• Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Kate the (Almost) Great

Chronic illness blog

  • Home
  • Start Here
    • About
    • As Seen On
    • Tags & Topics
    • Popular Posts
  • Blogging Resources
  • Freebie
  • Shop the Blog
    • Products for the Chronically Ill
  • Contact & Work with Me
    • Ads and Sponsoring
  • Follow
  • Holiday
    • Gift Guides

in Health &middot August 14, 2020

Mental Health And COVID-19: How I’ve Been Managing Mine

We are 6 months into COVID-19 being a big deal in America, or at least yesterday, August 13th, was 6 months into me putting myself in lockdown. As I have a very suppressed immune system, I have to take COVID-19 extremely seriously, and in March, my rheumatologist told me that I had to do everything I possibly could to keep myself safe. Between living through the COVID-19 era and having generalized anxiety disorder, my mental health has been something that I have to actively work on. The CDC describes mental health as “our emotional, psychological, and social well-being” (x). In this post, I’m going to share what I’ve been doing for my mental health and COVID-19 in the world.

I am not a mental health provider, or a medical provider of any kind.

Times are hard for everyone right now, for a variety of reasons. In this post, I'm talking about mental health and COVID-19, but specifically about life during the pandemic and not about your mental health if you have COVID-19 (I can't speak to that experience). I'm an immunosuppressed person with generalized anxiety disorder, so the pandemic is extra stressful.

Mental Health and COVID-19: What This Means

What does “mental health” mean?

The thing I see occasionally online is people who think mental health equals mental illness. But mental health is like physical health in that it is a thing that everyone has, even though it wasn’t talked about a lot publicly until recent years. Or at least, it wasn’t a term used until recent years.

The CDC agrees that it is separate from mental illness and says, “Although the terms are often used interchangeably, poor mental health and mental illness are not the same things. A person can experience poor mental health and not be diagnosed with a mental illness. Likewise, a person diagnosed with a mental illness can experience periods of physical, mental, and social well-being” (x).

So you can have no mental illnesses but go through a really tough time that makes for not-awesome mental health.

For example, no one has a great time during their college finals season. It’s super stressful. If you live in the dorms, you’re also moving out either for winter vacation or for the summer. You’re also saying goodbye to your friends for a little while and you might be heading home. So pretty much everyone feels awful mentally – aka their mental health is bad at that time – without having a mental illness.

Free printable to prepare you for chronic pain medical appointments

But how can COVID-19 affect mental health?

Gosh I feel like the bigger question is how couldn’t COVID-19 affect mental health?

We are in a world-wide pandemic, the likes of which haven’t been seen in at least a century.

In the US, at least, we’re still in lockdown.

There are people who basically refused to be in lockdown, which is making this last even longer.

There are people who refuse to wear masks, and many more who aren’t wearing them correctly.

(And in the US, many states and areas reopened way too early. )

There are still people who don’t believe COVID-19 is a real issue.

You get the picture.

And that’s just COVID-specific info!

The CDC says, “During and after a disaster, it is natural to experience different and strong emotions. Coping with these feelings and getting help when you need it will help you, your family, and your community recover from a disaster. Connect with family, friends, and others in your community. Take care of yourself and each other, and know when and how to seek help” (x). I don’t know about you, but a world-wide pandemic like COVID-19 definitely counts as a disaster to me.

mental health and COVID-19, mental health during the COVID-19 pandemic, COVID-19 pandemic, COVID pandemic, mental health and COVID, mental health, mental health and coronavirus, mental health coronavirus, mental health in covid era, mental health in coronavirus era

How I’ve Been Managing My Mental Health During COVID

Staying on top of my mental health has been doable, but it definitely has to be intentional. I have generalized anxiety disorder, which I’ve talked about in the past, but my mental health is more than my anxiety disorder. I’m going to talk about how I’m managing my mental health and COVID-19, which is sometimes anxiety-disorder related and sometimes general-life-in-COVID-19-world.

Here’s what I’m doing!

Try to stick to my normal routine as much as possible – This is a little bit tricky, but not too much for me because I’m already a lot of a homebody. So I get up at around the same time I did pre-COVID-19; I do my same morning routine; I’m going to bed a little later than usual, as I don’t have to get up early to take the T to work so I feel okay watching 1 more episode of whatever TV show I’m watching; I try to do the same nighttime routine; you get the picture. Routine is so key for me to manage my anxiety, so I’ve been trying to stick to mine as much as possible.

Force myself to get out of the house to go for walks – I am very fortunate to have been home in Maine since March, and we’re in a very rural town, so I can leave the house to go for walks very safely (with mask in pocket, of course, as although I’ve literally never been close enough to someone when out walking here that would require a mask, I am on immunosuppressants). Doing this has been so beneficial for me as it’s good to get out of the house that you’ve basically been in constantly for 5.5 months, in addition to being in my favorite place in the whole world. I was doing this in Boston in March before coming up here, and it was even more beneficial there for me because I was in an apartment.

Try to do yoga a few days a week – While going for walks is great for the mental benefit of getting out of the house, doing yoga or strength-training exercises is also ideal for me for actual exercise. I’ve worked hard to build muscle over the last year and to get used to regularly exercising for my POTS. Doing yoga several times a week helps me stop the constant monologue in my head that is my anxiety disorder during a global pandemic, so it’s beneficial to my mental health that way, but also the fact that I’m doing something physical helps me feel like I’m not losing all the progress of my POTS exercise protocol.

POTS exercise protocol diaries

Keeping therapy appointments (virtually) – In general, it helps so much to be able to talk to a professional about everything. The biggest help to me has been having a place where I can talk about all the things that I know are ridiculous for me to be anxious about. But that was pre-COVID; it is extremely rational be anxious about COVID-19, so I’m dealing with that plus my normal anxiety levels. There are different types of therapy, and it’s probably best for the therapists to decide what type you should do. Additionally, you might need to meet with several different people before you find someone who is best for you, so if you’re having a hard time clicking with someone, move on.

Reducing Twitter use – I love Twitter, but in recent months it is invading my life too much when I’m not on the app. To help with that, I turned off my Twitter push notifications, and I try to log off of Twitter a couple nights a week. That is helping me sleep because I hadn’t realized how frequently I try to wind down my night and then find myself opening Twitter. Both of these things have helped a lot!

Focusing on work – I will fully admit that this isn’t the healthiest, but I’ve been focusing a lot on work so that I don’t have time to feel sad about all the people who don’t seem to care about masks or all of the people who have had, currently have, or will have COVID-19. Between my day job and this blog, I’ve had plenty of work to do. Especially because we’re in the middle of my day job’s busiest time of the year!

How has COVID-19 affected your mental health?

Like this post? Check out:

Chronic Illness and Mental Health, 10 Simple Self Care Methods That Will Improve Your Life, The Art of Managing Anxiety

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.

Share this with your family and friends:

  • Share on X (Opens in new window) X
  • Share on Facebook (Opens in new window) Facebook
  • Share on Pinterest (Opens in new window) Pinterest
  • Email a link to a friend (Opens in new window) Email
  • Share on LinkedIn (Opens in new window) LinkedIn
  • Print (Opens in new window) Print
  • Share on Tumblr (Opens in new window) Tumblr

Related

Previous Post: « The Best Food Substitutions for Common Intolerances
Next Post: How To Track Blog Traffic in Google Analytics »

Reader Interactions

Trackbacks

  1. Mental Health and Chronic Disease Management: What You Should Know says:
    May 25, 2021 at 7:04 am

    […] Mental Health And COVID-19: How I’ve Been Managing Mine […]

    Loading...
    Reply

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Primary Sidebar

Kate the (Almost) Great® is a chronic illness lifestyle blog. It is a resource for chronic illness patients and their loved ones.

  • Bluesky
  • Email
  • Facebook
  • Instagram
  • Pinterest
  • Threads
  • TikTok
  • Twitter

Categories

Health
Lifestyle
Writing & Blogging

Pages To Start With

  • About Kate the (Almost) Great®: Meet the Health Blogger
  • As Seen On
  • Contact & Work with Me
  • Follow
  • Health Blog Resources I Actually Use + Recommend
  • Newsletter
  • Popular Posts
  • Privacy Policy & Disclaimer Policy
  • Products for the Chronically Ill: My Recommendations
  • Shop
  • Start Here
  • Tags & Topics

Search

As an Amazon Associate I earn from qualifying purchases.

This blog uses affiliate links. Thank you for supporting Kate the (Almost) Great!

Sign Up for the Newsletter

Please wait...

Thank you for sign up!

Most Popular Posts

  • The Products I Loved (And Wanted) in Grad School
  • What Sjögren’s Syndrome Is: A Beginner’s Guide
  • The Lifestyle Changes I Made for My Rheumatoid Arthritis
  • What Does Arthritis Pain Actually Feel Like?
  • 9 Arthritis Products That Help My Rheumatoid Arthritis
  • What Every POTS Syndrome Patient Needs for the Summer
  • Beginner’s Guide: Rheumatoid Arthritis Flare Up
  • What Is the Difference between Osteoarthritis and Rheumatoid Arthritis?
  • Seronegative Rheumatoid Arthritis Diagnosis: What I’ve Learned


Bluehost.com Web Hosting $3.95

Health Union Patient Leader Certification

Support KTAG

If you like what I do, please support me on Ko-fi.




Footer

Sign Up for FREE Instagram Challenge

Get 25 FREE Instagram prompts for chronic health creators!

You can unsubscribe anytime. For more details, review our Privacy Policy.

Thank you!

You have successfully joined our subscriber list.

Get your FREE Instagram challenge here 

and 

For just $5 get your copy of my ebook Take Your Blog (And Income!) to the Next Level with code "greatest".

.

Kate the (Almost) Great

Chronic health lifestyle blog

Lets Go!
  • Facebook
  • Instagram
  • Pinterest
  • Twitter
July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
- Disability Pride Month ⁣
- Juvenile Arthritis Awareness Month ⁣
- the anniversary of when I was diagnosed with autoimmune arthritis at age 19 after 9 years of symptoms ⁣
⁣
As you can imagine, that makes me very aware of my disability via juvenile arthritis⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
⁣
#DisabilityPride #JuvenileArthritis #RheumatoidArthritis #AutoimmuneDisease
There are a lot of reasons why you shouldn't doubt There are a lot of reasons why you shouldn't doubt someone's chronic illness, but this is one of them. ⁣
⁣
I'm always amazed by how people can have the exact same illness or set of illnesses and still have different experiences. Sure, there will be similarities, but which symptoms are the worst, what medications you respond to, and your quality of life can vary significantly. ⁣
⁣
It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: Kate takes a selfie. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
⁣
#ChronicallyIll #RheumatoidArthritis #Endometriosis #Fibromyalgia #POTS
This basically sums up my summer so far: Harley, a This basically sums up my summer so far: Harley, a sewing project, and my foot in a cast⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣ ⁣
⁣
ID: Harley the golden retriever has his head on Kate's lap. Also on her lap is an in-progress needlepoint project and Kate's leg (in a walking cast) is elevated.⁣
⁣
#Osteoporosis #RheumatoidArthritis #GoldenRetrievers #Needlepoint #Needlework
Week 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

1️⃣ Foot checkup! Walking boot is on occasionally from now until September 
2️⃣ Boston 
3️⃣ IVIG
4️⃣ Dentist 🦷 All good! 
5️⃣ Not a filter - this was the Boston area the second half of the week 
6️⃣ Physical time!

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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⁣⁣.

⁣⁣⬛⁣⁣

IDs:
1️⃣ Kate takes a selfie in a doctor’s office
2️⃣ Looking at TD Garden, the bear statue for the Bruins, and Zakim Bridge in the background 
3️⃣ Looking at tubes coming out from under Kate’s clothes. There’s a Kindle on her stomach
4️⃣ Kate takes a mirror selfie before leaving
5️⃣ Medford Square looking like there’s a yellow filter over it
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
Also, if this is how you’re finding out, I’m sorry Also, if this is how you’re finding out, I’m sorry. I’m fortunate enough to have a lot of people who care about me and this is the fastest way to tell everyone. 

Video: Kate talks to the camera while putting on makeup. There are captions. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
Week 27 of 2026 Weekly (Delayed because last Sund Week 27 of 2026 Weekly

(Delayed because last Sunday was baaaaad)

1️⃣ Due airport difficulties, we got a few more days with Emma. Harley was THRILLED!
2️⃣ Beautiful bird/squirrel visitors
3️⃣ A beautiful Maine summer day

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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⁣⁣.

⁣⁣⬛⁣⁣

1️⃣ Harley the golden retriever putting his front legs up on Emma’s legs to demand hugs.
2️⃣ A bird feeder and hummingbird feeder on a deck. There is a hummingbird at one and squirrel at the other.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
Reminder: you can be proud of your disability comm Reminder: you can be proud of your disability community while wishing your body cooperated more⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
 ID: Screenshot of a thread post. The background is dark teal, and it's written by katethealmostgreat. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
⁣
#DisabilityPride #ChronicallyIll #InvisibleIllness #Disabled #Disability
I don’t know the exact date of my RA diagnosis, bu I don’t know the exact date of my RA diagnosis, but this is from right around then in July 2010. ⁣
⁣
When I was diagnosed, I had been having symptoms for 9 years. ⁣
- 9 years of foot pain (partially from tarsal coalition)⁣
- Arthritic damage in said food⁣
- Carpal tunnel off and on for several years⁣
- And more⁣
⁣
I was finally diagnosed because I woke up one morning and was unable to open my jaw more than 8 mm. It turned out that I had horrible arthritic damage to my TMJs, which got me off the waiting list at MGH rheumatology. I left that appointment with an autoimmune arthritis diagnosis. ⁣
⁣
The fact that July is not only my diagnosis anniversary but also Juvenile Arthritis Awareness Month has always seemed right. I may not have been diagnosed with JA, but given the amount of arthritis I had along with my many years of symptoms, it's generally accepted that I had it. ⁣
⁣
This year marks 16 years since diagnosis and this fall marks 25 years since my symptoms started. It's pretty weird that so much time has already passed!⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: Kate at 19 at Fenway Park for a Red Sox game. ⁣
⁣
#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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?⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
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".⁣
⁣
#AutoimmuneDisease #RheumatoidArthritis #PsoriaticArthritis #AnkylosingSpondylitis #JuvenileArthritis
Follow on Instagram

Copyright © 2026 · Kate the (Almost) Great · Design by Studio Mommy

%d