Showing posts with label women. Show all posts
Showing posts with label women. Show all posts

Tuesday, August 16, 2016

My Mom's a Witch!




There's a story I love to tell people about when my kid was really little. There was a social worker involved in our lives at that time (because of me, separate blog post ENTIRELY but you know I'll write it eventually), and my kids were living with my sister. The social worker, a very unfunny woman with NO sense of humor, asked Spawn I about me.

"Mom's a witch," Spawn I said, totally deadpan.

"What do you mean, she's a witch?" asked Sorry Sally the Social Worker.

"She can make people disappear," said Spawn I.

"Who did she make disappear?" This from Sorry Sally.

Pause. Deadpan still.

"Daddy."

My daughter claims not to remember this exchange, but I sure as hell do. I was in the next room, and I nearly dropped my coffee cup all over the kitchen floor, and I damn near choked on the coffee that was pouring forth from my nose and sticking in my throat. I had to step out the sliding doors into the freezing cold backyard to keep Sorry Sally from hearing the gales of laughter that were issuing forth in a gurgly fashion, combined as they were with the regurgitating coffee. It was the way she said, "Daddy," in that matter-of-fact five-year-old's voice. 


Despite my shitty parenting, my kids have grown up to be wonderful young women.But the fact of their success as young adults has little or nothing to do with my parenting, because, due to my addiction and mental health issues, my sister had to step in and raise them for me. I won't go into personal details about the hows and whys, because I don't want to embarrass anyone, but I didn't see them again for 10 years. And a lot happens in 10 years. But they were never once, not for 10 seconds, off my mind or out of my heart. And they were never very far away, no matter where they were, and that was because of my faith.

My elder daughter was under my roof until she was five; and it was a Pagan roof. The little one was only with me for a year. I'm quite sure that neither of them remember living in a Pagan household, and my sister converted to Lutheranism from Catholicism when she married her second ex-husband, so the girls were raised in what passed for a "Christian" household. I won't chime in here with my opinion of people who rally Christ to their sides while doing all manner of clearly un-Christlike things. That's also for another post. But Spawn I seems to now be leaning toward a more naturalistic approach to spirituality. I don't abide with telling kids what they should or should not believe; I think the best thing is to let them sort through it all (and there's a lot), answer their questions as they come up, and hope that they make the best choice FOR THEM.

Spawn I believes in God, that much I know, but so do I, just not the Judeo-Christian God that looks like an aging wrestler with a gigantic beard. She moves through this world coming from a place of pure love for all living things. She respects other people, nature, and all those who come across her path, whether she actually likes them or not. And that's really all I could hope for as a parent. She and her sister make me proud, even though I have no right to claim pride in how they've turned out.

Pagans are different from other religious types because we don't proselytize. I can guarantee that no witch has ever knocked on your door trying to sell you on "signing up." We don't have buildings with stained glass to advertise our place in the community, and we don't have parochial schools (although I know of a few who insisted on home-schooling their children because they lived in the Bible-Belt, south of the Manson-Nixon line, and they didn't want their kids around that - and I can't say I blame them, but we live in NY). We also believe that everyone is on the path that they should be on at that particular moment. So while I would love for both my girls to eventually embrace their birthright (which is what the Craft really is), it is by no means my top priority. The only things that matter to me are that they love and are loved in return, that they get hurt as little as possible (I'd like them to never get hurt, but life being what it is, that's never going to be possible), to learn from it when they do get hurt, and to find and keep happiness. That's it. No riches, no fame, no glory. Just that they be happy and at peace.

When and if they approach me wanting to know more about the Craft, I will be more than happy to answer their questions and, perhaps, down the road, welcome them into the fold. In the meantime, I told you at the beginning that they were never far away, no matter where they were. That's because, on my altar at home, the contents of which come with me wherever I call "home", are two shells. I picked each one of them up during my pregnancies, and I anointed them and set them on the altar. During the day, they are enclosed in a little red cloth bag that hangs nestled in my cleavage, over my heart. At night, they are on the altar, and when the moon is full it shines in on them through the windows, recharging them. Those shells are my girls, and they will always be with me, no matter where the tide blows any of us.

This is Spawn I in a recent photo. It's shocking that she looks so grown up, since I'm only 30.


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To find out how you can help people suffering from mental illness, and to help get rid of the stigma, please visit The National Alliance on Mental Illness to take the pledge, get involved, and make a donation.

For more information on mental health, please visit The National Institute of Mental Health.

Thank you for reading. If you liked this post, or any other posts, please don't forget to like and share. And please leave a comment if you're so inclined. As you can see, I have no followers - you could be the FIRST! (Who knows, you might get a t-shirt)


Tuesday, August 9, 2016

It's Nothing Personal



Before I get started, let me just say that I have no idea what happened to the formatting on my last post. It's all different fonts, and different font colors, and I can't fix it. Maybe it's black magic from another, less famous blogger. Or else I'm a techtard and I don't know what I'm doing. 

It"s probably the latter.

Moving along. For some reason that continues to escape me, still, people seem to think that when I write something, it's a personal attack against SOMEONE, usually them. 

It's not.

My last post, about Alice (she's in the hospital now, by the way, and has been for a week - I'm hoping she gets better soon because I miss the fuck out of her), seems to have ruffled a couple of feathers in the "professional" community. There are people who think that I was attacking them, their profession, their skills as practitioners of that profession...and it's simply not true. I don't know why these people didn't leave comments, since my comments are unrestricted, but whatever, that's their choice and I respect it.



I don't for one minute believe that anyone on Alice's treatment team has anything but the best intentions for her and I don't believe they want anything other than for her to get better. I just don't agree with the way it was gone about, and I have every right in the world to voice that opinion, here or anywhere else that I feel so inclined. Besides, the post wasn't strictly about Alice - none of my posts are about one thing or one person - it was about MENTAL ILLNESS and the fact that everyone is affected by it. Everyone. I was attempting to make people aware of that, to open the eyes of some who may not be aware that they could be in a position to help someone who's suffering. So if you read it, and you got upset, I'm here to tell you: It wasn't about YOU.

None of my blogs are personal, except for the ones that are about me. And I'm not as passive-aggressive as I used to be: If I really have a problem with you, believe me, I'll let you know about it, and I won't make little side comments in a blog that probably nobody reads. I'll call your ass. 

I wrote about Alice because, as her friend, roommate and fellow traveler on the road to mental wellness, I am not part of her "treatment team" and I have no say in her treatment because of that. I have told the people who ARE on her treatment team when I see things and hear things that "aren't right," but I do that when I think ANYONE in this house is decompensating (a fancy-shmancy term for getting sick). I know that they would do the same for me. But, because I'm on the other side of the mental health line, it's a rare occurrence that anyone listens to me, let alone does anything about it. Yes, it's frustrating. And that's why I write about it. Because there's a whole world of people outside of this house, outside of the "treatment teams" and the professional caregivers, and perhaps if I reach even one or two of those people, and some help is afforded to someone who needs it, that might make a difference.

So. That post wasn't about you, or your character, or your skills, or your abilities. If you were offended, I don't know what to tell you, other than that everyone who reads this blog is free to contact me via email, or to leave a comment on the post in question. Feel free to have at me.


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To find out how you can help people suffering from mental illness, and to help get rid of the stigma, please visit The National Alliance on Mental Illness to take the pledge, get involved, and make a donation.

For more information on mental health, please visit The National Institute of Mental Health.

Thank you for reading. If you liked this post, or any other posts, please don't forget to like and share. And please leave a comment if you're so inclined. As you can see, I have no followers - you could be the FIRST! (Who knows, you might get a t-shirt)


Saturday, July 30, 2016

Go Ask Alice


As many of you already know, I currently reside in a community residence for people with mental illnesses. I have a co-occurring disorder: addiction along with major depressive disorder, post-traumatic stress disorder (PTSD), anxiety disorder with panic disorder, and trichotillomania (trik-o-til-o-MAY-nee-uh) (a disorder that involves recurrent, irresistible urges to pull out hair from your scalp, eyebrows or other areas of your body, despite trying to stop). That last one took a long time to admit, but it's not the end of the world. Fortunately, I don't have any diagnoses that involve psychotic features. But one of my best friends does.

To protect her anonymity as much as I possibly can, I'm going to call her "Alice." She was diagnosed with schizophrenia in her second year of college. She's now 38 years old. We've known each other for three years, and lived together for two. Of all the people I'm friends with (and I have a lot of acquaintances, but not many who I count as friends), she's the most generous, thoughtful, funny, enthusiastic and supportive. I can always count on Alice to chill with me when I'm feeling blue, binge watch entire seasons of our favorite television shows (currently "Salem," we're on Season 2), co-sign my bullshit when I say that cake I bake myself has only 100 calories per (very large) slice, and tell me when my ass looks fat in a particular pair of jeans. She's a gem of a person. I've watched her struggle, and she was getting there. She was working and preparing to move to the next level of housing in this agency (the apartment program, where 3 women share a house, each with their own room, and no staff on site except for a few times a week). We've supported each other along the way, and she's just as happy about me moving to my new place (SPA housing, which is a little bit less intensive than the apartment program but not entirely on my own) as I am. 

But here's the thing with schizophrenia, and many other mental illnesses: you just never know when the shit is going to hit the fan. 

A few weeks back, Alice's medication regimen was changed. She'd been super, super sick and in the hospital for a few months (this was last year). While she was there, they put her on a completely new lineup of meds. When she got home, she was still a mess, but then, one day, out of the blue, the "Old Alice" emerged, and it was a joy to behold. She was absolutely fine. So why the doctor decided to ditch one of the meds that had gotten her back, I do not understand. That happens a lot when people with these illnesses manage their own meds - we think we're better, so we think we don't need the meds, when meanwhile, the meds are the reason we're better - but for a doctor to do it just baffles me. 

In the weeks following the change, I told staff repeatedly that I thought Alice was acting "off." She was just not herself, and it was clear that something was not right. I know that I'm not a psychiatrist or any kind of mental health professional, but I've been her roommate long enough to know when something is going on. Alice, of course, said she was fine. She always says she's fine. But she wasn't.

For the past 3 days, the girl has been gradually declining to the point where she now has almost no grasp on reality. She's talking to herself, in gibberish, she's singing to the paint, she's not sleeping. She had to quit her job. All of the staff here NOW agrees that something is wrong. Everybody thinks she needs to be hospitalized, except for the doctor, who says no. The same doctor that took away the medication that had made her stable in the first place.


Here's my thing. If we live in a house where there is staff in place to keep us safe, then shouldn't it ultimately be the decision of the staff whether or not Alice goes to the hospital? Or, at the very least, to the psychiatric emergency room, where she can be evaluated in person by a physician? Because her current psychiatrist has made this call based entirely on one telephone conversation, and not even a conversation with Alice, but a conversation with a staff member.  I mean, the girl hasn't slept in three whole days. I feel like, at the very least, they should bring her to the ER, sedate her, and force some rest on her poor, tired body.


The auditory hallucinations are probably the scariest thing, and they're the most common symptom in schizophrenia. The goal is to not only reduce the occurrence of "the voices," but to also teach coping mechanisms and reinforce that the person doesn't have to obey, or even acknowledge, the hallucinations. But I can't talk to Alice right now, because Alice isn't there.


It saddens me that her own doctor is so very adamant that she remain outside the hospital. I know why he's doing it - this particular doctor doesn't like to have any of his patients hospitalized, because it will reflect poorly on his choice to change the medication regimen that was working in the first place. Also, Alice is one of his "stars," because she was doing so well. But at what cost?


Whether you realize it or not, you know someone with a mental illness. We all do. Every last person in this country is affected in some way by mental illness, and we need to educate ourselves. Alice needs a voice right now, since her doctor doesn't seem to want to use his on her behalf. I am grateful that the staff at this house sees the need, and will probably just take her to the hospital by the end of the day. But how many are out there right now, alone, singing to the paint and not being heard? We all need to stand up and use our voices so that they can be heard.


For more information, please visit The National Institute of Mental Health's page on schizophrenia.  And for ways you can help to end the stigma and help give all mentally ill people a voice, please visit the National Alliance on Mental Illness and see how you can get involved. If you won't do it for me, do it for Alice. Or for the Alice that you may not even know you know - and love.