tag:blogger.com,1999:blog-4895604594896814289.post8093942023962771066..comments2023-08-20T01:37:48.791-07:00Comments on CFS Patient Advocate: Maija Haavistoconsuegrahttp://www.blogger.com/profile/05666537564189582035noreply@blogger.comBlogger4125tag:blogger.com,1999:blog-4895604594896814289.post-78512337208055277932013-02-17T21:02:40.882-08:002013-02-17T21:02:40.882-08:00I have been looking into becoming a volunteer chil...I have been looking into becoming a volunteer child advocate, however I am in an emotional turmoil trying to decide if is the right to do, since I've come from the same background. I am afraid to get too emotionally involved, but I know everyone's help is needed<br /><br /><br /><br /><a href="http://phlebotomytrainingpro.net/north-carolina/" rel="nofollow">phlebotomy schools north-carolina</a>Anonymoushttps://www.blogger.com/profile/06106007750484567313noreply@blogger.comtag:blogger.com,1999:blog-4895604594896814289.post-76016335526471677732013-02-15T04:00:50.909-08:002013-02-15T04:00:50.909-08:00If you were appointed Patient Advocate for a close...If you were appointed Patient Advocate for a close relative (parent, sibling, spouse, child, etc.) would you be able to carry out their wishes, including a wish to end their life if...? Would age or disability make a difference in your ability to serve as their patient advocate?<br /><br /><a href="http://phlebotomytrainingpro.net/north-carolina/" rel="nofollow">phlebotomy schools north-carolina</a>Anonymoushttps://www.blogger.com/profile/06106007750484567313noreply@blogger.comtag:blogger.com,1999:blog-4895604594896814289.post-1933994984816280362011-02-14T03:45:22.079-08:002011-02-14T03:45:22.079-08:00I have taken LDN for almost four years. I have C...I have taken LDN for almost four years. I have CFS, am 63. The LDN lifted a whole body weakness within a month. Many start, and then stop too soon. I will take LDN for life, because of all of it's benefits.<br /><br />Sara W.<br />North CarolinaSara W.https://www.blogger.com/profile/04522863392663242243noreply@blogger.comtag:blogger.com,1999:blog-4895604594896814289.post-78805684322917255472010-11-24T19:14:02.261-08:002010-11-24T19:14:02.261-08:00It's the first I've heard an ME/CFS patien...It's the first I've heard an ME/CFS patient strongly and publicly promote this drug. You'll read people experimenting with it here and there, but up to now, we in the U.S. haven't heard many great success stories. Maija's dozen isn't exactly a study, but it sounds like Finland will be giving such a go. She's obviously cognizant that she's writing on a deadly disease and that what's done a lot for her won't work for everyone, and there's so much more work to do. Thank you for posting!Anonymousnoreply@blogger.com