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@Gary Burgess just listened to episode 3, brilliant!! You are a gifted interviewer, you asked all the right questions, nothing was left out. I am so grateful to you for your work. Unfortunately, I am not on I tunes and totally crap at IT with my brainfog but is there anywhere simple I can go to...

Oh my God so well said. The negativity this week on forums by a minority was head wrecking and they are very vocal....the trouble is they sow seeds of doubt. Also as more signatures are needed for the Senate resolution to be passed, we all need to stick together. But no, nothing is simple in the...

Merryn's family are real heroes. Its so terribly sad but I am glad to see the truth being told.

Thanks Emily and all the team, ye are super!!

Sorry to keep asking questions, is there a deadline for signatures?

I have in laws in the U.K but the thought of asking them to help nearly sends me into a crash....but I guess I should try, I might wait another while before I take it on....

How many MP signatures are needed for the debate to go ahead?

Edinburgh was by far the best I have seen...it was brilliant. Just saw New York there, poor numbers....it didn't look like a great crowd. Its true we need our healthy friends but if they can't like an M.E related facebook post, there is little chance of them taking to the streets. Any post M.E...

I think we should all do one and let M.E Action take it from there...we ain't got nothing to lose...

Yes, lets all get our video clips sent to M.E Action..now is our chance

Thank you Gary so much and also Jen and Robert, love that song so much.

Absolutely ridiculous, Unger has no shame if she turns up at conferences this year still saying website is being updated. As we say in Ireland a shoe in the proverbial is what she needs. The CDC are partly responsible for the mess we are in, one would think it's high time to clean it up ....grrrrr

Ron Davis said at some point, I saw on a tweet earlier, we don't want to just treat this disease, we want to cure it. That statement used to fill me with hope in the past, not so much now.......it just seems a bit unrealistic.

That's hard to do. I don't post about M.E on my private facebook page only very rarely as I get no response and that hurts. People have no interest in M.E, have no idea of the suffering. So patients have to help themselves. As for 10% diagnosed, I question that. I diagnosed myself by googling...

The crowdrise is extremely slow....where are all the millions missing....even the smallest donation makes a difference...I hope it starts to rise...it feels like now is the time to push things forward...we need to seize the moment!

What a creep, he has zero remorse for all he has done and keeps driving it on.

@dave30th the weasel is out and dangerous

Prof Sir Simon Wessely is taking part in a three-lecture event at Seale Hayne, Newton Abbott, Devon UK. One of the lectures is on FND...........Functional Neurological Disorder............the new label given to UK ME patients. Can anyone attend? It is free...

How about using the Canadian consensus criteria.....we know so much, yet so many physicians know nothing...grrr

An absolute legend, contributes so much to our cause.