How do you plan your day and conserve energy? Are you a Spoonie?
Are you like me, and run out of energy after doing only a few things? You shower and are then worn out and have to rest? Or maybe you walk the dog and it’s just too much! And you find yourself turning down invitation to lunch (pre-COVID-19) because of no energy. I do. I hate having to say no to friends, going home early, or taking shorter walks. I feel like I lost so much and myself!
Then I heard about The Spoon Theory, developed by Christine Miserandino. It’s a way of describing, planning, and conserving energy units that you use during the day. On her web page, Christine how she explained her illness (lupus, an autoimmune disease) and energy levels to a friend. You are able to explain to others the details of your life as someone with an invisible disease or chronic illness.
For example, I start my day with a list of things I need to do (shower, make the bed, do some laundry) and then I add my list of things I want to do
(go for a nice walk, sew, bake something). When I put the lists together, I realize that I won’t have enough spoons (units of energy) to get through the day. So, I’ve learned , using The Spoon Theory, to divide up the have to’s and the want to’s and add in some rest periods. I probably won’t get everything done—there’s always tomorrow—but I also won’t get exhausted, achey, and cranky half way through the day! The Spoon Theory has made so much sense to me!
Have you thought up a way to use and conserve your energy throughout the day?
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@sueinmn Great examples, Sue!!
Hi Sue,
Thanks for your ideas! It was kind of you to reply. I plan to come back to your post to see what I can do. Kinda tuckered out now.
Wow. Not a great way to start the day. Why on earth would you put this here ?
@jcarndt, I can understand your shock when seeing @strongevergreen's post about end-of-life symptoms in isolation. @becsbuddy queried them and they kindly explained how considering end of life guides their living in a follow-up post. I encourage you to read it here: https://connect.mayoclinic.org/comment/961338/
Today is a beautiful sun-filled day where I live. The leaves on the trees from my window are yellow, but with the sunshine they look golden. There is beauty in the cycle of life.
Sorry, but I at 76 find humor in the remark about resting. Because that’s me! I ALWAYS have a list. But have gotten used (to some degree) to my reality: I am unable to complete the list! Sometimes completing an everyday chore will exhaust me suddenly. Have to rest. The day passes so quickly for we who are in this predicament. I get frustrated. But, then, and it’s the hardest part. I tell myself “everything is as it should be, and that it’s going to be okay.” It helps ME. 🙏🏼
I am trying to stay positive and always have a list to guide my priorities, but find I’m often “exhausted, achey, and cranky.” I get so frustrated! Yes, I’m early in the MG treatment process, but I can’t even get through a shower without resting. In fact, I’m sitting here in a robe right now trying to catch my breath. I still need to get dressed and take care of wet hair. Sometimes I just feel like crying.
I have the same problem. I get out of breath and my heart beats like a drum in my chest just making the bed. So, now I pull the sheet and blanket up and straighten it out, then I watch a little TV or play on my computer. When I am ready, I go back and finish it up. Some days I don't make the bed because I want to do a load of laundry. It's all about not minding doing it in stages. Give yourself a break. I think you are beating yourself up because you wish you could still do it like before. Well, guess what, you can; it's just doing it differently and ending up with the same results. Accepting that you have to do things differently than before is the hard part. Just remember you can do it. Good luck and keep smiling.
Thank you for the thoughtful reply and hug! I refer to the approach you indicated as "pacing." Without doing a little at a time, I simply would not get through a day. I don't mind doing things differently. What frustrates me, though, is that I get precious little done, anymore. You are absolutely right that I wish I could still do more! How do I get past taking a shower being the main event of the day? I really try to do something productive while resting like paperwork, reading, or working on a hobby, but I'm usually huffing/puffing and in pain. I hope this gets better as I get farther along in my treatment. Thanks, again, for you encouragement!
I’m a Spoonie too. I have several autoimmune diseases that zap me of energy. I also was recently diagnosed with idiopathic hypersomnia which is also known as Narcolepsy 2. So everyday I feel like I’m on cold medication (antihistamines) and have to prop myself up to stay awake.
I wake up tired and I sometimes use half my spoons just getting out of bed, and taking a shower. I then go sit in my recliner hoping for a renewal of strength. Usually, I fall asleep.
It’s very frustrating when I want to go out and do something but I just can’t muster up any spoons. I’m 74, and I certainly didn’t think retirement was going to be like this…
It's not energy. i don't have the fatigue people complain about (I'm in- I think- a Sjogren's flare.) I develop either painful symptoms, or in addition chronic coughing up mucous, hard to breath, so it's depressing but there's little i can do in the evening except watch TV with my husband. I have been making a to do list recently because my CONCENTRATION is bad and I forget importan things.
I do think listing must do and want to do could help. Thanks for the insight. I had a fairly decent day yesterday, hopong the azathioprjne will kick in - not sure if I will go in remission, but hoping this flare will die down. (Rheumatologist said I could go into remission but might take years- only diagnosed Oct. 2023, but probably had Sjogrens and was misdiagnosed until then- but that's a long story for some other post ). Thanks again for your insights.