As many of you know, living with a chronic illness is an evil roller coaster ride that you can never get off! I never really thought much about how hard it would really be. If you had asked me 10 years ago if there would ever be a time, where I would be limited with what I can do I would have laughed you right in your face and given you a very "colorful" answer. I have always been a typical go go go I'll sleep when I'm dead type of person. I would literally "spring" out of bed in the morning and do a whole day of work and then do a million activities after. There were very few days when I even sat down before it was time to go to bed.
Many of you regularly read my blog so I'm not gonna bore you with what you already know, but I've been having a rough go of it lately. I didn't realize what an emotional toll being sick takes on you. I feel like a totally different person now than I did 8 months ago, and I find many of us are going through this same thing.
Well my friends, I had "one of those days" today.
It all started at 3AM when the tornado sirens started going off and the wind sounded as if it would rip the side of my house off. A normal person's first thought is, "Wow I better get to the basement." Not this chick. I sat by the window and watched what was going on very closely because I knew that going down the stairs to get to the basement would hurt, because my knees are swollen and my stomach hurts so bad.
So I finally got to sleep at about 5AM. I was awakened at 9:30 by the husband walking in the door from work. (he's not supposed to get home until 3PM or so) So again, I was woke up. He got sent home early without pay because there was a power outage and the power never came back on. Normally this would be kind of a good thing, but given the fact that I'm unable to work right now, not so much.
So then, I had a rheumatologist appointment today. (enter scary movie sound effects here) So I go in there and find out that I have joint damage that I wasn't aware of before and I have to go back on the methotrexate shot. I know a couple of people who are on it as well, but for some reason my body hates it. So now I must inject myself with liquid fire that makes me feel like a puddle for 2 days after I take it.
I would never wish my pain on anyone, but the next person who gives me the "but you don't look sick" comment, I am going to punch them in the head and the stomach, then smack them in the face, then kick them in the knee. While they are down I am going to tie them down and say,"now, get up and go on with your day." When they say they don't think they can I am going to say, "Why not? You don't look sick."
Wednesday, April 20, 2011
Just one of those days..
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Thursday, April 14, 2011
YAY ME I WIN!!!
Posted by Rosie 1 comments
Back by popular demand!
Sorry about the fact that I've been kinda awol from my blog! I haven't been having a rough go of it lately and I'm not fortunate enough to have a laptop.
I've had a pretty bad day today even, but I decided to write and try to get my feelings out. Many people don't realize how much emotional pain comes along with physical illness. I used to always be a "glass half full" kind of gal. I still try to do this for the most part, even though it's annoying to some people at times. I've always felt like feeling sorry for myself or dwelling on the negative only makes things worse. Then came lupus....
I didn't realize how, something I've practiced my whole life, would become so difficult to me. Right now, I'm sicker than I have ever been in my life. The last 7 months of my life have been spent in a bed or a doctors office. Now, anyone with a chronic illness will agree, that a doctors visit does NOT qualify as a recreational outing. Right now, that's all I can do though. I was always a 100 mile an hour, "I'll sleep when I'm dead" kind of person. So this has been very difficult for me to adjust to.
I feel like my own body has yanked the preverbial rug out from under me and there's nothing I can do about it. So with that, I'm finding that the glass that I once saw as half full is either totally empty. Actually most days the glass is shattered on the floor.
I'm so thankful that I have friends and family to lean on. I'm gonna steal from my friend Monique in saying, there has been more than 50 times lately where friends and family have lent me their strength. I keep questioning myself. I cry almost every day and I try to hide it. I wonder through the tears if I'm strong enough to go on. Somehow I find the strength to keep pushing forward. It took me a while to figure out how, but it's all the people in my life and even just the people who stumble upon or follow my blog. You all give me strength every day. I just want to say thank you to all of you right now! THANK YOU!
Mo Mo, Fo Fo, Jo Jo and Po Po. (they all know who they are) You guys especially always give me strength and I'm so thankful. Thank you for always having a kind word, or just an "I understand" (because I know you truly do) What we go through is something no healthy person can get and I'm thankful I have you guys to "get" me!
You can find Jo Jo Mo Mo Fo Fo and Po Po on twitter
@lupusman
@falanya
@messyhappiness
@purplegimp
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