Thursday, 24 September 2015

Little Heartbeats PPROM awareness


You don't need to be alone any longer 

If you are dealing with PPROM
On bedrest, dealing with neonatal, dealing with PPROM baby loss 
then do get in touch with us by sending us a private message on our Facebook page here https://www.facebook.com/PpromAwarenessUK

Saturday, 12 September 2015

Thunderclaps to raise awareness



It takes one second to do, and mean an awful lot to us Pprom parents if you can support and follow our Thunderclap

Link is here 

https://www.thunderclap.it/projects/30730-pprom-awareness-in-pregnancy

take the time to watch our videos....

why this is important to us...



Watch our PPROM video here 



Guess what babies do survive, if the RIGHT Care is given 
watch here 


Our thunderclap is here --->>>>>


Thank you for supporting our cause 




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


Raising funds to make a difference

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? 



Friday, 8 May 2015

PPROM Thunderclap - what is thunderclap? #PPROM #Prematureruptureofmembranes before 37 weeks - #Pregnancy #MatExp

What is Thunderclap?
Thunderclap is the first crowd-speaking platform that helps people be heard by saying something together.
How does it work?
If you reach your supporter goal, Thunderclap will blast out a timed Twitter, Facebook, or Tumblr post from all your supporters, creating a wave of attention.
Who's using it?
From passionate individuals with a message to share, to organizations such as The White HouseLevis and the United Nations.
So hope that helps you decide to follow our #thunderclap 

“We are NOT the Only 1's & Our babies deserve the best possible chance to survive https://youtu.be/5x0O_kyX1cc #PPROMAWARE http://thndr.it/1brQ37W

SUPPORTERS
18 of 250
7% of goal supported
SOCIAL REACH
80,187
People
TIME LEFT
23 days
Ends May 31, 8:00 PM EDT

'Unless someone like you cares a whole 

awful lot,Nothing is going to get better. It's not.' 

Saying BY Dr. Seuss — 


Tuesday, 5 May 2015

Perfect Heartbeats Preterm Premature Rupture of Membranes In Memory of our Babies born sleeping

PPROM Awareness Video by Our Angel Mums

463 views

'Unless someone like you cares a whole 

awful lot,Nothing is going to get better. It's not.' 

Saying BY Dr. Seuss — 


To help us gain changes to the way PPROM is dealt with please Sign our petition: click to here to sign our Change PPROM petition

For anyone wanting to Donate, 

click here:-  

http://www.youcaring.com/nonprofits/little-heartbeats-raising-awareness-on-pprom-/337480

or to #UCLH Stem Membrane Patch Project via 

Just giving text PROM49 £1 to 70070 

or to any of our team giving pages, 

https://www.justgiving.com/teams/Ppromresearch

'Sinead Speakman 15.04.2010'

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...



Sinead Video 2


http://flipagram.com/f/QmHdmBEF92

Our latest Thunderclap click here to follow by twitter or facebook

SUPPORTERS
18 of 250
7% of goal supported
SOCIAL REACH
80,187
People
TIME LEFT
23 days
Ends May 31, 8:00 PM EDT


#PPROM #Prematureruptureofmembranes #watersbreaking #pregnancyissues #miracles #babyloss #breakthetaboo @PpromAwarenessU https://www.facebook.com/PpromAwarenessUK