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Hello from New Zealand!
Hello,
My name is Emma-Kate, I am from New Zealand and I have been invited here, by Mardy, to discuss FMS a little. I posted a blog entry about it the other day, and it's a subject I would like to retun to in the near future.
I have ME/CFS, with associated pain since I was 13 (I was also born with Cerebral Palsy), I am now 28 and although I remain unwell, I work a little as an Occupational Therapist, and an awareness education teacher, including giving the occasional lecture at our local medical school, and university.
I am really looking for different perspectives from people, experiences, things that others want to see written about (I don't have all the answers unfortunately), and would welcome any suggestions, feedback, or even people who would like to collaborate on writing a post, (Mardy and I worked on the FMS post).
The blog is simply a very objective demonstration about ME/CFS, and associated illness, such as FMS, and the purpose is to share information, provide education and promote awareness.
http://cfsandxmrv.blogspot.com/
http://apps.facebook.com/blognetworks/userpage.php
I hope everyone is well,
ek
This forum is provided to allow members of Lumigrate to share information and ideas. Any recommendations made by forum members regarding medical treatments, medications, or procedures are not endorsed by Lumigrate or practitioners who serve as Lumigrate's medical experts.


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The purpose of Lumigrate.com is to "Light the Path to Health and Well-Being", so to have a path through the Internet to New Zealand and someone as amazing as E.K. is so very cool! "Forums" area is for YOU.. US ... to all come with our knowledge and need for it and collaborate, conference, co-mingle, COMMENT.
CERTAINLY, go to ek's blog and facebook 'stuff' and let other's know! What one of my concerns has been as I saw how much momentum was going with facebook and the fibromyalgia community was there is a 'dilution' going on at the same time as there is MUCH more volume of information. People don't know where to go, they're often not finding valid sources ("Valid" inclues "not controlled by vested interests that might not want some information to get out"). Lumigrate's Forum ability and my vision for growths when the website was constructed allows it to accommodate LOTS of people coming here to write, read, post, link ... 'commune'. So please leave comments for ideas HERE so that people can see what you write -- comments on what EK writes here would be great but naturally on her blog or facebook is WONDERFUL too! The more you do with valid places and sources and direct others to them, the better! It can be your good deed for the day! ~~ Mardy
Mardy Ross, OTR Founder, Lumigrate "Lighting the Path to Health and Well-Being" Follow us on social networking sites such as: Twitter: http://twitter.com/lumigrate facebook: My personal page: Mardy Ross Fan Pages: Lumigrate, Lumigrate: Fibromyalgia, Lumigrate: Fibromyalgia Health Education and Counseling (Lumigrate Webucation is a 'personal page' replaced by fan pages but used for 'fun' still).