Tag Archives: rheumatoid arthritis

Pain

I am in a world of pain right now. Like, I seriously wanna cry. I was on my feet for waaaaay too long today cooking… I haven’t “cooked” since before my injury and now I see why. OMG! I couldn’t really take pain meds as I’m not stable on my feet and I was using knives. I always think back to the Final Destination” movies when it comes to things like that. Funny, I never thought about those movies while on the track doing roller derby. I can’t explain that.

That’s neither here nor there. Again, I am in a world of pain right now. Feels like someone is sticking scalpels (yes, plural), into the medial malleolus of my right tibia. I have a very high threshold for pain, as I am in pain almost everyday of my life thanks to my lupus and RA, so I normally don’t complain about pain; I push through it. No pain, no gain. But imagine, if you will, how easy it would be for someone with my pain threshold to overdo it, and perhaps injure myself even more.

Which is precisely why I’m done for the night! I will NOT be doing anything else that requires me to be on my feet; I’m horizontal from here on out. I just thought I’d share. Oh, and please do forgive me if I’m talking in present, past and future tense… I simply cannot bear to correct myself right now.

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Lupus is a minor inconvenience……

…sometimes and sometimes it can be the most devastating aspect of my life. My rheumatoid arthritis is rearing it’s ugly head today. Right now, I feel so sad. I feel depressed. I feel anxious. I feel sick to my stomach. I am inconsolable. I feel full. There are tears welled up in my eyes. My back hurts. My neck hurts. My legs are sore. My hair is falling out. I am fatigued. I am sleepy. My fingers are sore, thank God they’re not swollen today. I feel like my body is falling apart, like in that silly movie “Death Becomes Her”. 

My hair is VERY important to me and always has been. When it first started thinning, I didn’t let it bother me so much. My husband was surprised, as was I, that I was taking it so well. Well, today as I was flat ironing my hair and I see how much further my hair has thinned I am taken aback. I’m not sure if I can handle it so well this time.

For the last few years I have been able to “grin and bear it”, the pain that is. I have been consoled by the fact that although I felt like shit, I looked good and no one could tell that I was sick. I didn’t hide my illness. I just didn’t tell everyone because I didn’t want anyone feeling sorry for me or treating me differently. Well guess what? I need to be treated differently. I don’t have the same stamina that many women my age have. I cannot walk long distances sometimes and it’s not because of my shoes (I wear heels the majority of the time, my Steve Madden gym shoes even have a heel). Flats make my shins hurt because I’m not used to working the muscles used when wearing flat shoes.

I am trying to live my life one day at a time. Most days I feel blessed that my kidneys are not involved in my illness right now. My nephrologist, Dr. Keith Bellovich, is the greatest doctor. He tells me that I am very lucky that I am in the condition that I am in right now. This condition can probably be attributed to my eating and excercise habits. I normally don’t eat garbage, and I walk a lot, go swimming, rollerskate, and play tennis. All of these activities take my breath away and I usually have to take a break every 25-30 minutes, lest I pass the hell out!

I don’t even know where I’m going with all of this. I guess I just wanted to put what I’m feeling, no matter how nonsensical it sounds, into writing. I’m all over the place with my thoughts and this is because my feelings and body aches are all over the place. There is no rhyme or reason to what my body does. It is attacking me. I am not the enemy. Lupus is.