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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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SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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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: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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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 down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis only affects people as they age.⁣
Fact⁣
Arthritis can affect anyone at any age, including kids as young as 3.⁣
katethealmostgreat⁣
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#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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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 bunch of IVIG supplies, including a pump. ⁣
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#ChronicallyIll #ChronicIllness #ChronicPain #AutoimmuneDisease #Autoimmune
Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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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 An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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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. She's a redheaded white woman wearing a gray sweater and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #Fibromyalgia #Endometriosis #POTS
Week 16 of 2026 This week had EVERYTHING 1️⃣ Cr Week 16 of 2026 

This week had EVERYTHING

1️⃣ Cross-stitch during virtual mass 
2️⃣ Tuesday featured a 90-minute meeting during work and then an hour advocacy work call after my day job (both were good!)
3️⃣ Wednesday started at my foot doctor’s office and I left in a walking boot. Hopefully these 3 fractured bones will heal correctly this time 🤞🏻
4️⃣ Thursday started back at MGH for my annual neurology appointment + foot CT scan
5️⃣ Then I went up to Maine … 
6️⃣ to celebrate my grandma’s 85th birthday! 

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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 In the foreground is an in-progress cross-stitch piece. The background shows an open laptop streaming Catholic mass.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair and green glasses.
3️⃣ Kate takes a selfie in a doctor’s office. 
4️⃣ Kate takes a selfie in a car.
5️⃣ Kate takes a selfie snuggling with a golden retriever.
6️⃣ Kate and her cousins stand with their grandmother in front of a sign saying "Happy Birthday." 

#CrossStitch #ChronicPain #ChronicallyIll #InvisibleIllness
My face comes with subtitles, so .. ⁣ ⁣ ⬛⁣⁣⁣⁣⁣ ⁣ I My face comes with subtitles, so .. ⁣
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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 drinks coffee giving side eye. White text box reads "My Face When Someone Says 'You Shouldn't Need a Cane At Your Age'" ⁣
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#ChronicPain #ChronicallyIll #RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Fibromyalgia
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