Shmookitty's Updates

Back after voluntarily silencing myself for 24 hours. Bipolar is out of control and I’ve been very symptomatic.

Insomnia is hell. Last night I only had two hours sleep. Have been up since 1 am.

I dont know whether the bipolar symptoms come first, or the insomnia sets off the bipolar. Probably both.

I see my pnurse on Thursday and am gonna ask her for some low dose PRN Ativan. I’ve been on twice daily Klonopin for extended periods without tolerance or addiction.

Tried other options and am starting to feel helpless. I know many of us struggle with insomnia. Totally sucks. I’m already totally worn out from the sza…

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Formally gave up my drivers license yesterday. Someone who is as low functioning as I am, with multiple serious psych diagnoses, has no business driving.

Our DMV allows us to apply online to surrender a drivers license and get a regular ID card through the mail.

I feel very at peace with this decision.

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Oh…I feel so ashamed. That’s why I made this thread, cause I need someplace here to get this stuff out.

It’s no secret here that this has been a horrendous year for me. My mental heath was already fragile, but my husband of 21 years got VERY sick in the spring. Had a couple of really close calls that could have left me widowed. That blew up my symptoms even worse.

Anyway, there’s been four times this year that I’ve narrowly escaped going inpatient. I have been feeling really insecure and scared about this.

Today i researched the specifics of my hospital’s psych ward. Discovered that their ER has an 8 bed special unit for stabilizing psych patients. Which made me feel better that a) there’s a place where a psychiatrist is always available, and b) maybe I could get sufficient care if I have yet another emergency, without being admitted.

My mother called to check on me since the last 5 days have been horrible again. I told her I was slightly better, and that I felt a little more secure now that I know my emergency and inpatient plans of action.

She went OFF. Completely melted down and panicked and yelled at me. Dont even THINK of going to the hospital! It will just be really expensive and you can’t afford that, and they will undo what (my psych nurse) has in progress, and you’ll come out much worse, and it won’t help!! You DON’T want to go there.

Gee, thanks, Mom, like I’m not already frakking ashamed of how low I am right now and how I can’t come off weekly psych nurse visits for almost two effing years…

I just want to cry. :pleading_face:

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I’m sorry. My husband won’t allow me to go to the hospital. If I feel that bad, he wants me to not tell so I can stay home. It’s hard when others don’t understand.

I hope you can make it until Thursday, but if you can’t, I support you and understand if you show up at the ER

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My bipolar symptoms are out of control too @anon28552576

I texted my doctor and waiting for a response.

I really don’t want to end up in the hospital

I hope you find some peace soon

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@LilyoftheValley
@Wave

Thank you so much. I knew if I got that out here, people would understand.

It means so much to me to have both of you supporting me here. :hugs:

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@anon28552576

I’ve been very flat myself for the last month or two. I’m sorry to hear you are struggling. Stay close to this forum and try to remain positive.

These afflictions can be like rollercoaster rides…but eventually you do hit some level track. :slight_smile:

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Thank you @Patrick :blush:

Sorry to hear you’re in a down place too. Hope we both can find stability again soon.

I sent my mother a carefully thought out email. I feel better for having done it. I usually just sigh and shut up when she’s like this, but I guess I just hit breaking point with her.

Shes in such denial about the severity of my illness. That doesn’t help me at all. If she wants to support me, she can’t expect a candy as sed glazed donut fake version of me. This is reality. I can’t pretend to be fine when I’m not.

I actually see it as progress on my part to assert what I need and what is not at all helpful.

Signing off for the night. More hugs to all of you. Thank you again. I love this forum.

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Um, whut? I wouldn’t dare say anything of the sort to Mrs. M. (my wife). She’d yank my nardz off and feed them to me. Frealz.

There’s no nice way to say it, so I’ll say it: Your mom is a nasty ho-bag. I’m sorry you have to put up with that. I’m also concerned that you don’t have adequate insurance in case you are hospitalized and get a bill. That’s not good!

Hoping you feel better Shmoo.

:heart:

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@shutterbug

My mom is not really a bad person, she’s a Pollyanna who is in denial about how much worse my mental illness has become.

She was pretty awesome when I was diagnosed with multiple personality back in the early 1990s. Drove me to my pdoc biweekly and to a weekly hospital support group for DID patients. Was the only one who visited me in the three weeks I was hospitalized, and came almost every night.

I talked with Chris last night after I posted here. We decided that we kind of understand where she’s coming from, feeling out of control, and confronted with the reality that my illness is so bad.

I was in biweekly pdoc treatment for DID for several years. Every penny of it was self pay out of my trust account set up to pay for college. I couldn’t begin to drive myself there, so she always took me. She took me everywhere, as I was way too incapacitated to drive.

Then I actually had 5 years of relative “stability.” I held a higher level admin assistant job for 3 years, and divorced my first husband after 10 hellish years. She started to relax a bit that everything might be okay.

I had moved out from my husband in February 2002. Had met my current husband online on hockey message boards in 2001, and we had escalated to long distance romance before my 6 month waiting period passed where I could officially file for divorce.

I spent 11 days with Chris in Calgary in July 2022, and in August announced I was engaged and immigrating to western Canada. I wasn’t even divorced yet.

She was confused, but didn’t protest or try to stop me. My MI was in remission and I hadnt been diagnosed sza until early 2015. So she was worried but quiet about it.

My mental illness blew up again in late 2006. I was soon mostly out of work because I couldn’t hold my sh it together long enough to stay employed.

With the Canadian medical system, I never got the psychiatric care I desperately needed. So I just kept getting more and more psychotic, all the way on the other side of the country and up on the Canadian side of the border. That must have been really hard to watch, especially from that distance.

Then when I came back, I was even way worse than that. I was getting outpatient psych care from a teaching hospital. The revolving door of resident doctors never diagnosed me sza, but they pumped me full of drugs that never helped. At one point I was on 7 psych meds and still completely psychotic. Again, she felt helpless. I was geographically only 2 hours away, but I had pretty much lost all sense of reality.

Then the sza diagnosis in 2015. And you have all seen that just keep plummeting.

She thought things were bad in the 90s…now I had all those problems again, plus sza. We have a very small family - there’s just my mom, sister, and me from my family of origin.

If I look at it from her perspective, I’m sure she feels completely helpless and confused as to how I’ve been in weekly care with a great and dedicated pnurse for almost 2 years, but am still trying to get the right med cocktail, and I have never been worse than I am now.

She feels helpless. I think she’s trying to kid herself that I can still recover. But if I go back to the hospital like I did in the 90s, she feels like I’ll be totally lost again. Can’t be in denial about how much worse things are if I land at the end of the line in a locked ward again. That has a way of smacking everyone sober.

I guess you can probably relate if the same thing happened to your daughter and she was so far away in a different country and not getting help, then she was too far gone to help once she came back to the same state.

This is already horrendously long. But I’m starting to sober up from my latest string of rapid cycling, and I’m seeing things from her side. Obviously I am not doing it on purpose, but I’m her firstborn and have been putting her through hell since I first entered treatment in 1987. And I have never been worse.

About insurance, Chris works in a call center at the university hospital, and I have stellar insurance with a reasonable out of pocket maximum. A hospital bill would suck, but it wouldn’t send me into bankruptcy either. She paid $30k out of her divorce settlement when I was inpatient in 1993, so the prospect of 2023 dollars must scare the crap out of her.

Sorry so long. No one is gonna read all this, lol!

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Sorry to hear that things are so rough right now

You have a lot of strength to deal with all this

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@Joker
Thank you, my friend! I’m beyond happy that you’re doing so well now. Gives me hope.

Hugs to you and Mason. If ya wanna put a Mason pic on my thread, I wouldn’t mind… :hugs: :blush:

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That’s just adorable @Joker.

:heart:

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@Joker

Oh my goodness! And a tummy one too! Thank you! He’s a mood brighter first thing.

Well, it’s actually 11 am here, but I finally crashed after days of insomnia, so it’s first thing. Lol

If I lived in your neighborhood, I’d carry dog treats in case I bumped into Mason, and I’d treat you to a pastry and a cuppa. :blush:

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Smooth kitty I’m so sorry that you can’t sleep. I understand your problem better than most folks cause I had really bad insomnia for 20 years on Ziprasidone but now one year after dropping that pill I sleep like a baby. I cannot advice with what to do but I’m sure you and your doc will find a sustainable solution to your insomnia problem.

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Oh, we’re keeping that one.

:grin:

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Lol @shutterbug

@Ghosts
Yeah I’m on 160 mg of ziprasidone, and may have to go up again.

When i was on it in 2012, I couldn’t stay awake! Now I can’t sleep! Same med, same dose. But different cocktail so maybe that matters. :blush:

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There are just as many drug reactions as there are people on the surface of the earth and besides I was on 240 mg. Ziprasidone most of the time.

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I may be headed there too! We’ll see. This is my 7th day on 160 and I’m not impressed yet. It’ll be a good med, but I am already prepared to go over the FDA max of 160 that I’m already on.

My pnurse is reassuring me I’ll be okay, and I need a high dose of anything because I’m “very complex.” :wink:

I see her every Thursday, so we’ll see if she bumps me up again. I definitely need a sleep aid tho.

I just want to feel better. I know it will never be perfect, but better is all I’m asking for. :blush: