OK .... I watched the Q&A on Mets BC on Monday and it was very interesting. The 4 presenters on the right (in the pic at the top) were a part of the discussion. Not sure who the lady on the left was, in the pic.
Over 1000 watched the Webinar - so obviously not all questions could be addressed. Neither Wendy's nor my question was addressed ..... but Annabel said at the beginning, that questions would be 'answered by email' .... but no-one that I've spoken to has had this happen yet.
I am keen to watch it again, tho!
https://www.youtube.com/watch?v=Td-ejQkoF7sThey have also sent out a survey to take re the program & any ongoing Webinars - to see what you would like to see 'covered'.
I've messaged them as to whether the questions on the registration form were going to be addressed separately. I hope to hear back soon.
I thought that a fair bit of the discussion was more on 'how do you know if you've got Mets' rather than addressing those who already have Mets & are looking for treatment answers. Specially for those at the 'pointy end' who may be on their 'last option chemo' (after trying several treatments), with poor quality of life, who are looking for research/treatment answers NOW. Their wish may be for better quality of life, over & above 'quantity' & wonder if they could go back to a previous treatment which, altho not 100% effective on the cancer, was at least holding it at bay, whilst allowing for better quality of life - ie able to get out & do 'normal things' rather than being forced to stay at home with nausea, neuropathy or gastro ruling their lives.
I am interested to hear YOUR take on it, if you watched it. if you missed it - check it out in the link above?
What did YOU get out of it?
I may have missed bits too, as I had to leave the screen a few times to attend to hubby .... so will definitely watch it again, when I can.
take care xx
@Mez_BCNA - could you copy this over to the Mets Group, please?