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in Health &middot February 19, 2014

Chronic Pain and God

Although I don’t talk about it much on here, I am a practicing Catholic. My religion has played an important part in my life, and more than just the obvious parts. If you’re new around these here, you may also be unaware that I’m a chronic pain patient who deals with arthritis and fibromyalgia. I talk about my invisible illness and arthritis on a regular basis, because it’s an important part of my life. What I don’t always talk about, though, are the many different ways I live with it instead of living as it. I’m not sure if that makes sense – I’m talking about it not being all of my life as long as it is a part of my life.

My friend Kenzie is a high school student who also deals with autoimmune arthritis. God also plays a large role in her life, although she’s not Catholic like me. A few months ago I sent her a story about my religious experiences with my health, and I wanted to share them publicly so that others who are trying to keep believing in God and His works while dealing with a bad situation – health, family, school, relationships, life in general – can see them and hopefully be inspired to some degree.

The story starts almost 5 years ago, when I was a high school senior and was in my 7th year of pain already. Let me take you back to January 2009 …

With 2 ankle surgeries under my belt, I also had 2 years of doctors not believing my pain, not knowing what was causing my pain, and, in general, a lot of misery. I finally found an orthopedic surgeon who believed me. We knew that my first surgery hadn’t worked – when my dad saw him in December 2013 and caught him up, he said that with RA the surgery didn’t stand a chance – but we didn’t know what else caused my pain. We scheduled surgery to fuse my ankle but to also do a scope, which is when they put a camera inside and take a look around. Long story short, we had no idea what was wrong and were absolutely positively desperate.

At the time, I was teaching religious education once a week to third graders. I was always involved in my church (like I mentioned, I’m Catholic). Our priest wrote me a recommendation for the Catholic colleges I applied to and the woman who ran the church was the mother of one of my best friends. The night before my surgery was one of the nights I taught, and after all our students had left the priest offered to perform the Anointing of the Sick on me, one of the Catholic sacraments.

When he performed the rite, I felt an immense sense of peace and calm and hope settle over me, for the first time in years. I can’t properly describe it. In short, I felt God.

When I had my surgery the next day, they found: tarsal coalition (original ankle condition), destroyed cartilage, and arthritis. They also fused my ankle. This surgery was the most important surgery I have ever had. It pointed me in the direction I needed to go (rheumatology) and gave the proof that I wasn’t crazy and imagining the pain like so many insinuated. This gave me the confidence to stand up for myself to other doctors in the future.

Not only did the Anointing of the Sick give me peace, it gave me answers. I fully believe the surgery would not have gone as well without it.

Fast forward 2 years … I had been diagnosed with arthritis and was in that deep pit of despair again because nothing was helping and the pain was getting worse and the arthritis spreading to more joints.

I decided to go on Catholic retreat, and one of the many activities there that we all participated in was Adoration. Adoration is when you sit with the Blessed Sacrament and pray for an extended period of time. I was having such a hard time and as I sat in the room with Jesus and thought and prayed I kept getting upset. Why me? Why was this happening? How could a loving and just God do this to me?

I started sobbing, completely and totally breaking down – thankfully I was not the only person in the room doing this; Adoration can be a very emotional experience – and as I started to come out of it, I felt it. That same combination of peace and calm and hope. The same exact feeling I experienced during the Anointing of the Sick. I felt God and Jesus and the Holy Spirit.

I haven’t felt that way since. I have only felt it those two times. But I know without a doubt that this is God’s plan for me. He is here, guiding me, leading me through everything. Yes, He gave me tribulations. But He was there when nothing else was. He was there, I felt his presence, when I had these two deeply emotional, religious experiences.

That’s the only way I can explain it. He was there.

Everyone is entitled to their own beliefs. But I know for certain that God is with me and this is His plan. I don’t believe it. I know it.

Like I said, everyone is entitled to their own beliefs. But please don’t leave comments challenging my experiences. If this happens, I will turn comments off.

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. Helene says

    February 19, 2014 at 3:52 pm

    What an amazing story!! I am so glad to hear this, I am a catholic too but really anything that helps you through something hard or painful is a good thing.

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  2. Neisha says

    February 19, 2014 at 4:21 pm

    My faith is very important to me as well. It's so awesome to have God's peace in hard times.

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  3. Cassie Lee @ Sage the Blog says

    September 10, 2014 at 1:26 pm

    AMEN. I love stories like this and you are so brave for sharing it here!

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Trackbacks

  1. Kate the (Almost) Great | Boston Lifestyle Blog - Pain and Cold Weather: Dealing with Chronic Pain this Winter says:
    October 7, 2017 at 6:44 pm

    […] Preparing for Chronic Pain Medical Appointments + Free Printable To Help, 10 Tips To Manage Your Chronic Pain This Summer, Chronic Pain and God […]

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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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