Here we go,
MaryF
Thanks Mary. Do you know where in the programme the interview is? Dave
Keep scrolling down the page and you will see a little film, it show bite size chunks of the programme, like recipes and things, keep going down until you see it. MaryF
Thank you Mary.
Thanks Mary
Thank you.
Thanks Mary, I had tears in my eyes watching, and lovely to see the positive outcomes diagnosis can have for some people, especially Karen and her family in this instance.
Thanks Mary - a shame the focus is still only how this condition affects pregnancy. There needs to be emphasis on how it affects every day life - sad but true most people like myself only get diagnosed thru recurrent miscarriage - but I was then left untreated for 15yrs
my health really went downhill - and thought I had MS and temporary paralysis.
This disease affects your entire body (and men too) its not just a pregnancy complication
Yes I hear you, but the article on the programme, was due to it being National Baby Loss Awareness Day, however the information is getting out there now, whether it be our members actually going to the press as ambassadors and doing articles in the paper or slots on the tv or radio! Also a few months ago via a debate on our condition in The House of Lords. The serious need to educate the medical profession further etc.
Yesterday's article was slanted towards miscarriage and still birth. I am sure more information will become widely available. In my own case i went to the papers, and I also distributed books on the condition in my local area, to medical staff involved with either myself or the children.
My own son has the condition and my late father had it, also probably my brother! He has had a stroke and has very marked symptoms, but it has not shown up in tests, however mine did not for years.
Best wishes. MaryF