Click the bright blue link (just below) to read the full news article.
Hi everyone, Claire here, Editor of Sleepydust.
If you suffer from M.E, Chronic Fatigue Syndrome or Post Viral Fatigue Syndrome then this could help you…
Here's the story:
Recently, I've put a video together, that explains what's in the Sleepydust ME/CFS course, and how it can help you.
Check Out The New Video Here…
More on New Video Launch About Sleepydust's Online Course…
Click the bright blue link (just below) to read the full news article.
Can you help spread the word by telling other sufferers, your friends, and family about Sleepydust?
Through it's various web pages, ezines, course, videos, and audios, Sleepydust continues to help sufferers and their friends and family, all around the world. If you have found the information on Sleepydust helpful, I would be very grateful if you'd consider telling others about it.
I built Sleepydust because I wanted to provide people easy-to-understand information about Post Viral Fatigue Syndrome, M.E., Chronic Fatigue Syndrome and Fibromyalgia. And moreover, to provide hopeful realism to sufferers who have lost hope of ever improving their quality of life. Because it is my utmost belief that there certainly is hope.
Can you help to spread the word about Sleepydust?
More on Want To Support Sleepydust? Here's How!
Click the bright blue link (just below) to read the full news article.
You can now post your thoughts, reactions and views on the topics we talk about on this blog!
Yep! The Sleepydust Newspaper is now totally interactive, and we want to hear your opinions! All you need to do is…
… click on 'comment', which can be found below every article post, and then… well… comment away!
More on Why Not Have Your Say?
Click the bright blue link (just below) to read the full news article.
Do you have a MySpace page? A blog? Maybe you run a web site or a forum?
Now you can help to spread the word by hosting the latest news on your site. Just click on the link that says 'Grab This Headline Animator' below…

↑ Grab this Headline Animator
Want To Do Your Bit?
More on Host The News On Your Blog Or Site
Click the bright blue link (just below) to read the full news article.
Hi Guys,
Hands up all those who've heard of MySpace! 
Aw, c'mon, I know there are more of you than that. Let's try it again…
Hands up all those of you who've heard of MySpace!!
Hey, that's better !
Ok… so, hands up all those of you who've got a MySpace page!
More on Come Join Us Over At MySpace!
Click the bright blue link (just below) to read the full news article.
As you may or may not know, we've now launched the Sleepydust ME/CFS video on YouTube.
— SIDE NOTE — Not only that, but we've now made it free for anyone to show their visitors the ME/CFS video, on their own site [More…]. Neat huh? — SIDE NOTE —
But now we need YOUR help! We need your votes!
More on Vote For The Sleepydust Video!
Click the bright blue link (just below) to read the full news article.
There's no doubt about it - we can make more of a difference as a collective. That's why we've made our ME/CFS video available for FREE, for YOU to host on YOUR OWN sites, forums, and blogs…
More on Do You Have A Blog, Or Run A Web Site Or Forum?
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Click the bright blue link (just below) to read the full news article.
The Free Sleepydust Online Video has finally been launched!
The video aims to help the friends and family of ME/CFS [including Myalgic Encephalomyelitis , Chronic Fatigue Syndrome , and Post Viral Fatigue Syndrome] sufferers understand the illness and what their loved ones are going through.
More on Launch! The Free Sleepydust ME/CFS Online Video Now Available!
Click the bright blue link (just below) to read the full news article.
Hi all
Thank you to everyone who sent in their questions for the Dr Mickel interview. We'll be collating the questions, picking the best and/or most popular ones, and recording an interview with Dr Mickel in the next few weeks. Once it's available, we'll let you know via the Newspaper and Emagazine.
And so now we have a different question for you!
What would YOU ask Lesley Martin? Lesley suffered from ME for 5 years. She recovered gradually using complementary medicine and self-help and now works as a qualified Nutritionist and Kinesiologist in the Buckinghamshire area (UK).
She has treated many ME/CFS and Fibromyalgia sufferers over the years.
We’re planning to record an interview with Lesley and want to hear from you! Do you have any nutrition-related or diet-related questions about your ME/CFS or Fibromyalgia? Or do you have any questions about kinesiology?
This is YOUR chance to ask a qualified nutritionist and kinesiologist, who has first hand experience of ME/CFS (having been a sufferer herself), and who is experienced in treating ME/CFS and Fibromyalgia sufferers . Put forward your comments and questions and we’ll pick the best questions and ask Lesley for you on your behalf. The interview will be recorded and will be made available to everyone for free.
Send us your questions and comments for Lesley Martin, here (please make sure you state that your message is for the Lesley Martin interview):
http://www.sleepydust.net/ask.html
Claire
Editor of Sleepydust
P.S. If you’ve already ordered the Sleepydust Online Course, then you'll already have access to a whole lesson (split into 3 parts), dedicated to nutrition, diet and ME/CFS.
http://www.sleepydust.net/recover-from-me-cfs.html
Click the bright blue link (just below) to read the full news article.
What Would YOU Ask Mickel Therapy's Founder?
We're planning to record an interview with the founder of Mickel Therapy, Dr David Mickel. For those of you who have no idea what Mickel Therapy is, it's a 'newish' therapy that has been making waves in the ME/CFS and Fibromyalgia communities. If you've already ordered the Sleepydust Online Course, don't worry, there's a whole lesson dedicated to explaining the basic concepts of Mickel Therapy.
Mickel Therapy claim that they can 'cure' ME/CFS and Fibromyalgia, and indeed, I have received so many positive recovery stories from sufferers, that I felt it would merit further investigation. But it's not without its controversy! And there seems to be lots of confusion surrounding it - what is it? How does it work?…
So this is YOUR chance to ask the founder. Put forward your comments and questions and we'll pick the best questions and ask them for you on your behalf. The interview will be recorded and will be made available to everyone for free.
Send us your questions and comments for Dr Mickel, here (please make sure you state that your message is for the Dr Mickel interview):
http://www.sleepydust.net/ask.html
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
Would you like to submit a review to us about a therapy you've tried, or a book you've read? Both positive and negative reviews are welcome!
Or perhaps you've found a treatment or supplement that really works for you and would like to submit your recommendation to us?
Click here to find out more…
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
Do you have ME/CFS- or FMS-related news to share with the community? Are you a charity, a researcher or scientist? Maybe you're a sufferer and have found a news item which you think might newsworthy?
This blog, The Sleepydust Newspaper, is where we post about ME/CFS- and FMS-related, international and national news. Some of the news items that are posted in the Sleepydust Newspaper are also mentioned in the popular Sleepydust Emagazine too. So this is a great way to announce your news and to spread the word.
Feel free to submit your news item below.
Here are a few guidelines:
* We will only consider news items which are related to ME/CFS and/or FMS in some way. This includes anything that might affect (or interest) ME/CFS and FMS sufferers, such as changes in government/state benefits.
* We have a large international readership, so we welcome national news items. Since we are a UK web site, we tend to focus on the United Kingdom, but news items about events / research in other countries are welcomed. Please note that we will not consider news items about local events unless they are notable, large events that are of general interest to the ME/CFS or FMS community at large e.g. a large ME/CFS conference with notable guest speakers would certainly be considered.
* We tend to consider news items that are 'of the moment'. No old news please!
* Please check recent postings made at Sleepydust Newspaper before you submit, to see if it's already been mentioned or not.
* To stay up to date with the latest newspaper posts (and to see if your news submissions have been posted), please subscribe to our RSS feed [more…] or sign up to be notified by email [more…].
To submit a news item click here…
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
Sleepydust receives many requests from companies, therapists and authors who would like us to review their products and services. Some wish to send us samples for our visitors to review. Others ask if I would review their product on Sleepydust, as Editor.
You can now find out how you can go about requesting a review of your product/service on Sleepydust here…
All the best
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
Sleepydust receives many enquiries from companies, therapists and authors who wish to advertize their products and services. You can now find out how you can go about advertizing on Sleepydust here…
The new page explains how you can start advertizing on Sleepydust immediately (for a matter of pence), and provides a form through which you can contact us if you are looking for more 'high-profile' advertizing.
Click here to find out more…
All the best
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
I'm planning on writing a few freebies on M.E. /Chronic Fatigue Syndrome (CFS) and Fibromyalgia (FMS). There are a few ideas, but I need to know which you'd be most interested in. So…
… here's another poll!
I'd be very grateful if you could vote!
If there's a real favorite, I may dedicate more time researching it and turn the favorite into a paid ebook, but for the main, I'd like to create freebies to get the word out about Sleepydust.
If you have any ideas of the type of information you'd like to see as ebook freebies, please do mention them in the 'any comments' box in the form linked below. (The freebies need to be information-type products that can be downloadable via the internet.)
Click here to vote for which ME/CFS & FMS freebie you'd prefer!
Thanks all!
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
I'm updating some of the review pages in our book review section at the moment. The first to be updated is one of my favorite fiction books of all time:
J K Rowling's Harry Potter And The Prisoner Of Azkaban
If you ever decide to buy any book mentioned on Sleepydust, please click through to the online shop via our links.
That way, Sleepydust will receive a small contribution, which will help to maintain this web site & to keep it going!
Thanks all!
Click here to read the updated review page of the Harry Potter And The Prisoner Of Azkaban book!
All the best
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
The main page of the Book Reviews section has now been updated!
If you do plan to buy a book…
… then why not help support our work by clicking through on our Amazon links and buying from them? That way, you get your book, and Amazon gives us a small contribution which helps us to continue the work we do here at Sleepydust. We would be very grateful for any support you can give us. Every little helps!
Audio books in particular are great for Fibromyalgia and Chronic Fatigue Syndrome sufferers because they are often too exhausted to read. For the audio book section (soon to be updated) click here!
And you can check out the updated Fibromyalgia & Chronic Fatigue Syndrome Book Reviews page here!
Claire
Editor of Sleepydust
Click the bright blue link (just below) to read the full news article.
At the moment, there are small ways in which you can help support the work we do on Sleepydust.
Every little helps and we would really be grateful for any support you can give us…
Check out this page to find out more…
Claire
sleepydust.net
Click the bright blue link (just below) to read the full news article.
We plan to launch a ME/Chronic Fatigue Syndrome & Fibromyalgia Support Group Directory (world-wide) on the sleepydust web site and we would love YOUR support group to be a part of it!
Click here to submit your support group details…
If you are a member of a local ME/CFS or FMS support group, we would be very grateful if you could let your Support Group Manager know about this page!
Claire
sleepydust.net