top of page
Search

Part 2 tips

  • Writer: Katie Tolbert
    Katie Tolbert
  • Jan 17, 2021
  • 6 min read

This is Part Two of the things illness and disability have taught me. I didn’t intend to do a series, but it turns out I’ve learned way more than I realised. Which is gratifying, in a ragged, dim glow silver-lining kind of way. Also with huge thanks to everyone who has shared their own learning and knowledge.


NB, for those who don’t know, Spoonie is a term some people with chronic illnesses or disabilities use to refer to themselves. It comes from Spoon Theory, a method of communicating how your illness or disability effects you.


Fatigue is a common thing many poeple face with disabilitys and all kinds of disorders.

That makes it incredibly hard to do basic things like take care of yourself, your house, your relationships, your work… Basically, all the things we need to do to maintain a healthy life style.


So I’ve devised some ways of keeping on top of things to the best of my ability. Some of these are theories, and some are practical shortcuts.


If you’re here reading this, I hope it’s because you’re looking for this kind of thing, because there’s nothing worse than unsolicited advice. And, obvious disclaimer: this is stuff that works for me (sometimes). I don’t speak for anyone else. I’m never going to tell you what to do. I’m just sharing because, as I said in the first post on this topic, it’s stuff I wish I’d known long before now. So here goes.


Pick your battles


I’m kind of an mixed person. (I can hear several of you laughing). Yep. It’s not something I really like about myself. A lot of it has to do with being upset at how my illness has taken over my life, and a lot of it has to do with the fact that the world is a bit crappy .


It’s hard not to take all of that on. But I’ve learned how much it costs me. Sometimes, it can be a good driving force for getting shit done. And other times, it just wipes me the fuck out. There’s a lot of truth to that saying about choosing the mountain you die on. For every action there is an equal and opposite reaction, and however much energy you spend on anger, you’ll pay for it. So the fight has to be worth the fall.


Take advantage of good days


Other people might tell you not to do this. They will tell you about pacing yourself, and the “boom and bust cycle,” and I’m not going to say that those things aren’t true. But what I have found is that it’s absolutely vital for me to do things when I am having a good day, and to rest when I’m having a bad day. And that may mean pushing myself a bit on good days. I’m ok with that. I would rather push myself a little further on good days, and allow myself to rest a little more on bad days, than spread it out. Because trying to do even a little bit on bad days can suck. And doing lots when I feel good makes me feel awesome.


So don’t feel guilty about letting housework pile up or whatever. Rest when you need to. And when a good days comes, then do it.


Let others help


For god’s sake, let others help. (I’m swearing at myself here, because I still can’t seem to learn this one). They want to. It really sucks seeing someone you love struggle. It’s frustrating as hell when they won’t let you assist.


Obviously, there’s caveats and grey areas to this. Sometimes, it’s really important to your sense of self-worth to do things for yourself, even if you’re going to pay for it later. Sometimes, you need to push yourself to find out what your limits are.


But a lot of the time, something that’s going to hurt you, or take you hours, can be done by someone else much more easily. And they will feel happy that they were able to help, because there’s so much they can’t do. They can’t take your pain away. But they can give you a ride to the doctor. Or make you dinner. Or take you to swimming or physio or the grocery store.


(The next step to this is not just letting others help, it’s actively asking for it. But that’s like level five ninja stuff and I’m not there yet).


The difference between Rules and Guidelines


This might not be so relevant if you don’t struggle with perfectionism or PTSD or OCD or something. But for me, learning the difference between what I considered Rules, and what could be Guidelines, was a big step forward in coping with my illness.


You could call this Needs versus Wants. Your Must-Haves versus your I-Can-Live-Withouts.


Whatever terms you want to use, it’s about knowing what you really need, and what you can learn to let go.


I’m not good at letting go. I like to have everything just the way I like it. But when you’re exhausted and in pain, that’s not always possible. So I ask myself, for example: is it a Rule that my sheets have to be changed every Sunday, or is it a Guideline? Is it a Rule that I need to reply to this email today? Is it a Rule that I do this washing now, or can it wait? This question allows me to relax around things just enough so that I don’t wreck myself over every little thing.


SHORTCUTS


Food


-You know what’s great? Smoothies. And milkshakes. Cos you can fit a whole lot of nutritional shit in them, and they are easy to eat. So if you can’t fix a whole meal, whiz up a banana and some peanut butter and some yoghurt. A stick mixer is a good investment, then you don’t have to clean a whole blender.


-Drinks like Complan are good too. Not to replace your diet, but just to make sure you’re getting enough of all the vitamins and shit. You can add the powder to a smoothie.


-MICROWAVES. Did you know you can microwave a whole ear of corn, then just peel it and eat it? You probably did, becauseyou probablygrow upwith one. Most vegetables can be cooked in the microwave. The frozen pre-cut kind are the easiest.


-Snack. If you snack a lot, you can keep your energy consistent, and you don’t have to make as big a meals either. Have a snack drawer by the bed so you don’t even have to get up. (I have one. Don’t ask me what’s in it).


-EGGS. Eggs go in the microwave! They’re your friend.


Housework


I struggle with this, Some things to do:


– Wash dishes in the morning & mid eveningif I can, because at night it hurts too much to stand over a sink


– Sweep instead of vacuum when I can because vacuuming can be hard


– Having said that, one satisfying thing to do while you’re sweeping is sweep the cobwebs off the ceiling. That way when you’re laying in bed they don’t annoy you. (Maybe that’s just me).


– Housework is an Ask For Help area. Shortcuts include ones where you involve other people to make the job quicker and easier.


Self care


It’s kind of hard to write this one, because self care looks different to everyone. For me it includes a questionable snack draw. It also includes:


– Making sure all my medications are lined up in the cabinet so I can take them straight away when needed. A shortcut here could also be a pill sorter box.


– A checklist of prescriptions pinned on the board so I know when I need repeats ahead of time


– Hot water bottle and/or wheat bag and/or electric blanket


– Self care for me can include not looking like a zombie even though I feel like one. Makeup is a minefield for me. I never learned to do it properly. But I’ve figured out what is easy to apply and makes me look ok: Mascara, mat, eyeliner (easier and quicker to apply, and more forgiving in that it doesn’t enhance dark circles, and it doesn’t look terrible if the lines aren’t perfect because you’re weak or shaky or whatever), light blush so I don’t look like death warmed up, and lip gloss. I don’t wear foundation most of the time, which is good because I don’t really know what the difference is between that and concealer and bb cream and highlighter and whatever else there is.


– For days when washing your hair is too much: use dry shampoo and leave in conditioner. Or just tie it up.


That’s all I’ve got for now, but if you’ve got things to add, please let me know. It was really great that people did that with Part One of this. Crowdsourcing survival is just another shortcut, I guess.

 
 
 

Recent Posts

See All
Fibro

One of the most common symptoms of fibromyalgia is widespread pain. This pretty much means that we feel pain from head to toe...

 
 
 
FNDwhat it is an how it works

Functional neurological disorder – formerly called conversion disorder – is more common than multiple sclerosis yet remains a...

 
 
 
My story

My rare disease Storys My name is Kate & I have FND. AMPS, HSD , & a under developed Cerebellum to name my rare disorders. The beginning...

 
 
 

Comentários


Post: Blog2_Post
  • Facebook
  • Twitter
  • LinkedIn

©2020 by Kat FND journey . Proudly created with Wix.com

bottom of page