The ME Show

That’s my experience too..no negative thought patterns, no fear of using energy on the rare occasion that I get any. I have hopes and dreams and remain positive.

 

Excellent show. I thought the shorter format worked well, it deals with issues and leaves you coming back for more.

Also a good way of introducing points , enabling further updates/ detail to be explored at a later date.

 

Me too. I had to get the all clear from a psychologist / neurologist / psychiatrist before I could go to the university hospital in Berlin to get my ME diagnosis. My GP is also a specialist in psychosomatic disorders (I only found out when it was too late!) and has given me the all clear in that regard too. Presumeably Michael Sharpe, never having met me, knows better. After all, I'm an ME sufferer, and that's all the proof he needs.

 

....not to forget that the least thing you or anyone else need is clinical evidence of things not only working but causing direct harm in the short run, but a lot more critical in the long run and for overall prognosis.

 

Hi Nellie. I haven’t so far. Let me looking into it, see who’s there and see what’s possible. I’ll let you know what I manage. Thanks for flagging it up.

 

I won't mention that I did suggest this in an email to Gary a while ago....

 

@Gary Burgess . Just listened to this week's programme and then posted it on my fb page. Excellent programme. You are really good at drawing in the listener. Thank you for your work.

 

Morning all. A happy bank holiday to you (if that’s a thing?!). Episode four of The ME Show is now live.

I speak to Jane Colby from Tymes Trust, a charity for children with ME. A truly fascinating interview about their work but also saddening revelations about some of the situations those children and their parents find themselves in.

www.meassociation.org.uk/podcast

I hope you get chance to have a listen - and please share far and wide if you can. Thank you.

 

Another excellent show, @Gary Burgess!

I've never heard Jane Colby speak and I was very impressed. A wonderful person to have on the side of children with ME (and their parents).

What struck me especially was when she pointed out the irony that those who call this disease 'chronic fatigue syndrome' don't accept that it can be chronic and that if it continues in a child, something else must be wrong.

 

Good to highlight the work of the Tymes Trust. I notice that Jane was careful not to name the sources of the particular unhelpful dogma on ME that she talks about - I think I can guess who she means though.

 

Excellent show Gary, thank you.

 

Excellent show @Gary Burgess

 

Another fantastic episode. Thank you Gary!

 

Good episode @Gary Burgess
Tactfully and sensitively done- a difficult task given the subject.
It is a Kafkaesque life some lead, i' m sure they will appreciate this

 

Really good Gary, thank you.

 

Excellent podcast, Gary.
Managed to subscribe to it on iTunes (which I don't otherwise use) with the intention of rating and reviewing but apart from a drop-down menu choice of "loved" or "dislike" - obviously I ticked "loved"! - I can't find any other way to rate or review it. Any tips anyone?

 

In iTunes, go to Podcasts -> Library -> Shows -> ME Show

On the page for the full show, rather than separate episodes, you should find reviews and/or options to post a review (this is based on the podcast app, might be slightly different in iTunes)