Charles Shepherd and Jen Brea on Breakfast Time tomorrow

AMAZING!!!

(should I merge this thread with the one above saying it's going to be on tomorrow?)

They just plugged Unrest big time!

And they DID NOT give any psychobabblers ANY airtime.

They took everything that Jen & Charles said and nothing else!
 
Done. Pretty good. And the fact the BBC aired it is ... amazing. They must sense they need to switch to the winning side.

The one thing I think PwME and advocates always get wrong is when describing PwME as feeling exhausted after exercise, because fit people feel exhausted after exercise too - the innocently uninformed will just say, well yes so do I. It's not so much about the getting exhausted, but so very much about the disastrous recovery pattern - that is one of the key discriminators; I don't really know why that is not made clearer, as it is one of the most crucial things to get across, especially in a short piece.

But though a long paragraph above, overall it was excellent as an awareness piece.
 
Not knocking it at all. Great progress for the BBC. But, so frustrating waiting through a lot of junk that could easily have been cut or shortened while waiting for it, then it only getting such a short time.
That was my thought. Chatting with the weather lady whilst she danced a little jig, had me thinking, yes, that allows you to shave another 10 sec off the interview!
 
Thank you for posting the youtube link, @Arnie Pye !

I just watched it. They both did an amazing job!

I appreciate that Charles Shepherd elaborated on the more general issue of autonomic dysfunction (not just POTS) along with listing so many of the other ME symptoms.

Just to give one example, when I was first sick I got the drop in blood pressure but not enough increase in heart rate to be called POTS (postural orthostatic tachycardia syndrome). If I had only done the simple standing test, and not a tilt table test, the test would not have shown POTS. And a simple standing test is not enough to show NMH (Neurally Mediated Hypotension, aka Neurocardiogenic syndrome and other names).

Now I have both NMH and POTS. But on my first tilt table test my diagnosis was only NMH, not POTS.

Note: Please forgive me if I'm not using the latest terminology for different types of autonomic dysfunction - it's confusing and seems to depend on which doctor is doing the talking.
 
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