Guest guest Posted March 1, 2008 Report Share Posted March 1, 2008 forwarding ................. Hello and welcome to the 'A Hummingbirds Guide to Myalgic Encephalomyelitis' e-newsletter for February 2008 I hope this newsletter finds you and yours doing as well as possible. I have a handful of new updates to tell you about this month. ----- The 'Treating Myalgic Encephalomyelitis - The Basics' paper was updated. Many new links were added and the treatment examples section was fully updated and now provides more detailed information on this topic. New treatments mentioned include: Alpha Lipoic Acid, N-Acetyl Cysteine, sublingual ATP, sublingual vitamin B12, antioxidants, digestive enzymes, Malic acid, D-ribose, medical quality (carefully fitted) compression stockings, Betaine, Turmeric (Curcumin), DMAE and low dose daily aspirin. Before trying any of these treatments however (or any treatments) please do read the various cautions given in this paper FIRST. See: _http://www.ahummingbirdsguide.com/treatingmethebasics.htm_ (http://www.ahummingbirdsguide.com/treatingmethebasics.htm) (A big thank you to those M.E. patients who offered suggestions and constructive criticism for the updating of this paper, it was much apprciated as always!) ----- Minor updates Minor updates were made to the following papers (and their summaries, where applicable): 1. The Ultra-comprehensive Myalgic Encephalomyelitis Symptom List _http://www.ahummingbirdsguide.com/themesymptomlist.htm_ (http://www.ahummingbirdsguide.com/themesymptomlist.htm) 2. What it feels like to have Myalgic Encephalomyelitis: A personal M.E. symptom list and description of M.E. _http://www.ahummingbirdsguide.com/whatmefeelslike.htm_ (http://www.ahummingbirdsguide.com/whatmefeelslike.htm) 3. Myalgic Encephalomyelitis is not fatigue, or 'CFS' _http://www.ahummingbirdsguide.com/fatigueschmatigue.htm_ (http://www.ahummingbirdsguide.com/fatigueschmatigue.htm) 4. Practical tips for living with Myalgic Encephalomyelitis, and _http://www.ahummingbirdsguide.com/helpyhints.htm_ (http://www.ahummingbirdsguide.com/helpyhints.htm) 5. A day in the life of severe Myalgic Encephalomyelitis _http://www.ahummingbirdsguide.com/adayinthelife.htm_ (http://www.ahummingbirdsguide.com/adayinthelife.htm) ----- Reminder: Would you like to see your M.E. story on a M.E. YouTube video? For more information see: _http://www.ahummingbirdsguide.com/newmevideo.htm_ (http://www.ahummingbirdsguide.com/newmevideo.htm) ------ That's it for this month! Next month I very much hope to be well enough to write again publically about the sham so-called 'Fair Name' campaign (and the ill-advised use of the unhelpful and unscientific term 'ME/CFS' generally by advocates). This campaign makes a mockery of legitimate advocacy, and we must join together to oppose it; M.E. sufferers *and* patients who do not have M.E. but have been misdiagnosed with 'CFS' alike. It serves neither of our best interests and indeed will only increase confusion and make the problems much worse. We must not let another 20 years be wasted! Too many of us have had our lives needlessly destoyed by mistreatment, abuse and neglect already, and there have been more than enough needless deaths... For more information on this topic see: _http://www.ahummingbirdsguide.com/cfsmustbeabandoned.htm_ (http://www.ahummingbirdsguide.com/cfsmustbeabandoned.htm) and _http://www.ahummingbirdsguide.com/whatisme.htm_ (http://www.ahummingbirdsguide.com/whatisme.htm) All the best, as always, in your ongoing battle with M.E. or your loved one's battle with M.E., until next month, (Also please note that, unfortunately I am not able to reply to all of the emails and Guestbook entries I have received and also that some replies will be very delayed. I am more than 6 months behind with my email. My apologies. A big thank you to everyone who has written though, especially if it was with suggestions for the site or positive comments.) Jodi Bassett -- A Hummingbirds Guide to Myalgic Encephalomyelitis: _www.ahummingbirdsguide.com_ (http://www.ahummingbirdsguide.com) Do not for one minute believe that CFS is simply another name for Myalgic Encephalomyelitis (M.E.). It is not. The CDC 1988 definition of CFS describes a non-existing chimera based upon inexperienced individuals who lack any historical knowledge of this disease process. Any disease process that has major criteria, of excluding all other disease processes, is simply not a disease at all; it doesn't exist. M.E. and CFS should be separated as definitions. They are not the same. Dr Byron Hyde MD 2006 -- ----------- A HUMMINGBIRDS GUIDE E-NEWSLETTER NOTES: 2. If you'd like to change the email address your newsletter is sent to, just e-mail me your new details and quote the same number given above. 3. Permission is given for you to forward this e-mail provided it is unedited. If you do so however, can you please make sure to delete my e-mail address from the top of the e-mail so I don't end up added to spam lists. Thank you. 4. If you have received this newsletter as a forwarded e-mail and would now like to to the newsletter yourself, see: www.ahummingbirdsguide.com/websiteenewsletter.htm for details. 5. To read past newsletters/site updates see the 'What's New' section on the website at: http://www.ahummingbirdsguide.com/whatsnew.htm Quote Link to comment Share on other sites More sharing options...
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