Sunday, January 10, 2016



Why I Don’t Always Want Your Help

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    I have been sick for twenty years. My diagnoses are Sjogren’s, Mixed connective Tissue Disease, and Fibromyalgia. My chart also says Inflammatory Arthritis. I think that’s redundant at this point, but it gets me my number one medication. Anyway, the point is, I’m sick and it’s not going away any time soon.
    The point also is that all my conditions are degenerative. They get worse over time. And I have had them a long time. So yes, I am much worse now than when I started. And that’s OK. That’s what I prepared for. I don’t like it. But I always knew it was coming.
    Which leads me to this: there are things that I used to be able to do that I can’t do anymore. A lot. More than I actually care to admit really. Like the standard arthritic inability to open jars of any kind. I’m an Italian who cannot open sauce jars! Oh! And there’s this... We’re old school. My car does not have power windows or locks and my fingers just don’t have the grip anymore making me an inadvertent victim of child safety locks on my own car doors! I am waiting for the day I lock myself in!
    I also can’t carry stuff anymore. Not just up and down stairs, but almost anywhere. I am ‘Queen of the Dropsies’. Whether it’s losing my balance, too heavy, or my insanely weak hands; I drop everything unless it’s strapped to my body. Which I have actually done with bags of groceries. That did not go well.
    So with these issues (and more) after twenty years of being sick, you’d think I’d be grateful for any help I can get. But that’s not always the case. And here’s why: With all I have lost the ability to do over the years, I need to know there are still things I can do.
    Don’t get me wrong here, I appreciate help. Especially when my body is in full blown attack mode. But on days when it’s calm, I need to feel normal. It’s important for my psyche. And I need to be useful. That may be one of the biggest things I have lost-my purpose.
    You see, I have struggled all these years not to give in to this disease. I tried to do everything I could not to let it show. I raised a family, I held a job, I cooked and cleaned. I know I didn’t do it all well, but I did it. And over the years, I slowly gave up things here and there that hurt the worst or I just could not do anymore. And I accepted it because I was able to keep doing the big stuff.
    But that changed a few years ago when I had to stop working. It changed even more last year when I had to go on disability.  Just like people are identified by what they do for a living, those of us on disability tend to be identified by that word and all of its negative connotations. Like getting something for doing nothing or being paid while sitting around and doing nothing. Being purposeless.
    So now I still struggle against this disease. But not to keep going and do everything. I know my limits and I accept them. I struggle to keep my identity. To keep my purpose. And a big part of that is continuing to do what I can when I can. So although I appreciate all the offers of help when they come, please understand that when I don’t accept them, it’s because I need to be doing it myself. I need to be purposeful. And for this short time, I need to be normal.