Do you have Fibromyalgia  or Chronic Fatigue Syndrome? Sign up please.   In the registration, You decide which questions to answer.   Click the button at the bottom of this page to begin. Together there are more than a million Canadians with FM & CFS/ME.  Together, we can make it easy for researchers to find us, at low expense, and in larger numbers.   Researchers tell us that finding patients for their studies is time-consuming and expensive.  Finding alot of patients for a large study is not practical.   By rallying voluntarily in this database, we can make it free, fast, and easy for researchers to find people, to make bigger studies possible.   What Happens: 1) When a researcher contacts us, we contact you.   2) We send you the researcher's invitation, by email.   The researcher is not copied on the email, and does not get your contact information in any way. 3) The researchers simply hope you will contact them. When you get our email, you can choose to contact the researcher, or not, each time. Your Information's Privacy, further: Your information will be kept confidential by FM-CFS Canada, and will never be sold or shared.  That is our pledge and Board policy, and is in compliance with law. FM-CFS Canada will be the only organisation to contact you using the information you provide here in the Patient Registry.   Please note, we may invite you to vote on matters, we may invite you to rally on some matter or event, but mainly and in practice since 2003, this Patient Registry is a way to send invitations from Canadian researchers.   Finally, please note, we don't contact everyone for every research request.   This database is a free way for you to help researchers, to help the cause, fitting with your schedule.   Would you agree? We will achieve our greatest advances through research!     Thank you for your participation! FM-CFS Canada