| This is a copy of a letter I have written several times now. When I was first diagnosed with FMS there was very little information; now there is a deluge of it to wade through which is almost as bad. I am listing a few sites which may be of use to you and if you have any questions feel free to contact me. Mitsou http://fibrohugs.com/ (This is a twenty four hour chat site which is helpful for those moments when you need to make contact with someone in a similar situation) http://www.sover.net/~devstar/( This site is by Dr. Devin Starlanyl and has accurate information that you can use in various situations) http://www3.sympatico.ca/me-fm.action/ (Canadian disability information) http://www.remedyfind.com/( THis site lists different medications and people's reactions to them) http://bcorsa.freeyellow.com/coping.html ( This site has a great number of practical help sites) http://www.nosscr.org/faqind.html (US frequent questions regarding disability) http://pw1.netcom.com/~schweit2/wecan/decision.html(favorable FMS finding for disability US) http://www.sunflower.org/~cfsdays/ss-disab.htm (obtaining SS with FMS) http://www.immunesupport.com/fms_research/articles/fm_contag.htm (disability checklist) Mitsou |