We could blame the way we are on our personalities saying “This is just the way I am or I have always been “that” way. If “that” way has gotten in the way of jobs and relationships maybe you should think about getting to the root of “that” way. WHY are you the way you are?
You could blame your parents, your childhood, your past experiences, and your illnesses. When it comes to some of our negative and damaging ways, it’s not so much about who’s fault it is as much as it is about who’s responsibility it is to change those ways. You are not a dog and you can be taught new tricks. Instead of assigning blame which gives us a way to justify our behavior or relieves of us of responsibility, I propose the idea of citing these things or people as sources. They are the root causes branching out into our thoughts, actions, and words. What are the “sources” of my behavior? What are the “sources” of my feelings and thought patterns?
It is a matter of will, choice,and work. Real work. A real look at the source but, the real WORK begins in the effort to change those thoughts which will change those feelings and replace those actions with new and improved actions. The work is NOT easy. Sometimes help has to come from a spiritual figure or professional help to assist you in the unravel of those tangled roots and put new tools in front of you. This overhaul is a long haul and can take years to improve. I’m still untangling roots!! I don’t want to keep producing spoiled and rotten fruits in my life. I want to cut the root that produces the bad fruit.
It must be nice to be not have to work 40 hours or not to work at all. It must be nice to receive food stamps or assistance. I wish I got food stamps. I wish I didn’t have to work.
It never ceases to amaze me the dumb and thoughtless things that fall out of the mouths of human beings in relation to the unknown situations or hardships of other people. I don’t know if I am get older and less tolerant of ignorant statements. Standing in line, the woman in front of me paid for her food with food stamps. After she left, the cashier says to me, “Must be nice not to have to pay for food. I wish I had food stamps and could sit at home.” Before I knew it I responded “Really? You wish would lose your job or due to an unforeseen illness or accident be rendered unable to work and take care of your family so that you wouldn’t have to pay for food and sit at home?” Silence.
Must be nice to wonder where your next meal is going to come from. Must be nice to fall on hard times or be marked as disabled. Must be nice to feel like a loser because you receive government assistance and everyone in line thinks you’re a leech. It must be nice to worry about your family’s future. It must be nice to all of a sudden have it all and lose it. It must be nice to work all your life and retire and can barely make ends meet.
No, it must be very stupid to say things without thinking about how a person ended up where they are. And for all you don’t know, it just may be a temporary set back. Be careful what you wish for this could be you.
Thank you. You’re Welcome.
I have a really bad cold and if you have RA or an autoimmune disease you know having anything that will further compromise your immune system is a disaster. I woke up feeling like crap. I thought to myself: “What is this?” It’s not RA. It’s not Fibromyalgia either. “What the—-?” One minute I felt chills and the next minute I was hot. I hope it’s not the flu. It wasn’t. It is a cold. A nasty, disgusting, cold.
Well, today my fever stayed away and I had some strength. I decided to cook. I didn’t cook yesterday. Chic fil A it was and whatever one could find if they got hungry later. When you have RA you strategically cook. You want it quick and you want it delicious. So here is the quick meal I threw together in 30 minutes.
I cooked steaks on an electric grill (the old George Foreman) and stir fried some veggies. My daughter wanted rice and the complete meal was done in less than 30 minutes. I was not on my feet long. Only for the stir frying (3-4 minutes) and when I seasoned the steaks. The grill did the hard work and I sat down. I didn’t eat much of my steak but I ate all of my veggies. My appetite comes and goes with this cold. However, leftover steaks and veggies become and omelet in the morning. 🙂
I can’t do that because of my toe.
I can’t do that because of my hip.
I can’t do that because of my knee.
I can’t do that because I am in a wheelchair.
I can’t do that because I use a cane or walker.
I did “that” or tried “that” and it didn’t work.
I can’t because I have RA, Fibromyalgia, Lupus, Osteoarthritis…etc…etc…etc…
Okay, first of all (and yes, I am doing that sassy rolling the neck thing with my hand on the hip), you can’t tell me I don’t understand because to some degree I do. So not to offend the sensitive soul of one with an autoimmune disease, let me talk to myself for a second.
Nikki: You can’t or you won’t? You can’t or does it hurt? You can’t but what can you do and don’t say nothing because you can do something. You can’t or are you afraid? You can’t or you feel as though “they” may be “looking at you funny?”
Well, Nikki (YOU), you have to change your attitude first of all. Yes, I know you went through or may be going through the “why me phase” or experiencing “B.A. nostalgia” (Before Autoimmune). But, listen, you have to become the very thing mentally you were before and that is a fighter or warrior. If you never were that then you must become one or you will speed up the process of the toil it takes on your body. Nikki (YOU), you can not or will not go out without a fight! You are the ROCKY of your illness.
So how can you improve your attitude?
- Prayer works miracles
- Meditation works wonders
- Positive quotes on the mirror or your nightstand that relate to attitude, inspiration, etc
- Instead of always searching for the bad things about your illness or disease search for people who are living successfully with it and draw from their ideas and perspective
- List or say five things you are grateful for every day morning or night
- Drink more water (just thought I would throw that in there)
- Eat healthier because you will feel better physically and it will help you feel better mentally
- Face your fears about your illness or disease and think more about what you can do than what you can’t do and be forever grateful for that
- Try it again and again and again. Try something new. Create an exercise of your own.
- Cherish the good moments, spurts of energy and use them to your advantage. Don’t worry about “I will hurt later” because what I have found is you are probably going to hurt later anyways.
Today is Rheumatoid Arthritis Awareness Day and I must admit for the last 5 years I have not really publicly displayed anything on this day. Sure from time to time I would share a post about RA but, really I didn’t want anyone to know I had it. And when I did talk about it, it was as if I were just as invisible as the autoimmune disease itself. This is my first year fully, okay, 85% embracing this day.
I decided to see it as a day to say HEY, WE ARE HERE. EVERYWHERE. LIKE…ALIENS THAT LOOK JUST LIKE YOU working in your office, at your schools, etc. ( YOU KNOW THE WHOLE “BUT YOU DON’T LOOK SICK” COMMENT WE GET 🙂 BUT NO 🙂 ). And by aliens I mean this foreign illness has invaded our bodies without warning or permission. Straight from the “OTHERLAND” (MOTHERLAND).
It’s a day to explain to you it’s not “JUST ARTHRITIS” and it affects more than your bones. It can affect your heart and lungs and rarely, the brain. It also likes to bring along with it Fibromyalgia, Osteoarthritis, Diabetes and a “party of five” of other things. It interferes with friendships and every type of relationship there is.
It’s a day for others to learn a little bit more about what I go through daily.
So, last night I was going to go a bonfire, earlier this week I was suppose to go to an open mic poetry night, I also was asked to attend a business meeting but, as you can guess, none of that happened. I noticed last night that not much of anything has been happening even with careful planning. It hit me this morning “like a ton of bricks” (as I heard an old man say frequently and often thought that could be painful), maybe how you use to manage your pain is not working anymore. Your plan (manual) needs to be updated to match the increase of activities in your life or the slowing down of activities in your life. Those of us in this community know how much energy it takes to do the daily basics, keep a clean house and clothes, take care of a family and self, plus work and then other things outside of that. Even with all of the careful planning sometimes Dr. Evil (that is what I call RA) has other plans for you! (Muah ha ha ha….NOT FUNNY) and so you have to work around it or go to sleep! It is a juggling act with no applause and sometimes you feel like you are waking up to a circus of what to do now and what to next and what not to do. So, today I will take some time and see where it is I am going wrong and how can I not only manage the pain or fatigue (physically) but, manage the illness itself (mentally)….better.