You may have noticed that I did not refer to this post as “Reactive Arthritis” like my previous post, rather “My Arthritis”. That’s because I have apparently surpassed the healing period for Reactive Arthritis and my arthritis has now transformed. Although the rheumatologist has informed me that I don’t fit perfectly into one specific type of arthritis, she said that I am most closely aligned to seronegative rheumatoid arthritis. If you are interested in finding out more about rheumatoid arthritis, take a look at this Arthritis NZ brochure.
When I went to see the rheumatologist, she was able to do an ultrasound on my joints and we not only confirmed that the inflammation is in my knees and ankles but we also saw that it was in elbows, which I was completely unaware of. The inflammation was also in my ankle tendons, rather than the joint, which was interesting to find out as well.
As a result of my consult with the rheumatologist I’m now on a new treatment plan (unfortunately much larger than I would have liked) called Triple Therapy. This seems to be the standard attack on rheumatoid arthritis and it’s hopeful that it will start helping me. The unfortunate side is that it takes three months to kick in, so I’m also still taking steroids as well. The steroids have certainly added a dramatic amount of fluid weight gain to my body, especially around my face. It’s hard to deal with, but I’m pushing through it knowing that once I’m off the steroids it will eventually go away.
So what does this mean for me now? I have to keep taking the medication – currently, an average of 18 tablets a day (including a couple that my mum is giving me, like turmeric tablets) and in three months time I will see my rheumatologist again for an update. Unfortunately, the Triple Therapy drugs have some nasty side effects, so I have to keep a close eye on them as well and there is also a chance that the disease may spread to my back. I purchased a small notebook to help me keep track of anything unusual because three months is a long time to remember small details!
Due to some of the drugs’ side effects, I also have to get a blood test every month to make sure that everything is okay. It’s a lot to take on, but I’m trying to focus my energy on more positive things like going to social events and reading fun books. It can be hard some days, especially when I’m in pain, but it’s important for me to keep my head high and continue to live life as normally as I can.
If you have any questions about what I’m going through or would like to share your own story – flick me an email, I’d love to hear from you!