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Conditions > Juvenile Arthritis > Juvenile Arthritis and Fatigue
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JA and Fatigue

What to do when weariness weighs down your child

By Linda J. Brown

The boundless energy of youth, that spark that keeps kids on the go, is something that fatigue steals from many children with juvenile arthritis (JA). And though it may require a bit of detective work from you, your child and your physician to get to the cause of your child’s fatigue, there are many things that can be done to alleviate fatigue and return the twinkle to your child’s eyes.

Some children with arthritis are very affected by fatigue while others are not. But in general, those with active disease, especially during flares, are more likely to feel fatigued. Kids with pauciarticular and oligoarticular disease don’t seem to have as much of a problem with it.

What causes fatigue?

Fatigue is a complex beast and several factors may be responsible for your child’s fatigue. These can range from his or her body’s way of dealing with the disease to inability to get good sleep.

“When the disease is active, we think it has to do with the toll of chronic inflammation on the body,” says Carol Wallace, MD, associate professor of pediatrics, University of Washington and Children’s Hospital & Regional Medical Center in Seattle.

Iron deficiency (anemia) can also produce fatigue. Keeping kids’ arthritis under control is important in this regard because chronic inflammation impairs how well the body utilizes iron and can worsen anemia. Jean Kotowski’s 12-year-old-son Danny from Naperville, Ill., was diagnosed with systemic juvenile rheumatoid arthritis (JRA) when he was 9 years old and he was very anemic.  “As a young boy he always seemed tired and when we took him in for his kindergarten they noticed he was anemic,” says Jean. “We checkup didn’t realize it then but that might have been the start of everything with Danny.”

Another likely cause of fatigue is pain. “I think pain makes you very tired,” says Marisa Klein-Gitelman, MD, associate professor of pediatrics and head of the division of rheumatology at Children’s Memorial Hospital in Chicago. Pain and inflammation often seem to be linked. However, Dr. Klein-Gitelman points to children whose arthritis is not active but who have previous hip or knee damage and are in pain on a regular basis. Even without inflammation, they feel fatigued. In these cases it seems pain is the trigger.

Getting good Zzzs

Poor quality sleep can certainly cause fatigue in anyone but can be particularly tough for kids with arthritis. Research has shown that compared to healthy kids, children with arthritis often “have more difficulty falling asleep, they wake during the night and have difficulty falling back to sleep, and they wake up early in the morning and can’t go back to sleep,” says Sharron Docherty, PNP, assistant professor, Duke University, School of Nursing in Durham, N.C.

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Farzin Fardin
31 May 2010, 09:06
Hi All
My son was diagnosed with JIA while he was about 13 in 2007 although he had some painful joint scenarios prior to that but doctors were not sure, as the usual treatment what they gave him was Naprosin and Methotrexate tablets. In 2008 his doctor started a new medicine which is called Enbrel in the form of injection, the injections are easy and if done well not painful at all, he was continuing to take Methotrexate tablets for about six month which has been eliminated thereafter. The Enbrel is not a kind of cortisone so does not have all the side effects of cortones and it was like a miracle for my son. He is 16 years old active boy now who plays Rugby and used to go to Karate classes and were very good at his fights winning some State titles.
The joint pain never returned and he is comfortable with injection which is going to gradually be reduced.
I wish you all a good treatment and hope.
Regards'
Farzin
Theresa (IL)
26 May 2010, 17:20
My son was diagnosed with granulomatous dermatitis when he was 14 months old, in late 1999. In February of 2003 at 4 1/2 years of age he was diagnosed with granulomatous arthritis which we discovered was unknowingly present back in 1999-2000. On Christmas Day of 2003, I received an email from his dermatologist confirming he did in fact have Blau's Syndrome. While he was in 2nd grade (2006) he had his first uveitis flare up. It has been a long road, trying different medications to find what works best for him. Over the years he’s been on Vioxx, Enbrel, naproxen, Relafen, and Zantac.

Currently, he goes in every 4 weeks for Remicade IV infusions, weekly takes methotrexate, and daily is on Erythromycin for the dermatitis, Diclofenac (anti-inflammatory), and folic acid. I’ve lived the fear and anxiety of being a parent to a child taking these medications.

While every case is different, my son will be celebrating his 12th birthday this summer. He plays basketball, baseball, swims, skateboards, rides his bike, and if you didn’t know he had this disease you wouldn’t even be able to tell. He’s not as agile or quick as his peers, but he gives it his all.

11 years ago, there wasn’t near the information available as there is today. Hang in there mommas and dads. Put life into perspective, and take comfort in knowing at the end of the day your child is at home and sleeping under your roof. All it took was one trip to Children’s Memorial for me to see that what our family is going through is an inconvenience or challenge; not terminal.
Dee
07 May 2010, 03:35
My 11 year old was diagnosed as polyarticular Juvenile idiopathic arthritis in Sept 2009 (that's a mouthful). We made sure he knew what each individual word meant to help explain what he has to kids in his school. We started with Humira in November. I can't express the difference, not only in his physical well being but his emotional as well. We take bi-monthly injections. I give them and he sings with his sister what starts out as "Mary had a little Lamb" then ends as something silly since the shot take a few seconds to inject. He also takes methotrexate and folid acid. He is very active and doesnt want to be held back but tires quickly. He is always the first one asleep and often falls asleep in the car between activities. He needs to learn to pace himself. We are grateful for the support he gets not only from the Doctors but family and friends as well.
Jan in WI
16 Apr 2010, 13:15
My three-year old daughter was diagnosed in September 2009. She takes a weekly Methotrexate injection - we do it on Tuesday evenings, when both parents are home and her older sister is around for support. It always involves some crying, but we encourage her to pick which leg and wipe it with the alcohol swab so that she is part of the process. We often have to hold her tightly to get the injection in - but we do strong hugs afterward...and generally allow for some sort of popsicle, lollipop or TV show (her older sis gets the treat too as long as she cheers and shows support). We've all made the connection that the shots help with the pain - so that makes it a bit less traumatic to go through this each week. It's tough, but definitely doable. Good luck!
ariz
23 Feb 2010, 16:14
Im 16 years old and I have to inject Methotrexate every week. Its very hard dealing with, I am terrified of needles. At the same time I have people who support me and encourage me to have hope and keep going with my treatment...Im doing so much better now! :)
Cathilyn
24 Jan 2010, 23:10
Our little girl will begin the Methotrexate this week. Let's continue to share our experiences as they occur.

Thanks.
Ewa
14 Dec 2009, 18:05
My 9 years old daughter was prescribed Methotrexate by injection.Can anybody share the experience of giving this to the child
Thank you

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