Our Life with Juvenile Arthritis: My Daughter’s Ninja

I told you I wrote a post! Ha! Here it is…a little update on my daughter…

As many of you know, my daughter has Juvenile Arthritis. She was diagnosed at the ripe old age of two, when I was VERY pregnant with Ev. You can read her story HERE.

kids get arthritis too

My KGAT awareness bracelet. 

She has been through a few procedures, including a joint injection and an MRI, both under sedation. She has endured countless blood draws and doctors appointments and even had to have both physical and occupational therapy. She was on an injectable chemotherapy medication for almost 2 years to suppress her immune system, and it did it’s job: it quieted her disease and eliminated the inflammation in her little body. However, she also paid a price for this. The medication made her terribly sick to her stomach. Even THINKING about the medication made her gag. She began hiding from us when it was “shot night” and would cry and BEG us not to give her her medication.

As you might gather, this was very taxing on our family. There were tears (and not just from her). There was anxiety, guilt, and sadness.

But her disease was doing well, so we stopped her medication. And we enjoyed 6 full months of non-medicated “remission.” She was doing great, feeling great, and our family was happier as a whole.

A few weeks ago, however, that all changed. I noticed a joint on one of her fingers looked odd…sure enough it was swollen. This particular joint, the one closest to the fingernail, had never been swollen before. I emailed her doctor first thing the next morning, and she called me right away.

We were hoping maybe this would be a short term flare due to a virus, but unfortunately the swelling never went away. We went in to have her pediatric rheumatologist check her over, and we found that her knee was also inflamed, as well as a toe. Ironically, just the week before I noticed the swollen finger, she had told her dance teacher that she could not jump on her “juvenile arthritis leg” but I just thought she said this because she has recently been learning more about her illness and she was using words to talk about it.

DSC_9741-1

E the day she told her dance teacher she couldn’t jump on her “juvenile arthritis leg.”

But I was wrong. The monster we call JA was back in full force, and attacking her tiny little body again.

You see, JA is an auto immune disease. E’s immune system is SO GOOD that it not only fights off common viruses like a ninja, but it doesn’t seem to know how to stop and continues on to attack her own tissues.

E rarely gets sick. She did not get a fever until she was over 2 years old and her JA had been diagnosed. The only time she gets a fever, is when she is VERY SICK. Like, ear infections and lung infections sick. I’m telling you, ninja like immune system.

If only the Ninja knew when it was time to chill out.

So now, we are going to try a different medication to help calm her immune system. Hopefully it will not make her so sick and it will get her back into a remission before too much damage is done.

Because even though E never complains of pain, we can see her compensating. She is favoring her good leg again. Sometimes she has a slight limp.

It makes our hearts hurt. Because we know her body is being damaged. And we can’t fix it.

Esella is one of over 300,000 children with Juvenile Arthritis. Unfortunately, so many children go misdiagnosed/undiagnosed far too long. Then when they DO get diagnosed, it can be very scary territory. There is such scattered information online and you never know what to believe. Many doctors simply are uninformed as well, which makes diagnosis and treatment that much more complicated. When E was diagnosed, I immediately started looking for information online and was disappointed in what I found. I wanted more!

I wasn’t the only one who noticed there was a need for more information out there. My friend Kim, and fellow JA Mom x2, has written a book called Living with Juvenile Arthritis: A Parent’s Guide. I’m just finishing it up and soon I’m going to tell you more about this great new resource. If you are a parent with a child with JA or a professional who works with children with JA, this book is a must read. But more on that VERY soon!

We go today to learn how to mix and administer her new medication. Wish us luck!

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About Katie

Katie is a licensed, credentialed and certified pediatric speech-language pathologist and mom to three (5, 3 and 9 months). Her passion about educating, inspiring and empowering parents of children with all abilities led her to start her blog Playing With Words 365 where she shares information about speech and language development, therapy ideas and tips, intervention strategies and a little about her family life too. Katie has been working in the field of speech pathology for 9 years and is certified in The Hanen Centre’s It Takes Two to Talk ® and Target Word ® programs and holds a certificate in Applied Behavior Analysis (ABA). In addition to blogging and being a mommy, Katie works part time in her small private practice in the San Francisco Bay Area. You can follow her on Facebook, Pinterest and Twitter.

Comments

  1. Katie, I can only imagine the mommy pain that you are going through. I wish the best of luck and much progress for your little girl. Only wish there was something I could do to help. Your blogger friend, Katherine

  2. Jennifer at Purposeful Nutrition says:

    Wow, that is very challenging. Have you considered or explored taking her off gluten? Have you heard of the GAPS diet? It is a healing diet with no grains or sugar to allow the gut to heal and is particularly effective in dealing with autoimmune diseases. There is also the paleo autoimmune protocol which is a similar diet, which is really an elimination diet to see what foods are causing the problem with the person.

  3. Wishing her well with her new medication! I hope it’s just what she needs! Hugs to all
    Carrie Manchester recently posted..Super Duper Speech!My Profile

  4. Hoping for a speedy recovery and less tears all around!

  5. Peg Franklin says:

    Katie please know that people in RI are thinking of and praying this new medication works. She is a strong, beautiful little girl. Prayers to all for strength

  6. I wish your daughter a speedy recovery. Arthritis is no fun, especially for such young children. Positive vibes and prayers sent your way!
    Varya @ CWOV recently posted..Silent Monday: Mother-DaughterMy Profile

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