The history of NF is complicated and the development of genetic testing was needed for researchers to realize that there are in fact three forms, but this fact is not even commonly known today by all doctors since NF is rare and in some cases not even identified at all. The results are a common issue of inaccurate diagnosis of the wrong NF form and individuals not receiving the proper testing for treatments needed.
Watch and read medical developments from NF2 doctors. Learn what treatments people with NF2 have opportunities to gain access to for better quality of life.
There is no cure for NF2. With each fact learned in research and each new treatments to manage some issues are made, it leaves patients, doctors and researchers asking even more questions. This link includes some of the newer questions about NF2, in hopes researchers will focus on these concerns in further treatment development or that doctors will answer questions during NF seminars or papers.
The Medical Documents link is a collection of the sources used to build the NF2 Information and Services website. Since research developments can change facts on any page in up to date sources, new sources are constantly being reviewed to be included and update facts.
Facts that will be included with the Science Education facts include; Neurology, Oncology, Otology, and Genetics. Knowledge of what will be included in this section are to help people with NF2 have a better understanding of science to help ask better questions when seeing doctors.
Disclaimer: Neurofibromatosis Type 2 - Information and Services, www.nf2is.org, is not run by medical experts, affiliated with
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the accuracy of other sites to which this site links, or of sites that link to this site. - Read More
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