There's a national neurofibramotosis foundation in NYC. If you use any of
the web browsers, you can get their web page.
Good luck.
Leslie
On May 07, 1996 09:11:06 in article <Neurofibromatasis>, 'Jim Stewart
<infoweb at ozramp.net.au>' wrote:
>A relative of mine has a disease called neurofibromatasis. The local
nursing
>and
>medical staff ahve little or no experience with the disease so I am
looking for
>>any sources of information on the disease, I am not a medical
practitioner. Can
>>any one help?
>--
>| |\ | |^^^^ |^^^^| \Jim / |^^^^ |^^^^)
>| | \ | |___ | | \Stewart / |___ |___/
>| | \ | | | | \ /\ / | | \
>| | \| | |____| \/ \/ |____ |____)
>Internet/Intranet Soloutions http://www.infoweb.com.au>Phone 61 3 9209 6969 Mobile 0419 381 105 Fax 61 3 9898 0303
>Email infoweb at ozramp.net.au--
Leslie E. Packer, PhD