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Welcome

Neurofibromatosis Type 2 (NF2) is a genetic disease that strikes every 1 in 25,000 people. It can be inherited or spontaneous and does not discriminate based on race, sex or even environment. While the disease is not completely rare, it is rare enough that the average NF2 patient may encounter few, if any, others with the disease in their lifetime.

The NF2 Crew was formed to address this issue, members correspond with and meet other NF2 patients from around the globe. A most often heard phrase from new members is, "I didn't think anyone else was like me, I fit in here!" We exchange everything from information on treatments and research to trivia and jokes. One of our goals is accessibility and we offer a variety of Internet-based communication mediums.

Some very good sources for additional NF2 background are AdvoCureNF2, Children's Tumor Foundation, Neurofibromatosis, Inc., and Wikipedia. We also have many NF2 related resources on our Links page.

If you are interested in joining the NF2 Crew, please click Who We Are in the left menu, then Join the Crew.

Disclaimer: We are not medical experts nor affiliated with any health care organization or any other company. No information on this site or obtained from NF2 Crew members should be treated as medical advice and should only be used in conjunction with consultation by a medical professional.

 

VERY IMPORTANT NOTE TO ALL MEMBERS: Only after you login will the Members button appear for you. In that section you will find additional features, including the (Yahoo) Group Lists.page, the Photo Gallery, the member Profiles (you can update and edit your own), Crew Chat, as well as access to the Message Board.

If you are having trouble retrieving your password because your email address has changed from the one in your profile, please Contact Us for help. We can fix that for you! Also, if you just forgot your username, please contact us.

 
2006 NF2Crew
Some content used with permission.
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