• Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Kate the (Almost) Great

Chronic illness blog

  • Home
  • Start Here
    • About
    • As Seen On
    • Tags & Topics
    • Popular Posts
  • Blogging Resources
  • Freebie
  • Shop the Blog
    • Products for the Chronically Ill
  • Contact & Work with Me
    • Ads and Sponsoring
  • Follow
  • Holiday
    • Gift Guides

in Health, Uncategorized &middot July 10, 2015

A Note on Living with Acute Chronic Pain

This post was originally written on my phone on Wednesday, July 1, 2015 when I couldn’t sleep.

 

It’s 9:41 on a Wednesday and I have been trying to sleep for almost 2 hours. My body has been sluggish and weak all day – well, more than normal, at least – and I need lots of sleep. Preferably 10-13 hours. But once I try to actually go to sleep, I can’t.

 

A Note on Living with Acute Chronic Pain - Kate the (Almost) Great

 

I’m not dealing with sleep issues. I’m dealing with pain. I only have one more narcotic pain pill left because the prescription I tried to fill earlier in the week had expired. And that’s because we had a mix up at the doctor’s office and they gave me an old script that I never filled. So tomorrow I’ll trek back across the city to get my script, go back to my local CVS, and hope that the new pharmacy interns don’t treat me like a drug addict.

 

That’s nothing against that, really. My local pharmacy has 2 full-time pharmacists (they have their pharm. docs), some full-time techs, and the rest are pharmacy students interning. The interns recently changed over for the summer semester and they don’t know me yet. The rest know me. They know that I take 25 pills a day and fill a legal (and needed ) opioid prescription every month. But the interns are trying to combine what they’ve learned in their classes, what the law tells them, what they’ve heard about people filling narcotics, and their brand new practical experience. They don’t know yet that I’m not a drug addict – I’m a patient with a highly active and severe case of seronegative rheumatoid arthritis who is waiting for the trimester’s chemotherapy to kick in.

 

I have arthritis in 58 joints and it’s currently running wild while I wait for last week’s chemo to kick in. It won’t for another 2-3 weeks, so in the meantime, I’m just trying to get by every day as much as I can. I still haven’t completely recovered from my chemo yet – my appetite hasn’t returned and I’ve been overly exhausted for 6 days. Today was my first day back for work. the absolute last thing I want while dealing with all of this is to be treated like a drug addict looking for their next high.

Buy The Essential Grammar Handbook, an ebook based on my experiences as a high school English teacher. For just $10, you can dramatically improve your writing, and therefore your life. It contains rules, explanations, examples, and practice.

Sign up for the monthly newsletter! Become one of the greatest people you will ever meet and get a recap of the best blog posts, extra writing tips, and free downloads. I will never give your email address to anyone or use it for any other purpose without your express permission.

Like this post? Check out:

Preparing for Chronic Pain Medial Appointments + Printable To Help, How Chronic Pain Patients Use Opioids, Being a Chronic Pain Patient in the Opioid Abuse Crisis

 

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.

Share this with your family and friends:

  • Share on X (Opens in new window) X
  • Share on Facebook (Opens in new window) Facebook
  • Share on Pinterest (Opens in new window) Pinterest
  • Email a link to a friend (Opens in new window) Email
  • Share on LinkedIn (Opens in new window) LinkedIn
  • Print (Opens in new window) Print
  • Share on Tumblr (Opens in new window) Tumblr

Related

Previous Post: « A Reintroduction
Next Post: Spoonie Spotlight: Anna Evangeline »

Reader Interactions

Comments

  1. Natalie B. says

    July 16, 2015 at 2:44 am

    As a Certified Addictions Counselor, I so hear you on this subject. The pharmacies, while trying to follow State and Federal regulations, have seriously hurt people who truly need these medications. I'm hoping your experience was okay.

    Loading...
    Reply
  2. Tori Gabriel says

    July 31, 2015 at 5:32 pm

    Hi Kate,

    Thank you! I’ve just read your posts on the linky and it’s nice to know I’m not alone. I have Crohns Disease and it’s badly flared at the moment. I felt so relieved to read your words. Off to FB now to “like” you so I don’t miss another post.

    Loading...
    Reply

Trackbacks

  1. On Living with Acute Chronic Pain: Please Don’t Treat Me Like a Drug Addict! | myRAteam Blog says:
    July 30, 2015 at 5:27 pm

    […] post originally appeared here and is reposted with […]

    Loading...
    Reply
  2. How To Increase Blog Traffic says:
    September 17, 2015 at 8:25 am

    […] Controversial post (about needing narcotics) […]

    Loading...
    Reply
  3. Kate the (Almost) Great | Boston Lifestyle Blog - How To Get Blog Traffic: My Blogging Advice To Actually Grow Your Blog says:
    February 2, 2017 at 8:01 am

    […] A Note on Living with Acute Chronic Pain […]

    Loading...
    Reply
  4. Resources for the Freshly-Diagnosed Chronic Illness Patient - Kate the (Almost) Great says:
    March 22, 2024 at 11:54 am

    […] A Note on Living with Acute Chronic Pain […]

    Loading...
    Reply

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Primary Sidebar

Kate the (Almost) Great® is a chronic illness lifestyle blog. It is a resource for chronic illness patients and their loved ones.

  • Bluesky
  • Email
  • Facebook
  • Instagram
  • Pinterest
  • Threads
  • TikTok
  • Twitter

Categories

Health
Lifestyle
Writing & Blogging

Pages To Start With

  • About Kate the (Almost) Great®: Meet the Health Blogger
  • As Seen On
  • Contact & Work with Me
  • Follow
  • Health Blog Resources I Actually Use + Recommend
  • Newsletter
  • Popular Posts
  • Privacy Policy & Disclaimer Policy
  • Products for the Chronically Ill: My Recommendations
  • Shop
  • Start Here
  • Tags & Topics

Search

As an Amazon Associate I earn from qualifying purchases.

This blog uses affiliate links. Thank you for supporting Kate the (Almost) Great!

Sign Up for the Newsletter

Please wait...

Thank you for sign up!

Most Popular Posts

  • Seronegative Rheumatoid Arthritis Diagnosis: What I’ve Learned
  • Beginner’s Guide: Rheumatoid Arthritis Flare Up
  • What Is the Difference between Osteoarthritis and Rheumatoid Arthritis?
  • What Does Arthritis Pain Actually Feel Like?
  • What Sjögren’s Syndrome Is: A Beginner’s Guide
  • The Products I Loved (And Wanted) in Grad School
  • 9 Arthritis Products That Help My Rheumatoid Arthritis
  • The Lifestyle Changes I Made for My Rheumatoid Arthritis
  • What Every POTS Syndrome Patient Needs for the Summer


Bluehost.com Web Hosting $3.95

Health Union Patient Leader Certification

Support KTAG

If you like what I do, please support me on Ko-fi.




Footer

Sign Up for FREE Instagram Challenge

Get 25 FREE Instagram prompts for chronic health creators!

You can unsubscribe anytime. For more details, review our Privacy Policy.

Thank you!

You have successfully joined our subscriber list.

Get your FREE Instagram challenge here 

and 

For just $5 get your copy of my ebook Take Your Blog (And Income!) to the Next Level with code "greatest".

.

Kate the (Almost) Great

Chronic health lifestyle blog

Lets Go!
  • Facebook
  • Instagram
  • Pinterest
  • Twitter
There's beauty everywhere, not just in the Maine w There's beauty everywhere, not just in the Maine woods. (Shocking to me, I know.) ⁣⁣⁣
⁣
There's beauty in little things, medium things. There's beauty in ordinary things. ⁣⁣⁣
⁣
In the first cup of coffee of the day with the sun shining into the kitchen. ⁣⁣⁣
⁣
In a completed checklist.⁣
⁣
In a freshly cleaned house. ⁣⁣⁣
⁣
In discovering a new-to-you genre of television that you LOVE. ⁣⁣
In quiet moments with people you care about. ⁣⁣⁣
⁣
There's beauty everywhere. ⁣⁣⁣
⁣
⬛⁣⁣⁣⁣⁣
⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⬛⁣⁣⁣⁣
⁣
ID: A beautiful lake and a mossy bank. ⁣
⁣
#MaineLife #207 #MaineLiving #IGNewEngland #Vacationland
Weeks 15 of 2026 Weekly Just trying to get throug Weeks 15 of 2026 Weekly

Just trying to get through!

1️⃣ IVIG time
2️⃣ I got a hair cut last week and then I looked nice at one point!

⬛⁣⁣⁣⁣⁣⁣

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⁣⁣.

⬛

⁣⁣⁣⁣⁣⁣1️⃣ Looking at Kate’s lap. There’s a pump with tubes attached that go under Kate’s shirt.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair wearing a navy dress with flowers, a silver Celtic knot necklace, and green glasses. 

#ChronicallyIll #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #IVIG
FAQ: What Is Subtalar Fusion Surgery? Background FAQ: What Is Subtalar Fusion Surgery? 

Background: I have tarsal coalition and rheumatoid arthritis and had subtalar fusion in my left foot in 2009 and in my right in 2018. While this was started because of the tarsal coalitions, it is a surgery that can help rheumatoid arthritis, too. 

Video: Kate talks to the camera. There are captions. A black text box at the binning reads “FAQ: What Is Subtalar Fusion Surgery?”. 

#TarsalCoalition #RheumatoidArthritis #SubtalarFusion #AutoimmuneDisease
There will be times when you do everything you can There will be times when you do everything you can to feel better and it won't work. That's not a failing on your part.⁣⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⬛⁣⁣⁣⁣⁣
⁣
ID: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣
⁣
#RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Endometriosis #Fibromyalgia #SjogrensSyndrome
Weeks 13 and 14 of 2026 Weekly Had some rough pai Weeks 13 and 14 of 2026 Weekly

Had some rough pain days in here so I didn’t do a lot and I combined the weeks in 1 post!

1️⃣ Hematology appointment 
2️⃣ PCP, after which an x-ray showed stress fractures in 3 bones 
3️⃣ Tea and cross-stitching

⬛⁣⁣⁣⁣⁣⁣

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⁣⁣.

⬛⁣⁣⁣⁣⁣⁣

1️⃣ Looking at Kate’s lap. There’s a medical bracelet on her wrist and a Kindle on her lap.
2️⃣ Kate takes a selfie in a doctor’s office. She’s a white woman with auburn hair wearing a black t-shirt, silver Celtic knot necklace, apricot mask, and green glasses.
3️⃣ Looking at a table on which is an orchid, an in-progress cross-stitch project, and a mug of tea.

#ChronicallyIll #RheumatoidArthritis #CrossStitcher #DisabledAndCute
Background: I have tarsal coalitions and rheumatoi Background: I have tarsal coalitions and rheumatoid arthritis in both of my feet, and I’ve had resection surgery and subtalar fusion surgeries. I am not a medical professional and am sharing my experience! 

Video: Kate talks to the camera. There are captions. Text reads at the beginning “FAQ: What Was the Recovery from Tarsal Coalition Surgeries Like?”. 

#TarsalCoalition #RheumatoidArthritis #ChronicPain
We've all made this mistake once (or twice or a hu We've all made this mistake once (or twice or a hundred times ...) ⁣
⁣
⬛⁣⁣⁣⁣⁣
⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⬛⁣⁣⁣
⁣
ID: Kate smiles at the camera. A white text box reads "No two chronic illness patients are the same, but we've all given ourselves flares by overdoing it on a good day". ⁣
⁣
#InvisibleIllness #ChronicallyIll #ChronicPain #SpoonieLife #ChronicIllness
SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣ ⁣ It can be rea SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣
⁣
It can be really easy to feel like chronic illness has taken over everything about you and that all you are is a patient. ⁣⁣⁣
⁣
You might be different than you were before you developed symptoms, but that doesn't mean that everything about you is different, even if everything about your life is different. ⁣⁣⁣
⁣
There is no one aspect of our lives that defines all that we are. That's true for LITERALLY EVERYONE! No one is just one thing. We're all many, many things. ⁣⁣⁣
⁣
For example: yes, I'm a chronic illness patient, and yes, I talk about it a lot online. But I'm also someone who is passionate about education, who played 1-3 instruments for 12 years, who is obsessed with her home state, who reads a ridiculous amount of historical fiction, and who has been writing in some capacity for decades. ⁣⁣⁣
⁣
Even if all you know about me is that I'm a chronic illness patient, that doesn't mean that all I am is a chronic illness patient. ⁣⁣⁣
⁣
⬛⁣
⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣⁣⁣⁣⁣⁣⁣⁣
⁣
⬛⁣
⁣
ID: Kate takes a selfie. She's a white woman with auburn hear with a blue sweater, green scarf, and pink glasses.⁣
⁣
#RheumatoidArthritis #Fibromyalgia #Sjogrens #Endometriosis #POTS
PREPARING FOR SUMMER WITH POTS⁣ ⁣ Summer is right PREPARING FOR SUMMER WITH POTS⁣
⁣
Summer is right around the corner. Here are somethings I'm doing now to make it easier. ⁣
⁣
1️⃣ Finding my many fans and making sure they're charged⁣
2️⃣ Increasing my sodium intake ⁣
3️⃣ Making sure I have plenty of @cure, my preferred electrolyte supplement⁣
4️⃣ Getting back into the habit of using Tachymon, the app I use on my watch as pictured here. I have it set to notify me not only when my heart rate gets high, but also when it has changed by a fair amount. Here, it shows my heart rate is 150 and the change from my recent average (104) is 45.6. With POTS, the problem isn't only an increase, but a quick increase. ⁣
⁣
What are you doing to prepare for summer with POTS? ⁣
⁣
⬛⁣⁣⁣⁣⁣
⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
⬛⁣⁣⁣
⁣
ID: An Apple watch showing a heart rate of 150, recent average of 104, and change from that average of 45.6. A white text box reads "Preparing for Summer with POTS". ⁣
⁣
#ChronicallyIll #PosturalOrthostaticTachycardiaSyndrome #Dysautonomia #POTS #SpoonieLife
Follow on Instagram

Copyright © 2026 · Kate the (Almost) Great · Design by Studio Mommy

%d