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You are here: Home / Coping / Magnesium for Fibromyalgia

Magnesium for Fibromyalgia

Last Updated: November 28, 2020

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.

Magnesium for Fibromyalgia

Some of the earliest recommendations that I received for Fibromyalgia involved magnesium. A friend suggested epson salt baths and my chiropractor suggested taking magnesium supplements. Since those early days, I’ve read many studies that confirm that most of us with Fibromyalgia are low in magnesium and can benefit from some sort of supplementation.

There are a ton of different magnesium supplements available in different formulations. Some are easier on the stomach than others, some are easier to absorb. I personally prefer magnesium malate as it seems to have far less of GI issues than some others.

How Magnesium can help fibromyalgia symptoms

Starting with Magnesium

When you begin taking magnesium you’ll want to start with a low dose and slowly increase. If you begin having loose stools or diarrhea you are likely taking too much.

While daily supplementation can certainly help reduce muscle spasms and reduce pain overall, you may find that topical magnesium can help with almost instant relief. I find that a warm bath with epson salts (which is basically magnesium salt) can help me relax and help reduce pain.

However, some people don’t do well with baths for a variety of reasons. In those cases, or when a bath just isn’t an option, a magnesium oil or lotion can be just the trick you need.

A few weeks ago I received this email from Antonietta:

Through the fibromyalgia support group, I learned how well topical magnesium oil or gel actually works to sooth Fibro pain, and much more so than any pain med or Fibro specific med ever did.

For me, all of those prescriptions were an exercise in futility and roller coaster ride of hope and despair when each one failed.

Hence, when I was first diagnosed with fibromyalgia a dozen years ago, I wish someone had told me about how soaking in Epsom Salts baths (with baking soda for it to be more gentle on your skin) and/or using topical magnesium gel or oil works to provide temporary relief of Fibro pain.
 
When I realized that Epsom Salts are magnesium sulfate, it clicked in my head how my grandmother and mother used Epsom Salts while I was growing up and how they swore by it. I have found using topical magnesium oil or gel to be like having an Epsom Salt bath but without the bath part as there are times when my body just doesn’t want to cooperate with getting in and out of one. 
 
The only thing is to never use magnesium oil or gel on freshly bathed skin or else it will sting. It has to be used on closed pores only, and never ever applied on the same day you shave your legs.
If you haven’t already added some form of magnesium to your supplement regime then I would highly suggest doing so. If you find that oral supplements aggravate your stomach and you can’t handle baths then definitely try a magnesium oil or lotion.
 
A combination of the three is ideal for me as the oral supplement keeps the spasms away and the pain low overall, the baths are great for relaxing before bed and help me sleep, and the lotion has been helpful for localized muscle pain.
 
I’ve not tried straight oil because I shave my legs pretty much every day that I shower and I just didn’t want to find out if it would sting. The lotion has not had that effect for me.
 
 
I’d love to hear more about your experiences with magnesium, or other natural ways you’ve found to reduce your pain and/or fatigue.
 
Related Posts:
  • How I reclaimed my life from chronic illness
  • 10 Ways to distract yourself from chronic pain
  • The fibromyalgia treatments that have helped me most

2 Comments Filed Under: Coping, Fibromyalgia, Tips and Tricks, Treatment Tagged With: chronic pain, decreasing pain, supplements

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. Connie says

    July 11, 2019 at 8:01 pm

    I was on vacation and I was hurting so I took a HOT Epson salt bath every morning and another one every night and I managed to walk 26 miles in 7 days. Never did that before and probably will never again. LOL I was thankful I found something to get me through it.

    Reply
    • Julie says

      July 12, 2019 at 12:17 pm

      The things we do on vacation. I just returned from Chicago and on the light days I did 8-10 miles! That first night I was hurting so bad, and I’ve been in rest mode for several days since returning home.

      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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