Showing posts with label JRA. Show all posts
Showing posts with label JRA. Show all posts

Mar 2, 2010

Meet Jessica, you will be so glad you did!

Presently there are around three hundred thousand children living with Juvenile Rheumatoid Arthritis. I have just recently became friends with a 15 year old young lady named Jessica. Jessica was diagnosed with Juvenile Rhuematoid Arthritis at the age of two years old. I met Jessica on facebook where she was kind enough to share her story with me. As you will soon find out, Jessica is an amazing young lady with a huge heart. Tears rolled down my face as I read her story and everything that she has had to go through. Even though I have never met Jessica, she is very special, I think you might agree too! Because it is important to me to put a face to this disease, Jessica has agreed to let me share her story with you! After reading this, you may agree that the "small" things in life that seem so bad just might not seem so "bad" afterall! Please continue to pray for Ayla, Jessica and all children living with this disease.

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My journey with JRA begins at age two. One afternoon, my mom came home from work to discover that my right knee was very swollen. Alarmed, my mom took me to the Johns Hopkins Hospital ER. Within a week, I was diagnosed with Pauciarticular Juvenile Rheumatoid Arthritis. My case was referred to Dr. Sills who placed me on Naproxen, Methotrexate (an aggressive chemotherapeutic agent), Prednisone (a harsh steroid), and Folic Acid (to thwart some of the effects of the Methotrexate) to combat the disease. After a few months my disease progressed and I had inflammation in virtually every joint in my body; Dr. Sills labeled my disease as Polyarticular.
Around age four, my mom and I relocated to Florida. There, my care was referred to Rheumatologist, Dr. Rivas-Chacon, at Miami Children’s Hospital and Ophthalmologist, Dr. Miller. Soon after the move, it was recommended that I see an aqua therapist and a physical therapist. We quickly became acclimated to my new schedule which included AT and PT visits three times weekly, eye exams once a month, rheumatologist visits and blood work every other month and, of course, meds every day and injections once a week. Within six months of enduring this treatment plan, the majority of my inflammation was completely gone. I was taken off the Prednisone and my doctors agreed it was safe to end the AT and PT and lower my dosage of MTX. I had achieved my first remission!
Every time I went to see the Rheumatologist, he decreased my MTX dosage more and more, until a few months later, I experienced a flare-up, beginning in my right knee. As the disease progressed, Dr. Rivas-Chacon amplified my MTX dosage and suggested I have two cortisone injections in my knees without any form of anesthetic. I underwent this procedure and experienced no benefits whatsoever. This infuriating cycle of getting better, then flaring-up continued for years. Throughout this never-ending rollercoaster ride I was never taken off of Methotrexate; yet, I remained very active through dance, karate, and soccer. I was always doing something!
Around age 11, I experienced yet another flare-up, and my MTX dosage was, again, increased, but this time my liver had a nasty reaction to the drug, and I found myself almost confronting a liver biopsy. The dosage was promptly lowered in hopes of showing improvement. My liver quickly recovered, but my joints didn’t. With the help of Prednisone, my disease went into remission. This remission lasted three lengthy years! It was great! Though I still had to take my MTX and Folic Acid, I didn’t suffer any pain from the JRA.
I am now fifteen years old, and just about two months ago, after we all thought I conquered the JRA for good, my right knee became inflamed. But, that wasn’t my biggest dilemma. I was just diagnosed with osteoarthritis (due to the damage the JRA had already done to my joints) and malalignment of the patella in my right knee, both of which cause me discomfort. In addition, I was recently referred to a cardiologist and nephrologist due to hypertension, shortness of breath, and chest pains. Plus, I’ve had a few episodes of nystagmus, so my ophthalmologist referred me to a neurologist. The past two months have been packed with doctors’ appointments, scans, ER visits, blood work, tests (including a thirty-day cardiac monitor), EKG’s, and echocardiograms; and in addition to MTX and Folic Acid, I shortly found myself taking Lisinopril, Zofran, and Naproxen. After all of this: still no diagnosis.
As I reminisce on my battle with JRA, I can remember the pain, the doctors’ appointments, the shots, and the pills, but I don’t recall ever feeling upset about it. It truly didn’t bother me. I think that’s what amazes me the most about children; no matter how bad things are, they are always blissful. We can learn a lot from little warriors like Ayla. And although I’m not happy I have JRA, I believe I have reaped many benefits from living with it. Having JRA has taught me to have empathy for others who are in pain, not to sweat the little things in life, and to be thankful for my wellbeing; sometimes I may not feel healthy, but there are many others who have it a lot worse. It has also given me the opportunity to meet a lot of great people and learn a lot of things. Whenever I go to the Rheumatologist’s office, I show the medical students how to do things! As for the future, I plan to beat my JRA (and keep it away forever), become a Pediatric Rheumatologist, and find a CURE for Juvenile Rheumatoid Arthritis.

Hope Ayla and everyone else is well!
Take care,
Jessica


Feel free to leave Jessica a word of encouragement, I am sure she will be reading this post :)

Thank you so much for taking the time to read about something that means so much to me!

Jul 9, 2009

Ayla featured in online magazine article

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Ayla was featured in an online magazine, "Therapy Times" this week. The author of the magazine was doing an article on Juvenile Rheumatoid Arthritis and found my blog about Ayla and asked if I would care to have Ayla featured in it. It is very informative and I thought everyone might be interested, especially all of the JRA mothers out there. Being that this is also National Awareness Month for JRA, I thought this was so appropriate! Click here for the link
Thank you Stephanie, you did an amazing job putting a face to JRA!


Baby StepsChildren with arthritis can lead active livesBy Stephanie Twining 07.06.09
Article available online at: http://www.therapytimes.com/070609JuvenileArthritis

Mar 1, 2009

Ayla's Update

On Friday we packed the car and headed to Cincinnati, Ohio with BOTH kids this time. My mom usually watches Brennan for us but she has taken a lot of time off of work lately, so we decided to take him with us. The 3 1/2 hour ride there went pretty well, both kids did well even though Ayla did want me to change her movies like every 10 minutes. Anyway, that is okay, at least she wasn't crying. Normally she would be miserable and would cry just about the whole entire time.

When we got to the hospital, John dropped Ayla and I off and he and Brennan went driving around for a little bit, got gas, ate lunch, changed dirty diapers..etc..we knew it would be a long day and Brennan would not last in a Dr's office for three hours.

The Occupational therapist saw Ayla first and was mostly concerned with her right elbow. This joint has always bothered her since the beginning and it is still a little swollen and has limited movement. There were also a few fingers that were swollen. She did a few exercises with Ayla and left and then we waited for the Dr or the physical therapist to come. Thankfully we were in the physical therapy room because Ayla had every ball that she could find out playing with them and she walked up and down a staircase they have oh about a few hundred times..lol..I was glad that it kept her occupied.

This was Ayla during her appointment





The fellow Dr. came in and did her usual exam, history etc and then the Pediatric Rheumatologist came in and did her quick exam. Although Ayla has been doing extremely well lately, she still has some swollen joints noticed upon exam. Both knees, rt ankle, several fingers, rt elbow all looked swollen to the PR. Also her right jaw is affected with arthritis and she was diagnosed with TMJ. They want us to try a treatment called Iontophoresis which is a treatment that is done in physical therapy.
Iontophoresis uses an electric current to push a chemical compound through the skin. Most often a steroid such as dexamethasone. Okay, this requires 20 minute sessions for three days a week for a period of several weeks. Okay people not to sound negative, but this ain't happening!! There is no way that Ayla will sit still for 20 minutes and let someone rub a wand over her cheek, nope not in this lifetime. Ayla freaks out when they take her blood pressure.. I can only imagine.. anyway, after talking to the Dr, we are just going to watch her TMJ and when we got back in May if there are no improvements then we may have to at least TRY the Iontophoresis.

Because of the swollen joints and TMJ, the Dr suggested that we go to weekly Methotrexate injections instead of the oral route. With the injectable route we know that she is absorbing 100% of the medicine and we may get better results. We are going to do this for four months, in four months if there are no improvements then we will talk about adding another medicine, most likely enbrel, which is another weekly injection. So please keep Ayla (and us) in your prayers as we begin this part of our journey. John will be giving her the injections and I know this will be hard on him. We are going to start next Saturday so I will keep everyone posted as to how it goes. We are also weaning her off of her prednisone so I pray also that this will not cause a setback . She will be completely off in four weeks. The Dr. also wants us to talk to our pediatrician about an iron supplement, Ayla is anemic which we have known for a while, but evidently some of her iron studies came back low.

While the Dr came in, John and Brennan also joined us. It was a three ring circus in that room with Ayla and Brennan. They were bouncing balls everywhere and going up and down those steps. It was almost comical as we were trying to talk to the Dr and keep our kids from hurting themselves at the same time. The Dr at one point said, " Um, you can take Brennan out in the waiting room where he is less likely to hurt himself, if you want". How funny!

It was a three hour long appointment and we still had to see the Physical Therapist after the Dr left. The kids (and us) were exhausted to say the least when the appointment was over. The drive home was okay, the kids only slept an hour so they were pretty cranky. Our next appointment is in May so we are going to try and stay the weekend and do something fun with the kids, like the zoo or Kings Island.

Ayla's current meds
Naproxen 125mg/5ml- 3/4 tsp 2x day
Ranitidine 15mg- 1.6ml 2x day
prednisone 15mg/5ml- .5 1x day
folic acid 1mg tab- 1x day
vitamin 1x day
calcium suppplement- 1x day
methotrexate- .3ml oral- next saturday will start injections