Editing Gillian Anderson (section)

===Neurofibromatosis===
Anderson is an honorary spokesperson for the [[Neurofibromatosis]] Network. She often holds auctions with the profits benefiting the Neurofibromatosis Network.<ref>{{cite web|url=http://www.nfnetwork.org|title=NF Network}}</ref> Her brother Aaron died from [[Neurofibromatosis type I]] in 2011.<ref name="Grand Rapids Press" /><ref name="US25">{{cite web|url=https://celebrity.yahoo.com/news/gillian-anderson-25-things-dont-know-164500184-us-weekly.html|title=Gillian Anderson: 25 Things You Don't Know About Me|date=February 7, 2015|work=[[Us Magazine]]|access-date=November 9, 2015|archive-date=August 10, 2015|archive-url=https://web.archive.org/web/20150810070414/https://celebrity.yahoo.com/news/gillian-anderson-25-things-dont-know-164500184-us-weekly.html|url-status=dead}}</ref><ref name="NW98"/> In May 1996, Anderson addressed the [[United States Congress]] urging for more education and funding for neurofibromatosis research projects.<ref>{{cite news |last=Winslow |first=Harriet |date=June 16, 1996 |title=THE PRIVATE SIDE OF THE X-FILES' ' QUIET STAR |url=https://www.washingtonpost.com/archive/lifestyle/tv/1996/06/16/the-private-side-of-the-x-files-quiet-star/d8850c16-3fb4-4714-a9aa-7332cd199d0c/ |newspaper=[[The Washington Post]] |access-date=October 5, 2015}}</ref> She partners with ''Doodle 4 NF'' – an annual fundraiser for the Neurofibromatosis Network.<ref>{{cite web|url=http://www.doodle4nf.org/why-doodle|title=Doodle 4 NF Website}}</ref> She also supported the Children with Tumours organization and the [[Global Genes - Allies in Rare Disease|Global Genes]] movement, which is devoted to helping children with neurofibromatosis.<ref>{{cite web|url=https://globalgenes.org/gillian-anderson-for-the-global-genes-projc|title=Gillian Anderson for The Global Genes Project|work=globalgenes.org|date=July 23, 2013|access-date=October 5, 2015}}</ref>