Joy lies in the fight, in the attempt, in the suffering involved, not in the victory itself

(Ghandi)
Showing posts with label trichotillomania. Show all posts
Showing posts with label trichotillomania. Show all posts

Tuesday, October 13, 2009

why is the last mile the hardest mile?

Three weeks ago Dr A gave me a prescription for an atypical antipsychotic, and tonight I started taking amisulpride (aka Solian). I wasn't keen to start a new medication while Doc was lazing on a beach in Portugal, but really, the last week has been hellish and I'm hoping for some kind of miracle. It's a low dose, but it's possible that it will help to stablise my moods and help with the trichotillomania, binge eating, angry freakouts, etc. When he wrote the script Dr A said it could keep me up all night, or help me sleep, and I'm desperately hoping it'll be the latter. So damn tired, so sick of the nightmares I'm having.

I took a personal day off from work today, after waking up with that utterly helpless feeling, knowing I would not be able to summon the strength to face the world. I spent the morning writing a list of all the crap I have to worry about, which (weirdly enough) helped. I'm now attempting to prioritise these things, and will work through them one at a time. Sigh. My dog had to have $500 worth of x-rays a couple of weeks ago, after rupturing her cruciate ligament jumping down from her groomer's table for goodness sake! Whose dog DOES that? So unfortunately, my divorce is temporarily on hold. But I still plan on doing it as soon as I save up the money again. I have also contacted Mr Ex regarding a few loose ends, possessions, etc, and it felt quite decent to be assertive. I am still overwhelmed with resentment and anger about a lot of things regarding our marriage/his lies. And I suppose one day that will all have to be dealt with.

I logged on here today and found I had one less follower. Nick Drake just the last straw, huh? LOL. My friend Kate once mentioned how easy it is as a blogger to place stock on who has you on their blog lists, and who follows you, and she is (as usual) right. It sucks that someone abandoned me while I was down!! I'm kidding, but you know what I mean, right? I have another friend who warned me, and rightly so, about the indulging in melancholy music when I'm already feeling low. I'm terribly prone to that, so have avoided all tear-jerking emo type music today! Apart from the blog post title, which is courtesy of Morrissey.

One of the bright moments in the last week has been my kick arse friends, in the real world and the virtual. It helps so much to know other people know what the black dog looks like, and how persistently he hangs around hoping for some scraps of sadness. Another bright spot was seeing Whip It - a movie that may be responsible for my unattractive and clumsy entry to the sport of roller derby!! If only I could a) skate, b) think of a good derby name and c) wear fishnets without resembling an overstuffed bag of oranges. LOVED the movie and am determined to live the tagline - BE YOUR OWN HERO!

Thursday, September 17, 2009

you're an angry blade and you're brave

A small update post-conference. It's been, it's done, seemed moderately successful apart from the usual technical glitches and no-shows. Sir J has moved on to his next "gig", and I am enjoying a well-earned day off.

Tomorrow I have to go and have the MRI I've been avoiding most of the year. Dr A has often said it would be useful to see what effects, if any, my lupus has had on brain function (and, ergo, depression, headaches, mania, moods, etc). I guess it will be interesting to know if any lesions are present, not that there's much they can do about them. Maybe it will turn out that I have a cabbage in my head instead of a brain haha.

Increasing my dose of fluoxetine has not helped my OCD or binge eating at all, and Dr A is suggesting a mega-low-dose anti-psychotic be added to the mix. I would then reduce to my previous low dose of fluoxetine, as the Abilify (or whatever) will be activating enough. The meds merry-go-round is so annoying, and confusing. But it would be good to not be a slave to the trich and binge rituals... Any feedback or advice from y'all would be welcome, as I know Abilify is something lots of folks have tried. Apparently the risk of weight gain is less than with other a-p drugs?

So much going on, no wonder I find it hard to sleep through the night. I am determined to not start medicating for sleep, though, as I know it's a hard road to come back from. This may sound like a negative post, but I'm feeling well. Relieved the work situation will now wind down slowly until December, when the Foundation closes for a month.

(Angry Blade - Iron & Wine)

Saturday, March 28, 2009

The Reinvented Self

The week continues on it's merry (somewhat TOO merry perhaps?) way. Sweeping the patio, walking the dog, cooking, cleaning, job interviews. It's all go at the L Ranch. There's a small and hellishly contrary part of my brain that is fighting it, still. I am trying to resist the inevitable analysis...is this energetic and cheerful person actually ME? Is it "normal" for me to feel hopeful, positive and motivated, all in one day? Is this one of those SSRI-related manias I've heard so much about? All I can do is be vigilant and document any out-of-character behaviours.

The medication is also supposed to have a positive effect on impulse behaviours; sadly so far my trilogy of tragedy (derm, trich, binge) are still firmly in place. But I have been able to go three or four days without harming in these ways, so I think the CBT is helping there. I am trying to distract myself and find other outlets. This week I started drawing, which I've always wanted to try - bought one of those "Drawing For Dummies" type books and so far I'm loving it. I am typically BPD in that I adore new hobbies haha!

Dr A has written a referral for me to have an MRI - apparently lupus/SLE can cause brain lesions and other nervous systems problems, and in 10% of lupus patients the disease causes personality disorders, depression and/or psychosis... Um, maybe that's something I would have found useful to know 5 years ago? Twenty years ago?? I seriously doubt that my lupus has impacted upon or caused my mental illness. Even if it has, the treatment (for the vasculitis or lesions) is masses of corticosteroids, which I refuse to take. But the knowledge will be powerful, just the same. I can't believe that the rheumotologist, haematologist, allergy specialist and previous psychiatrists have never mentioned an MRI...