The Government

Being Cripple Is Annoying

~ shawnaborman ~ Leave a comment

Hello, hello! How’s everyone doing this lovely Wednesday? Things here are usual. Medicaid has decided it’s that time of year to prove I’m still worthy. Poor. Cripple. Whatever. So, I spent most of the day filling out a 20 page form. None of the answers has changed except how much Social Security I get, but I still had to trudge through the entire form anyway. Now, I just need to take a picture of my ID and get copies of my bank statements from April through July. Easy enough, right? But no. My bank just overhauled their system and even though everything was supposed to be up and running on Monday, they don’t have online access to any statements but June. Ugh. If that’s not up today, I’ll have to call them and convince them to email the statements to me. Once I get those, I’ll send everything to my CLASS case manager and she’ll fax it to Medicaid on my behalf so they’ll realize I’m on that particular program and hopefully not argue with my eligibility. If they had told me a week ago (before my bank decided to “improve” things and I could have just downloaded the statements) or waited until October, which is when I usually have to renew, I probably wouldn’t be complaining. I just hate having to call people. And I hate redundant forms. I just hate the whole process of being reminded I’m a poor cripple leeching off of society. Anyway, it’s late and I don’t feel like coming up with something nice to ramble about. Here’s a pretty picture by Yuumei instead of a real post.

Never Mind

~ shawnaborman ~ Leave a comment

Howdy, howdy! How’s everyone doing this first Wednesday of July? I’m annoyed as feck for two reasons. One I won’t talk about yet, because it’s an ongoing thing and I don’t want anyone involved to stumble upon a rant about it. Yet. The other thing is Medicaid bullshit, but it’s late (after 10pm because we also had visitors), so I’m not even going to write the rant I was planning. I’ve spent far too much time on the phone the last few days because no one knows anything. Tomorrow (today), will be another wasted day. So, I’m going to go eat and spend the next hour or so watching TV.

A Little Rant

~ shawnaborman ~ Leave a comment

Howdy, howdy! How’s everyone doing this lovely Wednesday? Not a lot going on here. Just stupid government crap regarding my benefits. I can’t entirely blame the government for all my stress this time, because everything up until today was something else entirely and the people involved already know I’m not happy about how everything went down. Let’s just say stuff hasn’t been getting done in a timely manner. But today (Tuesday), I’ve spent far too much time trying to justify needing another hour of care every day. And I get it. The government doesn’t want to give just anyone benefits. They’re like giant companies that way. “You want healthcare and to be able to afford rent and food??? Damn commies.” But also, look at me. It’s pretty freaking obvious that I need care. I promise I’m not just a mooch. If they’d let me earn more than $1900 and change a month without screeching about taking my Medicaid away, I’d even try to be a productive member of society. But no. They don’t allow you to get to a stable place before they rip away the benefits that keep you alive. Just stay poor. Ugh. But that’s a different rant. Let’s get back on track.

I’m on a program called CLASS. They offer various services, but I only use the healthcare assistance service where they pay (actually Medicaid pays) for someone to take care of me. When I first got on the program at 18 after a ten year waitlist (yeah, no one even remembered signing up when we got the letter saying I was cripple enough for them), they only paid for outside help to come in. Eventually, they started paying family members, so Dad gets paid to take care of me. With all the prices on the rise and the fact that home healthcare works hadn’t gotten a raise in a ridiculous amount of time (because, you know, the Texas government), Dad requested an extra hour a day (no, he doesn’t get paid 24-hours a day because apparently the government thinks cripples are robots who just power down and require no assistance for far too many hours a day/night… as if normal human beings don’t have to pee or worse during sleep time, so cripples certainly don’t). But he’s up to 14 hours a day and the government is balking at a 15th hour. They’re forcing us to justify the request instead of just looking at my file and seeing my diagnosis (an incurable disorder that gets worse over time) and the fact that I have never asked for anything I don’t need and realizing that yeah, she needs help. It doesn’t help that they don’t reach out to me directly. There’s a middleperson. Things get lost in translation.

Anyway, it’s almost 8:00 and I’m getting hungry, so I’m going to stop ranting. But anyone who says cripples don’t work for their benefits and just get handouts have never had to deal with the government (state or federal). Fighting for shit I need is an entire job in itself. They should be paying me, but then they’d probably kick me off everything anyway. Blargh.

End of Year Rant

~ shawnaborman ~ Leave a comment

Hello, hello! How’s everyone doing? Are you ready for the coming year? Things here are annoying, so I thought I would vent a little. It’s nothing super important or life and death or anything. It’s just irksome. The government is involved, so of course everything is taking way longer than it should and it’s all a giant hassle when it should be easy peasy. They’ve had years to streamline the process, but they have not. Just like with everything else they’re involved in. Things shouldn’t be this complicated. But anyway…

Some backstory. Dad started collecting social security this year. Well, according to a lawyer we went to when we made our wills (he specializes in cripple stuff), since I’m cripple, I should’ve been eligible to receive some benefits when Dad started collecting. We knew this, but we didn’t know what all we would have to do when the time came. So, when the SSA said we needed to complete a form for me to receive the benefits, we searched high and low on the website for it, but couldn’t find anything. Ugh. We called on July 23rd to find out what to do. Long story short, I would need to set up a phone meeting and answer some questions (no mention of a form), but there were no appointments available at that time. They would be in touch.

Fast forward to October when Dad starts receiving his benefits. We still haven’t heard anything about my appointment, though we have been calling at least once a month to make sure no one has forgotten. The nice SSA people all assured me it was just a matter of waiting, but that I won’t be penalized because they know I’ve been in touch and trying my best to move things along. The waiting game continues until Dad gets a super weird letter and calls them again himself in November. The lady he talks to thinks the wait is ridiculous as well and puts him in touch with a woman who sends our issue up to her bosses.

Are we, though?

At this point, Thanksgiving is upon us along with the rest of the holidays. More waiting. Then, yesterday I get an email from an ssa.gov email address that contains the correct national phone number to call back, so I open it. My appointment has been scheduled! For February… at like 9 in the morning despite my requests for an afternoon appointment. Whatever. I will make it work. And I will call today to confirm that the appointment is legit, that they have my correct contact info, and who I should call in the event that no one calls me.

Again…

But seriously. Why has it taken over six months just for an appointment? And there’s no guarantee that the appointment will be the end of this process. It probably won’t be, because at that point, they’re probably going to give me trouble about keeping my Medicaid, which will start another cycle of drama. I’m dreading that one even more than this whole mess. Why do they make everything so complicated? Ugh. Wish us luck. I’ll be back next week with my regularly scheduled book review. As always, feel free to share your thoughts and stories here or on my social media pages!