I had a panic attack attempting to delete a few people from my Facebook. Some of them family. It’s never easy deleting family from facebook. It’s never easy deleting anyone from Facebook. I never thought I would have such a hard time. So much so, that I would have a panic attack over it. Well, I covered all my bases, you know, should I give them a “head’s up”, or should I just not give them any notice.
I won’t go into detail what happened, but social media is so anxiety inducing, because there’s no face-to-face interaction with the person. In my mind, I feel like the face-to-face interaction is easier to deal with because you see the emotions of the person, you hear their voice, and then afterwards you can deal with their real-time emotions of the aftermath of the situation. Keyword is real-time. With texting, Facebook, instagram, twitter, etc, and the like, you’re dealing with the delay of the person’s emotions. They may have calmed down in the aftermath of a situation if something has gone wrong, or they may have gotten angrier and things have boiled in their head. OR you could be that person texting angrily and that other person could be busy and have no clue as to what’s going on and didn’t even get your text/message.
This could all be the same for something positive that has happened. I was personally speaking from my situation as if something has gone horribly wrong.
My anxiety and panic attacks get pretty bad. I admit I usually run to my medicine. I’m trying to find other ways to calm myself. I can find peace of mind through music and distraction. Not so much reading, as my mind races when I am anxious and panicky. Dancing helps. Distraction is a big helper. Distraction through television, music, and sitting outside. Which is about all I can think about right now. I am finding more as I go on to recovery.
I am finding that I am becoming more anxious as I recover. I did not expect that. That blindsided me.
My medications have been taking a toll on my brain or my mind.
The Haldol has been causing cognitive dysfunction within my brain. I can’t think straight, I can’t comprehend what to other people are saying, I can’t understand some of the most simple of things. All because of the Haldol. Antipsychotics are a hell of a drug. They are a hell of a class of drugs meant to rule your mind.
Lately, I haven’t been able to keep up with small tasks like taking care of my animals/pets. Taking them out? I
forget. Feeding them? I forget. It seems almost scatter-brained. That’s the best word I could come up with.
adjectiveadjective: scatterbrained; adjective: scatter-brained
- (of a person) disorganized and lacking in concentration.
I am scatterbrained for the time being. Under the control of so many medications, I dont know where my mind is going to, or where it’s headed. I need a 5 year long term plan.
I was diagnosed with Schizoaffective disorder when I was about 15. It changed to Paranoid Schizophrenia when I was 21. It has went between Schizoaffective disorder and Paranoid Schizophrenia off and on since I was 21. Depending on what doctor I saw or if I went to a hospital and saw a psychiatrist there.
Only a handful of people know, which include obviously my providers, and my immediate family.
I look at that sentence and I think, “Wow, just my immediate family, why?”. Well, it’s a private matter, yes, but no one else would understand. There would be stigma, right? Both, yes. I’ve already had stigma from other family members, and people who aren’t family.
It being National Mental Health Awareness Month it’s hard to fathom that with all the kinds of change that’s happening in 2015 (and even in the recent past) in this great world, that the kind of change that I wish would happen hasn’t happened. The awareness for mental health and mental illness. It’s hard enough as it is to get my immediate family to understand my struggles with my illness, so there’s no way I’d be able to get anyone else to understand a lifetime of struggles or even a day or frame of time of struggles. I feel like why even try. That’s how I feel right now in my life. But, I wouldn’t stop spreading the awareness for others’ awareness. For others being able to have a spread awareness for their extended family family or friends or other people.
My parents are more open to me than ever, but it took a long time, many years to get here, and that’s sad in itself. They didn’t trust and didn’t want me to go to mental health providers at all. They still don’t really trust doctors in general. They belittled me for awhile, and one parent belittled my appearance because of the side effects of the medication: the weight gain. I cannot post my real feelings through some social media because of all of this, but I digress. My extended family will never truly understand my struggles. Will they ever know my illness? Maybe someday some will, if I tell them, but that’s my buisiness ultimately, and i’m not one to share my illness openly, BUT those that are mature enough to take on my buisiness and know me well enough, I might just tell them. I’m not sure about everyone’s family, but…I don’t feel like my family will ever be ready to hear it. And it makes me really sad.
I was so happy to be apart of changing the stigma of mental health in this country and around the world. I felt honored to be apart of the NAMI commercial that took place in Dallas, TX. It was absolutely freezing with 30 degree weather!
Here is the behind the scenes look at the commercial that comes out in May for Mental Health Awareness Month 2015. For more info you can go to my page on Mental Health Awareness and NAMI’s Mental Health Month 2015 page. Thanks for watching!
I’ve been pushing myself to get out and do more things and push away my feelings. It’s really broken me down. I’ve not just had more episodes, but probably more episodes because of this, because of pushing myself to my limits. Past my limits. I’ve been pushing myself to go to college, socialize, take criticism when I can’t (from family/friends, and take demands), etc. It’s really starting to wear on me. It’s making me more emotional and breaking me down.
My clinic, my nurse practitioner lowered the dosage of my sleeping medication and I haven’t been sleeping. I need that sleep. Every hour I can get, I need it. For my mental health. I really do. It’s so incredibly vital to me. So much so. I used to shun sleep. I thought it was for the weak. I was becoming psychotic without it. Even without just a normal amount. I naturally can’t sleep. So I grew to think that people that did sleep were naturally, just, weak.
I’m not sure if having a full schedule is good for me. I really need downtime. I need that 2-3 hours where I have nothing to do to regain my sanity. To relax. To think. I like being busy. Just not sure that is the life for me where I have something to do every second of the day. It’s just not something that I think is good for my health, because it’s very stressful, and I can only imagine what it’s like for someone else with schizophrenia or schizoaffective disorder, or another severe mental health issue.
This issue hasn’t exactly got me tossing and turning yet, but I’m almost there. It could be called something of a “Quarter-Life Crisis”. Not sure if it applies to me. I am though going through some sort of existential crisis.
I am 24 years old. I will be 25 in some number of months (not too long from now) and I realize that, yes, I am getting older. I’m getting further and further away from my high school years. I graduated high school at 17. I went to college that same summer, of that same year, because my parents thought it was a smart idea. That’s a whole other story.
Well, at 24, I’m still in college. That’s not a bad thing, and it’s not a good thing. It’s not a good thing by society’s standards, but because of my mental health and many hospitalizations I went through, and the down times I had, It’s not a bad thing. It shows my resilience, my willingness to succeed and keep going, and persistence.
I’m studying philosophy right now. I love it! I especially love existentialism. Philosophy drew itself to me while going through the tough periods with Schizoaffective disorder and growing older, and thinking upon suicide, and “Where am I going in life?”. I’m still new to it, I’ll admit. Everyone starts somewhere in Philosophy, I was told.
So, where am I going in life at 24 going on 25, 26, 27, 28, 29…etc? I just see time ticking away away, whereas I just saw time sitting still when I was younger. I’ll still give the fact that sometimes I still do see time stand still, but then I look away and look back and it has passed. So there’s a whole new realization. I feel as if I’ve wasted so much of my time being hospitalized. I know I couldn’t have done much to stop that, but I still can’t help but feel like it’s time wasted. Especially the down time from medication. The sleeping all the time, mostly. Sleeping up to 12-16 hours a day at one point. Even once as to sleep 24 hours straight, if my memory serves me correct. That’s another thing. My memory. Where are my memories from my early twenties? My mid-to-late teens? Nothing but withered away from medications into oblivion. I feel lucky I even took a few pictures. I take a lot of pictures nowadays. Partly because I feel like my memory will be abolished from medications, but then I want to remember even the littlest things when I get even older. With all this technology around me why not use it?
The fact that I can even see a bit of time still standing still, somewhat, I feel shows I’m still youthful. Although, I don’t want to waste this youthful time doing nothing, or what I perceive as doing nothing. I want, and need, to fill my time up with memories, events, church, educating myself, and having a lot more (healthy) fun. Just ANYTHING besides being hospitalized. Anything besides that.