beset by Satan
in all his
diverse forms –
but the most
persistent of all
is the government.
beset by Satan
in all his
diverse forms –
but the most
persistent of all
is the government.
Am I the only one that thinks it is kind of messed up that you pay into Medicare all your life, and then, when you finally get coverage (either through age or proven disability), you still have to pay monthly plan premiums, deductibles, and don’t receive even basic care like prescription coverage without buying additional plans?
I know if you are impoverished enough, some of these fees can be waived or you might qualify for Medicaid to help out, but since I am married and my husband brings home a lower, middle class income, we don’t qualify for any of that help. I can understand why some benefit recipients choose not to get married! They pretty much penalize you for it.
I’m not complaining because I am the worst off in the world (I know I’m not). I guess I was just surprised to find out what the reality of receiving Medicare coverage is actually like. It honestly isn’t much different than commercial insurance in all the ways they find to charge you more for necessary healthcare.
Man, I’m pretty bummed today. I was supposed to go ghost hunting at a local cemetery with a paranormal investigation group, but yesterday my earache turned into a raging ear infection and between the ear pain and the nausea from the antibiotics, I had to choose to stay home and rest. I guess there will likely be other opportunities, but still wish I could have gone.
Among other news, my first SSDI payment got messed up and didn’t come. Took me two days and multiple phone calls to multiple agencies to get it solved and will hopefully get my payment within the next couple weeks. I had a huge meltdown over the whole situation Thursday, which probably didn’t help my immune system and may have contributed to my current infection. I can’t help but notice that my already weak immune system takes a nosedive when I’m stressed or upset.
Even thinking about it now makes me mad lol. The worst part was that the automated phone answering systems would NOT let me talk to a live person for the longest time! Ugh. It was like a labyrinth to find my way through to talk to a living, breathing human. I realize this post is pretty negative and maybe a bit whiny lol, but that’s where I’m at today. Hope you are all feeling better than I am at the moment!
Sorry I didn’t update you all yesterday after the hearing, but I was just too exhausted mentally, emotionally, and physically after the stress of the day. Overall, I think the hearing went ok. It didn’t start out very well since my husband and I had trouble locating the right building and ended up walking through the thick, slushy snow so far that I had an asthma attack, started crying, and was totally soaked from the knees down by the time we actually found the right building. The roads were bad too from the snowstorm and parking was almost impossible since none of the parking lots had been cleared yet.
Once we got into the building, I had a few minutes to recover from the asthma attack and calm down at least. I also had about 15 minutes to meet with my lawyer before the hearing to go over everything again. During the hearing itself, I was quite nervous. I was doing a lot of rocking back and forth (“stimming” in autistic terms).
I think I only had the nerve to look at the judge two or three times the entire hour I was in there. I mostly stared at the microphone and tried to block out everyone else there while answering questions. That seemed to help my social anxiety. I think I did a decent job answering the judges questions…and she asked a lot. I never lost control of myself, although in my closing remarks I did tear up a bit and got a little emotional talking about how hard it had become for me to keep a job due to my physical and mental disabilities.
Unfortunately, the judge did not tell me her decision yesterday. I will have to wait to receive the official verdict letter. On the positive side, my attorney did say afterwards that he thought it went great and even on the off chance that the judge gave a negative verdict, he thought I had a strong enough case that he would appeal that. I hope it doesn’t come to that though, God only knows how much longer that would make the whole thing drag out…and quite honestly, we need the money as soon as possible, especially since I just got a $1,500 ER bill (our deductible sucks).
I am often disheartened by the cold commercialism of society. As I watch the rise of the giant corporations and mega conglomerates, I feel like life in general is becoming less conducive to humanity and relationships and more about flashy advertisements and raking in the money. Those few people running the world don’t just seem to be garden-variety-greedy anymore, they seem to be Scrooge-McDuck-diving-into-a-swimming-pool-of-gold-greedy.
Recently I was walking around a Walmart, my head almost swimming from all the useless stuff trying to attract my attention, when I suddenly had the impulse to go around the store and ask every employee I could find whether they believe Walmart really gives a shit about them as a person, or if they think they are viewed as a replaceable number only. I resisted the urge, but as someone who spent a short amount of time working as a greeter at Walmart, I can almost guarantee that if the employees answered my question honestly, probably none of them would say the corporation gives a damn about them. And that microcosm of Walmart, represents an entire world of similar sentiments.
Ok, so I had another subject planned for today’s post, but I need to rant a bit, so I’ll save that topic for later. I hope you won’t mind listening to my frustration today.
So, I’m part of a group on Facebook for people with certain mental issues, and I have noticed many of the people in the group getting social security disability solely for those mental issues, which I happen to share. I am not upset that they got disability for their problems, but I can’t help but compare it to my own situation and feel angry at how I have been treated by the system.
I’ve been fighting for several years to try and get disability benefits, my worst conditions that affect my ability to work are: Bipolar Depression, Asperger’s, PTSD, social anxiety disorder, fibromyalgia, chronic fatigue syndrome, IBS, degenerative disc disease and bulging discs, chronic bronchitis/ear infections, and severe plantar fasciitis. ALL THAT and yet I am still fighting! It pisses me off because I know people who got it much quicker for SO MUCH LESS or just ONE of my conditions. And none of these conditions are light, even the last rejection letter from social security said the conditions are indeed severe…and yet I got turned down AGAIN? I have a plethora of medical evidence and have tried to follow medical advice to the letter. What more can I do???
I DO have an attorney (my 2nd actually), and I am now waiting for a court date, the 2nd time I will have to go to a hearing for this. The last judge I got had a record for barely approving anyone, which seems unfair in itself. How can it be a fair system when some judges approve a majority of people and other judges approve hardly anyone? Were it not for my husband, I would likely be homeless by now.
To make matters worse, one person in the Facebook group insinuated that plantar fasciitis and chronic ear infections/bronchitis aren’t severe enough to affect your ability to work long term. Well, I’ve had the plantar fasciitis for 15 YEARS. I’ve seen specialists, done meds, physical therapy, long-term steroid therapy, custom orthotics, cortisone shots, nothing helped. Doesn’t seem like it will magically get better at this point. It is so severe I have a noticeable limp and have almost passed out from the pain at times when I was forced to be on my feet for long periods of time.
As for the recurring infections, I’ve had chronic ear infections and bronchitis for many years, often getting up to six within a six month period. I’m now on my 3rd course of antibiotics this year (2018) for the chronic ear infections and bronchitis. Again, I’ve seen specialists, tried a host of medications and other treatments (both medical and alternative) and nothing has worked so far. The amount of antibiotics I have had to take has led to issues with antibiotics not working as well anymore, worsening IBS symptoms, and even episodes of MRSA, C Diff, and colitis which I had to be hospitalized for. These are not minor, fleeting problems.
To make matters worse, I have TRIED to work while fighting for disability. The last job I had (working only two days a week) I was let go from for missing work too much due to medical issues, most of which I was in the hospital or ER for, so they know I wasn’t just “faking”. I also tried being a greeter at Walmart, since it is about one of the only places that actually hires really disabled people and I couldn’t even do that due to my social anxiety, depression, and other health issues. I am not even fighting for welfare here, only the benefits I worked for over the years!
Kind of a downer subject today, but it is something I feel like I need to say. Please note I am not in any immediate danger, nor am I planning to hurt myself in any way. This is simply a post about WHY I would likely commit suicide if I ever did. I am sharing this in the hope that others will come to care about these issues and learn to empathize with people like me.
If I were to ever commit suicide, there are two likely scenarios why, and both have a lot to do with our often selfish American culture/government and the view that many people have that everyone should just “fend for themselves”, regardless of their actual ability to do so. I honestly cannot see myself committing suicide simply because of depression, loneliness, bipolar, Asperger’s, fibromyalgia, chronic fatigue syndrome, or any of the myriad other struggles I face on a daily basis. I have survived those things for years and will likely continue to do so. However, if I did ever kill myself, here are the two likely culprits:
*Art by Maranda Russell
Admission time…I LOVE a good conspiracy. JFK. Roswell. 9/11. The Illuminati. Skull and Bones. I love it all. Sometimes I think conspiracy theorists can go too far (Sandy Hook being a hoax comes to mind), but overall, I’m willing to view evidence either way and see why people come up with the conspiracy theories they cling to. Sometimes the evidence makes me highly suspect foul play, even if I can’t prove it. And that’s the thing, I will tell others I suspect a potential false flag, but I won’t make a proclamation that I know the truth for sure. Of course I could be wrong. There are some things I do not believe were false flags that I could be wrong about too of course.
So with the Las Vegas shooting, I have been taking in media from a mainstream perspective as well as watching some videos and supposed “evidence” that the shooting may have actually been a state sponsored false flag (false flag does NOT mean it didn’t happen, just that the government planned it). I have not been convinced either way. The footage of gunfire possibly coming from the 4th floor is rather fascinating, but not conclusive proof. Of course motive is a question whether you believe the media narrative or the false flag narrative. False flags normally are done to demonize a group of people, give an excuse to start a war, or distract from something else the government doesn’t want you to notice is going on. With Trump in office, God only knows what they might try to distract us from!
Regardless of whether things like this are crazy people gone rogue or some kind of sinister plot cooked up in Washington, I do support banning high capacity assault weapons. In my opinion, normal people just don’t need access to those weapons. Of course, that doesn’t mean I trust the government either, but heavily armed governments vs heavily armed rebels just ends up with dead people everywhere. I like to believe there is another way to make change, which definitely needs to be made. I’ve studied how the US government supports terrorism around the world and it convinces me they are undoubtedly capable of inflicting such things on their own people should it suit them.
So yes, I do enjoy a good conspiracy and might post about them, but that doesn’t mean I am putting aside all skepticism. I’m just skeptical about both sides.
(The below was written out of simple outrage from what I have seen happen to fellow human beings who are genuinely too sick and weak to work, but are expected to wait years for any help from the government programs they have paid into all their lives. I am fortunate to have other resources to survive on while unable to work, but not everyone is so lucky. Many homeless you see on the streets are actually disabled veterans and citizens who deserve so much better…)
Applying for government benefits, even those you have worked for and earned yourself, can be a ridiculously long, complicated, and humiliating process BECAUSE they design it to be so. They want to break you down, make you give up, make you give in. They expect the sickest and weakest among us to jump through hurdles on command, knowing it is almost an impossibility unless there are others propping us up.
Honestly, I think they hope that you will die on your own before they have to do a damn thing. I can picture Uncle Sam with fingers crossed, hoping you buckle under the stress and poverty, or even end up taking your own life from the hopelessness and despair of feeling useless, discounted, and vilified by a media that touts how “easy” it is to fool the system and labels those who are disabled as leeches or lazy.
Apparently discrimination laws don’t apply to the government either, since they clearly indulge in age discrimination, something every lawyer will blatantly tell you up front. Even publicly, you can find legal representatives in the field explaining why you are simply fucked if you dare get too sick before age 35, 40, or even 50. So if you are a young adult or middle aged person struggling with a chronic illness or severe pain condition, you had better tell it to get lost and come back in 10 or 20 years. Yeah, that works. After all, young people aren’t allowed to be sick or disabled.
You know, it is really funny, that many of the same people who are so public about being pro-life are also always trying to cut social safety net programs like disability or make them harder to access. If they could, I think sometimes that the government would perform adult abortions on those too weak or sick to continue to prop up their sick, twisted system. Getting rid of us all would be so much easier, wouldn’t it?