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Ava A., Age 3

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Ava A.

Over the past year and half, my daughter went from a happy, walking and playing little girl to a child who hated shoes, socks and suddenly couldn't move her knee and fingers. 

Over the summer of 2009 we thought maybe she had sweaty feet, and that was the reason she hated shoes and socks. But as the fall neared, we noticed she always had high temps over 101, sometimes reaching over 103. My little girl was suddenly often tired and hated the cold weather, she was walking funny. We thought it was because she just wasn't used to wearing shoes. We were also noticing that with her hands and fingers, she stopped bending them. She kept them pointing in a "C" shape with her thumb. Always a runny nose, temp and always sweating. I was always calling her pediatrician. Always on antibiotics because her urine had white cells, lymph nodes behind her ears were swollen as well. 

Then suddenly in January of 2010, she stood up, screamed and tried to walk. Her knee gave out and popped out. She couldn't walk; we rushed her to an ER. They told us it was broken and put her in a splint. The next day we were seen by an orthopedic doctor; telling us it was nothing. At this time, my little girl has been through so much. It continued this way till January of 2011. It happened again a year from the date, but worse. Her foot and knee were turned in and her knee had overgrown and looked like a grapefruit. Again, we saw the orthopedic doctor. Once again more X-rays. Again, telling us it was nothing. 

No longer taking these answers, we went to the pediatrician. Ava's pediatrician referred us over to New England Medical Center. We did blood work, ultra sounds, X-Rays. It all came to light. Years of her having GI problems, temp, etc. After doing her bone marrow test, she did not have cancer. Ava had Polyarticular Juvenile Arthritis. We were seen by a specialist (rheumatologist), Dr.Lopez. Now we were told what we would have to do.

As her mother I was scared to know that my beautiful little girl was gonna have to go through so much. I would rather have Ava out of pain and be happy playing, running and jumping than a life with flares that seem to get worse and worse for her. Dr. Lopez informed us it will take time to figure out what works for her medication wise. We went through different kinds naproxen, indocin. Then we went to prednisone, fluoric acid, and methotrexate (injections chemotherapy); those 3 seem to calm her flares down. It did take time but now it’s working. We are weaning her off the prednisone, which is great news. 

Ava is walking and jumping when it doesn't hurt. We had a very hard time finding physical therapy and occupational therapy for her age. I never gave up. I made many phone calls and finally found someone to help her. We enrolled her in gymnastics (which she loves) and it’s one of the best therapies, along with swimming at the local pool with her grandparents. Ava is getting back to being a happy little toddler, dressing up in fairy and princess clothes with her heels.


Ava A.

Over the past year and half, my daughter went from a happy, walking and playing little girl to a child who hated shoes, socks and suddenly couldn't move her knee and fingers. 

Over the summer of 2009 we thought maybe she had sweaty feet, and that was the reason she hated shoes and socks. But as the fall neared, we noticed she always had high temps over 101, sometimes reaching over 103. My little girl was suddenly often tired and hated the cold weather, she was walking funny. We thought it was because she just wasn't used to wearing shoes. We were also noticing that with her hands and fingers, she stopped bending them. She kept them pointing in a "C" shape with her thumb. Always a runny nose, temp and always sweating. I was always calling her pediatrician. Always on antibiotics because her urine had white cells, lymph nodes behind her ears were swollen as well. 

Then suddenly in January of 2010, she stood up, screamed and tried to walk. Her knee gave out and popped out. She couldn't walk; we rushed her to an ER. They told us it was broken and put her in a splint. The next day we were seen by an orthopedic doctor; telling us it was nothing. At this time, my little girl has been through so much. It continued this way till January of 2011. It happened again a year from the date, but worse. Her foot and knee were turned in and her knee had overgrown and looked like a grapefruit. Again, we saw the orthopedic doctor. Once again more X-rays. Again, telling us it was nothing. 

No longer taking these answers, we went to the pediatrician. Ava's pediatrician referred us over to New England Medical Center. We did blood work, ultra sounds, X-Rays. It all came to light. Years of her having GI problems, temp, etc. After doing her bone marrow test, she did not have cancer. Ava had Polyarticular Juvenile Arthritis. We were seen by a specialist (rheumatologist), Dr.Lopez. Now we were told what we would have to do.

As her mother I was scared to know that my beautiful little girl was gonna have to go through so much. I would rather have Ava out of pain and be happy playing, running and jumping than a life with flares that seem to get worse and worse for her. Dr. Lopez informed us it will take time to figure out what works for her medication wise. We went through different kinds naproxen, indocin. Then we went to prednisone, fluoric acid, and methotrexate (injections chemotherapy); those 3 seem to calm her flares down. It did take time but now it’s working. We are weaning her off the prednisone, which is great news. 

Ava is walking and jumping when it doesn't hurt. We had a very hard time finding physical therapy and occupational therapy for her age. I never gave up. I made many phone calls and finally found someone to help her. We enrolled her in gymnastics (which she loves) and it’s one of the best therapies, along with swimming at the local pool with her grandparents. Ava is getting back to being a happy little toddler, dressing up in fairy and princess clothes with her heels.

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