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in Health, Uncategorized · January 2, 2015

Leaky Gut and Anemia

Hey, guess what? I’m leaking.

Literally.

Leaky Gut Syndrome Kate the (Almost) Great

Let me back up a bit. As you probably know if you’ve been following me on this blog or on social media, you know that I have rheumatoid arthritis and fibromyalgia and I’ve been in pain since 2001. Well, one component of my health that has been generally unaddressed is that I’m anemic and have been for a very long time. We first found out my junior year of high school (8 years ago), and since then I have tried everything possible to fix it.

But nothing worked and I remained stably anemic since then. With my more serious health concerns and frequent ER trips for pain, it was pretty much ignored. No one was really concerned except for my mother. Would we have been concerned if I hadn’t been dealing with other issues? Absolutely. But that wasn’t the case, and I just didn’t have room in my brain to think about something that had become just a part of my normal life.

Over the past year or two, my mother started talking about the anemia more and more. While I completely understood, I felt that I should focus on other aspects of my health. Then I started seeing a chiropractor. His goal is to help me with my fibromyalgia pain and my joints that tend to float out of their designated spot in my body. So when we first met, we talked about my fibromyalgia treatment.

He suggested that I see a naturopath who he knew. Since the whole point of me not working now is to get my health in order, I was on board.

Leaky Gut Syndrome Kate the (Almost) Great

The appointment was incredible. We talked about my medical history, looked at my blood under a microscope, and just generally had a whole bunch of medical revelations.

1. My body is constant in flight-or-flight mode.

2. I definitely 100% have RA (shocking, I know)

3. I most likely also have leaky gut syndrome

Fight or Flight – What Happens To Me

Essentially, my body is just constantly on edge. I’m always moving at least a little bit. My eyes don’t dilate properly. This may have to do with my anxiety or may be due to some medications that I’m on.

What I Need To Do

I get to wear sunglasses even if it’s mildly bright so that I don’t “damage my eyes” or some nonsense. (Note: actually not nonsense.)

Rheumatoid Arthritis – What Happens To Me

Like I said, we looked at my blood under a microscope when it was fresh and when it was dried. Also, as soon as he pricked my finger it started bleeding significantly. As in he asked if I was on blood thinners. So that’s great.

The red blood cells were stuck together, which is not supposed to happen. That doesn’t allow nutrients to be absorbed. There were brown spots in the dried blood, which means yeast. And there was a white cloud, which means inflammation.

What I Need To Do

Continue with my RA treatment, but I’m also trying to be better and eat an anti-inflammatory diet, which I’ll talk more about later.

Leaky Gut Syndrome Kate the (Almost) Great
Leaky Gut – What Happens To Me

Leaky gut syndrome is also known as increased intestinal permeability. It is something that doctors are recognizing more now, but still don’t know a whole lot about it. The problem is that the gut is the biggest immune system organ (how weird is that?), but it isn’t completely understood. It has been mentioned a couple of times to me over the past few years, but never seriously addressed or considered.

What happens is that the lining of the small intestine doesn’t work properly and it can let substances into the blood stream, hence the name “leaky gut.” So it’s a cycle: there’s intestinal inflammation of the gut lining, which leads to nutrient malabsorption, leading to an immune response. So the immune system responds, causing GI issues and food intolerance, which leads to autoimmune disease, which starts the cycle all over again by causing intestinal inflammation of gut lining.

This means that I could have been dealing with this for a very long time and it could have caused the arthritis. That just blows my mind.

What I Need To Do

Treatment for leaky gut involves cutting more foods out. Like I said earlier, I need to really stick to an anti-inflammatory diet. So some of the foods I’ll cut out will be only gone for a few months while the gut heals and some of them will be gone for good. My naturopath will be giving me a full list of what I should and shouldn’t eat when we get some more tests back from the lab.
The steps are that 1) I’ll remove food and factors that damage the gut, 2) replace them with healing foods, 3) repair with supplements, and 4) rebalance with probiotics. I already don’t eat gluten and dairy, but I’ve now cut out corn and soy. Soon, I’ll cut more out, maybe including sugar and grains.
Leaky Gut Syndrome Kate the (Almost) Great
As a whole, I’m excited. I’m excited to feel better and to give my body a fresh start. I’ve felt for a while that I’m right on the edge of feeling a lot better, but my current treatments weren’t doing enough. This will hopefully settle things and make life a whole lot better. Ideally, it will also help me get off of some of the 23 pills a day I take. It’s definitely not going to be easy, but I know it will be worth it. 

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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Previous Post: « Either I Will Find A Way, Or I Will Make One
Next Post: Spoonie Spotlight: Leanne »

Reader Interactions

Comments

  1. Laura says

    January 2, 2015 at 7:45 pm

    Hi Kate! So sorry you've been dealing with all that! You might want to check out the FODMAP diet (Kate Scarlata's blog has a lot of info) – that along with cutting out gluten really helped me with my health issues!

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  2. Katie @ Chalk it up to Better Luck says

    January 2, 2015 at 9:51 pm

    I'm glad that you've possibly found the source of all your pain! I hope you start to feel better soon.

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  3. Natalie B. says

    January 6, 2015 at 12:01 pm

    I'm impressed with your dedication toward getting well. I too suffer with fibromyalgia, chronic fatigue syndrome, and anemia. It's not easy. Several years ago I learned that I am always in fight or flight too. My anxiety comes out by always moving my fingers. lol What really helped with my anxiety was CBT (cognitive behavioral therapy). I, literally, reprogrammed my brain into thinking differently. Weird huh? I sincerely hope you're on the way to improved health. 🙂

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  4. Marla Rogers says

    January 6, 2015 at 5:40 pm

    I'm so happy you've made such a big health revelation! I hope 2015 sees you heal :]

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  5. hi says

    October 5, 2020 at 9:25 am

    I go to see day-to-day some blogs and sites to read content, however
    this weblog provides quality based articles.

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    Reply
  6. REBECCA LYNN BAILEY says

    September 27, 2021 at 10:11 am

    Hi Kate,
    If you have leaky gut you may also have b12 anemia, which contributes to anxiety and a lot of other cognitive conditions like brain fog, fatigue, memory issues as well as nerve issues etc. Worth checking out

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    Reply

Trackbacks

  1. Beginner's Guide: Autoimmune Paleo Diet | Kate the (Almost) Great says:
    February 15, 2024 at 3:20 pm

    […] autoimmune paleo – or autoimmune protocol diet or some variation thereof – is the belief that leaky gut is the cause of autoimmune illnesses. By eating this particular diet, the thought is that you can […]

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Some things I've done for this so far:⁣ ▪ Gett Some things I've done for this so far:⁣
▪ Getting professional haircuts on a regular basis⁣
▪ Got a Kindle and therefore reading more⁣
▪ Making bread regularly, even though I'm bad at it ⁣
▪ Doing my best to keep houseplants alive⁣
▪ Regularly looking for more recipes to try making and not relying on the ones I already have⁣
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I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣ID: Screenshots of thread posts written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat. ⁣⁣The background is dark teal. All text is here, with one paragraph per image:⁣
"I realized recently that, big picture, this is the best my health has been since I got sick. When I got my infection in 2018 that impacted my whole body until 2023, I wasn’t diagnosed with one of my illnesses and 3 of my diagnosed ones weren’t controlled to the level they are now.⁣
So this year my quasi-resolution is being nice to myself and focusing more on thriving than existing. Because I can, for the first time maybe ever, thinking about thriving *and* existing."⁣
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#AlmostGreatLife #AlmostGreatHealth #ChronicallyIll #SpoonieLife #ChronicallyAwesome #InvisibleIllness #ButYouDontLookSick #LivingWithIntention #Disability #Disabled #Spoonie
Some housekeeping! 1) I am not sponsored. 2) These Some housekeeping! 1) I am not sponsored. 2) These were recommended by my foot surgeon. When you have RA affecting most joints and tarsal coalitions, good sneakers are essential. 

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Video: 3 pairs of HOKA sneakers on wood floor. Kate’s hand picks up one and tosses it out of view. White text reads “My Hoka system” and there are captions in a black box. 

#AlmostGreatLife #TarsalCoalition #RheumatoidDisease #RheumatoidArthritis
In July 2025, it will have been 15 years since my In July 2025, it will have been 15 years since my RA diagnosis. Here's how I've changed since then!⁣
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(And I'm not talking about how my health has changed!)⁣
▪ I trust myself and my instincts a LOT more⁣
▪ I understand my body's limitations AND the best ways o get around them to have the life I want⁣
▪ I love using mobility aids as they make my life a lot better⁣
▪ I cook and bake a lot more⁣
▪ Work-life balance is not an option for me: it's a requirement⁣
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How have you changed since your diagnosis?⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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ID: Kate sits at a desk with her head in her hand. On her desk are notebooks and pens. She is a brunette white woman wearing an olive dress, gray stone necklace, and round tortoiseshell glasses. ⁣
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#AlmostGreatHealth #RheumatoidArthritis #arthritis #SpoonieLife #healthblogger #autoimmune #autoimmunedisease #chronicallyill #healthblog #chronicallyill #disability #disabled #invisibleillness #DisabledAndCute #spoonielife #RheumatoidDisease
Week 18 of #2025Weekly ⁣ ⁣ This week was prima Week 18 of #2025Weekly ⁣
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This week was primarily about getting things set and wrapped up before a heavy appointment week, including my infusion, next week. ⁣
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1️⃣ Meal prepping (the finished product of this salad has a lot more ingredients, including protein, but it doesn’t looks as aesthetically pleasing once they’re in there) ⁣
2️⃣ Started the week at the doctor and with a cortisone shot in my knee. He was very impressed with me and I had to point out that when you start your cortisone shots with some in your ankle area - which has a lot more stuff in it and requires being done under x-ray) your knee is truly nothing.⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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1️⃣ Cut up vegetables in a clear glass container⁣
2️⃣ Kate takes a selfie in a doctor's office. She's a brunette white woman wearing a green t-shirt, blue mask, round tortoiseshell glasses, and silver Claddagh necklace.⁣
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Drop your suggestions in the comments _______ Drop your suggestions in the comments 

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Video: the view of a sun setting over a lake as seen through the trees. Upbeat music plays. Top text reads “How To Deal with Unsolicited Advice”. Then a series of messages pop up. The are: 
“Sorry, my mom said I can’t do that”

“Didn’t you hear? The new pope said that was heresy.” (Ideal if you’re not Catholic)

“I have to wait until mercury isn’t in retrograde, and it’s always in retrograde”

“My psychic said that will kill me”

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Having decades-long health problems sometimes mean Having decades-long health problems sometimes means coming across something in your health history that you completely forgot about⁣
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I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣ID: Screenshot of a thread post written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat. ⁣⁣The background is dark teal. All text is what’s above the first black square.⁣⁣⁣
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Here are some ways I practice self care, aka talki Here are some ways I practice self care, aka talking care of myself AND who I am as a person separate from illness⁣
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This is my Wonderful Things jar. Every day, I write down something wonderful or good that happened that day. ⁣
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I know it looks like I'm forcing Harley to sit like this, but he was making this face before I put my arm around him. Dog snuggle time is the best!⁣
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I got a Kindle this year and it has been amazing. It's so much easier on my body than lugging around books and it makes borrowing from the library a lot easier.⁣
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Yes, I share this all the time, but filling my pill boxes every 3 weeks make it so I stick with all of my medications. But the self-care part of this is that I don't have to take the time to refill a box every single week.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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IDs: ⁣
1️⃣ A glass jar on a desk with a lot of multi-color post-its inside⁣
2️⃣ Kate has her face in a golden retriever who is slumped onto her. They're in a teal room with a red rug. Kate is a brunette white woman wearing red pants and a gray sweater.⁣
3️⃣ A Kindle on dark mode in Kate's lap⁣
4️⃣ 3 open pill cases on a yellow bedspread ⁣
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What I Bring To the Doctor _______ Video: a pa What I Bring To the Doctor 

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Video: a pan of an exam room. White text reads “What I Bring To the Doctor ” and the “1. Planner/notebook
2. List of current medications 
3. Notes on my biggest concerns and questions 
4. My kindle for wait time” 
The intro to Maroon 5’s Priceless plays. 

#AlmostGreatHealth #ChronicIllness #ChronicPain #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #Endometriosis
💃🏼 Week 17 of #2025Weekly 💃🏼⁣
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1️⃣ She’s married!! ⁣
2️⃣ She married the best person in the world for her!!!!!⁣
3️⃣ I got dressed up! ⁣
4️⃣ The reality of doing fun things with chronic illness and pain is that then you have to recover from the fun things. It took … a while. One million percent worth it, but this is why I don’t do big events on a regular basis. ⁣
5️⃣ And then I had to be a person again for an appointment!⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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IDs: ⁣
1️⃣ Kate stands hugging Emmie. They're both white woman. Emmie is in a wedding dress and Kate is in a red dress and wearing round tortiseshell glasses.⁣
2️⃣ Kate and Emmie stand next to Matt, Emmie's husband. He is a white man.⁣
3️⃣ Kate takes a mirror selfie. she's in the same red dress but now also wears a jean jacket and holds a cane and mask.⁣
4️⃣ Kate takes a selfie while giving a thumbs up. She looks tired. She's now wearing a pink flowery dress. ⁣
5️⃣ Kate takes a mirror selfie. She's wearing black shorts, a gray shirt, a jean jacket, a blue mask, and black aviator sunglasses. She has a bag over her shoulder and holds a cane.⁣
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#AlmostGreatHealth #AlmostGreatLife #ChronicallyIll #InvisibleIllness #SpoonieLife #RheumatoidArthritis #RheumatoidDisease #Autoimmune #ButYouDontLookSick #AutoimmuneDisease #SpoonieLife #InvisibleIllness #DisabledAndCute
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