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Symptoms > Fatigue > Instant Energy Boosters
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Instant Energy Boosters

By Jodi Helmer

You wake up exhausted, and then drag all morning. In the afternoon, it takes several cans of soda for you to be alert enough to slog through a mile-long to-do list. And when the evening rolls around, the only thing you have enough energy for is a date with your favorite sitcom stars. Sound like a typical day? You’re not alone.

“We have an epidemic of exhaustion in our culture,” explains Judith Orloff, MD, psychiatrist and assistant clinical professor of psychiatry at the University of California, Los Angeles. “We need to learn to take charge of our energy levels and tap into practices that make us feel vibrant and happy.”

Instead of dealing with all-day exhaustion and forgoing activities because you don’t have the stamina, learn some tricks for getting instant energy boosters:

Turn up the tunes. Listen to your favorite CD on the way to work, or sing along to “Elmo and Friends” with your grandkids. Researchers have found that listening to music helps boost energy and stimulates positive thinking.

Straighten up. Bad posture can slowly sap your energy. According to the International Chiropractors Association, slouching requires your muscles to work harder to hold up your body, and that can lead to fatigue. Just 15 minutes of reading or typing in a slouched position strains the neck, shoulders and upper-back muscles.

Take a break from work every 30 minutes. Go for a quick walk around the office, get a glass of water or do a few slow stretches to get your blood flowing. Practice good posture by ensuring that your shoulders and hips are aligned, and your head is straight. At your desk, sit in a chair that provides good lower-back support, and keep your knees slightly higher than your hips.

Do a minimeditation. Setting aside time to do minimeditations throughout the day can help when you’re overwhelmed by demands at work, dealing with a needy friend or just feeling stressed about the state of the world. Meditations help refocus your thoughts and create positive energy.

Dr. Orloff, the author of Positive Energy: 10 Extraordinary Prescriptions for Transforming Fatigue, Stress & Fear into Vibrance, Strength & Love (Harmony, 2004), recommends finding a quiet spot with no distractions, sitting in a relaxed position with your eyes closed and taking deep, slow breaths. Focus only on breathing in and out. As outside thoughts enter your consciousness, acknowledge them and then refocus on your breathing. Do this for three minutes.

Wear red.
On days when you’re feeling sluggish, try wearing a colorful sweater or scarf for an immediate pick-me-up. Studies indicate that color has a huge impact on energy level. Red, in particular, has been shown to improve mood and alertness.

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ann
01 Sep 2010, 04:33
If the sunshine seems to help you but being out in the sun may be a bad idea, talk with your health care providers (dr, pharmacist, etc.) about taking a Vitamin D supplement, especially in doses of 1000 IU or more. Recent research has found it to be important in many processes in the body, not just avoiding osteoporosis. It can even help fight off depression (in conjunction with other treatments). I've had 2 doctors in my family recommend it to me and it seems to be helping. Still having problems with fatigue, though. Not sure what all I have yet although I know I have OA, lung problems, and possibly Sjogren's Syndrome.

Cheryl, I'd check with my dr. and/or a pain management specialist about a different medication for OA; I've had to try a number since I can't tolerate NSAIDs other than Celebrex (but have GERD, partially due to it). There's more out recently and more coming.

I'm at the point again (had both knees replaced a while back) where I think I'm going to have to go on painkillers again but am hopeful I'll be able to tolerate one of the new ones or Celebrex again (if I can have surgery to relieve the severe GERD that I have). In the meantime, I resort to heat &/or cold treatments, my treasured electric blanket (whole-body heating pad!), and chocolate-as-needed. It's so nice that chocolate helps up the endorphin level for us chocolate lovers!

I'm so glad to find this site; there are tons of good hints and lots of hints, help, and support from the posters, too. I've picked up a number I'm going to try soon, too.
Betty
23 Aug 2010, 11:00
There are 3 generations of Arthritis; my mother, diagnosed at age 67; me at 41 and my daughter at 11. I pray my granddaughters ( I have 2) will be free of this curse but fear they too will be afflicted.

My mother has RA, Osteoarthritis; I have RA, OA, Fibromyalgia and Sjogren's. My daughter has RA, Lupus, Reynaud's, Sjogren's and Scleroderma. Pain is no stranger to our family.

We have all been treated and handled our disease very differently. My mother was given Aleve and for years this worked. But this year, 15 years later, she began medication for depression and anxiety as well as plaquenil. She became extremely ill and hospitalized because of the medication and is now taking nothing except for tylenol p.m. and uses Voltarin Gel for pain.

I on the other hand have been on various mediations for 20 years from OC meds such as Aleve (when it was prescription only) to plaquenil and methotrexate. I have tried the diets, exercise and meditation programs too but with little result. Recently, I have gotten pain relief from Methotrexate, Celebrex and Cimzia. I no longer take Ultram or vicodin for pain or plaquenil. To sleep and for anxiety I take Trazadone and Ambien. I continue to be stiff most of the time and fatigued. I was always busy and doing for others and realizing that I now could hardly care for myself caused deep depression early on and continues to visit on occasion. I am 62 (was 42 when diagnosed) and tend feel like the best years of my life were wasted on pain, anger and fatigue while I went from one doctor to the next and visited labs. But then I think of my daughter and how she has had to live with this most of her life.

My daughter has dealt extremely well making lemonade out of lemons. It was tough in school because she was so fatigued but looked completely healthy. Growing up in So. CA learning the dangers of the sunshine (unable to enjoy the beach or go to Disneyland without fearing a seizure or days in bed as a result ) was the most difficult for her and missing out on school activities, dances etc. When most young people were participating in after school activities she was home sleeping. However, she used this time researching how she could benefit from alternative medicine, meditation, exercise and counseling. She took classes at the community college on nutrition and yoga. She became a medical assistant and then a medical esthetician working in the field of dermatology (today part-time). Like I said, lemonade...! Working in the field of medicine offered her the opportunity to obtain information from patients as well as doctors. Until recently she was successful in staying off medications she so desperately wanted to avoid. However, unfortunately, the inevitable finally happened. She is on plaquenil and medication for depression and anxiety as well as eye lubricants for the Sjogren's. She believes she has prolonged her life and avoided other complications by staying off medication for as long as she could. 25 years later we are so grateful she applied such tenacity and effort into her own care and it worked so well for her.

Obviously not everything works the same for everyone, but lots of help can come from doing the "most" for ourself through group chats or support groups; or meetings, exercise groups, and learning as much as we can about our condition, medications and side effects. When I was diagnosed, unlike when my daughter was 5 years earlier, I was without medical insurance so learning through my daughter was my saving grace. When she was 11 and so ill, I often asked " WHY HER GOD" .... Years later I got the answer.

I sincerely wish everyone who reads my story gains hope and inspiration to find the right "formula" for them. It has taken me years literally to learn i "can't" spend 2 or 3 consecutive days shopping, cleaning, gardening or even with family. I need a rest every 2-3 hours. I can only drive during certain hours or I may doze at the wheel.... Life changes and so must we. As resistant as we try to be, at some point we must given in .... but NEVER give up.

Happy 2 B Moving (at a snails pace)... ;-)
Betty


Erle Pieratt
13 Jun 2010, 13:09
I have had RA for 11yrs. I took methotrexate for 9 years. It worked very well. At first I had flu like feeling, but after a few weeks it gradually went away. Then after 2 months of taking methotrexate I got relief. I still had flair-ups but I adjusted and moved on. I have found good diet of low fat, exercise, low stress and lots of rest makes a big difference. plus being around positive people and limited sunshine all makes a big difference. I understand your pain!!!!! Last year the methotrexate stopped working, so we added Enbrel. In march of this year I ended up in ER with major pain. I have enlarged spleen and cancer. I stopped all meth and enbrel and pain stopped. The CLL -cancer is slow growing type. Just stated on Orencia and I pray that RA and cancer will be controlled. Thank you all for sharing your stories, I hope my comments helps someone??? God Bless you.
Alanna
04 Jun 2010, 17:26
i am so glad that I have found a support group of people that has RA and what we go through on a DAILY DAY!!! I love all the comments and I will put them into actions. I Have been DX with RA 2 years, and the first year I suffer trying to get this illnes under control... Please keep sharing your experiences with me and others.
Lisa
14 May 2010, 09:21
I have RA but have only been diagnosed since mid April, but I've certainly had and understand the whopper fatigue and migratory pain and stiffness that comes with it. My GP prescribed me xanax to help counter my depression. It really helped! I only take 1-3 .05mgs a day, but when I start having the RA blues I take one and it often stops the downward tailspin and can actually start me on an upswing again. I also take 1 of the xanax and sometimes a pain pill before bed and I now sleep EVERY night. I don't know why this drug works so well for my RA symptoms.....but it does. I'm on methotrexate which is now beginning to work after 5 weeks but I'm still in a wait and see pattern. Before I had this disease I had NO IDEA what fatigue really ment.....not a clue. I hope some of you can get something to stop the tailspin...even if just for a few hours a day it will make life worthwhile again.
Amanda B.
29 Apr 2010, 13:11
I have RA and Sjogrens an autoimmune disease that attacks moisture producing glands and causes a lot of other problems. I have had problems almost all of my life and I am 31, I have had stones in my gallbladder, both kidneys, both parotid glands, and I do believe there are some in my tear ducts and those glands, I have gallstones still forming in my liver, which come out and cause problems every so often. But the main problems are the horrible joint pain and the fatigue that makes me do face dives into my computer, food, and even in mid-sentence while talking. I even think I could fall asleep while standing up. My knee caps are wierd they wiggle around, which causes the cartlige underneath to be damaged. My other joints are almost always inflamed and painful. Just getting up and dressing is a major under taking, I just want to be able to get my cleaning done and be able to sit down without passing out. I can't watch TV, or enjoy anything with my daughter, go anywhere, or have a life.
I have a lot of patience but this is really getting the best of me, I can't do anything I enjoy all I do is sleep, I really can't even eat because of the Sjogrens my teeth are just about gone. Dry mouth caused my teeth to literally crumble away, which is extremly painful, I have had 7 pulled and need all but 4 pulled. I am looking into dentures but they may not work, implants may be the only answer. I really don't know what I am going to do. I quit taking pain meds almost 2 years ago, because the docs kept telling me that they were making me hurt more, and making my teeth fall apart, and causing all my problems, but low and behold someone finally did the right thing and did some blood work and poof, found what was wrong. I was right all along there was one main problem causing all my symptoms.
Sorry to vent but I just hope it helps someone else. So in the event that you have dry eyes and dry mouth and they are not medication related, you may want to ask your doctor to test for Sjogrens Syndrome. It also causes problems with liver, kidneys, thyroid, and other organs. Do a search to learn more, most docs don't know about this disorder.
SILVIA GMURRAY
22 Mar 2010, 08:23
i HAVE A GRANDDAUGHTER DIAGNOSED WITH jia,POLYARTHRITIS, AGE 3 IN aUSTIN AREA. lOKING FOR OTHER FAMILIESIN THE AREA WITH SIMILAR CONDITION. THANKS, sILVIA
Lionel Logan (use 'Bluesman329')
10 Mar 2010, 21:00
I have had osteoporosis a few years and recently contacted arthritis. Do I have osteoarthritis? I exercise moderately and walk and so far, Thank God, no pain. My Doctor wants to give me prescription. My Pharmacist suggest 'Flexamin-triple strength' or 'glucosamine/chondroiton/MSM' pills which he says helps rebuild cartilege. Says If I need pain relief; ibuprofen pills or capsation.
Your ideas or experiences, please.
(...The e-mail address that I signed up with is no longer valid 'twcny'...).
I hope the answer will be in 'comments' in the e-mail
Kay
05 Mar 2010, 09:21
I have osteoarthritis and osteoporosis. I have tried to get help from my doctor, a chiropractor, and by exercising at the local "Y". My family doctor prescribed a pain med (which I don't take; it just masks the problem). The chiropractor visit gave me temporary relief. The exercise helped somewhat. I can't believe in this day and age we can't go somewhere for a diet and exercise program (and whatever else the "professionals" deem will help us) geared to our individual problem. If there were such a place, the average person probably couldn't afford it! I have come to the conclusion that my inground pool is the only thing I can resort to for exercise in the summer. I took care of my mother for 20 years. She was paralyzed from a stroke and she also had arthritis in her hips and hands as I do. I would also be interested in the heredity aspect of arthritis. I am now 63 and so discouraged I could just give up! I, too, have always been a go-getter and a hard worker, but I'm just worn out from this arthritis. I am sitting here crying after reading all the distress it has caused for so many people.
francine
18 Feb 2010, 07:35
I have osteoarthritis in both my hands. My dr keeps testing me for RA - which thankfully has not shown yet. I have had fatigue for years. I was treated for candida at one point. I changed my diet - no sugar and no processed foods at all - and drank a great amount of water. It helped. Once I get going I am normally ok - but there are days I just don't have the energy at all.
char
13 Feb 2010, 11:49
i work in a production place. We don't get to take tunes or breaks when we want we have one at nine-fifteen, lunch at eleven thirty and another break at one forty-five.....we don't necesarily get out of work at three thirty neither. we have a certain target every hour that we have to meet....so what can i do to boost my energy at work other than have hot chocolate or pop at break??? No radios, mp3's, Ipods or phones allowed except at breaks.
Rudy Rogers
27 Nov 2009, 22:45
I have had R.A for 5yrs.I on humira & methotrexate.this messes with my lungs.they will sometimes give me L-tab 3 pills a day and I'LL take 4 or 5 in a day.they don't get it. its like having a BAD headace with a bottle of asprin in front of you your going to try to get out of pain.I cry out to god to please heal or let me die!I can take some pain It's that it's every day of my life.if I do day that pains not got me in tears,I'am so tired just wore out.It's not living.your energy boosters.don't work for me.If I just fell my pain one weak.I promise any one would understand.I realy wont that. I'AM sorry for going on.thanks for your ears.R.ROGERS
Peggy
15 Nov 2009, 17:59
A friend told me to try taking a high dose of Guaifenesin (the main ingredient in Mucinex sold in drug stores)for Fibromyalgia fatigue. My doctor said there is no proof it works but that it couldn't hurt. It gave me instant energy..not like the old days but now I'm up more than I'm down.
Yvonne
14 Nov 2009, 08:08
I too have exhaustion all day long. My Mother-in-law had bone cancer and passed away from this. She used to say that she was so ehausted she felt like she could die. I have Fibro and Psoriatic Arthritis. I feel everyday the way she described feeling. I exercise and do not feel any better. It just makes the pain and exhaustion better for about 1hr.. My doctors don't address it either. I take Humira and methrotrexate. Nothing gives me back my energy.
Lisa
06 Nov 2009, 17:28
WOW!!!
This is the first time i have been to this site and it`s wonderfull to hear that im not just getting old and lazy.
I did1nt relize that the fatigue is from the RA. I am an E.M.T. and work 24 hour shifts which are getting harder and harder to make it through a day.I have been thinking of changing jobs but at least i do get a chance to lay down and rest at work. but when i get 48hrs off i end up sleeping about 36 of that just to be able to go back to work.Sometimes i feel like i`ll never have the energy again to do the things i want and enjoy.
THANKS FOR LETTING ME VENT
Leeann
04 Nov 2009, 21:15
I was diagnosed with RA 6 months ago. Fortunately, I work in a large clinic that has the best rheumatologist around. So, I get a lot time to talk with my RA doctor and she also has RA. For the fatigue I have been taking weekly B12 injections, an otc Vitamin D 2000iu daily, and a rx drug called Provigil. My doctor also uses this drug for her fatigue. We like it because it does not make you jittery, and for us does not have any side effects. It's not a magic pill, however. I began the Provigil after I had been so exhausted I would nod off at work, and while driving. The medicine didn't make me feel brand new like I could run a marathon, but it did give me enough energy to get out of bed. I had been feeling so tired I would lose focus at work, and leave all the household chores to my boyfriend. Now, I still feel tired but I don't struggle half as hard to get out of bed like I did.

As to the article, I find these tips extremely useless. There is no way the writer could have any idea the fatigue you suffer with RA. This magazine should hire some writers with RA. Or ask experts on RA to write articles.

I also like the comment made about having things family members could read. This disease is invisible to the common person. I wish I could have something to give to friends and family so they can know how I suffer physically and emotionally. I hate trying to describe to people about how much I'm suffering bc I don't want to come across as whiny. Although, since I'm only 24 years old and am expected to have all the energy in the world, I would like people to understand why I can't keep up with them. I fear people thinking I'm lazy when actually I am working very hard and busting my butt.
JUDY
03 Nov 2009, 15:23
I talk to my physician all the time about the fatigue and he just says he doesn't know why it is not relieved with the Humira. I have been on Remicaid and Embrel and they were changed because he thought it might help but overall I don't feel that he realizes how bad it is-that maybe it is depression or maybe I need to exercise more. I get so frustrated!
John
03 Nov 2009, 10:01
I just read Larry Fluellen's question about the sun and RA...I have RA and Fibromyalgia...I decided one day several years back to start sunning for relief because the sun always seemed to make me feel better and it lasted once I started to do it regularly. I built a private sun deck and began sunning on a daily basis..weather permitting. It does get a bit cold in Louisiana in winter. I still made the most of the sun even on chilly days I spend a hour or so sun bathing. Since my fibromyalgia affects most of my body, I began nude bathing in the privacy of my private sun deck. I have been doing this since I was about 48. I am now 62 and the sun still helps me a lot. When I have to go long periods without sun my aches get worse.
I am aware of all the sun risks, but since I am not all that fair I tan easily and do not burn. However, I have found that the best way for me is sun exposure starting with only a few minutes (say 15) to start and once my skin tans increase gradually to up to two hours of full body exposure. I guess one has to measure the risk. If your skin needs protection, certainly use it. I tan and use no type of blocker only skin creams to keep my skin soft and moist after sunning. It seems that all the types of radiation from the sun is needed for me or at least, I might say, since I don't know which ones to block I choose not to block any. Please use any cautions you deem necessary to protect from skin cancer..but sun does help in the way I do it...for me and others I know...Larry you might like to consider sunning for a short period until your body gets used to it and working up to 2hrs or so. I have stayed longer, but if I start to feel discomfort, I stop. Our bodies are all different as far as reaction to exposure to sun is concerned, again, take sensible precautions. You know your skin condition..but the sun will help you. I hope this may help some who suffer as I do.
Sincerely, John
Neva
06 Oct 2009, 10:30
EXERCISE! EXERCISE! I have "lotsa" arthritis. In 1980 I joined the Y and have been exercising every since. I don't have to take any pain medication because the exercise takes away the pain.
Before the exercise I had taken 4 or 5 heavy pain medications in order to exist. Once I exercised, I hardly ever have to take any pain medication.
Marie
02 Sep 2009, 09:34
I don't think there's that much you can do about fatigue. In my case it's clearly linked to the medication I take. Sometime I find swimming can do some good, it's not as hard on the joints as walking or cycling. But basically the only thing that really helps me is sleeping enough.
Ashly
21 Aug 2009, 13:54
I enjoyed these tips and techniques but I don't believe you can get long lasting relief by doing just these simple things. I'm a waitress and have suffered for several years with hip and knee joint pain. I tried the chiropractor and it helped but for a short time, however the pain creeps back. I searched for a natural remedy, as I don't like taking medications, and I found the solution through a website: fastjointpainrelief.com
In fact, that site linked me to this site. I hope it may help others looking for relief.
Bette
19 Aug 2009, 02:18
While I agree that doing the things the article suggests does make some types of lighter fatigue better, for the really hard fatigue, the RA kind that makes my eyes cross, makes my body weak and limits so much of my life, I have not found any remedy. A four hour nap sometimes helps. Unfortunately most employers frown on their employees taking a four hour break to nap. And by the way, every employers I have ever had would frown on their employees doing anything but working every 30 minutes. They say that anything that needs to be done can be done on the two 10 minute breaks and a 30 minute lunch for a 8 hour day. While the tips can help a minute amount for a normal person, realistically helpful to a person trying to survive with RA they are not.
margaret
05 Aug 2009, 11:36
I have RA and fibromaylia I am so tired and hurt to move .I can not get out of a pool , can not walk . I take medictions vitamins not one thing helps . I sleep 12 hours a day and Iam still tired . So far not one thing has helped , can not walk good anymore.If anyone can help it would be great, thanks margaret
Cheryl
23 Jul 2009, 10:53
Hello,
I've been recently diagnosed with Osteo-arthritis in my back, what kind of pain relievers are out there instead of taking the perscription the doctor gave me, it's too hard on my stomach.

When will I feel like I havent been beat up every morning when I wake, I'm always sluggish and sore, does anyone have any suggestions, I could really use one, lol.

This is a great site too!

Thank-you
C.
Kate
14 Jul 2009, 11:50
I was diagnosed in 3 1/2 years now and the enbrel and humaria have not helped. I battle with the fatigue the most. I have to sleep a minimum of 12 hours to function. Does anyone have any tips.
Rosemarie
07 Jul 2009, 19:31
I agree with Anjela. I think the title is misleading and so the article is disappointing. I would love to exercise, but arthritis has worn away the cartilege in my knee and it is painful to walk around my house.
Josephine
25 Jun 2009, 16:51
What a relief!You just gave me an answer to my "Total lock of energy" Thanks.
Kim
21 Jun 2009, 15:14
It is such a relief to know I'm not the only one with this life-wasting fatigue. I'm newly diagnosed with RA and was diagnosed with Sjogren's almost 2 years ago. I've always had a lot of energy and I've been a can-do person. Now I feel like I have lead in my blood and fuzz in my brain and it is unremitting. Not only is the fatigue difficult for me to adjust to, my family can't quite believe it's real. When I've spoken to physicians about it, they side-step the question, perhaps because there isn't much they can do about it. So far what has helped me the most, other than the common sense guidelines of good diet, exercise, etc., is the validation I have received on this website. It's good to know that "fatigue is one of the most common symptoms of RA" - it's not just me. Perhaps there could be information sheets on this we could print out and give to family members/friends? Thanks.
Nancy
21 Jun 2009, 09:51
to larry fluellen-depending on what medicines you take for your RA, you should be very careful of sun exposure. My medicines make me sensitive to the UVA/UVB rays and I can get a bad sunburn quickly. My advice is to read the warnings that come with your prescriptions and/or ask your physician and/or check the various medical web sites for side effects of your medicines. I do know that the warmth from the sun feels good but too much is not good for anyone. Skin cancer from sun exposure is also a real danger-don't add that to RA.
Marcy
19 Jun 2009, 12:01
I hear you! I'm the editor of Arthritis Today. It's great to get this feedback. I'd love to hear more about how fatigue affects you and what advice you would give others.
rachel
19 Jun 2009, 11:16
I can definately agree with Angela. These do not hel ppeople with REAL honest to GOD fatigue. And NO ONE seems to understand!
kate
17 Jun 2009, 06:00
I identify with the fatigue and tiredness that people with arthritis have I have had this condition for years. So for me exercise energizes me and the pain in my knee, etc. is helped with physical therapy.
Marged
16 Jun 2009, 23:31
I thought these were excellent suggestions.
I copied them & sent on to several people &
plan to use them myself. Most of them I already
do. These are the kinds of things I like in
the magazine. I am not interested in the dangerous drug treatments coming from the pharmaceuticals and doctors. Alternative medicine is the way to go for most all our ills.
Marged
anjela
16 Jun 2009, 17:55
I can't believe whoever wrote this article has ever had real fatigue- It would have been better titled regarding tiredness- yes tiredness not fatigue.I have a neurological condition with crashing fatigue-I didn't know whether to laugh or cry at the suggestions. Take a walk....no a 'quick' walk around the office. Listen to Elmo(as if the fatigue doesn't make me woozy enough) If you ever had fatigue it doesn't allow for these things-
This remminds me of someone who said when I told them of MY fatigue how after a trip to Nordstrom or their spa they too feel exhausted.
Please let people who know about fatigue and reserve your tired recommendations for those just get tired or lazy!
Susie
16 Jun 2009, 14:18
What a great space to share experiences.
I've learned that feeling lazy is not lazinees, is depresion, I am exhausted thinking, working, etc.etc.
Yes! For a short perior of time, I read, I listen music, I excersice, meditate, and also I do have a short talk with God. Doing one of these things helps me to keep going in my life!
Sara Sesals
16 Jun 2009, 13:26
Thanks
larry fluellen
29 May 2009, 22:30
does long periods of time in the sun effect RA in an way.

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