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in Lifestyle &middot June 26, 2014

Each Day Is a Battle

If you’re looking for a post about staying positive while having a chronic illness/pain condition, you’ve come to the wrong place. If you’re looking for a happy lifestyle post, you’re in the wrong place (although that was the initial plan for today’s post). This is going to be negative and I’m not going to apologize for it because this is my life and I don’t want people to see what my blog and think that I’m always positive about living with arthritis. Yes, I try to be most of the time. But there are plenty of times where I’m not.

Living with chronic illness and pain sucks. There’s no other way to put it. It just really, really does. I’ve been in pain every minute of every day for 13 full years now. I’ve had 4 ankle surgeries. I’ve dislocated my knee at least 4 times. I’ve spent over a full year of my life on crutches. I’ve seen over 20 doctors – primary care doctors, orthopedic surgeons, ostopathic doctors, chiropractors, rheumatologists, and even a neurologist. I was a patient at Children’s Hospital of Boston’s pain clinic. I’ve been in and out of physical therapy since I was 10. I’ve had 5 or 6 cortisone injections. I take 20 pills a day and have infusions of chemotherapy once every 4 months.

I’ve gone through a lot. I’ve dealt with a lot. I deal with a lot.

Matthew 5 3

I accepted a long time ago that my life would be pain and doctors and medications forever. But somehow I found myself in the middle of a cycle I thought I was done with: the cycle of doctors telling me that they have no idea how to make my pain better because I’ve already done everything I’m supposed to do.

I dealt with this cycle for my ankle when I was in high school. After my second surgery (March 2006), I ended up going through a few years of doctor after doctor and no answers until my third surgery (January 2009), when they put a camera in my ankle and finding a whole lot of messed up stuff. Then, even though I went through the arthritis diagnoses problem in the spring/summer of 2010, it was a very short period of time and I had an answer fairly quickly. Now I find myself going through that awful cycle with my knee.

The physical pain I feel on a daily basis from my knee alone should be enough. But then you add all the emotional pain that goes along with doctors saying that all you can do is what you’ve already done, and there’s nothing they can do, etc. It becomes overwhelming and upsetting and simply too much to handle.

I don’t really know how to end this post. This is how I’m feeling right now. I had a doctor’s appointment on Monday with an orthopedic, and that appointment really upset me. I’m feeling extremely discouraged right now. I have a second opinion appointment in a few weeks with someone else because I just simply can’t accept that there is absolutely nothing they can do for me other than hope that my arthritis medication magically works better this time around.

This week has just really reminded me that this can be a battle. I battle my arthritis each and every day just by getting out of bed and trying to live a normal life. Sometimes the arthritis wins. This has been a week of that. I’m just not really used to the arthritis winning the emotional battle, as well. Unfortunately, it seems to be winning a lot of that recently.

Kate Mitchell battles arthritis on a daily basis
All happy before my doctor’s appointment because I have high(er) hopes for my immediate future. Hopefully I can bring back that state of mind.

7 Things People Forget About Me | Self-Publishing Series

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. suburban prep says

    June 26, 2014 at 1:19 pm

    I can relate to the pain felt on a daily basis.

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  2. Brittney, Breaking Free says

    June 26, 2014 at 1:42 pm

    Im sorry you're dealing with this, and its okay not to be positive happy go lucky 100% of the time.

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  3. Cece says

    June 26, 2014 at 3:16 pm

    I all can say is I'm sorry. I feel so sorry that you have to deal with it. It sucks and I'm glad you don't feel bad about saying so because it's totally your prerogative to do so. Don't give up. I hope that somebody comes up with something for you.

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  4. Alison says

    June 26, 2014 at 3:18 pm

    I'm so sorry that you're dealing with all of this pain and feeling so discouraged. I don't know *exactly* what you're going through, but as a fellow chronic illness/chronic pain sufferer, I can kind of understand. I hope that you can get some relief and that you find a team of physicians that will work together to help you feel as good as you can. I'll definitely be sending good throughts and prayers in your direction.

    I also really liked your "7 Things" video, although it was a bit blurry! 🙁 I'm also short (4'11") and do not have a "petite bone structure" either. Also, my husband is just over 6 feet tall, so we look kind of ridiculous, but in an adorable way. At least… that's what I tell myself. Adorable, not awkward! (I may be delusional.)

    Anyway, hope to see more videos from you soon, and I hope that you are taking care of yourself and feeling better.

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  5. Sarah Farris says

    June 26, 2014 at 4:43 pm

    I hope your appointment today goes well. I have chronic pain, but I can't imagine having it while I was so young–plus so many surgeries. You are hero! I know what it's like to leave the doctors office crying because they weren't able to help you, or have them be rude to you because they don't know how to help you. But, it's ok not to be happy-go-lucky about it everyday. I know that the pain has made me learn how to put on a really good "happy" face for a few hours, only to come home and just feel miserable. The show can be exhausting, too!

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  6. gayle @ grace for gayle says

    June 26, 2014 at 4:54 pm

    you have every right to feel the frustration full-on sometimes. thanks for being raw and real. truly hope this gets better for you. (((hugs)))

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  7. The Girl who Loved to Write says

    June 27, 2014 at 1:20 am

    So so sorry. You have every right to feel that way, and sometimes getting all that frustration out in the open is the first step to getting to a positive state of mind.

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  8. Marla Rogers says

    July 1, 2014 at 5:19 pm

    Keeping you in my thoughts ♥ You're a really strong person and I know you can get through this!

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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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