I work for days, sometimes weeks, up to my botox appointment to get everything possible done so that I can rest after my injections. I learned the hard way that doing housework spreads the botox, especially cooking and cleaning that involves repetitive movement. When the botox spreads, it not only fails to treat my condition, but makes my hand weak, so weak that I can't turn the key in an ignition, unscrew the gas cap on the car, or even clip my own fingernails. No fun, so I prep. I prep and freeze food. I do chores like a crazy women. I usually rush right up to my appointment, sliding in the door just when I am due. I liken it it to the nesting pregnant women do before they give birth, only I am not giving birth. I am receiving toxins into my body to release my muscles and prevent them cramping so hard it feels like I have wires pulling my fingers back into my skin.
I experienced a few moments of mental relief after getting my botox injections this time, but when I went to schedule my next appointment, I felt grief. I grieved the fact that I will have to go through this cycle all over again. I grieved that I had to schedule this appointment around a planned visit to a friend, as that visit requires toting my luggage around, and would therefore not be appropriate after botox, when my arm was supposed to rest. I grieved that this botox treatment cycle will be my life for the rest of my life, unless God heals me.
In some respects, these are little things. Focal dystonia is not a terminal condition. It's not cancer. I shouldn't die of it. While I cannot do repetitive motions for three days after botox, I can walk. I can run. Botox doesn't make me sick or ill overall (as do chemo and other such treatments). Other than a few tiny injection pricks and ongoing muscle atrophy from the injections, my arm does not look much different. My condition is chronic, though, and that brings with it some grief. Maybe that grief is more about the little than the big things, but it's still grief, and I am still needing to work through it. Maybe this is part of my sanctification process. Maybe this is part of my journey in practicing self-acceptance and self-compassion. Whatever it is, may the Lord help me through it, because only in and through him are all things possible.
No, I don't think that you can ever "get used" to a condition that prevents you from using one of your hands. Of course there are worse things, but this sounds pretty annoying/uncomfortable/painful.
ReplyDeleteI'm sorry that you're dealing with this. I'm sending all of the good vibes for your symptoms to decrease, for you to find an outlet to deal with the downtime after your injections, and for science to come up with a better treatment option/cure. And hey, miracles are also possible and welcome!
Thank you for your kind words!
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