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You are here: Home / Coping / The Flare Survival Kit

The Flare Survival Kit

Last Updated: April 4, 2016

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

Flares are rare for me, these days, and usually when they occur they don’t last more than a day. I believe that has a lot to do with learning to accept the flares when they come, and give them room. When I’m in a flare, I don’t leave my PJs, I don’t shower and I don’t work. I do, however, rest, relax, recover, and enjoy catching up on some TV or a good book. I keep my flare survival kit close at hand so that I have to do as little as possible and can recover as quickly as possible.

It seems like most often flares for me fall on a Monday. Usually, after a busy weekend I try to take it easy on Monday, but often even if I don’t plan for an easy day, fibro gives me no choice. 

When possible I try to take Sunday off to simply relax. There’s a difference between a relax day and a flare day. Relax days are taken intentionally in hopes of avoiding flares. Flare days require a little more TLC, and a few special items.

What's inside my Fibro Flare Survival Kit (image of med kits) Counting My Spoons

My Flare Survival Kit includes:

  • Hot Tea – I love a good mint tea, or a ginger tea. My new favorite tea lately though is Numi Organics 3 Roots Tea, with ginger, turmeric, and licorice. It’s soothing and tastes really good with a little honey added (I typically add a little honey to most teas).

 

  • Heating pad – Even though most of my flare days don’t typically include excess pain, there are times when it does. The area that tends to bother me most is my neck and shoulders, so I’ve been using my Relax Wraps re-heatable hot/cold therapy pad a bit more.

 

  • A blanket – When I’m not feeling well I’ve got to have a comfy blanket to wrap up in. I’ve got several in the living room that I really like, a lighter one for when I’m not really cold just want to cover up,  and heavier ones for when I need to warm up.

 

  • Fay Farms CBD Muscle Rub – When my shoulder or neck is acting up (or well anything hurts), I kind of live off of this stuff (or well I guess I live with this stuff on me). As I type this my shoulders are slathered in it.

 

  • Oska – It’s a bit unfair to include this in my flare survival kit as it’s really something I rely on daily. But, when pain flares up I do find that I turn it on a bit more often. Oska Pulse is an amazing product that reduces inflammation and improves blood flow – thus reducing pain. Take a look at my full review to learn more.

 

  • Netflix / Amazon /Hulu  – (aka good TV) I don’t know where I’d be without streaming television. I gave up cable a few years ago and it’s been a really good choice. With the various streaming options there’s always something good to watch.I try to find something funny that will keep me entertained. I enjoy light-hearted sitcoms as well as random competition shows like Cupcake Wars and, lately, Making It.

 

  • Tablet/ Kindle / Smartphone – When I’m not feeling great the last thing I want to do is look at my computer, but I can deal with my tablet. It’s great for keeping up with social media, reading a book, playing poker, and checking my email. If I’m laying in bed and don’t feel like dealing with the TV I can even watch streaming video on it.

 

  • Epsom salt baths – I take a bath with Epsom salts often before bed, but when I’m not feeling well I’m likely to climb in one in the middle of the day. It’s relaxing and the salts help ease muscle tension.

 

  • Patience – I have to have patience with myself if I want to get through a flare. If I push myself too hard or I’m not willing to just ride it out, the flare will last longer. Resting isn’t easy but as the meme that’s been going around says I have to remember that when I’m resting I’m still doing something very important – I’m healing.
We must have patience with our bodies on flare days. Show them love and kindness. Share on X
  • Chocolate – What? Did you really think I’d leave off the most important thing? Seriously. Chocolate is my comfort food. I may have given up gluten, dairy, and eggs but you’ll pry dark chocolate (usually in the form of Trader Joes Pound Plus with Almonds bar) from my cold dead hands.

 

  • Water – Hydration is one of the most important things I’ve found for keeping flares short. I’ve also found that not staying hydrated is often a culprit in landing me in a flare. So, when I wake up feeling bad I fill up my large water bottle and drink it down… then do it again.Recently, I’ve also learned that electrolytes make a big difference. Adding them to my water helps keep me hydrated and gets me hydrated faster. I really like the Ultima electrolytes because they don’t have artificial sweeteners and other crud I try to avoid.

 

Never under-estimate the importance of recovering on a flare day.

 

So, now that you know what’s in my flare survival kit, leave a comment below and share what items you can’t live without during a flare.

Never under-estimate the importance of rest ... and chocolate...to recover on a flare day. Share on X

Related Posts: 

  • What causes fibro flares?
  • How I shorten fibro flares
  • The ABC’s of bouncing back from a flare
  • A play list for fibro flare days

6 Comments Filed Under: Coping, Fibromyalgia, Tips and Tricks Tagged With: flares, recovery, relaxation

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. Teresa says

    May 2, 2022 at 7:59 pm

    My flares usually last 1-2 days. My go-to-comforts are my heating pads, Voltaren gel and compression gloves, ankle and elbow compression sleeves. Can’t do without any of these! Your articles have helped me so much!

    Reply
  2. Venessa Lacy says

    February 1, 2021 at 11:47 am

    Hi Julie! Fellow spoonie and chronic pain warrior here…Just finished reading your article and it was awesome! I’m fighting through a flare as I speak and your words were comforting and encouraging. It’s refreshing to know that I’m not alone. Gentle and warm hugs to you dear!

    Reply
    • Julie says

      February 5, 2021 at 11:40 am

      You’re definitely not alone. I’m glad I could help. What other things have you found helpful during a flare?

      Reply
  3. Sam says

    June 21, 2019 at 12:15 am

    This is really good list. I have tried something similar to the above except the electrolytes. I didn’t like the other electrolytes on the market because of chemicals and sweeteners I want to avoid. I will try these. I would also add Grace. Because it is so easy to be hard on myself instead of taking care of myself. Only rest will end the flare, but I can’t rest if I’m feeling guilty for taking a me day.

    Reply
    • Julie says

      June 21, 2019 at 11:05 am

      That’s why I like the Ultima electrolytes! So true on giving ourselves grace during a flare, and any time for that matter. We can be so much harder on ourselves than we’d ever be on anyone else.

      Reply
  4. Norman says

    April 6, 2016 at 10:50 am

    Shared to Facebook.com/MenWithFibromyalgia
    THANK YOU FOR ALL THAT YOU DO!

    Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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