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I am in a quandry as to what steps to take, if any, with this overwhelming fatigue and muscle pain I have had for 2 weeks now. I guess that this is a major FM flare...I suppose I have not had one this horrible before!!
I am sooo stiff in the mornings....I "warm up" in about an hour, but feel so very exhausted even though I have rested for 4--5 hours using my CPAP machine. I take 150 mg of trazodone for sleep. I am taking tramadol for the FM pain four times a day. It doesn't seem to be really helping...my muscles ache like I have the flu!!
I have been diagnosed with FM for many years.....This pain/fatigue feels weirder than normal. I have recently retired (disability) from teaching high school English, and have had major depression because of this life change. I am a diabetic with uncontrolled blood sugar due to taking high dose prednisone for polymyalgia rheumatica and temporal arteritis. I do not eat right...too many carbs and processed foods...mostly because I am too tired to cook!!
I can do a chore or take a shower for 15 minutes or less, but have to lie down for a few minutes afterwards just to keep going!!
I am so tired of being tired!!! There are so many things that I want to do, but it exhausts me just thinking about the effort.
I hope someone has some ideas for me to try. I know that exercise, even a little, will help. The sore muscles make me cringe if I do more than shopping-type walking in the store.
My recent blood work came back normal, except for elevated sed rate and c-reactive protein, which is due to the PMR. My vitamin D was fine, iron okay, and everything else normal. Could hormones be the culprit? I am having menopausal symptoms like night sweats and hot flashes occasionally....
Please tell me what I can do to reduce this horrible soreness and fatigue!!! Thanks for any replies.....
I will try a heated rice sock tonight for my neck. Can anyone tell me how to make body sock with rice?! LOL I could stitch two sweat suits together, fill with rice---that would be a good deal of rice, though----and heat it all up. I can feel the pain melting away!!!

Well, glad to know you read the toolbox post and got some good ideas...and glad the Vit. D is normal.
yes, one of the first things to try is stretching....I know it seems like the last thing you want to do...but we do need to get the blood moving...
Do you take vitamins? Even if your D is normal, you might want to take a D vit. pill. I take a mulit vitamin, a B-100 Complete, and a D1000mg. I think the B vit is essential for energy.
And lastly, you might want to consider asking your doctor about changing the meds to see if they are making you sleepy. I was on Cymbalta for about two years and it was working great, when suddenly, I was sleepy all the time. I got off the Cymbalta, and felt much less sleepy.
I don't know if it could be hormones or not...I went through menopause without any symptoms of it...strangely enough...After years of painful periods..one day they just stopped. However, that was about the same time I was dx with fm...so all of this could be connected...I just have no way to know.
So, try, if you must, getting a nap in...but set your alarm so you don't sleep too long. You don't want to be awake all night...
cece
I have learned how to "control my FM pain" by taking vitamins and supplements....so you might want to talk to your doctor about taking supplements.....I take magnesium and malate combination supplement....(found in vitamin store) Omegas, Super B Complex, Vitamin D and calcium, plus others....as I do have other health issues....these are the ones though that help me "control my FM pain"....now...I would like to tell you that I am NOT painfree....nor do I expect to be...but I am so much better than I was when I first got sick...
And it took me a long time to figure out what my body needed....there are no quick fixes....it takes at least 6-8 weeks for whatever you decide to try....before you can truly expect to "feel" a difference....I do take Prestiq for depression...and it does help me also....it keeps my emotions leveled out....so I no longer have any crying spells....like I did in the beginning...but this is the only prescription medicine that I take....
Gentle stretching and exercises help me also....and using a heating pad and taking hot showers with lavender bath salts helps me right before bedtime....as it helps the body to relax...
Sleep is so very important for us FMers...and we have to get the deep sleep....which I think is a big problem for a lot of us....I do not think I get enough of the right kind of sleep....
You are lucky that your Vitamin D level was normal....because a lot of us FMers have low Vitamin D and low Vitamin D does cause one to have additional pain...and it also affects other illnesses as well....be sure and keep tabs on this at least each and every year....remind your doctor since the Vitamin D is not a test that is normally included in the bloodwork that is done......depending upon what your level was....you still might benefit from taking a Vitamin D anyway....I know that the "normal" level varies.....depending upon the info you are reading....
I hope that you will find something that will help you soon....
Take care and good luck...
MiMi
I see you've already got some good advice and you ask a very good question.
While you're waiting for Dr. Pellegrino to respond, take a look at the tips he shares in his own discussion:
Fibromyalgia and Fatigue
Fatigue is part of FM, but it can be part of other chronic conditions you mentioned (diabetes with uncontrolled blood sugars, depression, polymyalgia rheumatica, temporal arteritis, meds including high doses of prednisone, dietary factors, sleep apnea, ?early menopause)
Wow, I looked over that list again! I'm thinking you may have more than just fibro contributing to your extreme fatigue flare-up! Your doctor(s) can work with you to try to get a handle on all your specific medical issues including fibro to try to stabilize your "baseline" to a level where you feel you can function better. Ask about possible hormone issues.
I try to find a successful "flare-up program" for my patients who may be at a stable baseline with their "maintenance program" until something comes along to exacerbate the symptoms. In Ohio, this "something" is often the seasonal weather changes (cold and damp) but can include trauma, stresses, infections, other medical conditions etc. The goal of the flare-up program is to find some combination of treatments (ie meds, injections, therapies, rest) that settles down the flare-up and allows the maintenance program to "take hold" again.
I hope this "makes sense" and I didn't distract you with "too many" quotations! Everyone is different and you and your docs can hopefully have some success in your unique situation.
"Dr. P"
the stretching plus try Yoga. I did tons of research & have added yoga & swim areobics to my routine along with mutiple vitamins. Fish oil & st. john's wart are 2 that I have found that have positive effects with FM. Good luck & hopefully you find something soon that works for you as each of us deals with it differenlty 
I did and presto!! no more pain like the fibro pain!! I couldn't believe it. Then I ate cheese one night and woke up hurting for a whole day. NO MORE DAIRY FOR ME!. I went to chocolate soy milk, and rice or almond milk. Just give it a try and see what happens. It may help you or it may
not, everyone is different.
You are not alone. I was a manager for 15 years before my fibro got so bad I had to go on fed disability. The fatigue is the worst and the pain is the second worst. Recently, my doctor put me on Strattera for the fatigue and it has helped cut it about in half. I also take cymbalta and celebrex for the pain and zoloft and abilify for the depression. Keep working with your doctor until you find the meds that work for you. Don't give up. There is a working combination of meds out there for you. You just have to be patient. One of the things I had to do was change doctors since my old doctor wouldn't work with me to find the right meds. If that's your situation, give it some thought. Best of luck. DaniGan
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