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Notes on My Routine


[Pi...]

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Alright, so here's some basic notes on my daily/weekly routine that have helped me through this process. :giggle:

Daily:

  • Morning: I do a quick 1-minute lymph massage (you can look this up on YouTube if interested). This gets the lymph flowing and helps with swelling. My left leg used to always be a bit bigger than my right and I had constant puffiness in my face, so this helped with that.
  • I make sure I get natural light in the eyes every morning to set my circadian rhythm, (not through a window!!) So I either go outside for 10-20 minutes or I use a S.A.D. lamp every morning. (This is important for sleep!)
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  • Pacing: In the beginning I would try to get as much done as possible in the morning before I 'burned out'. Then I realized that was causing me to burn out and that I needed to space out my activities with long periods of rest. (This is what they suggest for Chronic Fatigue Syndrome and I've found it helps). So I try to never be active for too long NOR sit for too long, but to evenly pace activity with rest.
  • I don't do more than one big outing per day and if I do an outing one day, I have a quieter day the next.
  • I move slowly and don't race around trying to accomplish something quickly because that increases tension.
  • I've organized a daily activity schedule that is a bit easy on a good day and bit challenging on a bad day and try to stick to it as much as I can, though there is also some variety. That way I know what I can practically accomplish each day and helps to prevent overdoing it.
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  • I have a daily nap if at all possible.
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  • I make dinner early (we eat at 5) for 2 reasons: sometimes I'm out of energy completely by 6 pm and secondly, I do intermittent fasting, which basically means I don't eat between dinner and breakfast. It's good for the digestive system to have a long break.
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  • I go to bed early (upstairs at 8 pm, one hour of tv by myself, then bed at 9). I put on orange glasses beginning at 8 pm to block blue light (important for sleep).
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Weekly:

  • I aim for 2-3 outings per week. (This would be different for others depending on where you're at). I think it's actually very important to get out and I'm at the stage where I have to really make a point of it or it's easy for me to stick around the house too much.
  • I do meditation from Monday to Friday and take the weekends off. (I'll talk about meditation more in a different post).
  • I have a light exercise routine that I add to very, very gradually. It is mostly yoga and walking. I found early on that I can't do anything aerobic, nor can I do weights. (More about this in another post).
  • I try to make sure I'm doing something with purpose and something fun weekly. Purpose can be posting on here, or planting a bee-friendly flower, or picking up a piece of litter, some type of prayer or anything that makes you feel like you're contributing some small thing to the world. Fun is also super important and not on most people's radar when they're suffering, but it can really boost "happy" neurochemicals. I do adult colouring books, crafts, play guitar and every Saturday night I have a 'Musical Bath'. I get in the bath and blast happy music and sing at the top of my lungs. (My family expect this! :LOL:)

In my future posts, I'll be breaking some of these categories down even further and going into more detail. Cheers everyone, hope you're all hanging in there!

 

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[Bu...]

Posted

Thanks @[Pi...],

I have almost no routines.  It's hard with my crazy insomnia induced sleep non-schedule, but this got me thinking about just doing some of the same things everyday as a start.  And thanks for the reminder about fun, I tend to forget that. ;)

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[Pi...]

Posted

@[Bu...] For me I found that I did a little better when I kept to a basic routine regardless of how I slept, rather than accommodating bad sleeps. Starts to help sort out the rhythms a bit. I mean, I don't feel top drawer, particularly in the morning. But I felt no better and often worse (more sluggish, brain fogged) if I tried to 'catch up' during the day. The insomnia thing is a massive challenge for sure.

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Thanks for the great advice I can and do most of these things, but it’s hard to stick to a routine. Benzos have left me so debilitated that it’s hard to know what kind of shape I’ll show up in the morning. I also have quite a bit of neuropathy in my feet and legs so it makes walking tough. I do use trekking poles to go for about a half hour or so. That seems to attributed to the benzos as it goes away when I have a window. 

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I am so OCD now as a result of the withdrawal that I have to stick to a routine and when it's disrupted, I feel very very anxious. I find walking to be very beneficial despite my neuropathy and I refuse to take gabapentin or lyrica for it. Just more drugs wrecking havoc with my CNS that I would have to withdraw from. I have started doing EFT for benzo withdrawal which seems to calm me down a bit. I am not to the point where I could take an outing other than go to an appointment. I am glad to hear that you can have fun. I listen to  a lot of classical music for recreational pleasure. And most critically, I try to stay in touch with new friends and old friends as much as possible.

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