*Deep Breath*
Sometimes this part of our life seems too painful or personal to write about, but then again I want to be able to look back on this. And I know there are other people going through similar situations who can relate to the difficulty of it all.
I feel like freedom is only just around the bend. My paychecks have finally started coming, and although they are only the smaller, training paychecks, the money is such a relief. It feels good to be able to pay most of the bills, even if I can’t handle all of them. It feels even better knowing that when my normal paychecks start coming in, we won’t have to borrow money anymore.
It feels even more better that once Todd finds a job, we’ll be able to have our own place again. I appreciate Sylvia letting us stay with her more than words can begin to say, and helping us get back on our feet… it’s the fact that we were ever off our feet in the first place that bothers me so much. I have always been such an independent person, and I hate depending on anyone for anything. This has been such a difficult, yet humbling experience.
The frustration I am currently feeling is palpable, bubbling at the surface in such a way that I want to go outside, clench my hair in my fists and just SCREAM. Good lord, can’t I just scream if I want to? I need a punching bag. I feel frustration in my fingers. Is this normal? I get so angry, so frustrated, that I feel like the only cure is to break my own fingers. Seriously, I’m a certified nutcase.
I’m so, so glad that I am getting this short break from school. I have taken on a bit of stress, with trying to get my FAFSA straight (on track with that), and re-applying for Medicaid/Disability. I found out that because I decided to abandon my last application out of guilt, shame, fear, whatever, that I missed out of the opportunity for them to help me with my medical bills from December until March ($86K). I’m a little confused, because I didn’t even know that I could get help with my medical bills until I got my letter of denial, saying that I could ask for a retroactive determination. When I went to ask for said retroactive Medicaid determination, thus help with bills, I was told that it was not possible.
The government makes no sense whatsoever.
Why wasn’t this information presented to me when I was accumulating these medical bills, put out of work, and dropped by my insurance? So many flaws in the system… I had no idea that there was this help out there for me. Even when I applied for temporary disability for being out of work, the application process was taking months and months, to the point where I couldn’t even handle the stress of the process! Phone calls, paper work, endless papers that needed to be faxed, endless information that I needed to gather, bank statements, bills, and I could barely handle it… and then they started scheduling doctor appointments. Dozens, it seems. This is when I backed out. I wish I hadn’t. I said to myself that I would rather be limited in the type of work I can do, and search long and hard for a job that will accommodate my problems (nothing physical or stressful) than go through this process and be a person on disability. I didn’t want to BE that person.
Certain jobs are out of the question for me now, through no fault of my own. I can’t lift anything, I have no stamina, I have no endurance, and I can’t handle high stress situations or customer service jobs due to anxiety, panic attacks, hyperventilating, tunnel vision and passing out. The stress from these types of jobs sends me into some sort of state of hypersomnia and depression where I can sleep 18+ hours a day. And that’s never enough.
However, I’m not that upset, because I didn’t know that Medicaid would’ve helped with my medical bills until it was too late. So yeah, I missed out on that opportunity, but what did I really lose if I didn’t even know I was losing it? At least that’s how I’m rationalizing it to myself. And I haven’t completely lost hope that I’ll get help somehow. There’s no reason for me to be upset. Even if Medicaid had helped, it probably wouldn’t have been a lot. And if I were to ever get my settlement, I would have had to pay back any money they helped with. It may even be better this way. Now, if I get a settlement, then I can just pay the bills off and not have to worry about paying back the government or Medicaid, because as of yet, they haven’t given me shit.
Another thing I have learned is there is a program for the “working disabled”. Basically I’ll still be able to work, but since my income is limited due to several factors, I can still get assistance, and most of all, Medicaid, which is what I really want. I don’t want “free money”, as some people assume of people… I just want health insurance without having to pop out a kid. I think I deserve that much.
I have too much pride to not work. I want to work… but I recognize that due to several factors, physical, emotional and mental, that my working and earning capacity is severely limited. Maybe this will change once I finish my Bachelor’s and I have more opportunities. The good thing is, I have now found a great job, where it isn’t exactly physical, except for playing and lifting a small child, and isn’t really stressful at all, unless you factor in a child’s future being in your hands.
I just have so much hope right now, despite everything that seems wrong and difficult and out of my hands. I feel like we are on the right track. It’s only been 3 months since we left Gaston. We may not have our own place by Christmas (like I had originally hoped), but it won’t be too long now.
And wanting and having our own place again… That’s another post entirely.
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