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$84,880 89% of target 850 Donors 5 days left Project ends on April 30, at 11:59

Well, I've had no reply, but the piece linked below refers to people from all over the world signing it, so I have joined them: Station: Manx Radio and Aiir Date: April 24, 2019 WebRadio: https://www.manxradio.com/news/isle-of-man-news/m-e-service-to-be-implemented-this-year/ Ref...

$72,834 76% of target 792 donors 7 days remaining

Now up to $70,726, 74% of total. 745 donors, 8 days left.

I will probably donate again if it seems necessary. I think (some) others will too.

I have trouble writing now. I don't know whether it's a visual or physical problem, or concentration problem, or maybe lack of practice? My writing used to be excellent - I won an award for it at school!

That's the first 20 years of ME, in case it wasn't clear.

Yes, I often read words incorrectly. I don't think it was that common in the first 20 years, but became common more recently.

I have no idea - sorry. I assumed not, but if anyone can find out, that would be great! I have found his email address and will ask him.

Source: Solve ME/CFS Initiative Date: April 19, 2019 URL: https://solvecfs.org/applying-for-an-award/ Applying for an Award --------------------- The Ramsay 2019 Application Cycle will be open on May 1st! You can view the scope and instructions from the Ramsay 2018 cycle here...

$65,835, 69% of total, 654 donors. 10 days left.

But maybe I was in a minority - before I got ME I decided to believe in ME, although I didn't know anyone with it. I decided that the consequences of my not believing in it would/could be worse than the consequences of my believing in it.

Station: Manx Radio and Aiir Date: April 18, 2019 WebRadio: https://www.manxradio.com/news/isle-of-man-news/petition-for-island-m-e-service-gains-traction/ Petition for Island M.E. service gains traction ----------------------------------------------- Craig Morris says sufferers are crying out...

Haven't got the time or energy to search for this, but: Yesterday, the New York Times published the March 13 Reuters report. See, https://www.nytimes.com/reuters/2019/04/18/world/europe/18reuters-science-social-media-specialreport.html...

I'm not aware that I have ever needed more anaesthetic than usual, and I have been a regular user for a long time. But I've never asked!

https://www.neurosymptoms.org/not-imagined/4594358022 "You don’t have a disease..."

Source: UK House of Commons Date: April 11, 2019 URL: https://www.parliament.uk/business/publications/written-questions-answers-statements/written-question/Commons/2019-04-08/242027/ Ref: http://www.me-net.combidom.com/meweb/web1.4.htm#westminster [Written Answers] Chronic Fatigue Syndrome...

Source: UK House of Commons Date: April 12, 2019 URL: https://www.parliament.uk/business/publications/written-questions-answers-statements/written-question/Commons/2019-04-04/240991/...

What do you think of this statement: "The reality is ME/CFS is a serious, heritable, neurological condition and I was shocked to discover subsequently that my grandmother had died from it aged 42." I had not heard of it being heritable. I wonder whether it was on her grandmother's death...

https://www.parliament.uk/business/publications/written-questions-answers-statements/written-question/Commons/2019-04-04/240991/ Sharon Hodgson To ask the Secretary of State for Health and Social Care, how much funding the Government has allocated to services used by patients with ME in the...