Main fundraiser photo

Ayda Faith Murphy

Donation protected

***UPDATE***


CAN EVERYONE PLEASE READ THE LINK AT THE BOTTOM OF THE PAGE. With the heaviest of hearts I have to say that beautiful Ayda Faith Murphy lost her fight on 20/04/2021

As you can all understand this is a devastating time for Carly, Ryan & Olivia so we’re slowly closing this page down  

Until all money has been transferred (this can take a little while as different banks have different rules) I will still have it open, there are currently donations being made to send the family somewhere to be alone at this horrible time to gather their thoughts so if you do still want to donate then that’s up to you & would be appreciated!! ♥️ No one should go through this so let’s show them all we’re still behind them!! #AydaFaithMurphy 



As everyone knows Carly & Ryan’s beautiful little baby girl Ayda Faith Murphy is extremely poorly in Hospital at the moment
We've all got to believe that this little miracle is going to come through this but until she does it’s costing Carly & Ryan an absolute fortune, especially as they’ve now had to leave her in the Hospital!! So with ferrying back & forth & food & petrol & sorting Olivia out, it’s bloody expensive!! 

I’ve spoken to Carly & she’s agreed (reluctantly) to let me do this, so below is a brief description of Aydas condition atm!!
Anything you can spare is going to help this lush little family so please share far & wide!! I’ve started at £500 but I’m sure we can knock that out the park!!! 


Let’s show Carly & Ryan that Bedlington are behind them all!! ♥️♥️♥️


Bowels all out ( Gastroschisis is a birth defect of the abdominal wall. The baby's intestines are found outside of the baby's body around the belly button area NORMALLY and is more common but Ayda’s condition is rare 10 cases worldwide hers are hanging on the left hand side of chest area (never seen this before)
also her heart is on the opposite side of the chest so rather than the left it’s sitting on the right and the heart has flipped completely over (doctors have said she has all the symptoms of a CDH baby Congenital Diaphragmatic Hernia but hasn’t got that)
And third thing is very very small lungs (hence being on life support)
All 3 things they have dealt with individually on sick babies but never 3 together they’ve said she’s definitely unique. ❤️
Survival is still single figures

https://www.facebook.com/686182428/posts/10159254019902429/

Organizer

Annouska Adamson
Organizer
England

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