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Fighting For Aaron

At the age of 11 Aaron was diagnosed with a very rare condition known as Systemic Juvenile Xanthogranuloma. The disease has affected his brain, eyes and bone. Systemic Juvenile Xanthogranuloma is a rare form of Histiocytosis that affects only 1 in 10 million children.

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Fighting For Aaron | fightingforaaron.com Reviews
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At the age of 11 Aaron was diagnosed with a very rare condition known as Systemic Juvenile Xanthogranuloma. The disease has affected his brain, eyes and bone. Systemic Juvenile Xanthogranuloma is a rare form of Histiocytosis that affects only 1 in 10 million children.
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1 fighting for aaron
2 search this site
3 aaron's story
4 systemic juvenile xanthogranuloma
5 other info
6 current fundraisers
7 contact information
8 report abuse
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Fighting For Aaron | fightingforaaron.com Reviews

https://fightingforaaron.com

At the age of 11 Aaron was diagnosed with a very rare condition known as Systemic Juvenile Xanthogranuloma. The disease has affected his brain, eyes and bone. Systemic Juvenile Xanthogranuloma is a rare form of Histiocytosis that affects only 1 in 10 million children.

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1

Systemic Juvenile Xanthogranuloma - Fighting For Aaron

http://www.fightingforaaron.com/aaron-s-diagnosis

Follow Aaron on Facebook. How You Can Help. JXG is a rare disease that belongs to a group of illnesses called H. 1) Cutaneous JXG, where lesions are only found in the skin and usually follows a benign course without treatment. 3) Ocular JXG: where lesions are present in the eyes of the patient and they may or may not be accompanied by skin lesions. Due to the infrequency of the disease and its misdiagnoses is very difficult to obtain accurate numbers of the people affected by it. However, its is roug...

2

Fighting For Aaron

http://www.fightingforaaron.com/home

Follow Aaron on Facebook. How You Can Help. Aaron has been diagnosed with a very rare form of Systemic Juvenile Xanthogranuloma which has affected his brain, his eyes, skin and bone. He's underwent 2 very long years of aggressive chemotherapy at Children's Hospital in Minneapolis, MN.

3

Aaron's Story - Fighting For Aaron

http://www.fightingforaaron.com/aaron-s-story

Follow Aaron on Facebook. How You Can Help. On March 30, 2012 Aaron was taken to the eye doctor when strange looking spots were noticed in his eyes. This was the beginning of a long, difficult road for him and our family. To rule out several conditions that could be causing the issues with his corneas. After being misdiagnosed by two separate specialists and being told it was an idiopathic (no known cause) condition, it was later discovered that these spots were actually lesions (tumors) in his corneas.

4

Report Abuse

http://www.fightingforaaron.com/system/app/pages/reportAbuse

By submitting this form, you are alerting the Google Sites team that this site has content that is in violation of our Terms of Use. Why are you reporting the content on this Site as inappropriate? This Site contains spam. This Site contains phishing. This Site contains malware. This Site contains sexually explicit material (like pornography or nudity). This Site contains content that is harassing me or someone else. This Site promotes violence or has hate speech.

5

Follow Aaron on Facebook - Fighting For Aaron

http://www.fightingforaaron.com/follow-aaron-on-facebook

Follow Aaron on Facebook. How You Can Help. Follow Aaron on Facebook. The most up to date i nformation regarding Aaron's progress and setbacks are. Posted on his Facebook page. If you would like to follow his journey, click on the button below. Or go to www.facebook.com /FightingForAaron. We absolutely love the support and encouraging comments left by our F.

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Fighting For Aaron

Follow Aaron on Facebook. How You Can Help. Aaron has been diagnosed with a very rare form of Systemic Juvenile Xanthogranuloma which has affected his brain, his eyes, skin and bone. He's underwent 2 very long years of aggressive chemotherapy at Children's Hospital in Minneapolis, MN.

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