Raising awareness of a life changing pregnancy condition can you help us raise awareness tonight ? We are nearly at 2000 views on our top video can you make it happen? also we are now short of 25 people for our social media thunderclap to work can you follow this tonight? our thunderclap page to follow https://www.thunderclap.it/projects/30730-pprom-awareness-in-pregnancy our donation page https://www.youcaring.com/nonprofits/little-heartbeats-raising-awareness-on-pprom-/337480 we are local to the area, and hoping to have a xmas show on soon too, just this week getting over surgery as just had a other baby loss, even though this time it was a missed miscarriage, the heartache is pretty hard to take in my blog http://miscarriage-nomoreheartbeat.blogspot.co.uk/2015/09/the-feeling-of-emptiness.html to date by raising awareness we have saved babies lives, we hope more can be saved by others helping to spread awareness and following our page https://www.facebook.com/PpromAwarenessUK https://twitter.com/PpromAwarenessU
We have shared this so many times, and we really feel very passionate about it, but no matter what we do, we just not getting funds in, running out of ideas, and wondering how do we change this, so we are gaining the support?
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Broke mummy's heart and why she is driven to do her uppermost to raise awareness & funds
Our photos is all we have of our precious first born baby Sinead, many find it too hard too look at, and many have made us feel that we should not be sharing, even lost friends through writing on the very first photo that we shared of her, The very first time we shared her was the day we gave birth to her and the day she lost her fight for life.... Which was the only ever time we shared her publicly..... We were made to feel this was wrong.....
but these are our memories, and we have taken the hard decision to share, as we took them to let the world know we gave birth to a baby....
Perfect nose, perfect hands, perfect feet
Fully formed and was every inch of us....
After we had a scan to confirm we had PPROM, with only sacs full of waters, we were refused to listen into her heartbeat again.....
We have never forgotten our daughters heartbeat.....
14 views
and we are not ashamed of our daughter because of our daughter we now raise awareness and we know it has saved at least 1 babies life, we want to save lots more.....
which is why this Stem membrane patch project means the world to us, and the reason why we now want to set up Little Heartbeats as a charity.
We are praying that wishes come true, and we gain your support today, so we can help other mums through their journey both miracle babies and babies born too soon
Sinead Video 1 - Our sleeping princess too beautiful for earth...