Well, Hello there. It's been a while. How've you been? I have purposely stayed away from here for reasons too many to write about. I cranked up the Pink Floyd and my creative mind decided to run the gamut on all I've been through over the years. I try not to go back too far because then it puts me in the negative place of asking all the why questions and being a person who hates negativity I stopped the crazy. I in turn whittled it down to the last two years, which then became the last year, give or take a month or six. Its been a rough summer to say the least or maybe more like a rough year but shortening it to summer sounds less stressful and painful, at least to me. It always amazes me how much my mind controls when it comes to pain. When I'm in it there are times it is excruciating and there the times it's doable and other times it's not, but I still believe the mind controls what we tell ourselves and after the painful times are done I can always convince myself, "It wasn't that bad." Plus I made it through to the other side of it." In the end that's all that matters.
It will be a year on January 3, 2017 since I started a new RA biologic drug called Humira. Yes, I know the actual and and I capitalized it since I had high hopes when I started it. Especially since I would see the commercials of people on the drug who where flying around on merry go rounds and had roses and kisses coming out of their asses. It was going to be the answer to all my pain and my life would be "normal" again, at least my normal. Funny, because my normal has been anything but for a long time. The joint pain, fatigue, answelling has controlled my life long enough. I thought, or at least hoped, after I started the Humira things would change but that's when the side effects took center stage, always an issue for me the side effects. Ugh. Humira does not play well with asthma/copd. My breathing became so bad I could hardly do anything without having to use my rescue inhaler, this on top of two other inhalers I was on. I called my rheumetologist and he said if this continued we would have to try a different biologic. The problem was just after that call I got a letter he was leaving and moving north, far north. Talk about a stab in the heart. I really connected with him and he was such a help to me over the few years. I was heartbroken. Now what? Over the years he had been my second rheumatologist and now I had to find another? I know it doesn't sound like a big deal but believe me it is. With all our complex medical issues we need a doctor who looks at us as a whole and finding one you mesh with can be difficult. In the meantime I stayed on the Humira and found a new rheumatologist. I have had three appointments witch him and I feel we are getting to that comfortable place with each other. I really like him and he listens to me and answers all my questions. Three months ago we switched to Embrel and wow what a difference with my breathing. I am off one inhaler and have been able to cut way back on the rescue inhaler. This is huge for me. You cannot imagine how exhausting it is not to be able to get air in your lungs it's unexplainable. All I know is I feel better and that's all that matters to me.
One other huge change is the level of pain I was experiencing. He gave me another cortisone shot in my knew three months ago when I saw him and the night time knee pain has significantly improved. This week was a cortisone shot in my hip for bursitis. I'm waiting for that to help more but it is an improvement during the day. Sleep can be hard when you are in pain. No sleep equals bad days for sure. The Embrel seems to be taking effect too because I am beginning to feel better as a whole. I woke up a few days this week and thought to myself. "I feel good." I cannot tell you the last time I have woke up thinking that. Fatigue and feeling sick all the time are just a couple of the symptoms of RA. I know people think it is just joint pain but it is so much more. It is a whole body issue. I could on with all the symptoms but why bore you with all that. I hope you get the point. The most importantly being if someone you know is ill please just believe them. I honestly don't know how anyone could make all this up. Have compassion, that's all. Like they say until it happens to you, you will never understand. True in all illness.
Changes are in the air and not just with the weather. I can feel changes coming on. I'm going to stay focused on that positive and not allow myself to look backwards too much and if I do I'm going to remember how far I have come in the past few months. According to my doctors the biologics can take up to a year to fully work so from here on out it can only get better. That being said I still have to take it slow. Pacing myself is how I get through all of this. It's so easy when you have a ok day to over do it only to pay for it for the next two or three days. I'm learning, slowly but surely but learning none the less. I only hope the same for you.