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in Lifestyle &middot March 23, 2021

My Morning Routine for Success

Start your day off with a morning routine for success – whatever that looks like for you! As someone with a day job, a blog, and multiple chronic illnesses, my morning routine is key to a good day. It helps me stay on top of my to-do list, do the social media check-in work that’s needed for blogging, and manage my body. So in this post, I’m sharing what success looks like for me (so you can see how my morning routine helps me achieve it), as well as what my personal morning routine is, and how to make a morning routine of your own.

Start your day off with a morning routine for success - whatever that looks like for you! In this post, I'm sharing what success looks like for me, as well as what my morning routine so I can achieve success.

What Does Success Look Like?

Of course, if you want your morning routine to help you be successful, you need to know what success looks like. That’s going to be different for different people!

For me, I need a morning routine that helps me ease into the day. One reason is that due to my rheumatoid arthritis, I feel a lot of stiffness in the morning.

My illnesses also mean that I need to make sure that I’m fully awake when I start work, as I experience a lot of fatigue. Some days, what happens in the morning won’t affect my day much at all, but those are the bad days. Personally, once I’m through the first hour or two of my day, I feel the best that I will the entire day and I will feel worse as the day goes on.

This also means that I want my morning to be productive. I can’t guarantee that I’ll be up to do anything at the end of my work day. This includes anything from cooking to a medical appointment or anything in between. If I’m going to cook dinner, I generally use a slow cooker, so in the morning I do all the prep and get the slow cooker ready. If I have a virtual medical appointment in the afternoon, I do any prep that I need to in the morning. If I need to have an in-person appointment, I’ll schedule it for the morning. You get the idea!

Because I start working at my day job at 8, and I work 6-8 hours a day, I try to do a bit of blog work in a 20-30 minute period in the morning. It’s crucial for my blog’s success for me to do even a little bit!

Finally, I would be remiss to talk about my morning routine without mentioning how important it is that I don’t miss my morning medications. If I want to feel okay in general and today specifically, I have to take all of my medications. This might feel obvious, but since I take pills 4 times a day and take anywhere from 30-40 pills a day (depending on my steroid dose or my allergies), it’s easy to miss a dose. That is not good. So I need to take a handful of pills in the morning and, ideally, drink 12 oz of water to set up my POTS for success.

A Day in the Life

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My Morning Routine for Success

6:20-6:30 – Wake up | I get up before 6:30 on basically all week days. I do, however, have to set 4-5 alarms for this because I have a history of sleeping through 3 or even 4. I’m an extremely heavy sleeper! Additionally, if I get less than 6 hours of sleep, my pain is significantly higher. My body is doing a lot at all times, and it really relies on rest.

6:30-7:00 – Ease into the day | This is the real reason why I wake up nearly 2 hours before I have to work; I really have to ease into the day. If I’m lucky, my morning stiffness only lasts around 30 minutes, but if I’m near to my RA infusion, it can take 2 hours. And on the really bad days, or on the days when I sleep less than 6 hours, the stiffness never eases up. I try to give myself 30 minutes to just zone out, catch up on miscellaneous stuff on the Internet, etc.

7:00-7:30 – Blog work | Every day, I manually pin for about 5 minutes, make 2-3 new pins for older posts and/or schedule new pins directly to Pinterest, and do a bit of interaction on blogger Facebook groups. If I have a new blog post, I promote that new post in addition to the other tasks. I try not to put pressure on myself as much as possible; if I don’t get something done before I need to get ready for the day, it’s not the end of the world.

7:30-8:00 – Get ready for the day | When I get ready for work, I put on my makeup, take my non-pill allergy and asthma medications, and then brush my teeth. I like to do it in this order so my makeup has as long as possible to set before I put my glasses on. I don’t wear contacts any more because of dry eyes due to my RA, and glasses really mess up makeup you have on your face, mainly your nose. 

8:00 – Take meds | My morning medications is the time of the day when I take the most medications at once. In addition to my normal medications, I take a higher steroid dose in the morning than in the evening. I also take a few supplements, namely Vitamin D3; sodium chloride, because POTS requires I consume more sodium than most people; Calcium, because my endometriosis treatment makes me at a higher risk for osteoporosis; and Collagen, as my skin, hair, and nails all suffer due to my Rituxan infusion. In addition, at this time of the day, I take 1 allergy pills, my POTS pill, and some of my meds for RA (Sulfasalazine) and fibromyalgia (Gabapentin).

I generally take my medications with sparkling water because a) I have to drink a LOT of water for POTS and b) Sulfasalazine has the grossest medication coating I’ve ever known. I’m not exaggerating; it’s orange and chalky and when I refill my pill boxes it leaves my hands and fingers covered in orange gross-ness.

Finally, before I start working, I also give my cat her medications. She is 18 and has a thyroid issue and chronic pain, so she gets Gabapentin in the morning, too! (She also gets a thyroid pill, which she prefers because it’s a pill in a treat instead of liquid.)

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Now that I’ve talked about what success looks like for me and what my morning routine looks like, let’s discuss how to make your own.

How To Make Your Own Morning Routine

Ask yourself what success looks like to you. If you can’t answer this question, you can’t concretely make a plan to achieve that success. There’s that old saying that a goal without a plan is just a wish. That’s definitely true!

Figure out whether or not you are able to wake up early. Not everyone is a morning person – which is fine! But if you aren’t a morning person or you have a lot of responsibilities (job, kids, school, etc.), then you probably want to maximize the time you have available in your morning.

Decide what you want to get done. Are you looking to write 500 words every morning? What about 15 minutes of yoga? Want to intentionally ease into your day? I can’t tell you what a morning routine for success is going to look like for you because I’m not you. Whatever you want to do in your routine, you want to make sure that it’s attainable. Don’t try to write 500 words in 20 minutes unless that’s something that you regularly do. Which brings me to the next point …

Figure out how much is reasonable for you to do in your morning routine. If you’re giving yourself 30 minutes between when you wake up and when you start working, you don’t want to over-plan your time. If you’re constantly struggling to do creative work in a short time span, then you run the risk of your creativity always feeling rushed. You want your morning routine to actually help you, so in general you should plan on doing a smaller amount of things on a daily basis, and on the days you have the time, do more.

What is your morning routine?

Like this post? Check out:

Self-Care Tips That Chronic Illness Patients Need, Resume Tips: 5 Tactics for Putting Advocacy on Your Resume, How To Actually Rest When You Take Breaks

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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Comments

  1. Kelsey says

    March 24, 2021 at 10:39 am

    I’m a heavy sleeper too! My husband and I have an amazing morning routine that I love but now that we have a brand new daughter in our lives I feel like it is always evolving! lol

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  2. Becky says

    March 25, 2021 at 9:56 am

    I had a decent morning routine going for a little bit but then the pandemic threw everything out of whack. Now I have to figure out how to adjust when so much about my job and my daily life is different. Commuting also throws a wrench into things, as the traffic can vary wildly – so I keep an eye on the GPS in the morning to see what things look like and if I need to leave earlier than usual or not.

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  3. Kait says

    March 25, 2021 at 5:15 pm

    Every time I read about someone’s morning routine, I’m like “that sounds like a nice idea, I should try it.” But my routine of hitting snooze five times and then scrambling to check my work email while making breakfast is what I always fall back into after a couple weeks. I like your idea about defining your own success, because it’s clearly not working for me to copy others!

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  4. Sue Jackson says

    March 27, 2021 at 4:57 pm

    What a wonderful post, Kate, filled with so much great information!

    I can relate to much of it – except the early wake-up time! I have ME/CFS and need a solid 9-10 hours of sleep at night, so 8 am is about the earliest I can manage. Otherwise, though I agree 100% – my morning routine is SO important! Like you, I am at my best in the first part of the day and go downhill from there, so I have to plan my most important work (I am freelance from home so more flexible) just after breakfast. Loads of pills here, too. I do a 15-min floor yoga routine (no standing – I also have POTS and another kind of OI, too) which really helps to work out the aches and stiffness from sleeping. And if I want to feel good, I need to have a healthy breakfast, which is especially challenging when I’m not feeling up to cooking!

    So glad you found a morning routine that works for you – thank you for sharing your experiences and expertise!

    Sue

    Live with ME/CFS

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  5. Courtney says

    March 29, 2021 at 10:35 am

    Such a great routine. I’ve been trying to wake up at 6 am so I can get an hour or two to myself to work out or work on my blog before my daughter wakes up. But I am really not a morning person so it is really hard for me to do it!

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  6. Mariya says

    March 29, 2021 at 10:44 am

    Thanks for sharing! This is really inspiring, I definitely need to start my mornings right otherwise everything just goes downhill from there.

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Trackbacks

  1. How To Be Good at Blogging: Blogging with Limited Time says:
    March 10, 2022 at 7:22 am

    […] But also, I need to wake up 1-1.5 hours earlier before I get ready for work because I deal with morning stiffness due to my RA. Getting up early means that the stiffness has worn off by the time I start […]

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  2. Tips To Make Independently Living with a Chronic Illness Easier says:
    May 31, 2022 at 7:23 am

    […] My Morning Routine for Success […]

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    February 13, 2024 at 4:16 pm

    […] Friends as an Adult: 12 Tips You Need, The Best Audiobooks I’ve Listened To, My Morning Routine for Success, 12 Boston Small Businesses To […]

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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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IDs:
1️⃣ Harley the golden retriever on a deck as seen through some plants
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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ID: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
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#ChronicIllness #ChronicPain #RheumatoidArthritis #Fibromyalgia #Endometriosis
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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ID: Kate takes a selfie in a doctor's office. ⁣
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#PTSDAwareness #ChronicallyIll #TarsalCoalition #RheumatoidArthritis #Osteoporosis
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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IDs: 
1️⃣ Looking at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
2️⃣ Birds arriving at a bird feeder as seen through a window

#ChronicallyIll #InvisibleIllness #ChronicPain #IVIG
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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#ChronicallyIll #InvisibleIllness #RheumatoidArthritis #Fibromyalgia
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! 

Video: Kate talks to the camera while holding a purse. She holds up individual items mentioned in the video before putting them in the bag. There are captions. 

#ChronicallyIll #RheumatoidArthritis #Osteoporosis #ChronicPain
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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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🤞🏻

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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