Robbie

Hi Rob. Morning here hence delayed response. 

Unfortunately here in the UK you can’t just decide to have a DCCV. You’d have to wait ages for an appointment to even discuss it. You’d be horrified as I didn’t even know who was doing my ablation up until the last minute as the consultant EPs decided to change their lists just before I went in! I can’t talk to the EP as no information was given to do that. They are like God! Not to be argued with unless of course you are a private patient. It’s very different and a real battle to try and get what you want done  

I did get to go to California to Costa Mesa back in 2011 when I decided to visit a clinic there for a treatment to help my MS. It cost £7,000 but unfortunately it didn’t work. It was lovely to visit the USA though. If I won the lotto I would certainly want to see your Dr Natale!

Thanks very much for your help though. I shall give it a go. 

Marty

 That sucks.  Alright good luck.  Keep me apprised.

Thanks. Will do. 

Both.

Thanks.

Adenosine and isoproterenol

I think you must be confusing my EF with Baba's. She's the one with the 69%. Mine is more like 60%. Pretty good, but nothing like hers, which is fantastic.

At least during an AF/AFL episode I would bet EF is reduced, but unless you've gone without treatment for so long that you're experiencing heart failure from it, I doubt that AF/AFL have much effect on EF.

That's pretty much what I thought.  60% is not good???  It's more than fine.

What was the topic? I notice sometimes it is in draft somewhere on the forum.  Click NEW TOPIC again, and maybe it will come back up.

I found it made numerous references to yourself and providing "links" if they exist thru clinic trials..portable monitors suck and very rarely should they be relied upon.  There probably has been no scientific comparsion studies vis a vie portable monitors....  should I leave you out?.  A lot of what I wrote while serious is also humorous.  want me to send u a copy of the unedited version??

Rob

ok