Support

JXG Roster
We have a JXG Online Support Roster to keep us connected and support each other. If you would like to join our list or wish to talk to someone, please email us using our "Contact Form" located at the top left side of this page. We also encourage you to visit the Message Board of the Histiocytosis Association of America

Our JXG Group in Facebook
Please visit our Juvenile Xanthogranuloma Online Support Facebook Page for another way to stay connected. There you can share your story with other JXG parents, upload pictures of your JXG champ and offer and receive support.

JXG Advocacy
We can write you an Advocacy Letter for your employer, family members, child care center, etc. that explains what JXG is. We also encourage you to ask for these type of letters to the Histiocytosis Association of America and your JXG Doctors.

JXG Support Group
We are currently seeking members to start a support group that meets online by using oovoo. If you are interested in participating, please email us using our "Contact Form" located at the top left side of this page.