This is a Really Real Extended Family post.
This is a post about being estranged from birth family.
This post contains politics, differing beliefs, pain of loss.
Today, my Facebook and photo memories were full of pictures with my niece and nephews.
Without planning it, my sister, the kids and I, tended to get together around this time every year.
I had 3 pictures in a row of me holding my first nephew. Each year around his birthday I was lucky enough to see him, and get a picture as he aged.
I had 2 pictures with my niece, a year younger than her brother.
One picture with the youngest, a year younger than his sister.
The last time I saw them was just over a year ago, before the pandemic was even a thing.
We would regularly talk over video chat. My sister lining all 3 kids up in high chairs at the table and sitting the phone where I could talk with them all.
My sister and I have very different beliefs. She is a conservative born again Christian, super into a her MLM essential oils and anti science including vaccinations, and I am super liberal and queer.
We managed to coexist. We avoided those topics. She didn’t seem to judge me for my life and the way I lived it.
As the election got closer, she began posting more and more about her beliefs.
She posted an article that someone connected queer folk to pedophiles. She posted articles against transwomen, and trans rights. She became more verbal with the beliefs that directly hurt me.
I distanced myself more and more, unfollowed her so that she would no longer show up in my feed. I’d occasionally check her page for pictures of the kids. I enjoyed watching them grow.
It’s been 6 months since a video chat. She had the kids call me shortly after my dad died, to give me something to smile about.
She posted and texted me around the time that Trump was getting banned from various social media outlets. Telling me that because of something she posted, they were shutting down her Facebook in 24 hours and I could contact her via text.
I didn’t respond, I knew that Facebook doesn’t give you warning, she was just feeding into the political bullshit.
A few weeks later she was back on Facebook, I knew because she was reacting to my posts again.
I realized I was censoring my posts, not wanting to start family drama, not wanting to alienate anyone, not wanting to call her out on her bullshit.
I added her to my restricted list, she can no longer see what I post. At the same time I did the same with my youngest sister, and made sure my mom was still on the list as well.
I’ve slowly gone no contact with the family I lived with for the first 17 years of my life.
I didn’t make some big announcement, I haven’t addressed any of it with them.
I last heard from my Mom on Christmas, we exchanged 2 or 3 mundane texts. Before that it was Birthday wishes from her.
She’s even further down that rabbit hole of QAnon. Her beliefs aren’t just against who I am as a person, they are downright scary. She jumps from one conspiracy theory to the next, I had to tell her point blank to stop sending me messages about them. It took her awhile to listen.
My youngest sister is doing well, as far as I know. She doesn’t advertise her beliefs so I have no idea where she stands, but she’s so involved with the other two that it just feels safer to distance myself there as well. Every few months she messages to see how I’m doing, but rarely responds to what I say.
It’s painful. The memories are painful. The fact that I have to sacrifice the relationship with my niece and nephews is hard, probably one of the hardest parts of this.
But, I have an amazing chosen family. I am surrounded by people who choose to love me for who I am.
And I’m thankful for that.
Stigma
Work in Progress
This is a Really Real Mental Health post.
This is a Really Real Health post.
TW: Mention of weight, exercise, and food choices, but in a body accepting way.
I haven’t written a long post in a couple of weeks.
Short posts detailing my current day to day stuff have been ongoing.
It’s a different way of communicating.
But less cathartic.
When I’m doing well I don’t feel the need to write the long, soul spilling posts that have become such a coping tool for me.
And I am doing well.
I’m slowly figuring out what is mood and mental health related, and what is habit learned by months and months of being depressed.
I’m working on not judging myself for either.
A couple of weeks ago I got on a scale to see if I was above the weight limit for something.
It’s frustrating that many things aren’t built for someone my size.
But, the truth is, I am bigger than many things allow for, and I’m accepting that it isn’t my fault.
I am allowed to exist as I am, and it’s sad that there are things that won’t accommodate me.
I’ve started speaking up. Letting professional offices, especially those in medical settings, know that they should consider having some seating without arms, seating that will accommodate all body types.
But anyway,
I got on the scale again recently, and realized that even with making conscious food choices, and moving intentionally, I haven’t lost any weight.
And honestly, I felt okay with that.
I’m moving around easier, I’m enjoying the things my body can do for me.
I’m working on stretching and strengthening the muscles and joints that help me get from place to place. I’m working on gaining more mobility,
more stamina.
Some days I’m still sleeping more than I would like.
My mood seems a bit better, and I’m more productive on the days that I sleep less,
but I can’t always get myself out of bed in the morning,
even when I go to sleep early.
And that’s okay.
I’m a constant work in progress.
Pushing myself gently to do a little more than I think I can.
But loving myself either way.
And when I can’t love myself as I am,
I accept myself as I am.
I remind myself of all of the things I have survived and overcome.
I remember that my body does amazing things for me.
Movement helps with that.
Especially yoga,
it helps me get in touch with my body and my mind.
It helps me push just a little bit further.
Also, the videos I’m following remind me that it’s okay to modify things in ways that fit my body and my ability that day.
They remind me that it’s okay to need props and items that help.
They remind me that every body is different,
every body has different abilities.
And that every body takes up space.
At the end,
in my Savasana pose,
they remind me to take up as much space as I want.
To open my body and feel comfortable, instead of shrinking myself.
It pertains to mental health as well.
So often we try to shrink our emotions and our symptoms.
We try to fit into a box created by the world.
Right now I’m feeling that I’m not disabled,
but that I’m differently abled.
Not everyone can open up and share their struggles the way I do.
Not everyone can see their vulnerability as a strength.
Not everyone can change lives by speaking their truth.
Well, that isn’t quite true.
Everyone will change lives if they speak their truth.
But speaking our truth is hard.
Accepting our truth is hard.
Accepting ourselves is hard.
Accepting myself is hard.
But I’m doing it.
And lately,
more than accepting me as I am
I’m loving me,
for who I am,
and for what I have to offer.
It may not be the type of productivity that this capitalistic world sees as valuable.
But I’m learning,
because of those around me,
that value isn’t just monetary.
Where do I begin?
This is a Really Real Mental Health post.
I’m doing some of the things, but there are so many things that are going undone..
I’m going to the gym every night.
But I’m not running the errands I need to run before the sun goes down.
I’m making more intentional food choices.
But I’m eating all day.
I’m cooking.
But dishes often pile up, and my stove top is gross.
I’m getting up early.
But then I’m napping most of the day.
I feel
better
I guess.
But there’s so much I still haven’t done.
The increased dose of my meds are working.
But they aren’t working enough.
Or, maybe this isn’t the bipolar or the depression.
Maybe it’s me?
Where does my illness end,
and my lack of willpower begin.
When does it become lazy, instead of ill.
But, writing this has me thinking.
Maybe,
I’m being too hard on myself.
Maybe,
everything doesn’t have to change at once.
Maybe,
I’ve spent so long minimally functioning,
that I can’t expect to reverse those habits in a week.
Maybe,
it is both mental illness
and me.
And all I can do is make the next right decision.
Keep moving forward.
Picking myself up when I stumble.
Doing what I can and slowly adding more
and more.
Maybe I just need to take it one day at a time.
Maybe I need to be nicer to me.
Just because
This is a Really Real Mental Health post.
I just felt like writing today.
I don’t have any real reason, anything pressing on my mind,
but I felt the need to put fingers to keys.
Earbuds in my ears, gentle piano music piping through.
My writing music.
I woke up before 4 pm today.
I’m already on my second cup of coffee.
I talked to my pdoc, and we discussed options.
Different anti-depressants that may be activating.
We’re restarting my Ritalin, something that the trauma unit discontinued.
And that’s when I started having problems with sleeping too much.
We’re also raising my antidepressant.
Hopefully this fixes it.
It will be a week or two before I know, she doesn’t use electronic prescriptions and will have to mail me a paper script.
She’s the best psychiatrist I’ve ever had, but at her age even a fax machine seems advanced.
She works for herself, no staff, just a tiny little messy office in an apartment building.
Of course, now she’s working from home. All of our appointments done via phone call.
I’m not even sure that she owns a computer.
I’ve wondered what will happen if she dies. Who will inform me?
Will I just suddenly not get the call at our scheduled time, and eventually I’ll find a new prescriber?
Weird thoughts that run through my head.
I’m starting on the preparations for the Florida trip.
Laundry is gathered, list is started, plans to clean out the fridge more completely for trash night tonight.
Tomorrow we will dig out the car and run some errands.
It’s still snowing.
Yesterday it was tiny little flakes, today it’s big and fluffy.
It’s supposed to rain and get icy.
Ew.
Snow days used to be the only days I took a break.
Running around for appointments and interesting things.
Plans with friends, the gym, long walks.
Snow days are just another day now.
I’m such a homebody.
Finding the balance between safety and using it as an excuse is just hard.
I haven’t found that point yet.
This trip is taking me way outside of my covid comfort zone.
But it’s with good reason.
And it will break the monotony that has become my life.
A monotony that so many people feel right now.
Ew.
Today my pdoc called me a lady.
I got that gross feeling that I get when I’m misgendered.
I don’t think I’ve ever told her though.
And by the time I realized I should say something, the moment had passed and we were on to other topics.
It’s hard to know when to say something, and when to just let it pass.
We’re heading south.
I know I’ll get “ma’am”ed and “miss”ed on a regular basis.
I’ll get that gross feeling but just let it go.
It’s easier that way.
I don’t get the weird looks and the lack of understanding.
Side Effects
This is a Really Real Mental Health post.
And a Really Real Medical Health post.
TW: Talk of weight, mention of suicidal thoughts, talk of marijuana use, talk of narcotic pain medications. (Also, side note, sorry I haven’t been as good about TW, I will go back to using them more frequently.)
This is super long, way longer than most of my posts (twice the length it seems), but, writing helps, and I have a lot to say this time. I totally understand if it’s too long to get through, thanks for reading this far.
I need medications to stay stable.
Medications come with side effects.
Side effects make it difficult to continue taking the medications.
I need medications to stay stable.
The Abilify really really helped me. It kept the suicidal thoughts tame enough that I could handle them most of the time. An extra 50 lbs later (more than 50, who am I kidding), I couldn’t continue taking it anymore because my weight and the fact that I gained it all back, was making me suicidal. It seemed dumb to stay on a medication to control my suicidal thoughts when the side effects were making me suicidal.
Around the time we were taking me off of Abilify, I started using medical marijuana. A few different doctors and my therapist had mentioned that it might help with this and that, and I figured it wouldn’t hurt to try.
It helped a lot once I found the right strains, I found that keeping a very low buzz was just enough to make me able to focus on work, I got more done in that few weeks than I had in awhile. It was easier to do the things that needed to be done, but at the same time I was facing a lack of motivation. I felt less anxious. I was sleeping better. My pain was almost completely controlled.
And I was eating the house again, because, munchies are a real side effect of marijuana. What’s the point of stopping a med that makes me eat too much, just to replace it with a med that makes me eat too much.
So I stopped it.
But now the lack of focus is back, the anxiety is back, the difficulty sleeping is back. My pain is back, too.
I’m on a few different medications for pain. The one I take every day is an anti-inflammatory. It helps, but not enough.
Earlier this year my primary put me back on Oxycodone, not necessarily daily, but on an as needed basis. It helps, a lot, but also I’m hesitant to take it. I didn’t need it at all when I was using marijuana. But now that I’m not using that, I’m instead falling back on the Oxycodone. It scares me. I was on it daily (actually, multiple times a day) a few years ago. I absolutely feel like dependency on medication isn’t always a bad thing (I’m dependent on my psych meds), and I absolutely feel that withdraw is something that happens with a lot of meds (stop taking a psych med cold turkey and you’ll see what I mean . . .actually, don’t do that.) Dependency on narcotics feels like a whole different ballgame. Maybe it is, maybe it isn’t. I don’t really want to go there, so I use it super sparingly.
I’m falling back on my Ativan more often, because it controls the overwhelming anxiety. Ativan is another one I’m super careful with. A thirty day script will often last me 6 months or more. But right now, because of the whole 2020 thing, I need it more often, and I don’t like that.
Oh, and I should mention my antidepressant and those side effects. It causes nausea. It’s bad enough that some nights I actually get sick a few hours after taking it. We’d like to increase it because it could probably work a bit better. But increased doses cause more nausea. What is worse, living with low grade depression constantly, or being miserable after taking the medication to treat it.
I’m stuck in this trap. All of the medications have side effects. Figuring out which side effects are worse than the ailment they’re treating is a constant conversation within myself and with my doctors.
I’m frustrated. I want solutions that don’t cause more problems.
I need medications to stay stable.
Medications come with side effects.
Side effects make it difficult to continue taking the medications.
I need medications to stay stable.
I Lived
This is a Really Real Widow post.
With some mental health thrown in, because they are completely entwined.
This time of year is incredibly hard.
Yesterday was the 7 year anniversary of a major accident that Kidlet and Parker were in. The pictures show up every year, reminding me of the horror of that day. Deep open wounds and the two people I loved most in the world strapped to stretchers. The screams I heard coming from my son in the ambulance that day are sounds I will never forget.
Sounds I never want to forget for the same reason I let the pictures show up in memories every year.
We survived that shit. Parker took a motorcycle to the head and Kidlet caught it, and they lived.
The reminders of Parker’s ankle surgery a few years back show up this time every year, too. It’s the beginning of the countdown to the day she died. That surgery and the restrictions after it were the final straw that broke her. Her death date is now less than 2 weeks away.
The last video I took just went through my memories the other day. The last photos will be any day now. The post where I tell everyone she died will be a few days after that.
I could delete them, block them from my Timehop memories. But I don’t.
We survived that shit. Kidlet and I lost one of the most important people in our worlds, and we lived.
I recently saw my first firefly of the year. The first was in Florida and I’ve seen one since coming home as well. It’s another reminder that it’s this time of year. A bittersweet thing as she was my firefly, it’s nice to have that reminder of her, but also, it means that day is coming.
Each year this time passes with a different set of feelings. The first year was a sense of urgency, a sense of needing to get to that one year anniversary so that it can just be over and done with. The lead up is always worse than the actual day.
Each year the pain has lessened. In earlier years I’ve felt the need to do something to remember her. A trip to the beach, normally. I’m not sure that’s so necessary anymore.
This year the reminders are there, but the feelings are different, yet again.
I’ve been trying to figure out what’s different, why does it feel so different.
And then it came to me. It feels less traumatizing this year. That’s the difference.
In the past it was a punch to the gut with each picture or facebook post, or even a just a general look at the calendar to see the date. This year it just is. It’s a calm, gentle reminder that it is part of my story. Part of my life.
Part of what got me to this point.
I’m super down on myself right now because I feel like I’ve undone years worth of work. Years of work that were so important as I tried to live in ways that Parker couldn’t anymore. I had to get better, I had to save myself, or losing her was in vain.
But this is part of my story as well. And that’s okay.
This is okay.
I’ll survive this shit. Life has thrown me curve ball after curve ball, and I lived.
I lived.
Blah
This is a Really Real Mental Health post.
TW: Mention of weight being a problem for me, but no mention of dieting.
First of all, I realize I’ve slowed way down on my writing. I’m writing some short stuff for the Facebook page/group I’m a part of, but mostly, my writing has just stopped. (Link to page and group in the comments.)
Second, everything I have written, for awhile now, seems to deal with either my weight, or work, and how hard both of those things are for me right now.
And I really did plan to make this post different, maybe come up with some more interesting topic, or something new. Except my weight, and work are the two things that are most difficult in my life. Everything else is just . . . there . . . it doesn’t really bother me.
I mean, the dishes keep piling up in the sink, and I can’t find the will to cook. Showering, and even brushing my teeth are chores that are difficult to force myself through. I’m sleeping for 12-ish hours a night.
If it sounds like depression and looks like depression it must be nothing. This is fine, everything is fine.

Well, I guess the other things are bothering me, they just don’t feel as pressing, or has as much of a sense of urgency about them. They are just part of my current normal.
I feel like I have no will power to just muscle through this stuff. Weight and work included. I haven’t been able to make the changes I need to make. I haven’t been able to stick to a schedule. I haven’t been able to just “do the things.”
But also, I know this will pass. I will get back into a routine. I will slowly change these new, unhealthy, habits, back into the healthier habits I had before. I will go back to thriving with a routine, and find satisfaction in a job well done. Dishes and menu planning and straightening up around the house will go back to being just things that I do.
My current meds, probably the higher dose of Abilify, are muting my emotions. In an effort to keep me from rapid cycling and ending up in a mixed mood episode, we’ve made life kind of flat for me. Yeah, I don’t get hypomanic, and the suicidal thoughts are mostly controlled, but the world is kind of grey and 2 dimensional. I don’t feel difficult things as strongly, but I’m also missing out on the bright colors of emotions I’m used to seeing.
This is fueling my depression, I’m sure. When the world seems flat and made up mostly of various shades of grey, it’s harder to see the positives and feel hopeful. It’s hard to be excited about life.
When there’s no sense of accomplishment when I complete a task, it’s hard to keep repeating that task over and over again.
But, mental illness is hard. It’s an everyday battle. The constant fight is draining. Even just riding the waves without fighting against them is draining.
This too shall pass. Hopefully some slow med changes will help. Hopefully the warmer months and more sun will help (If I can get myself out of the house.) Hopefully continuing to adjust to this new normal will help.
Hopefully.
If I can hold onto that hope, I’m winning the battle.
Wait, Weight, Wait
This is a Really Real Mental Health post.
And a Really Real Health post.
TW: Weight/dieting/exercise. Mention of suicidal thoughts with no intent or plan.
I hate my body.
It’s making me hate who I am.
And I’ve had a few realizations in the last couple of days.
First, I remembered that I’m on a high dose of Abilify. It made me gain some weight at lower doses but the weight gain has gotten so much worse at this increased dose. I think it’s a big reason for my whirlwind eating, and my craving of sweets. It’s the medicine that keeps the suicidal thoughts under control. We had to increase the dose when I was in the hospital, and we increased it again as I finished up with partial. I think it may be time to look into decreasing the dose, or changing to a different med.
Also, I realized I hate my body right now. I hate how I look. I hate how I feel. I hate how hard it is for me to interact with my environment.
I spent the last, however many, years looking at old pictures of me and comparing my round puffy face to the slimmer version it had become. I constantly said how much I never wanted to be that fat and gross. How horrible it was that I ever got that way.
How horrible I was.
It’s really hard to take good care of a body I hate. It’s hard to stick with changes because I don’t really feel like I’m worth it.
I also feel like nothing will change, and like I’ll always go back to this weight.
That thought makes the suicidal thoughts start. The idea that I can’t change this, and this is the body I’ll live in until I die, is hard hard stuff for me.
Often, when I think too much about forever fighting to stay mentally stable, I think that death would be better than fighting for the rest of my life.
Now, when I think too much about forever fighting to keep my weight under control, I think that death would be better than fighting for the rest of my life.
I started to list the things I was doing and trying to do, but honestly, those won’t matter until I go back to loving myself where I’m at.
I hate that I could say “I deserve to take up space” when I was 50 lbs lighter, but now I feel like I don’t deserve the space I take.
I hate that I could see how beautiful I am at one weight, but I can’t see my beauty now.
I hate that I feel like I need external validation.
I hate that the same people who praised me for losing weight, will judge me for gaining it back.
I hate that some of them will feel they can speak that judgement out loud.
I hate feeling like this.
I hate being like this.
I hate me.
I’m Tired
This is a Really Real Mental Health post.
This time last year I was intensely suicidal. I was tired of fighting the thoughts that so often wanted to kill me. I was tired of being in pain.
I was tired.
This year, comparatively, I’m doing really well. I don’t really get all that suicidal all that often. My pain is somewhat controlled. I’m relatively stable.
But.
I am tired.
I’m tired of being inside. I’m tired of not going to the gym. I’m tired of missing my friends. I’m tired of hearing about people who aren’t even trying. I’m tired of working. I’m tired of avoiding the world.
I’m tired.
I’m tired.
I’m tired.
And this time I know I’m not alone. I know there are lots of us that are tired.
And it’s still not fair.
None of us deserve this right now. None of us were prepared for it. None of us should have to learn to live with it.
But most of us are learning to live with it. We are doing what we’re supposed to do.
Those that aren’t, piss me off. The more we leave our houses the longer this will take, and it’s going to take a long while as it is.
Stay the fuck home.
I’m tired.
I’m tired of living in this world even though I’m not tired of living.
I’m tired.
I’m tired of not being able to write because there’s no life to write about.
I’m tired.
I am tired.
L-I-G! (Life Is Good!)
This is a Really Real Life Post.
Being able to be myself is nothing short of amazing.
I mean, yeah, being wholeheartedly me means I deal with some really bad depression and suicidal ideation. It means I spend days inpatient and weeks in partial sometimes. It means there are some really shitty times.
But it also means I get to be open and out there and vulnerable. I get to wear my wild skirts and bright hair. I get to tell my story in a way that helps others (and helps me at the same time). I get to laugh and cry and let my dorky hang out.
I get to spend time with people who are just my kinda people, instead of struggling to fit in with the people who aren’t.
I’m learning how important all of this is.
I trip down the sidewalk, I fall face first down the stairs, I spill food down my shirt, all on a regular basis. But that’s just part of my charm, even the bruises, scars, and messed up shirts.
I am anxious and moody and sometimes my memory is all kinds of shit. But I keep moving forward no matter what life throws at me.
I’m falling in love with my authentic self.
My imperfect, beautiful, self.
I wish I could see things from this perspective all of the time. I wish depression didn’t creep in and pull me under. Make me nervous and afraid. Make me sad and apathetic. I wish life was all roses and bright smiles.
But even my mental illness is part of who I am. It’s part of what makes me, me. It’s part of what makes me beautiful.
Even though sometimes I’m a beautiful mess.
I’m learning to accept all of me.
And that’s pretty fucking amazing.
I can’t wait to see who I’m becoming.
The best is yet to come.
(Someone save this post and send it to me next time I’m falling apart, please.)