Saturday, March 31, 2012

Jonathan Harnisch on Twitter

Dear Readers,

If you're interested, I'm adding my Twitter info for Jonathan Harnisch.

My bio [April 1, 2012] currently reads:

Jonathan Harnisch


@jwharnisch


2012: Recovering schizophrenic, accomplished writer, producer and musician, who blogs and podcasts about mental illness, New Age ideas and transgressive fiction.

2013: Celebrated Schizophrenic Creative Artist—Porcelain Utopiawriter, producer, musician, developer, blogger & podcaster; an evolving process of consciousness.

http://www.twitter.com/jwharnisch


Sincerely,

Jonathan Harnisch

Motivate Others

Via Scoop.it - Motivational Quotes and Images

If your actions inspire others to want to make more of themselves you are certainly doing the right thing.

Motivate Others!

Friday, March 30, 2012

To Be Still


The soul is the innermost being of man himself.


The soul is contacted when one learns "to be still."


If one will use his power of thought to become tranquil,


he will begin to be instructed by the God Source.


Jonathan Harnisch

Mental Health in Athletes

Fears for top athletes' mental healthWCBDBy: | AP WELLINGTON, New Zealand (AP) A leading New Zealand sports pyschologist believes mental health problems among professional athletes are "a great untapped well," and sports leaders say more should be... Via www2.counton2.com


March 2012

Jonathan Harnisch

Thursday, March 29, 2012

Schizophrenia Today

March 29, 2012



I'm sorry for the negativity but today and having schizophrenia has plain sucked.


Jonathan Harnisch

Letting Porcelain Utopia Go

UPDATE: March 29, 2012


Twitter: @jwharnisch



http://www.twitter.com/jwharnisch


"I'm considering letting my 1-year-old "baby" Porcelain Utopia: http://www.jharnisch.com/ go. I'll keep it online but going from 225,000-1 Million hits/day to 50-200. It feels like I perhaps lost my momentum? April 1st will be 1 year. 26,000,000 + change hits. But either way, it's fair enough. Did well. Hard to let go, but health seems to be declining as well. Love to you all."


Jonathan Harnisch


P.S. Already, I've been receiving many comments, Twitter DMs, Facebook PMs and e-mails since posting this on Twitter earlier this morning, reaching quite a number of you. Thank you, I will do my best; maybe to just slow it down a bit. I might benefit, in this case, to simply take care of myself first, if that makes sense, before Porcelain Utopia.


Warm regards to all of you...


—J.

Wednesday, March 28, 2012

Friday, March 23, 2012

Thursday, March 22, 2012

Porcelain Utopia » The Schizophrenic Lens: Angel-Demon-Human Dichotomy

Via Scoop.it - Porcelain Utopia

Demystifying Mental Illness from the Perspective of a Survivor...

Via www.jharnisch.com

Chevys, Fords, and BMWs

My wife, Maureen, posted the following blog on her page at http://www.maureencooke.com which is another terrific page, a lot of mental health insight, from the perspective of being married to someone with schizophrenia.

I'm taking more time off on this end, as I write my memoirs and some other "bigger" projects. -JH

<a class="StrictlyAutoTagAnchor" href="http://www.jharnisch.com/tag/crazy-people" title="View all articles about Crazy People here" >Crazy People by Maureen Cooke here" >Maureen Cooke:


http://www.maureencooke.com


Bay City, Michigan. 1958.



1958 Edsel: (c) www.free-images.org.uk

The Ford Motor Company released the Edsel, whatTime Magazine named one of the 50 worst cars of all time.


We are living on Litchfield with Grandma and Grandpa Foley. I don’t like living there. I like having my own house, my own room. I like making noise if I want to make noise, and Grandma and Grandpa Foley don’t like noise. And they are always cold, even in the summer, so they always have the furnace going, and I always have prickly heat.


But I like the kids on the block: Sean Finnegan, whose mother has bleached blond hair, owns a zebra-print chaise lounge, paints her nails rose-pink, and talks on a red telephone. She doesn’t even have a party line. And I like Kevin O’Brien because he lives next door to the funeral parlor, and the funeral parlor porch is the best place to play in Bay City.


And I like the uncles, who come over and drink with Grandpa Foley and Wight Dad. There’s Uncle Jimmy and sometimes Uncle Bob, whose head always looks round to me. I haven’t seen him in years, so I have no idea if his head was indeed round, but that’s how I remember him. He’s married to Aunt Joan, who’s now a friend on Facebook, and is an amazingly hot-looking 80-something. She attributes her looks to her smoking – says it kept her thin.


Uncle Jimmy’s married to Aunt Lil, who was always my favorite aunt; she lives across the street in a brown, frame house with a wrap-around porch. The house was meant to be an apartment, so there are three separate entrance doors, which, when I’m 6, I think is the neatest thing there is. And when Grandma Foley starts complaining that Aunt Lil can’t keep her house clean and is “just like the Mexicans” always buying television sets before buying a stove that works, I decide I don’t like Grandma Foley, that she just doesn’t understand fun when she sees it.


But because everyone lives so close, we have Sunday dinner – chicken. Grandma Foley puts the chicken on early in the morning – before 8:00 – and then we go to 9:00 Mass at St. Mary’s. It’s High Mass, my favorite because there’s chanting, and it’s all in Latin, and I don’t understand a word of it although I can say Dominus Vobiscum and Kyrie Elison. I will be 40 before I discover that Kyrie Elison is actually Greek, and I will find this out, from of all people, a convert.


Natural-born Catholics, in my opinion, should know more about the Church than converts, but that is a different discussion for a different day, I was talking about the uncles and Sunday dinner.


We’d eat about 2, when the chicken was done, which meant that when you picked the chicken up out of the pan – and it was always whole-body in those days – all of the meat fell off. Grandma Foley worried a lot about salmonella, trichinosis, and glass shards traveling through your body and piercing your heart.


But finally we’d get to eat: chicken and white bread with real butter – that she didn’t want me to pound, so it would be soft – and frozen peas and sometimes brussell sprouts, and always a pie: homemade crust with a chocolate pudding filling. Sometimes, on holidays, Grandma Foley made a lemon meringue but not for regular Sunday dinners.


And after dinner Grandpa Foley, the uncles, and Dad would start drinking. Usually beer. In the bottle. And then they’d smoke and drink some more. And Grandma Foley and Mom and Aunt Lil and sometimes Aunt Joan would clean the kitchen and mutter to one another about all the drinking because they knew where it was headed.


Dad worked at Ford that year; he was a salesman, and he drove a loaner – and, of course, it was a Ford. A Fairlane. Which would prompt one of the uncles to tell him – jokingly – he ought to work for Chevy because that company knew how to make a car.


The thing is, when people drink, the joking invariably turns ugly.


And my father would say that at least Fords knew how to build a transmission. Hoots of laughter from the uncles: “Yeah, and what good is a transmission without an engine?”


“Fords,” my father would say, “started the auto industry. If it weren’t for Fords, there’d be no Detroit.”


(Dad, there is no Detroit. Not anymore.)


Again hoots of laughter: “If it weren’t for Ford,” they’d howl, “there’d be no Edsel.”


And probably if my father hadn’t been drunk by then, he might have laughed. But drunk people – at least not my drunk uncles, grandfather, and father – have no sense of humor. He would glower at first, then say:


“And if it weren’t for Ford, I wouldn’t have a job. I’d be nothing but a deadbeat like you.” (This would be said to any of the uncles, regardless if they were working or not.)


And then the least drunk of the uncles would say, “You want a real car, one that’ll run forever, get a Checker. Just drop a new engine into it every 100,000 miles. Now that’s a car.”


To which my father would growl, “That’s a taxi.”


Then my Grandpa Foley would chime in: “Ford. Chevy. They’re all the same. The thing is, Wight, you’ve got a job.”


“And what’s that supposed to mean?” my father would yell. “You want me out of here. You just say it. Say it to my face, old man.”


And then Grandma Foley would come into the living room – that crowded, crowded, smoky living room with all the drunk uncles and the doilies on the arms of the couch – and she’d be wringing her hands: “JesusMaryandJoseph,” said as one word, “JesusMaryandJoseph, Emmet. Not again. They have no place to go.”


And my grandpa: “I didn’t say that, you old bat.”


And my father: “You want us out of here, you just say it. You just say it to my face.”


By now my grandpa was drunk and angry: “I want you out of here. You and your noisy brats.”


Which brought my mother into the fracas: “We have nowhere to go, Daddy.”


And my father: “Nobody calls my girls brats.”


And then Grandma Foley and the aunts and my mother would cry because the men were at it again: Drinking and fighting, and why couldn’t we all have a ‘normal’ Sunday once in a while? Like the Jews. You don’t see the Jews fighting.


“Of course, you don’t see the Jews fighting,” Grandpa Foley would yell. “It’s the niggers who fight. Joe Louis. Now that was a fighter. One hell of a boxer.”


And pretty soon, everyone would settle down and start talking about all those ‘niggers’ who knew how to fight, with my mother trying to shush them, trying to stop them from using the ‘n’ word, and then Grandma would tell her to stay out of it, at least they weren’t killing each other.


And all this – all those Sundays listening to the uncles fight and watching the women wring their hands is why I don’t like discussing cars. I don’t want to hear that Toyota is better than Nissan and Honda’s best of all and that the Americans can’t build cars like they used to. I don’t want to hear it. Ever. Listening to people discuss the merits of one car over another makes my stomach hurt.


Until I met Jonathan.


Jonathan had (still does) a 328IS BMW. A little silver car with a black leather interior. The first time I met him face-to-face was at the Long Beach here" >Long Beach Airport – tiny little airport, white stucco with blue trim – but close enough to the ocean that you can smell the water, what some people call the ‘salt’ but since it smells just like the Great Lakes, I think I’m simply smelling water. Or fish.


At any rate, it took four different attempts to fly me from Albuquerque to Long Beach here" >Long Beach. Jonathan tends to be impulsive, so the first time he tried to fly me out, it was 7:30 at night, and he decided he wanted to see me and bought a ticket for a 9:00 flight. We were “Skypeing” with one another. I told him I couldn’t make a 9:00 flight and to cancel the ticket. He told me I could so make the flight, and I said I couldn’t. I’d need to pack, and by the time I got to the airport, it’d be 8:45.


He hung up on me.


The second time he tried to fly me out was over a weekend when I had to work. He told me he’d pay me $1500 and that would take care of the “work.” I explained that it wouldn’t take care of the work because I’d destroy my credibility with the company, and I’d be fired.


The third time he tried to fly me out, everything was working great up until the actual day I was supposed to fly.


He called me that morning, whispering into the phone that he was in the psych hospital, that it was his schizophrenia, which I didn’t believe he had because the only people I knew who had schizophrenia were Michael Meyers from Halloween and maybe Jason’s mother from Friday the Thirteenth. (Odd, how I forgot that Uncle Lanny had schizophrenia. I guess we remember what we choose.)


Oh, and I knew those people from movies like Awakenings or One Flew Over the Cuckoo’s Nest, who shuffled around the ward, slack-jawed, and drooling, and I’d seen Jonathan on Skype, and I knew he was nothing like that.


So that morning when he called me to tell me he was in the psych ward because of his schizophrenia, I thought he was lying. Not about the psych ward, but about the schizophrenia. I thought he just didn’t want to meet me and that being in the psych ward was somehow preferable. And I thought he told me had schizophrenia because that would be (probably is) the worst diagnosis you can have if you’re mentally ill.


Kind of like the Rolls Royce of cars.


But, just in case, he was telling the truth and just in case he needed someone out there, I offered to still fly out, visit with him at the hospital. He turned me down, said he didn’t want me to see him like that. He wasn’t even in clean clothes.


So, okay. We’d delay our meeting.


He got out of the psych ward a few days later, called me, got me another ticket. The plan was to fly out early in the morning and fly back home that evening. That would work fine. We were getting along online and on the phone, but who knew how it would be in person? A day was probably all either of us could take.


We were in agreement about how long I’d stay.


But then he told me he’d send a driver to pick me up.


“No,” I told him. “I’m not flying out to meet a ‘driver.’”


“His name is Alan,” Jonathan told me. “He’s nice. He knows all about you.”


“I don’t want to meet Alan,” I said.


“I could send Guillermo,” Jonathan said.


“I don’t want to meet him either.”


“I don’t drive,” Jonathan said.


How could anyone in Southern California not drive? Jonathan explained that his Tourette’s made it hard for him to drive.


“Well, I still can’t have somebody I don’t know pick me up. This is already too scary for me.”


Finally, Jonathan agreed to get me. He told me to look for a silver 328IS BMW. Meant nothing to me.


I said, sure, is that like a big car, a small car, a what?


Small, he said.


“Like a sports car?” I asked.


“Two-door. M package.”


Still meant nothing to me. Figured BMW was like a Lexus or maybe a Ferrari. Expensive, I figured. And probably fast.


Night before I was to fly in, I went to Wal Mart, bought a pair of open-toed, high-heeled sandals. Jonathan had told me he liked feet, figured I’d get something pretty to wear.


I should have gotten something comfortable because there are no direct flights from Albuquerque to Long Beach. You have to fly out of Sky Harbor in Phoenix, and Sky Harbor is a very large airport, which means you have to walk really far to catch a connecting flight, which I could not do in those open-toed, high-heeled sandals. I had to walk barefoot, carry the shoes.


But still I made the flight, my heart pounding. Before I’d left, I’d confided in my friend Bridget, told her how terrified I was. She said, “What’s the worst that can happen? He doesn’t show and you’re devastated.”


Thank you, Bridget.


The plane from Phoenix to Long Beach landed. I put on the shoes I couldn’t walk in, got off the plane, and checked my phone: Jonathan had texted he’d be late.


I knew it I knew I knew it. He wasn’t coming. It was all a big joke, get me believing him, and then just leave me at the airport. I started to tear up.


He sent me another text: About 5 minutes out. Look for a silver BMW. 328IS.


Like I knew what that was.


I went to the front of the airport, stood around feeling self conscious, feeling sick to my stomach. He was lying to me. I knew it. I just knew it. He wasn’t coming.


And then the 328 pulled up. A silver hatchback. Looked like a Mazda or Subaru to me. Besides, what difference could it possibly make what kind of car he drove? As long as it ran.


He got out of the car dressed in a white t-shirt,  striped pajama bottoms, a navy blue sport jacket, and a turquoise, stove-pipe hat. He looked exactly as he had on Skype – eccentric and endearing. He took the suitcase out of my hand, wrapped his arms around me, and whispered: “See, this isn’t weird.”


No. It wasn’t weird at all.


Until I came out two weeks later, and he decided that since he had to go to the hospital to get his Lithium levels checked, and he didn’t want to take a taxi that should drive the 328, and although, to me, the car may have looked like a Mazda, I was aware that it was a trifle more expensive than one, and driving it didn’t sound like that much fun to me.


What if I did something to it?


For example, what if I bottomed out when pulling out of the garage? What then?


“Uh,” Jonathan said, when I did exactly that, “this car’s got a pretty low under carriage.”


“Okay,” I said, then turned onto Cherry, which had a great big street sign, screaming: DIP.


Bottomed out again.


“Shit,” I said. “I’m sorry.”


“It’s okay,” he said.


“I think you should drive,” I told him. “I’m ruining your car.”


“No, you’re doing fine.”


He was being polite. I wasn’t doing fine at all. I didn’t know where I was going, and I was terrified I’d run into something. At least, I knew how to shift. At least, I wasn’t stalling out in first or grinding the gears. At least, I had that going for me.


But still getting to St. Mary’s was no fun. I had no idea where I was going, which meant I was driving really slow, and the people behind me began honking. Plus, there were one-ways, and although I could see the hospital, I couldn’t figure out how to get there.


Eventually we did. We pulled into the parking garage. Keeping it in first, I climbed floor by floor to the top where we finally found a parking space. I pulled in, felt a slight lift to the car, thought nothing of it.


We found the lab where Jonathan needed his Lithium levels checked, came back out, got in the car, put it in reverse, and backed up.


There was a horrible sound of ripping metal.


“What was that?” I practically screamed.


“You tore the grille off,” Jonathan told me and began texting his old girlfriend (or rather friend with benefits, as he referred to her.)


“I did not tear the grille off,” I told him.


“Yeah, you did,” he said. “I’ve done it before. I know the noise.”


Still, I didn’t believe him. I got out of the car and checked. He was right. I’d somehow managed to park on top of the cement barrier (that was the slight lift I’d felt), and when I backed up, that cement barrier had torn off the grille.


I’d done exactly what he said I’d done.


I climbed back into the car; he was still texting that friend with benefits. I laid my head on the steering wheel. How in the hell could I afford to fix a BMW?


I hated the car. It was cursed. I was cursed. I thought back to all the uncles. No wonder they drank.


Cars.


They were nothing but a gigantic pain in the ass.



<a class="StrictlyAutoTagAnchor" href="http://www.jharnisch.com/tag/crazy-people" title="View all articles about Crazy People here" >Crazy People by Maureen Cooke here" >Maureen Cooke:


http://www.maureencooke.com


Jonathan Harnisch

 

 

 

Divine Love

Divine love brings exactly what you need to experience and progress in this moment.


—Kelly Howell

Wednesday, March 21, 2012

Porcelain Utopia Mobile Site

PU 1 HEADER


Re: PORCELAIN UTOPIA MOBILE SITE: WEEVER APPS


Providing Exceptional Service for Porcelain Utopia on Mobile Devices


Dear Readers,


Mobile Site Viewers—this is why!




Weever Apps


http://weeverapps.com/


Create powerful web apps, zero programming required!



And it’s free!


I just wanted to write an article, a blog post, as I’ve been thoroughly impressed with the traffic I have been able to drive to Porcelain Utopia via the mobile app in just under a month (thus far in March: 10 million hits). It’s phenomenal. And it really boils down to the fact that Weever provides a free app service that does have professional [paid] subscriptions, available, but as many of you, my following here on porcelainutopia.com / jharnisch.com might feel that your own personal website could use a better following, increased audience, or revenue, even just easier access to a WordPress-powered site on mobile devices—I have learned through other free services like Google Analytics that most of my readers these days log on to my website on mobile devices.


While I personally don’t care much for going on the web on my iPhone, I felt I owed it to my audience (and owing no money to Weever Apps, which helped;  I am extremely low on personal finances) but once I saw my site on my iPhone for the first time, I thought, “Whoa! It’s not auto-formatted for mobile devices as I thought it would have been like with Blogger and some other free websites. I ran a quick search on Google, for a plugin for WordPress that would provide an easier-to-read interface on mobile devices, and bang! There was Weever (http://weeverapps.com/) and it was free to try, so I tried it. I love it!


Having had programming skills since the second grade on the old Commodore PET computer, Weever requires no programming skills, and it literally took me 5 minutes, tops to set the whole mobile site up, mobile-friendly, and free, as is my art, and all that I do, I imported the ShareThis (http://sharethis.com/) plugin—again, seriously easy, and both companies provide outstanding customer service, if needed. Combined, these services have helped me incredibly as on occasion I will have a few questions, and with my illnesses, like Tourette’s and schizophrenia, it’s often difficult for me to get a sentence out, or communicate (on the phone, for example). I prefer email and both services have email support, with nearly instant response time. I wanted the option (and free!) to allow my audience to share my material across the web, and as it turns out most of my audience, comes from StumbleUpon: (http://www.stumbleupon.com) “the easiest way to discover new and interesting web pages, photos and videos across the Web”—via mobile devices, thus through Weever—


Often Porcelain Utopia will receive 225,000 hits with an average page view per hit being 5+. I think that it’s likely because I post material about so many different parts of me, artistically, whether it’s just a quote, a photo, a novel, song, movie, or a written blog. But the key, for me is to not be focused on the hits—it’s a matter of creative expression, and that being said I present my honesty and just 'lose the fear' of how my audience might respond, or not. I’m usually pleasantly surprised, the more honest I am, I’ll often think, 'Oh this is not 'good',"but I post such material anyway, and as they say, you never know what’s going to go ‘viral’—so I’m guessing that Weever has their own analytics service, but whatever the case I thought I owed it to the team at Weever to tell them thank you, you, with all the other free and easy-to-use services, from WordPress itself, to StumbleUpon, ShareThis and Google Analytics—If you want a site with an audience, while all I had wanted at first was to express myself, maybe reach just one person, and now I have over 25 million hits here on Porcelain Utopia and it’s not even been a year. I speak honestly, I use Twitter—over 12,000 followers (again Twitter is free, Facebook, and Google+, too--)


I just do what I do and Weever etc., has helped make it a cinch, altogether. To those who want a well-read site, who have perhaps have little or no experience, be honest and “real” in what you post—do your research, of course, learn from the pros, as they say, and use what’s already there—as most of it is free, at least to try! Weever, you are “responsible” for this last successful month, of “Wow!” hits, in particular.


I’m thinking I’ll write you through customer support and let you know about this post, as I am likely going to be “endorsing” (if that’s the right word)—giving thanks and due to my large audience now, to give a public thumbs up! to those (people, non-profits, and companies) who deserve it, and Weever definitely does!


Weever, if you do read this. Thanks so much! It does seem you are pioneering this mobile WordPress site phenomenon! As I often say these words, “You Rock!”


P.S. Just so you know, (Weever) if you would like to use this blog post, in any way—I’m a writer, but not 'the Best Writer in the World'—if you feel this blog post could help your company get into the hands of other bloggers, please feel 100% free to share or use my words, in your ads. There's no need to hide my name, etc., you did not ask me to blog anything about you—so I, too, hope this was “OK” that I even mentioned you, I just though I’d give credit where credit is due! And well, it’s overdue! Thanks again!


Sincerely,


Jonathan Harnisch




[caption id="attachment_8852" align="alignleft" width="125"]Porcelain Utopia Porcelain Utopia[/caption]

 

Monday, March 19, 2012

Our Need To Be Honest >> Porcelain Utopia


Our Need To Be Honest



How Are You?


Broken. Useless. Alone. Clueless. Confused. Betrayed. Fragile. On the Verge of Tears. Depressed. Anxious. About to Break Down. Pathetic. Annoying. I'm just a burden. Distant. Lonely. Bitter. Heartbroken. Rejected. Crushed. I Feel Like I'm Going to Just Fall Apart at any Moment. Empty. Defeated. Never Good Enough.


Fine.


Jonathan Harnisch

Saturday, March 17, 2012

Hyponatremia

RE: JONATHAN HARNISCH - DAY ONE: HYPONATREMIA

I thought about whether or not to blog, though to start with my definite need to thank you all for your letters of support and encouragement since yesterday's brief 'getting the news' blog. This does present an open door to unselfishly keep this topic of Hyponatremia or whatever it’s called as an open topic for this blog, this website—after all it is, of course, a perfect opportunity to blog but also to heal and to overcome. It’s perhaps relevant to the mental illness aspect as well as the “overcoming obstacles,” and documentation, of you will, of Porcelain Utopia; how I might get through this diagnosis by seeing the negativity as a challenge, an opportunity, and as something to share—adding more to the story of this complex, sometimes a mean, jerk, that I can be, an unpredictably a good person at times, and one who has and continues to go 'through the ringer,' as I call it, over and over again, perhaps more than one who is not diagnosed with the devastating illness I have been given—not to diminish another's so-called simple anxiety and what-not—as I say, it’s all matter of degree and how the individual perceives his or her own condition, situation, or stress.


I, of course, must continue to walk my talk. My whole mindset of this, forgive my language, but this crap, this “detour” in my own, already f@#ked up life, yet I do—I really do tend, these days, to grow through all of this—this life situation—as seeing more of the positivity and opportunity though the overall 'Utopia.' What I refer to as the tagline of PU reads: The 'Angel Demon Human dichotomy,' to me, it means something to the effect as I publish erotica and hard core rap, then all off a sudden, I seem to reach Zen, and angel-talk, then I vent, I get upset, I hallucinate, then I reach bliss—the rollercoaster of it all. Think about it: a real bad example comes to mind but take the nicest, good-natured person—for sake of this example, let’s choose the altogether/could-do-no-wrong Tom Hanks—let’s imagine (the idea) that in his private life—(even better, the Dalai Lama—!)—Let’s assume he’s got some kind of skeleton in his closet as we all do. He might dress in women’s clothing and has very explicit “affairs” in his personal life—OK? Maybe he does not, but, I have skeletons—I believe at this point they’re all public knowledge now, because I had been so closed up that it bothered me, and I don’t need to keep a job that’s on the line if I “tell,” I have nothing to lose—I have the 'ticket'—the opportunity to literally be that guy who can, but who I feel does, open up 100%. After all, I was addicted to crack cocaine alone: I therefore have (yet luckily I have no STDs etc., or unplanned children—but yes, I did all those things... I behaved 'like a crack head.' I was sure lucky as all hell I have no criminal record, etc., but I—let’s just say for now—I did all that. And lived to tell. Prostitutes, gambling, and drunk driving. I made out OK overall and have never injured anyone. I bottomed out, and learned my lesson. I changed and grew, and continue to do so. I am a writer (even the fiction) a lot because my experiences in these last 36 years have been unbelievably mind-blowing.


Nonetheless, this particular post is/should be perhaps more centered on my intent: about this new diagnosis, though Hyponatremia is more of a physical disease; this new battle in my life. Yet, let’s hope, as I do hope that it actually islikely nothing, after all…” I really do not have the drive this morning to write, nor to even be on the computer but I feel I owe it to you, and to update you all—all 30,000 to 300,000 people per day, to perhaps inform, and document the best as I can through this new process.


First hearing the news, then the panic process, the grief, to wanting to just 'die now and get it over with.' I’m sure my attitude will change over time, and as I’m likely destined to the ICU unit at some point, tests after tests, complex and frustrating for both doctors and patient, as the treatment involves a lot of trail and error aspects, testing, retesting, analysis, and decicions. The Mayo Clinic, my sociopathic family thus getting involved—though I no longer have any relationship with them. They simply keep and spend my $2 billion inheritance money stemming from that one forged signature and notary in 2009 which gave them their full 100% control, and this whole 25 million people in my social network—virtual, but it is real: real people. Real interactions; the whole point of the Internet and social networks. This site cost me $30 and zero dollars for advertising—so I do owe it to you and I guess in a way, to myself. I have been up all night reading, taking online crash courses on iTunes U and listening to medical podcasts, learning about all the medical terms, and information concerning this unfortunate diagnosis, which I did sign up for, you know, somehow, 'astrologically,' but I wish I didn’t.


I’m loaded up on prescribed as-needed PRNs/medication—tranquilizers, anxiety meds, even Klonopin—and I am still in panic mode—the whole big picture of Porcelain Utopia and what it means to me makes up my entire life and purpose—I don’t want time away from it. I’ve earned this and deserve it, and you all have sent me about 200 emails through the contact form overnight—mostly complete strangers to me, and a ton of doctors. Thank you.


Following, are some of my initial thoughts and notes. Whether or not this condition is able to treated in the end. I have already gone through a game plan with my wife and medical team: to start—deep breath, positive attitude and only one liter of water per day for 3 days, onto the first blood and urine analysis—boom: done. If I fail, I'll pick myself up, dance the “schizophrenic shuffle” [sarcastic humor] and re-start, re-set, re-group and re-try.


…Getting there, as I can and as I choose.


I had been drinking 4-5 gallons of water per day for the last two years, I am not supposed to drink anything else, nor diet poorly, so I do everything they say and now I have to eat junk food and sugar and not water, but instead sodas, and then do what I have to do: test after test, ICU, Mayo Clinic likely, and then it’s either a day, a week, or a year—who knows—that will end up seeming afterwards as, “Well, that was sure a waste of all our freaking time—”


Initial email:


“Hey Close Personal Friend/Medical Doctor: What do you know about Hyponatremia, without just being optimistic just because we are friends? I have been diagnosed with it, and would like to know of life expectancy and things since I'm not up for another disease (heart and kidney I think, low sodium, drinking too much water?) First they said rid the drugs and alcohol. I did 10 years ago. Then drink as much water as possible. I did that, too. Then lower caffeine. I did. Then sugar and salty foods. Now I'm supposed to eat junk food especially salt, and drink as little water as possible, even add sugar. I'm freaking out like WTF! you know? My wife and all the doctors and caregivers knew these past 2 weeks, and I was just told a couple hours ago, "at the right time for Jonathan since his day was going so well." Have to go in for all these f@#king tests, and sh*t (please excuse my language) I'm just venting because, just g@d d@mn it, you know? Chronic heart and kidney disease? Is that what it is? Can you let me know whatever you know? At the moment, I just want to die—right now—forget the wait time and suffering, yet not by suicide, of course—all my life I had wanted to die, until 2011. Now it’s 2012 and I might get what I had only-before 'prayed for'—just to get it the hell over with. You know? I am sure this is all a semi-normal reaction to receiving news like this. Thank you for hearing me out. –J.”


Immediate Reply:


“Yo! J.—


OK, Here is my advice given strictly as a friend!


Hyponatremia (as I think you know) means low levels of sodium in the blood.  It is important to remember that this in itself is a non-specific finding, meaning that the underlying cause of the condition must be discovered and treated. There are a SH*T-LOAD of things that can cause Hyponatremia. That is why your doctors want to do some more tests, so they can figure out exactly what is going on. Lots of the reasons are harmless and easily corrected, such as drug and diet adjustments. So all in all, I think you should take this seriously, but not jump to conclusions. Once the doctors know what is causing your sodium levels to be low, the treatments will present themselves. This is one of the things in medicine that all patients (and their doctors) hate, having to wait to get to the bottom of the problem. When is your next round of tests? Have they done any treatments so far?


So, in summary, take a deep breath, say your favorite mantra and focus your healing, balancing energy inwards. The whole world is sending healing vibes and love your way—Can you feel it? And that is a good approach to ANY medical question!:)


PEACE AND LOVE. I hope that helps!”


Facebook:


General Note to personal friends who wrote me loving notes: I thank you all:


“Hi Friends: I stayed up all night reading about this BS and talking with my doctor friends. I haven't changed my water intake. Thank you for the posts. I did not know so many cared as you do. Apparently, it’s relatively common (1%) and is in fact low sodium in blood. One of my early Schizo voices said I would die of a blood disease so it has been freaking me out, and still is. I already reversed diabetes, eat no sugar, dropped the caffeine, lost 100 pounds, survived Schizo, severe Tourette, trauma, brain injury, drug & alcohol addiction (10 years in January) overcame cancer in Mexico twice, and I still smoke and chew, and loss of all family, old friends and a gigantic financial fortune! —My old and gone Hollywood and Wall St. life—I did not “sign up” for this. It is frustrating and complicated for both docs and patient with this blood disease, I'm told, and likely I'll end up in ICU unit with 60% mortality rate, as I see it. I read a lot about it and contacted all I could in my social network with my mental heath work online. Basically they all said take a deep breath and stay positive. I slept an hour or two and just woke up. Thx. -J."


Will try to keep you posted. Thank you again for all your support and reaching out.


Sincerely,


Jonathan Harnisch



-via iPhone

Thursday, March 15, 2012

Mobile Update: Hyponatremia

FROM YESTERDAY/GROUND ZERO:


16 March 21012

Just heard news I've some kidney and heart disease: Hyponatremia-good day but was just given the news-total buzz kill-I'm going to die of WATER!??? I was just told about this "at the right time for me to hear"--Schizophrenia, etc., etc., & now this Hyponatremia nonsense-Just in that "freaking out about the news" moment. Yikes have I been thru the ringer.


More Info on Hyponatremia:  http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001431/


Sent from my iPhone


Next Porcelain Utopia Post on Hyponatremia http://www.jharnisch.com/hyponatremia-01/


STRESS: WORRY VS. CONCERN

STRESS:



WORRY=emotional/hurtful


CONCERN=intellectual/helpful


You choose...

Sincerely,

Jonathan Harnisch

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Hope is the Magic Pill >> Porcelain Utopia

[caption id="attachment_11666" align="aligncenter" width="600"]www.porcelainutopia.com www.porcelainutopia.com[/caption]

Re-post from 30 January 2012


CALL ME A NARCISSIST:


♥ Call me a narcissist but I'm amazed I can even write this simple status update-and so much more. ♥ Having a $X,XXX,XXX,XXX inheritance squandered (not by myself), overcome cancer (in Mexico, twice, and still smoke & chew, cancer-free), lost entire family to tragedy, overcome so many disorders (most noticeable: Schizoaffective & Tourette's)-now, resurfacing diabetes-lost 100 pounds (without exercise)-I'm coming on 10 years off severe alcohol & crack addiction. Thank U! That saves me a session with the doc!


I Love Life & All of U! ♥


Thank you to all who took the time to share the good ole Teddy Roosevelt post and the latest "Best Day of Your Life" piece. My audience and the public used to be my worst enemy, now my best friends--all of you, no matter where or who you are--I find it mysterious and spiritual and invaluable that we're all connected in some special way...


My left hand and leg are 100% numb due to low blood sugars (ironically not too high!). I struggle physically, and  dizzy as my illness makes me, as "crazy," eccentric, weird, funny, charming, with my very odd sense of humor, peculiar demeanor, which always seems to change:


"What's Jonathan Harnisch going to do next, say next?"


My Angel-Demon-Human/Inspirational/Sometimes "Erotic"/Transgressive/Being Real...


BEING MYSELF.


...HERE'S ENCOURAGING ALL OF YOU TO OPEN UP.


DON'T LET ANYTHING [AT ALL] BRING YOU DOWN. 


COUNT ON HOPE...


EVEN WHEN YOU'RE OTHERWISE SEEMINGLY


ALONE


IN THE WHOLE ENTERPRISE.


TRUST ME ON THIS ONE.


HOPE


"...It works. It does the trick. It's the "Magic Pill."


Jonathan Harnisch


FB JH pu sig Profile

So Here Goes



Restored Post from March 15, 2012


Blog Post from my wife Maureen Cooke's page: http://www.maureencooke.com about living with someone who is mentally ill.


So Here Goes:


A couple days ago, I posted The Go Ahead, in which I explained that Jonathan had told me to write as honestly and forthrightly as possible and not worry about hurting his feelings.





A dandified Jonathan

So here goes – and know that it’s still hard – because I still worry that some of what I write may,  indeed, hurt his feelings, and I don’t want to do that. And, yet, I would be doing a grave disservice to the credibility of these blogs and what I hope will be the memoir of my experiences with Jonathan.


So big intake of breath here, square the shoulders, raise the chin, and get started:


In July 2010, when Jonathan checked into Colorado Recovery, he was on, what I can only refer to as, a shitload of meds. He was on 3 different anti-psychotics: Geodon, Zyprexa, and Risperdal; he was on an anti-depressant: 80 mg of Lexapro, which in all likelihood, was responsible for the rapid cycling of his moods; he was on a mood stabilizer: Lamictal, a mood stabilizer; a tranquilizer: Klonipin, and, on his own, he was taking Benadryl, generally 10 to 20 pills a day. A few tabs of Benadryl would have helped eliminate the dystonia caused by the anti-psychotics, but in the quantities he was taking only attributed to the psychosis. SeeDiphenhydramine-induced psychosis, if you’re interested in the topic.


The staff at Colorado Recovery was able to get Jonathan on the right meds much more quickly than his doctor here in Corrales would have been able to do, treating him as an outpatient. Reducing psychotropic medication quickly needs careful medical supervision and is really better done as an inpatient. Still, as drastically as his medication was adjusted in Colorado, when he came home in October 2010, he was still on very high doses of Risperdal.


A couple problems with anti-psychotics: They cause weight gain, which in turn causes an increase in blood sugar, which in turn can cause metabolic syndrome. Anti-psychotics may be necessary, but they are not without significant, dangerous side effects.


In addition to the more dangerous side effects, the anti-psychotics can also cause lethargy, and schizophrenia and schizoaffective disorder can cause apathy, so initially, when Jonathan came home, he spent most of his day lying on the couch. Pretty much doing nothing.


One day, I came home from shopping and was carrying in bags of groceries. Jonathan stayed on the couch. He didn’t get up, didn’t offer to help, and, in all honesty, I’m not sure he even noticed I’d gotten home.


When I came into the living room, there he was lying flat on his back, headphones on, staring at the ceiling. He noticed me, took off the headphones, and then said: “I know you hate the apathy. I read inSchizophrenia: A Handbook for Families that it was the one symptom that families hated the most. Well, I can’t help it.”


And maybe I could have been more tactful in my response, but what I told him was, “No. Why would I care if you spend the whole day on the couch? It’s not what I’d do, but I don’t have schizoaffective.”


“It’s a negative symptom,” he told me. “It means I don’t have any interest in anything. And it’s not my fault.”


“Yeah, I know.”


“And you still blame me.”


“No, Jonathan,” I said. “No. I don’t. And the apathy? I couldn’t care less about it. What’s hard for me, what I don’t know how to handle is your negativity. Your assumption that I’m finding fault with you when I’m not. When I’ve never found fault with you. That’s what I have the hardest time with.”


The negativity is closely linked to the paranoia, so that for Jonathan to tell me that he knows the biggest problem I have is with his apathy, he’s making an assumption about me, and it’s an incorrect assumption.


However – and here comes the paranoia – my trying to talk it out with him doesn’t resolve the issue. He thought for the longest time that I was silently criticizing him for lying on the couch. (By the way, he no longer lies on the couch all day. Amazing what the right combination of meds, in the right doses, can do. Western med isn’t all bad.)


And because of the thought problems from the schizoaffective, he wasn’t really hearing me about the negativity. In addition, the negativity so frequently leads to paranoia that when he’s in that space, I can’t reach him.


The problem with the negativity – for me – is that by nature I am a positive person. I default to optimism, to liking people, to feeling hopeful. That is my natural state.


However, if I am around negativity or despair, such as the case with my Luther Dad (I think after my mom died, he sank into despair, which didn’t abate until he himself died in 1990), the negativity gets in. At a psychic or soul level.


If I am around negativity in short bursts, I can block the energy. I can take my mind and emotions elsewhere, but I don’t really want to disengage from my own husband, and yet I can’t afford to let that level of negativity get in. It’s not healthy for me, and ultimately it’s not healthy for him.


An example (and this is related to the medication issue, as well): I have been ill since the beginning of November with a flare-up of Hashimoto’s, which is an auto-immune disorder and which reacts very badly to stress.


And I have had a very stressful week, which began with my inability to get into the safe where I keep Jonathan’s meds. That was on Monday night. The stress that I was feeling about the safe breaking was causing my thinking to deteriorate, which made me weepy. I wasn’t thinking right. And I’d had a misunderstanding with Jonathan; I thought he was ignoring my request to help me try to get the safe opened.


Jonathan’s doctor, in the meantime, and one of his caregivers were wisely advising me to let the safe issue go until the morning. I couldn’t. That part of my brain that could pull me out of my own level of paranoia that Jonathan wasn’t willing to help me was also making me “decide,” as I told both his doctor and caregiver that if Jonathan wasn’t willing to help me get the safe open, then I wasn’t going to replace the meds, as the doctor suggested, or let the caregiver help me in the morning.


I told them both that if Jonathan wasn’t willing to help me, then he didn’t need his meds.


See? My mind isn’t working right. Even as I was saying it, I knew my mind wasn’t working right because Jonathan needs his meds.


Then I decided what I’d do is stay at a motel for the night (I was already in my pajamas and thought that was a good thing because that way I wouldn’t need a suitcase.) Then I thought that checking into a motel in my pajamas was a bad thing, so I figured I’d go for a drive. It was 15 degrees out, and the roads were icy. And a friend texted me ALL IN CAPS to please, please be careful that the roads were treacherous.


It was about at this point that I sat down and cried.


Because of the Hashimoto’s, or something else, it is taking me a very long time to recuperate from that level of stress, so when I saw my endocrinologist the next day, I was still stressed, still weepy, so when she asked me how I was feeling, saying I looked sad, I started to cry.


This is not a doctor who handles crying. She excused herself, telling me she had to check on a client and would be right back. When she returned, she told me that my thyroid levels wouldn’t be causing such emotional lability, and she would prescribe Armour, but she didn’t want me to take it until I coordinated with a holistic psychiatrist.


I felt dismissed and frustrated and a lot like I’d never be well again. I cried all the way home.


When I got home, two of the caregivers listened to me and hugged me and suggested I call my therapist, which I did. My therapist, in turn, suggested I see an integrative physician, who may be able to help me get to the bottom of what’s going on with me.


However, the stress of Monday and Tuesday left me still stressed on Wednesday and a bit stressed on Thursday. I’m not at my normal baseline. I’m limping.


Thursday, Jonathan had a manic episode, which led to his being angry with his doctor and which led to him texting me that she never listened to him, didn’t believe that he needed to increase his meds, and the he didn’t want to see her again. That he was done with her.


It is his doctor’s opinion, and mine as well, that my being ill, especially with my emotions being so out of whack, results in a loss of predictability in Jonathan’s environment and exacerbates his symptoms, and as uncomfortable as those symptoms may be that before Jonathan’s meds are increased permanently, we should wait until I am better to see if that helps bring Jonathan’s symptoms back under control.


My position, just as I already indicated, is that psychotropic medication has serious, dangerous side effects. My own uncle died from a heart attack at 40 because he was diagnosed with paranoid schizophrenia back in the late 50s, when patients were routinely given huge amounts of anti-psychotics, which led to my uncle having metabolic disorder, which killed him.


I don’t want that for Jonathan, and I’m sure his doctor doesn’t want that either.


But when Jonathan gets in that space, it feels to him as if no one is listening to him, no one is hearing how horrible he feels, and there is no way for me, when he’s in that space, to reach him, to reassure him that I do care how horrible he feels, but that a permanent increase in medication is not the answer right now.


I am not opposed, nor is his doctor opposed, to his increasing his meds; however, she (and I) want to make sure that a permanent increase is absolutely necessary.


Seeing Jonathan uncomfortable, seeing him manic and paranoid and angry, is stressful for me. In October, before all this thyroid stuff started, I was able to maintain the equilibrium necessary for me to ride this out – to reassure him without being drawn in to that level of negativity about his doctor.


Now, it’s additionally stressful because it requires more physical energy for me to accomplish that. I won’t see the new doctor until January 3, and, in the meantime, I’m in a holding pattern.


So this morning, when I got up, Jonathan was already awake. He told me he’d read my Facebook post from yesterday, in which I’d written it had been a long day in a long week. Jonathan said, “That was because of me, wasn’t it?”


I told him, “No.”


He then started talking about one of the caregivers and how horrible she had been to him; he called her a name, and I stopped him, told him that I desperately needed a positive day. That I could not go to any negative space today, so please if he was angry, tell me he was angry, but don’t call anyone names, especially someone I like.


“See,” he said. “I knew that post was about me.”


I sat down with him then and explained to him what had happened on Monday, how that had carried over to Tuesday, how dismissed I felt by my doctor, and how hard it was to keep being my own advocate for my health care.


He asked if I were being resistant to the suggestion that I need psychiatric care. I told him ‘no,’ that I’ve been in and out of therapy for nearly 40 years, and that I wasn’t opposed to taking a psychotropic drug if I needed one, but that I wanted to get to the bottom of what’s been going on with me, and that a psychiatric problem, such as depression, would not cause my vision to be blurry and sometimes double, would not cause an inability to regulate my temperature, and that I needed a doctor who would get to the bottom of what was happening to me physically before I would start drugging what I see are the emotional symptoms of an, as yet, untreated auto immune disorder.


So…. what I’ve been going through for the past few months, and what I’ve written here, is what it’s like in thereal world” of living with someone with a serious mental illness.


This is no Benny and JoonThere is no quick fix. No cool music from the Proclaimers. No Johnny Depp doing Buster Keaton impressions. Living with someone with a serious mental illness is hard. It can be done, and people can thrive, but it is difficult; it requires commitment, emotional resiliency, and a tremendous amount of outside support.


So thank you to:


J’s caregivers,
His doctor, 
His therapist, 
and my own therapist.


With their help, with their support, I feel hopeful, even as I recognize I am still out of whack and will probably continue to be out of whack for at least the next few months.


Thank you.


Thursday, March 8, 2012

OVERCOMING ADVERSITY

[caption id="attachment_2009" align="aligncenter" width="535" caption="Demystifying Mental Illness from the Perspective of a Survivor"][/caption]

Difficulties strengthen the mind, as well as labor does the body.


-Seneca




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REACTIONS TO SCHIZOAFFECTIVE DISORDER

Thank You to Healthy Place http://www.healthyplace.com for sharing this insightful video about schizoaffective disorder on your website:



"How My Family and Friends React to My Mental Illness"


[youtube http://www.youtube.com/watch?v=xD0_9Vawffw?rel=0]

- Jonathan Harnisch

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Monday, March 5, 2012

Self Approval


012
As one of my friends posted this morning:

"I Guess I Feel Pretty Super Today!"


I Agree...it's a Great Day Today!

Sometimes this kind of thinking really keeps me going:

"Today I will let go of my need for approval and my need to be liked. Instead, I will choose to like and approve of myself. The people who count (including me) will respect me when I'm true to who I really am."


—Melody Beattie


Sunday, March 4, 2012

Turn it Over to the Universe


"If you turn it over to the universe you will be surprised and dazzled by what is delivered to you. This is where magic and miracles happen."


—Dr. Joe Vitale

Saturday, March 3, 2012

Invisible Children

PU 1 HEADER

Via Scoop.it - Schizophrenic & Caregiver: Featuring Jonathan Harnisch

To see real time reports on LRA activity in the DRCongo, Central African Republic and South Sudan visit: www.lracrisistracker.com To learn more about Invisible Children's recovery efforts in the post-conflict regions of northern Uganda AND our work...

Via www.youtube.com

[caption id="attachment_8852" align="alignleft" width="125"]Porcelain Utopia Porcelain Utopia[/caption]

Thursday, March 1, 2012

TO LEAVE THE WORLD A BIT BETTER

“To laugh often and much; To win the respect of intelligent people and the affection of children; To earn the appreciation of honest critics and endure the betrayal of false friends; To appreciate beauty, to find the best in others; To leave the world a bit better, whether by a healthy child, a garden patch, or a redeemed social condition; To know even one life has breathed easier because you have lived. This is to have succeeded.” 


[caption id="attachment_4257" align="aligncenter" width="192" caption="Ralph Waldo Emerson"]American Essayist & Poet[/caption]

-Ralph Waldo Emerson



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GRATEFUL TO BE ALIVE

‎"By embracing pain, fear, and challenges with gratitude,


I discover the real value and meaning of my life.


I am so grateful to be alive."


-Dr. Darren R. Weissman

This again, is the Best Day of My Life! Please take the time to consider that it might be yours, too.


-Jonathan

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