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in Health &middot November 3, 2015

How To Save Spoons When Cooking

Pssst – scroll down to the bottom to learn how you can enter to win $500!

I love food, I love cooking (after all I was training to be a pastry chef before I had to drop out because of my health). Granted, these days, I couldn’t be happier than with an afternoon of cooking shows (hello, James Martin makes everything better). There’s nothing that beats actually cooking real food that doesn’t just exist on my TV-screen, though. Most of the time, I make pretty boring ‘I have to do this to eat’ things, smoothies for a couple of days, green juice for the rest of the week.

Eggs, two, fried, for dinner. A slice of melon and a cup of iced latte for breakfast. Yoghurt and a squeeze pouch of strawberry-banana puree for dessert. Pretty mundane stuff that isn’t very creative, to say the least. Boring but still taking up energy. Sometimes, especially before getting regular IV saline (and this summer when I didn’t have a useable vein left in my body) I have to get someone else (A.K.A. my mom) to help me. Going from spending a day working on a bazillion tiered cake or a boatload of chocolates was hard but I’ve been able to find ways to help me save energy and even make things just because I want to.

Here’s how:

How to Save Spoons While Cooking

1 – Do everything in a certain way. I know it’s boring. It just saves so much energy when you don’t have to think about the way you’re going to do something when you’re actually doing it. This can apply to anything, not just cooking. The way you get dressed, brush your teeth, wash your hair … It’s also a big help if brain fog is a problem, you can even write it out and stick it somewhere you’ll see it.

2 – Think about where you put everything in your kitchen. Do those pans you use every day really need to be in that awkward spot behind a bunch of other things in that far away cupboard? Put the things you use most often in easy to reach places, close to where you’re going to use them. Pans near the stove, glasses and mugs near the water pitcher/cooker. Think about putting tea or coffee supplies in the same cupboard as a couple of mugs (or put a mug near your coffee machine).

3 – Use machines. If you’ve got them or can afford to buy them, use them. Use a blender or a stick blender to mix things. You can even make pancakes and warm sauces with a blender if you’ve got a high-powered one (like a Vitamix or a Blendtec). Use a food processor to do everything from making dough, to slicing and chopping vegetables. Stand mixers (like a Kenwood or a Kitchenaid) are great for whipping up cream, kneading or making meringue. Use them for anything that needs whisking for more than 10 seconds. You can even use a stand mixer with the paddle blade attached to shred chicken in about a minute. Use a slow cooker if you won’t be able to keep an eye on what you’re cooking the entire time. Chop and peel all the ingredients, add them to the slow cooker, turn it on and leave it for at least 4 hours.

Spoon Saving Checklist
Click this picture to get the checklist!

4 – Consider the utensils you use when you’re cooking. Can you get a lighter pan? I like a simple stainless steel pan for pretty much everything. Cast iron pans work great. They’re a good idea if you could do with a bit more iron in your diet, but they’re a lot heavier and more difficult to lift. You want something you can actually, safely lift off the stove when it’s filled with something hot. Same goes for knives and chopping boards; can you get lighter versions of both if that would help you? You can always keep a chopping board on the counter, that way you don’t need to start dragging it across the kitchen when you’re ready to start cooking.

5 – Break the recipe up. Find moments in the recipe where you can take a break and come back to it, later. Print the recipe and read it through, are there ways to break it up in smaller pieces? How much time will you need for the recipe? Can it be done in a reasonable time frame (however long that is for you)? Can you prepare some things beforehand? Things like chopping and peeling vegetables or defrosting something to go in the recipe, can be done a day beforehand, for example.

7 Ways To Make Cooking Easier

[bctt tweet=”How to save spoons while cooking plus a free checklist.”]

6 – Freezing the basics. Spend some spoons preparing basic recipes like tomato sauce, soups, stews, bone broth, and freeze them in small containers to have a meal (or part of it) ready, quickly. Smoothies and juice freeze great as well.

7 – Bonus tip: You don’t have to stand up for any of these tips; you can sit down or even lay on the couch while peeling vegetables, etc. Pull up a chair next to the stove when you’re making something that needs stirring. Sit on a good level next to the stove so you can see inside the pan. That’s also to make sure you won’t tip a hot pan of whatever it is you’re making, onto yourself.

To sum things up: Do everything in a certain way, use machines, consider the utensils you use when you’re cooking, chop the recipe up in different parts, freeze basic recipes, and take a seat.

Download The Ultimate Guide to Spoon Saving Cooking Checklist!

Sarah is an integrative nutrition health coach from Belgium. As a result of living with gastroparesis, dysautonomia and gluten intolerance, she now uses her health coach and pastry chef training to share recipes, tips and tricks to help others live as well as possible despite their own dietary restrictions.

Thanks, for the post, Sarah! I bet this will help loads of spoonies who love to cook but hate to lose energy for an entire day in the process. You can find Sarah here. I’m currently recovering from my infusion, but I’m still on Twitter! And if you follow me, you already have one entry to enter to win $500 in cash. Enter here!

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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  1. Heidi Knepper says

    November 3, 2015 at 9:59 am

    great post!!

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  1. How To Be a Global Citizen says:
    November 5, 2015 at 8:01 am

    […] the meantime, check out Emmie’s blog Illness to Wellness, Sarah’s post from Tuesday on making cooking easier on spoonies, and Sarah’s […]

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Dos and don'ts for when someone in your life is di Dos and don'ts for when someone in your life is diagnosed with autoimmune arthritis! What are some that you would add?⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: "So someone you know was diagnosed with Autoimmune Arthritis". Under the Do column (indicated with a green checkmark) is:⁣
"As how they feel about it⁣
Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
Under the don't don't column (indicated with an x in a red circle) is:⁣
"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
Assume nothing about their lives has changed⁣
Conflate autoimmune arthritis with osteoarthritis⁣
Pass your cold to an immunosuppressed person".⁣
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#AutoimmuneDisease #RheumatoidArthritis #PsoriaticArthritis #AnkylosingSpondylitis #JuvenileArthritis
Weekj 26 of 2026 Weekly Scenes of a summer week Weekj 26 of 2026 Weekly 

Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣⁣⁣

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2️⃣ Kate takes a selfie
3️⃣ A duck with little ducklings following on a lake
4️⃣ Harley coming up to Kate. Her legs are out on an ottoman, 1 foot in a walking cast, and an in-progress needlepoint project
5️⃣ Looking down at a Mahjong table with the game set up
6️⃣ A kayak on the shore of a lake 

#MaineTheWay #MaineSummer #Needlepoint #MaineLife
Living with chronic pain is really hard. You’re wi Living with chronic pain is really hard. You’re winning every day you’re still here.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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I've been spending a fair amount of time at my foo I've been spending a fair amount of time at my foot surgeon's office this year, and boy has it been messing with my head. ⁣
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I spent a lot of time from 2001-2010 dealing with my left foot. Long story short, it took until this foot surgeon saw me in 2010 after fixing this foot for me to be diagnosed with rheumatoid arthritis. But I spent those 9 years going from doctor to doctor, having surgery after surgery, trying to figure out what was causing my pain and to fix it. ⁣
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Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
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I spent from age 10 to 19 unsure what exactly was wrong with me and in huge amounts of pain. We thought we figured it out, and then something else happened. ⁣
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We know exactly what is wrong with this foot this time around: in 2024, I got 3 stress fractures, and no one put me in a boot. They almost fully healed before breaking in 2025, and then the same thing happened in 2026. ⁣
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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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PTSD is a bitch.⁣
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(PS - if you want to know why I'm going back to this guy when it messes with me, it's because I don't trust anyone else to fix my foot.)⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣⁣⁣

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1️⃣ Looking at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
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What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and more. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: ⁣
Things I Do Every Day for My Chronic Illnesses⁣
Take pills at least 4 times a day⁣
Don’t eat gluten, dairy, corn, soy, or eggs⁣
Sleep 7+ hours a night⁣
Consume 80-100 grams of protein, 120 mg of calcium, 5-10 grams of sodium⁣
Wear a mask whenever I leave the house⁣
Do pilates 4+ days a week⁣
Work from home⁣
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Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

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There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: A Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣

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IDs: 
1️⃣ Kate takes a selfie. Her new glasses are thin silver circles
2️⃣ An in-progress cross-stitched alphabet in a special hoop stand that Kate is sitting on.
3️⃣ Kate takes a selfie in an infusion chair.

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