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in Health, Lifestyle &middot May 23, 2023

The Restorative Power of Nature

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in Health, Lifestyle &middot May 23, 2023

The Restorative Power of Nature

While I’m recovering from surgery, several other health bloggers are stepping in. Please enjoy this guest post from Suzan!

Scientific studies have found that time spent in nature—even for as little as five minutes—reduces stress, improves creativity, reduces self-criticism, and increases kindness. Spending time outdoors also has measurable physical effects, including reduced inflammation, improved mental clarity and memory, and reduced stress response. It even improves immune function, as measured by the improved function of the body’s natural killer cells, with quantifiable improvements lasting 30 days or more after time spent in nature. These are all very real physical improvements that everyone living with a chronic illness certainly needs.

Aside from scientific research, I know from my own experience that spending time outdoors feels rejuvenating, peaceful, and centering. Before I had ME/CFS, I loved outdoor activities, including long hikes, canoeing, camping, and backpacking. Much of that is beyond my limits now. However, my husband and I still enjoy camping (at our own slow pace), and various treatments for ME/CFS have allowed me to manage short hikes and kayaking. Spending time outdoors is still among my favorite things to do.

Even when I can’t be active, I still have a goal to spend at least 10 minutes each day outside. I lie in my reclining chair on our back deck, looking up at the sky and listening to the birds, and I instantly feel more relaxed. That small amount of time in nature in our own backyard makes me feel better.

Here are some ideas for how you, too, can experience the restorative effects of nature, even if you are mostly homebound.

Just a Few Minutes Outdoors Helps

Some research studies show positive physical and mental changes in people after only five minutes outdoors, so it doesn’t take much to make a difference! Try lying in a reclining chair or hammock in your yard/garden, patio, or deck. Just that simple change of scenery—from reclining on your normal bed or couch to reclining al fresco—can make you feel better and help you to tune into nature.

Leave the Devices Inside

Although I admit I do sometimes bring my laptop outside to write, you’ll get the most benefit from leaving the phone, tablet, laptop, and other devices inside. I usually don’t even play music when I am out on our deck because it drowns out the sounds of nature. Instead, bring a book or a crossword puzzle out with you, or just grab your pillow and maybe a blanket—and relax.

Immerse Yourself in Nature

With the electronic devices left inside, you can concentrate more fully on nature. You may be surprised at how much of the natural world you can experience from simply lying outside your home for a few minutes and at how restorative it can feel. Gaze up at the sky, noting its unique colors and the variations in light and shadow. Watch the clouds move across the sky, and observe their different types and shapes. Notice how the sky after a summer storm looks entirely different from the sky on a clear fall day. Look at the flowers and trees, appreciating their different colors and shapes and how they change with the seasons.

Listen for the sounds of birds singing and the breeze moving through the leaves of the trees. Smell the air. Breathe deeply and notice the aroma of dry fall leaves, damp earth after a spring rain, or the fragrance of summer blooms.

Focus yourself entirely on the natural world around you, blocking out the incessant noise of our modern life. Even just a few minutes of fully immersing yourself in nature can reduce stress, improve your sense of well-being, and bring positive physical changes.

If you can’t manage a few minutes lying outside, then open a window near your bed or couch (or just look through the glass) and try the same exercises to focus each of your senses on the outdoor world. Studies have shown that simply looking at pictures of nature has positive effects.

Managing a Longer Outdoor Experience

More extensive time spent outdoors beyond your own yard can bring even more and longer-lasting improvements. That might be too much to manage for some people who are severely ill and housebound. However, many people with chronic illnesses can handle a longer or more immersive experience outdoors, especially after treating aspects of the disease and incorporating effective illness management to allow you to be more active without relapsing.

If you can manage it, take a stroll along your street or neighborhood and notice the trees, flowers, and sky. Even in a familiar place, you can appreciate the changes in weather and seasons. For a change of scenery, try going to a local park or nature center and taking a short walk.

If a walk is beyond your limits, ask a friend or family member to push your wheelchair along a paved path or to take you on a drive through the country. Roll down the window, breathe in the fresh air, and enjoy the sights and sounds of nature.

After treating orthostatic intolerance (OI) and wearing a heart rate monitor, I discovered I can handle a little bit of kayaking. Since it is done sitting down, my heart rate doesn’t jump up as high as when I am walking, and I can rest and just float whenever I need a break. Many parks with lakes or ponds rent canoes or kayaks. If you can’t manage paddling on your own, ask a friend or family member to bring you along in a tandem (two-person) canoe or kayak. Being out on the water is incredibly peaceful and calming.

If you’re up for a more extended outdoor adventure, you might want to try camping. Camping in our pop-up camper and spending more time outdoors than I can at home makes me feel relaxed and content. You don’t have to go far, either; look for local, state, or county parks with campgrounds. Many state parks and private campgrounds offer rental cabins or trailers, or you can rent, borrow, or buy a camper as your home-away-from-home. All public parks have handicapped campsites, and many have at least one wheelchair-accessible trail. You also provide your own food when camping, which helps when you have a restricted diet.

When camping, stick to your normal routines as much as possible. For me, that means an early bedtime and an afternoon nap. We also bring portable lounge chairs so I can recline around the campfire or with my book.

One of the best things about being away from home (even if it’s just a local park) is that I am away from all the usual household responsibilities. I can focus all my energy on relaxing, having fun, and enjoying my surroundings. I love my small daily doses of nature on my back deck, but spending a few hours or a few days immersed in nature elsewhere is truly rejuvenating.


Every chronically ill person is different and has unique needs, even if we have the same disease, but we can each find our own ways to incorporate nature into our lives. The payoff for a little time spent outside is huge, in terms of both emotional well-being and physical health.

So, go ahead! Put away the device you are reading this on and indulge in some time outdoors. Your mind and body will thank you.

Excerpted from the book, Finding a New Normal: Living Your Best Life with Chronic Illness by Suzan L. Jackson 

© 2020 Suzan L. Jackson

Suzan Jackson is a freelance writer whose work focuses on topics related to health, family, travel, and media reviews and has appeared in many magazines, websites, and anthologies. She has had ME/CFS, an immune disorder, since 2002, and also has Lyme disease. Both of her sons also became ill with ME/CFS in 2004. Her younger son is now fully recovered, after 10 years of mild illness. Her elder son, who recently started his first full-time job, still has ME/CFS as well as three tick-borne infections. Sue and her sons improved their conditions with a number of treatments. She runs several support groups, both online and locally, to help others. You can connect with Sue on:

Book: Finding a New Normal

Chronic Illness blog: Live with ME/CFS 

Book blog: Book By Book 

Twitter: @livewithmecfs

YouTube: @SueJacksonDE

Facebook: Live with ME/CFS

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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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🤞🏻

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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.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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