Accepting And Enjoying Life, Just As It Is

“Let go of the tendency which we all have to want things to be different from how they are right now, and allow things to be exactly as you find them. Allow yourself to be exactly as you are.”

-Jon Kabat-Zinn, Guided Mindfulness Meditation

AcademicQuite often, when I am in a flare, I began to distance myself from the things that I really enjoy doing. When getting out of bed, grooming myself, and getting dressed sometimes equal “doing too much”, it’s easy to start crossing off items from my list of daily activities. Even some things that don’t require too much physical activity, such as reading, listening to music, and watching television, can sometimes require more concentration than I might have during the worst days of a flare.

But once I finally do start getting better, as I have been doing over the past few days (even though I am still only at the beginning of what will sure be a long recovery), I love to (oh so cautiously) add activities back into the fold. It’s a double-edge sword that must be approached carefully. I know that doing just a little bit more allows and encourages my body and mind to get closer to a place where it needs to be, but I’m also aware that doing too much too quickly will only increase my chances of relapse. (If this were Cirque du Soleil, I’d be limping along on the tightrope!)

Towards the end of this past December, when my rheumatoid arthritis started to have a larger-than-usual effect on how I was able to teach my college courses, I consoled myself with the knowledge that a six-week vacation was just around the corner. During the past few weeks, as my pain and disability continued to worsen, one of the aspects that I took comfort in was the fact that I did not have any professional responsibilities until the first week of February. The timing of this latest flare was working in my favor and I was enjoying my break, so I couldn’t complain too much…but I did start to miss the joys associated with teaching, learning from, and interacting with my students. As I began to emerge from my flare just a few days ago, even though I knew the coming weeks will continue to present certain challenges, I was once again looking forward to going back to work.

My return to the academic world actually arrived one week sooner than expected, and I couldn’t be happier!

This past Thursday, which was just my second day into a very slight improvement of my overall condition, I received a phone call from my university. The dean wanted to meet with me to discuss the possibility of me taking on some additional responsibilities in the coming academic year. (Oh, and the meeting had to be that same evening!) The first thought that passed through my head was that there was no way I could do so in the state that I found myself…but I asked for a few minutes to think things over.

I consulted with my physical therapist (who was actually at my house giving me ultrasound treatments at the time) and my husband. Both of them encouraged me to attend the meeting; they thought that it would be good for me to put my mind on something other than my illness, and that even though I needed to be careful it would be good for me to get out of the house. (The meeting place was not going to be on campus, but at a more accessible coffee shop closer to my house…the culture where I live is one where important discussions are often conducted outside of a formal business environment.) I called back and confirmed my attendance.

A few hours later I sat in the coffee shop, elated, as the dean described his plan for me to become more involved with a special graduate degree program that the university offers. My vision of the future was once again full of excitement and academic curiosity, and my feelings of hesitation and concern about my rheumatoid arthritis quickly began to fade away. He had been informed of my health situation, so we had a brief discussion about my rheumatoid arthritis and how I continue to learn to manage the limitations of my illness with my willingness and ability to teach. We finished our meeting with an agreement to move forward with the proposal. The timing of my new courses has not yet been formalized, but just this morning I did participate in the orientation/welcome meeting for the new graduate students.

I continue to give myself plenty of time to rest, and will continue to do so in the coming weeks, even after I return to work. I continue to give myself extra time to get ready in the morning, and pad my travel times between Point A and Point B. I move forward with a new found confidence in asking for special accommodations when I need them. I am not placing a deadline on this current period of healing. If my current state is actually my new normal, I’ll just continue to figure out how to incorporate it into my life.

I’m pulling myself forward, but I’m not pushing myself too hard. Even though I continue to experience considerable levels of pain, for the first time in the past few weeks (months?) I can finally say that I really do feel good…and I continue to learn that feeling good is about so much more than just the presence or absence of pain. Even though my rheumatoid arthritis will always be a big part of my life, there will always be room for so much more. Being reminded of this is such a wonderful feeling.

Stay tuned…for the next adventure of Rheumatoid Arthritis Guy!

6 Comments
6 comments
  1. Cathy says:

    Yay! This is such a beautiful post RA Guy. We are so much more than RA and your good news is a reminder of all the other wonderful things we are. Congratulations on everything!

  2. Wren says:

    “…and I continue to learn that feeling good is about so much more than just the presence or absence of pain.”

    This is a profound lesson, Guy. I’m happy for you as you move forward, “working with yourself” and taking such great joy and satisfaction in the life you’ve made for yourself.

    Sending smiling, warm hugs your way.

  3. Jules says:

    I must ditto the above posters- it’s such great news that you are on the mend an have such a terrific plan beyond your RA. I truly believe that when we have something positive to concentrate on, we are miles ahead of the game.

  4. Lana says:

    I know what you mean about needing more time and concentration during flares. They can take a lot out of you. I am glad to see the flare has lessened and that you have returned from vacation in good sprits. I have recently taken on some more responsibilities as well but the weird thing is that before my diagnosis, I had a lot more responsibilities and commitments so I am just trying to incorporate them back into my life. Good luck to you with this new thing you are doing…I am sure that everything will work out. Like you, I believe that RA is a part of my life, but it is not the only one part. Take care and be good to yourself.

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