We have passed another milestone for members joining on here, now we are past 6,000, best wishes to you all.
youtube.com/watch?v=lmIFXIX...
MaryF
We have passed another milestone for members joining on here, now we are past 6,000, best wishes to you all.
youtube.com/watch?v=lmIFXIX...
MaryF
You know how you want to celebrate... but then realise you're not quite sure what you are celebrating?!
So that's 6000 reasons for more research? Yay!
Thanks Mary. That video is the perfect celebration.
Wow thats great. It would be interesting to break it down my membership by country. Loved the year im 40!
Great now we all have to teach at least one doctor each about what it is and that it's out there and they need to get educated about it🎈🎈👀🎈🎈💕
I see many doc's to put it mildly -and even the nurses- i always talk about it ,some ask for info of which i direct then to the site for the general public - still all kinds of info on there . i have helped with the Dia. of 3 woman in my 7 years with APS Their Doc's knew they had a blood disorder BUT that was it and directing to our knowledge on the sites and telling them what to do for tests has proved to work -- The Doc'd just don't know . England it seems to me is the only country that has it tested in young woman if i read it correctly. If every one of us talk about it to any Medical - insurance people the word does get out and that seems to be something we all can do .The best being the aps sites. like ours { not the health unlocked } but the general site . I have had positive feed back from the ones that actually did visit it . so that's a good hing . My nurses in my PCP'S office are MORE up on the APS than almost all of the DC's . I talk to them at 2 or 3 times a week basis . So it does work grteat ideas above and great job Mary on the video . Thank You