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Cure |
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Dr. Philippart is an essential member of Jaxon’s team. He has first hand experience in treating SSPE, and has taken a personal interest in Jaxon’s wellness. He truly believes in quality of life. Read more about him….. |
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Related Links |
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There is a plethora of information on the world wide web that discusses SSPE. Below are just a few which we have found informative. |
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SSPE Association, Istanbul, Turkey This website has over 700 kids registered with SSPE and is full of hope and tips. If you try this link, you may find it toggles back and forth from English to Turkish on the various pages. Be patient and poke around for the information they are providing. |
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Jaxon’s |
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Jaxon’s Cure P O Box 152 Port Orchard, WA 98366 360.876.2837
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Maxi Maxi and his family are in Germany. Maxi's family and Jaxon's family are in contact with one another, sharing experiences and supporting one another in a way that is creating a bond between these two families like no other! It's a great website, check it out! |
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Dr. Blume is Jaxon's primary Neurologist. She works at Seattle Children's Hospital and is a vital member of Jaxon's medical team. She has treated Jaxon since the onset of the SSPE symptoms and has provided exemplary care. |
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Mission Statement Jaxon’s Cure is a non-profit organization specifically established to raise awareness and find a cure for Subacute Sclerosing Panencephalitis (SSPE), a rare degenerative disease of the central nervous system caused by an altered form of the measles virus. Funds raised will be directed towards research, cure development, and awareness on all issues related to SSPE. |