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You are here: Home / Medical Studies / 5 Part Treatment for FMS/CFS

5 Part Treatment for FMS/CFS

Last Updated: March 30, 2011

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.

Many of the top online nursing schools are beginning to realize the challenges of treating fibromyalgia and chronic fatigue syndrome. They are teaching students about a variety of options, including the SHINE program. SHINE stands for sleep, hormones, infections, nutritional supplements and exercise. Well-trained nurses are an essential part of administering any FMS/CFS treatment program.

I just read this interesting article about the “SHINE” 5 part treatment plan for FMS/CFS. I’ve only really worked (and my Drs have only suggested I work) on 3 of these 5 areas. Most of our treatments typically focus on Sleep, Nutritional Supplements & Exercise. This treatment plan also includes treating with Hormone therapies even when blood tests may show no deficiencies, and treating underlying Infections.

I’ve often wondered about the potential for hormone / thyroid imbalances even with normal tests, as many of the symptoms related to FMS also appear in thyroid disorders. In talking to a couple of my doctors, it seems that some doctors do believe that more aggressive treatment is necessary for those of us with Fibro, and that perhaps just because our tests may be “clear” doesn’t mean that we don’t need treatment for something. Sometimes the symptoms speak more than the tests. Thinking about this, it reminds me of the issues I had with my gall bladder several years ago. Test after test showed it was fine, but the symptoms were definitely there. Had this been 20 years ago a doctor would have taken my gall bladder out on symptoms alone. 20 years ago doctors were able to treat symptoms, now thanks to insurance regulations they have to run a test to have something on paper to show why they are treating us. I think we rely too much on tests that may or may not be correct, especially when most of them are known to be fallible.

I can’t help but wonder if those of us who have doctors who are a little more aggressive in our treatments are also the ones who are seeing the most improvement. Then again, if you keep doing the same old thing, you are going to keep getting what you’ve always gotten.

Leave a Comment Filed Under: Medical Studies, Treatment Tagged With: chronic fatigue, chronic pain, sleep

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.

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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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