Broken and Damaged

broken-damaged

I’m trying so fucking hard, but man, I have no idea what the hell is keeping me going. Yesterday was such a battle and I’m afraid of a new day, mainly because I blacked out twice yesterday. Unfortunately, my appointment can’t be moved up because I’m a new patient, so I just have to pray that I’ll get answers next month, or at the very least, some new ideas.

Here’s hoping today is a better day, in every way.

 

The Aftermath

*Potential trigger warning*

I survived, and I’m always sorry when I do. Always.

Last week, a member of my family overdosed on prescription medication. It wasn’t painkillers or anything like that. In fact, I have yet to look the drug up, but I do know what it isn’t. It’s not lethal if you’re taking it responsibly, but it can be deadly if you’re being an asshole or you take four instead of one. That’s true for a lot of drugs we deem “safe”, which is precisely why the pharmacy tells you that if you can’t remember if you missed a dose, skip the dose, don’t double-up.

We don’t know yet if it was intentional or accidental, but she doesn’t remember what happened. I wish I could say the same. It took me roughly twelve hours to talk two different family members down over what happened. I’ve felt deeply depressed, unhappy, mentally, emotionally, and physically drained ever since. I’m in such a dark place and as I sit here, I realize no one has noticed.

I remember when I tried overdosing. I’d had enough and I wanted out. This was long before my Fibromyalgia diagnosis, and honestly, it was unnecessary back then, I just couldn’t tolerate what i was going through with zero support (much like I feel now). I can say with absolute certainty that no one noticed what I did and no one knew I did it. Even now, no one spends enough time with me to notice if I’m sick or not acting like myself because they don’t know me well enough to know what’s normal for me. I can’t laugh or be goofy or do anything without it being criticized or psychoanalyzed. I could do so many truly dangerous things and I am certain no one would notice. When would they have the fucking time?!

I’m not content living a half-life. I’ve spent the past few weeks in so much pain, I didn’t realize until yesterday just how badly I want it all to stop. The daily struggle. The forcing myself to get out of bed when I really shouldn’t be moving at all. The emotional struggle. The blackouts are so bad that I don’t remember most of today after eating breakfast and I’m concerned, because I think I hit my head at some point. My skull is on FIRE and aches so bad, I’m freaking out. I’m tired of forcing myself out of the house to do far too much because the one person who knows me best and knows exactly how to help me is hundreds of miles away and I haven’t seen him in a year and a half. The financial struggle is never-ending, and realizing that I’ve been unhappy before, but this is a whole other level of miserable is the icing on the cake of misery. This is something that cannot be broken with a positive attitude and smiley faces. This can’t be fixed with kind words and someone being polite. This is serious and every time I turn to someone for help, I’m given their equivalent of a gigantic middle finger. If someone does help me, they hold it over my head like a weapon. It makes it worse because helping someone should mean that you care, not that you show them hatred.

I do have a doctor’s appointment coming up, but it’s mostly for a diagnosis. A new one, because the old one is almost five years old and things change, including me. This is a fresh start and I don’t know if this doctor and I will click or not, but he’s only getting one chance to show me who he is and what he can do to help me.

Five years ago, I was in a different financial position, and while I was struggling emotionally, I kept it in check as much as humanly possible. I was making things work. My life came tumbling down less than six months later. Horror after horror, and I am suffering for it every single day. My doctor never billed me for my last appointment. He knew I had no insurance that would cover the visit at the time (Hell, the only thing my insurance was paying for back then was monthly medication and the occasional ER visit. My primary care doctor, at the time, was months away from dumping me as a patient when I needed help the most.) and that things with me were not okay. I never saw a bill from him. If he’d sent one, I would have paid it, but sitting here today, struggling, I see it as a major act of kindness in a world where there’s so little of it. In sixteen years, he’s probably bought a car or put his daughter through private school for a full year based on what I did pay him, so I don’t feel guilty about it. When I found out in late 2015 that he never put Fibromyalgia into my chart when he diagnosed me, thus making me look like an idiot and making me question exactly what the hell is wrong with me, I damn sure felt even less guilty. I was shaking with rage, and I still am. That one absent-minded mistake cost me DEARLY. And here I am, back at square one.

I feel like an insane basket-case, just waiting to explode. I’m looking at the pile of problems in front of me, which I cannot solve. I’ve got nowhere to turn for help, and I am scared out of my mind. I can let certain things go, but the realization of this particular problem and how important (and potentially damaging it could be) is making things worse. I suspect knowing that since yesterday is what caused me to blackout today. The stress is too much for my body. Stress can be so damaging, we don’t always know exactly how much stress we’re dealing with, until it’s too late.

Unlike many people, I’ve always understood the level of emotional pain it takes to make a person say “I’ve had enough.” I also understand the level of mental and physical pain it takes to say “No more. I can’t do this.” Most people never act on it, especially when they’re talking about it for several years to family and friends, but the people who, like me, keep it inside, are the ones more likely to act on their thoughts. There’s no fascination involved, we’re just done.

Today, I am 100% DONE. I have no idea how I’ve survived this far and I’m tired of worrying. Of not sleeping. Or praying and feeling like I’m all alone. There’s only so much hurt, disrespect, abuse, and abandonment one person can handle.

Will tomorrow be better? I don’t know. I never know. I can pray, and I am going to reach out for help to see if someone will have my back this week, but ultimately, once I’ve exhausted all options, I don’t know where I’ll be.

I’m praying for better days, but I feel lost and completely abandoned. The level of emotional pain for that is off the charts.

This is the aftermath of loss, grief, abandonment, abuse, and other things you may never heal from. No matter how strong you are, no matter how hard you try, there are some things you can’t do anything about. For me, that hurts almost as much as seeing how meaningless I am to others.

Most people would say “It’s the Monday blues.”, but those people don’t understand I feel like this almost daily. That’s not okay.

copyright © 2017 by Lisa Marino & Blackbird Serenity, LLC. ALL RIGHTS RESERVED.

 

Hearing ‘If You Need Anything, I’m Here’ As Someone With Chronic Illness

https://themighty.com/2017/05/how-to-help-sick-friend-not-in-hospital/

People say this to me often, but they’re about as emotionally present as a flea. They don’t call, they don’t check in, they don’t ask if there’s something I CAN do and agree to join me, etc. It’s always about them. It’s like being invisible, just like my illness. I don’t exist, unless someone wants or needs something, and suddenly I’m this amazing, brilliant person. I didn’t think it was possible to roll my eyes so much, but it IS, and it’s because I find it offensive and rude.

Maybe it’s because I am a writer, but I believe words have immense power. Use them wisely, and please, check in on people. Just because they’re not hospitalized doesn’t mean they’re not isolated and/or hurting deeply. I spend 95% of my time completely alone. I’m not even sure why I have a phone most days. It would be nice if people weren’t so self-centered, but since they remain as they are, I’ve decided to remain who I am.

The Countdown

Every year, usually around mid-April, is the countdown reminder from every company I’ve ever done business with, or might do business with in the future, that Mother’s Day is fast approaching. Last year, it angered me to the point where I unsubscribed from about 20-30 different mailing lists. I just couldn’t take it any more. The e-mails were daily. Daily. Sometimes, there were three or four a day. How much more business do these people need to drum up?! Was it a slow year?!

This year, Mother’s Day falls out on the day when I normally do my big grocery shopping, which requires hitting three different stores, usually, to acquire everything on my detailed list (which I usually organize by store, so I don’t forget anything major). If I keep my head down and I just focus on that list, I should be able to avoid as much of the hoopla as possible, but the pain in my heart will never go away.

There have been years where I couldn’t even get out of bed at the mere thought of facing other people on Mother’s Day. And the worst part is; Few people acknowledge this or discuss it. I refuse to be one of those people.

It’s unbelievably rude when people dismiss your feelings, especially in regard to something like this. When someone tells you to “get over it”, it might actually be wise to consider the source and/or re-think your relationship with that person. Being dismissive of someone’s pain, be it physical, mental, or emotional, is never acceptable.

Being a Motherless Daughter is painful. There is this enormous piece of me missing, and I assure you; no one gives a damn. No one else’s life stopped after my mother’s death, no one else mourns her daily, and that makes it so much worse in my eyes.

I remember how I felt at her funeral. I probably know her eulogy by heart because I only had a few days to write it, but every word was from the heart. I did her proud. I try to keep making her proud every day of my life.

The things I could talk about with my Mom are now things no one else on this planet would understand. Instead of having a person laugh with me and enjoy my insight and sense of humor, I am criticized for having a sense of humor that others do not understand or appreciate. Technically, that’s their problem, not mine. There are so many times I want to tell her about something going on, and I can’t. I know she is looking down on everything happening in my life and is now the “All-Seeing Eye”, but I really hope she sees how I am being treated and the character of others. I hope she sees and does not forget.

My mother always taught me to forgive, but never to forget. “Forgive for yourself,” she’d say, “So you don’t have to carry the hurt and allow it to harm you, but don’t EVER forget.” Forgiveness has become downright impossible in the wake of her passing and other terrible things that have occurred since that fateful day. There are always things you can never un-hear, un-see, un-learn, etc. There’s far too much you cannot forget. My mother was a nice, kind, caring person. I’m not all that nice and my kindness and ability to care is limited.

My Mom used to tell people she couldn’t remember what she wore two days ago, but that “My daughter remembers EVERYTHING.” My short-term memory is shit, but my long-term memory is eerily accurate. So you can question me, but don’t, for a single second, try telling me I’m wrong. I’m many things, but wrong isn’t one of them (I have a key-chain that says that verbatim.). Not when it comes to most things. And I openly admit when I am wrong, which many people won’t ever do.

Last year, right around the start of this month, is when my blackouts began (at least I’m pretty sure that’s when they started. In fairness, it took a few months before I was aware that I had lapses in time each day.). Is it somehow tied in to my mother’s passing and all the other death that has effected my life in the month of May? It’s possible. I have an appointment at the beginning of next month and I will certainly ask the doctor if he thinks it’s a possibility. If it’s not something triggering me, then it is something neurological, and that’s even scarier to me. I doubt an MRI will show damage, but psychologically, I suspect it’s a form of trauma manifesting itself.

I wish there was a measure of sensitivity surrounding this subject, but there really isn’t. I can attend the local Motherless Daughter event, or I can stay put and mourn on my own. I don’t think I can actually focus on other people’s stories at the moment, so it’s probably best I just isolate myself, except for the fact that I am ALWAYS isolated and alone. The effort I put forth not to be is always slapped down, always insulted, and is never good enough. The more negativity I hear, the more triggered I become. Someone might think they’re paying me a compliment, but I know an insult when I hear one. I’m NOT stupid, and I will walk away or disengage when a person is acting like an asshole or just plain being disrespectful.

One of the reasons people like and respect me is because I’m always the same person. Whether it’s on the phone, in a letter or e-mail, interacting on-line, or when you meet me or spend time with me; I don’t change. What you see and read is precisely what you get. I’ve had friends tell me precisely how much they enjoy that and respect it because they never have to worry how I am going to be because I’m always myself. When my friends spend time with me, they don’t understand why anyone wouldn’t love me. I am most at ease and most myself when I am with them. I wish they didn’t all live so far away, but I do have a very close friend visiting next month from California and I am SO excited to spend time with her! We met through my writing, as well as hers, and have been friends for five years. It seems like a much longer time period because of the bond between us, and I’m really looking forward to whatever adventures we get to share. Right now, having something to look forward to is all I’ve got. I don’t really know what I will do after she goes home. 😦 I do know I will miss her, though.

I might not write anything on Sunday this year, and if I don’t, I hope everyone will understand why. I might reblog something I’ve written in the past if I have the time to search, but if I am silent, I hope no one will take it personally.

I am still recovering from last week’s Urgent Care visit for my migraines. My IV “wound” is nearly healed, but I learned my lesson in regard to how to handle this horrible pain from here on in. I hope the neurologist I see is a good one and that he will have answers for me. I’ve been doing extensive research to make sure I go in armed with information to try and come up with a plan that we can both agree on.

And so, the countdown begins. On the plus side, I’m glad to be writing in a successful, productive way. For those of you who’ve been super supportive of this project (Lillian & Steven), please know how much it means to me.

Have a lovely Friday, everyone!

copyright © 2017 by Lisa Marino & Blackbird Serenity, LLC. ALL RIGHTS RESERVED.

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