The ME Show

Very good - thank you @Gary Burgess and Dr Shepherd.

 

Good question. I do not know but will go ask.

 

Really enjoyed the show @Gary Burgess. Do you prepare the questions? They’re good..relevant. Really looking forward to next week with Carol Monaghan MP.

Makes you wonder if Andy Burnham (Mayor of Manchester) would be good to approach to see what influence he could have. He attended Millions Missing at Manchester. I think he knows the ex Loughborough MP (think Andy Reed) who’s wife has ME (Sarah Reed). I think Sarah is part of MEAction but I could be wrong..just thinking out loud with a foggy brain.

Anyway, fab show, I’m really loving it.

 

Thanks @dangermouse. That's really kind.

I've always approached interviews the same way: read up some, but not loads, on my interviewees and don't prepare questions. But I do often list things I want to cover and then mentally tick them off as I go. I much prefer them to feel like conversations, so tend to ask things based on what I've just heard. By not overly reading up, I tend to avoid assuming knowledge during the chat.

Thanks, too, for the interview suggestion. I've committed to 10 episodes for series one and have the guests lined up. After that, I will review the project with the ME Association based on whether anybody listens and finds it useful/interesting (hope so), how I'm managing setting up/recording/editing/publishing them (good so far), and whether they and I would like me to carry on.

I'll add Andy to the series two list. Keep thinking out loud... it's appreciated.

 

I hope you continue to do the shows @Gary Burgess they are the first of this kind, that I’ve come across, that are relevant, interesting and informative whilst forming a kind of connection for people with ME.

Yeah, I think Mayor Andy Burnham (for the reasons @NelliePledge highlighted) would be a good ally for the ME community.

 

Morning all. Episode three of The ME Show is live.

This week I speak to SNP MP Carol Monaghan who led the Westminster Hall debate about the Pace trial. Listen for free online or via iTunes at www.meassociation.org.uk/podcast

If you're able to spread the word and share that link elsewhere, that'd be amazing. Thank you all.

 

Excellent show (I prefer the shorter length). Jane Colby next week......looking forward to that one!

 

@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 rate your show? I thought Carol was fantastic, another angel on our side. Also, I much prefer the shorter version of the show

 

Thank you, @Sunshine3. Don't worry about your IT skills. That you have listened is more than enough for my liking. Really good of you to take the time to do so.

 

Brilliant 3rd episode @Gary Burgess

 

@Gary Burgess Here's a listener from Germany – all of the first three episodes were amazing, thank you! And thanks to the ME Association for supporting this show.

 

Just catching up with this project now and I have to say! Wow, BRILLIANT work Gary! You've got just the right voice for this. All works really well. Keep it up.

 

Thanks for working on this. Marking to come back to listen to when I've got a bit more time.

 

Listened to the 3rd episode last night. It was great hearing CM speak with the passion and indignation that we all feel and combined with jen’s Speech was quite inspiring.

Well done @Gary Burgess another good one. I think these are going to become quite good awareness tools to send to family and friends. I’ve added it to my to do list to send the links out.

 

Even Michael Sharpe is listening:
https://twitter.com/user/status/999367123775483909

 

Wow, these are fantastic, @Gary Burgess, you are so good at this!
Excellent guests, skilled interviewer, clear and simple format--just grand!
Thank you so much

 

I think MS is too far gone ..he seems to be lost amongst the smoke screens he’s created. He is now tying himself up in knots. Nice that he’s listening though.

The thing I don’t get is what behaviours he thinks are at play? I was tested for depression and anxiety before they gave me a diagnosis ...no problem here? I’m still positive I haven’t lost the plot...what I really need is a treatment that helps me with my ATP, not parlour tricks with no clinical evidence to support them, or even worse clinical evidence that proves they don’t work.