worry about his health pushes down on me. I don’t know what to do. I do know that I am so scared of losing him.

  His second round of chemo went well. He was only at the hospital for three days, and came back home on the third day. He hasn’t experienced any side effects. He’s just awfully tired from fighting so hard. I am so proud of him for being so strong. His strength makes me want to be strong, too.

  I am having a hard time fighting the worry, though.

Whew, glad that’s all off my chest now. I really need to stop bottling everything up and keeping it to myself. I have a hard time vocalizing the worry, though; I force myself to carry it all on my own.

If you’ve read this all the way through, thank you. I’m so glad that you were here to listen. Now I want to return the favor. Tell me, how are YOU doing?

This time last year, I was stressed out. I thought I wasn’t graduating because of my advisor’s bad advising. Just when I thought things couldn’t possibly get any worse, they did a 360 and got better.

When Michael came over for dinner on Christmas Eve and gave me my promise ring, they got even better. I closed the year with a great dinner at Outback and with a positive note.

This year, I don’t know what’s coming or how the story is going to end. Much like last year, I’m scared. But last year’s worries pale in comparison. I’d go back and not graduate, if that meant making this year better.

I’d like to hope that things will turn out okay, just like they did last year. But this year it isn’t as simple as meeting with a Dean of Academic Affairs and reviewing paperwork. This year, a better car won’t make my problems go away. A promise ring won’t fill my heart with warmth. Instead, my heart is heavy and full of dread.

I know I should be more positive, because — as last year proves — things can work out. They can turn around and be BETTER again, in the blink of an eye.

I guess I’ll have to wait and see what Santa brings me.

I am not doing too well.

I’ve spent the last two weeks in a fog, kind of just moving through the days. I’ve been a little better today but I can’t shake the feeling that this is only the eye of the storm.

In high school, the best parts of my days in shop (I went to a technical high school and spent my four years in Culinary Arts) were the mornings and afternoons. First thing in the morning, I would come in and fill a little bowl with chocolate chip cookie dough as it was being made by Chef I. He got so used to me snitching cookie dough that at one point he started having a bowl ready for me. (And then Chef Z and later Chef M tried to shut me down, but that’s another post for another day.)

After a day of cooking, we would eat together. If you worked on Faculty Range, in Bake Shop, or in the Dining Room, you got to eat the good stuff (as opposed to being on Cafeteria side, where you made lunch for the whole student body). My favorite thing to eat for lunch was a few slices of bread with butter and a big bowl of sauce. (And to think I stayed a size 3-5 throughout my high school career!)

I haven’t had homemade bread since.

This afternoon, while wandering around on Lifehacker at work, I found a post on making fresh-baked bread quickly and easily. I scribbled down the recipe — 6 cups of water, 3 tablespoons of salt, 3 tablespoons of yeast, and 13 cups of flour — on a Post-It and stuck it in my purse.

As soon as I got home, I set to it.

I split the recipe in half, since the Lifehacker post is for a one- to two-week supply of bread that you ideally bake a loaf every day. I dissolved 1 1/2 tbsp of yeast and 1 1/2 tbsp of salt in 3 cups of hot water (I remembered from Culinary that the hot water makes the difference).

Then I stirred in 6 1/2 cups of flour.

After the dough started to come together, I stripped off my rings and kneaded the dough with my hands. The scent of it was intoxicating.

When it reached the right consistency, I patted it into a neat little ball, scraped dough off of my fingers, and went to the sink to wash my hands. I didn’t get far before the urge to try some of the dough came over me. I pulled a little glob off of my left hand and popped it into my mouth. I knew instantly that I hadn’t fucked up the recipe; it had the perfect bread dough taste, with just the right amount of salt. I scraped as much dough off of my hands as I could and ate it before washing them, it was that good.

Then I put a towel over the bowl the way Noni always did when I watched her make dough and set it to rise.

If all goes well, I’ll have a nice hot slice of homemade bread with butter tomorrow morning before work with Noni, Popi, and Biz Noni. I might even put some grape jelly on it. My mouth just waters thinking about it, and my heart warms just a little bit.

That gaping hole is still there, but with little things like hot fresh bread and cards from my good friends online and off, it is a little less raw.

I’m VERY goal-oriented, but I tend to take on HUGE things and pile myself with too much to do. Recently, I’ve tried to break that habit by setting smaller goals at smaller intervals. Every month I set a few small goals that are more achievable and less stressful.

Last month, I tried to:

• Write a novel — and FINISH it, dammit!
• Finish designing Freaking Bookworm.
• Give Perpetual Smile a face lift with a customized design.

I managed to write about 60% of Secondhand Mom, my NaNoWriMo novel. I also started working on Freaking Bookworm. With a whole lot of life thrown at me all at once (chronic pain/disease getting worse, work, and finding out that my Popi has cancer), I got pretty slowed down on these goals. BUT — and I say “but” very loud and proud — I did accomplish a lot. I got very close to two of my three goals, so I can’t complain.

With everything that is going on, I need something to focus on, WITHOUT OVERWHELMING MYSELF EVEN MORE. I have a hard time not overloading myself. The last thing I need right now is to send myself to the ER for a nervous breakdown. BUT — and I say “but” very loud again — I need goals like a junkie needs heroin. I’m a goal junkie. An overachiever, if you will. So, how to get my fix without overdosing?

There is a LOT that I want to do right now, a LOT that I need to get done, and a LOT going on in my personal life. The wants I need because I need to try to stay as happy as possible. This means satisfying the muse (writing the novel, working on personal side projects, etc). The needs, well, they need to get done because my clients want their shit done, rain or shine, whether my fingers and toes are attached or not. Plus, I’m broke and I need some money. The chaotic, shittiness of my personal life needs to fuck off, but it’s there nonetheless. That part of my life cannot be changed. I’m having a hard time with that, too.

So, goals. Right. Getting back on track.

• Go to my writers’ group, every week. This will encourage me to keep writing, be it THE NOVEL or other stuff. It’ll also keep me sane.
• Spend lots of time with Popi. Make him laugh.
• Buy a camera and start taking tons of pictures of the people I love, because for some reason there are no recent pictures of anyone.

There. Simple enough, right?