You are very welcome. I am glad these info help. Please look after yourself and stay positive. There really is a lot of us about , some better, some much worse but we are all here for each other....
Hi These forums are great for getting in touch with people who understands and listens and the odd 'rant', but every one is different. I am not sure whether these links are allowed on here but here...
CFS is covered under the DDA in UK, not sure how it works in America. However the law is only as good as the persons who 'interpret' it. There is no guarantee to how long you get to stay in work...
PS. There are lots of very active UK forums too....
Hi I think that there are quite a few from uk, as I am. I only visit this Forum once in a blue moon. I know it is difficult, especially if you've had this before it was even 'recognised' as an...
Hi Your experience sounds like mine and probably many other people. I was so frustrated with this PVSyndrome on my sick notes but no real 'medication' was offered to me. Then 6 months I get another...
Hi I am still struggling at work especially when stress. So far my employer is following the advice suggested by the Occupational Health as it is covered under DDA. I am going part time next year but...
Hi Jewelrylady I've taken your advice and trying to explore different forums on the web. I've only started joining forums this March because of this illness. Before I don't have broadband except at...
Thanks denise I normally get the new one as it is a large practice where the experence doc is not necessary better! I know because when I had an operation in 2002 I went to see the eldest doc and he...
Hi jewelerylady I've been to the doc and mentioned melatonin, unfortunately the one I see before is no more and he is one of these new trainee doc who just will not give me a straight answer one way...
Hi Denise Thanks for the advice. I am quite new to this, only diagnosed last Summer. I am on 20mg citalopram anti depressant. I have been thinking whether I should ask gp to increase this to help...
Hi I am struggling with getting back to work from 2/3 hours each day to more? Anyone with similar experiences? How do you cope? And any success stories? I would welcome any pointers/advice. My worse...
Hi I am newly diagnosed in the summer with cfs. I just know that if you have flu like symptoms for a long time they called it post viral and then if this doesnt go away in 6 months and all your blood...