Joseph's lifesaving surgery

I didn't want to put this post up but it's the last thing left I can do or we can do for our little boy so far the NHS is finished with baby Joseph surgically. The surgery my boy had on the 4th July as a first attempt at a staged repair of his heart didn't work unfortunately so they don't want to risk another surgery and it worsening his condition, they placed a stent in in hope that the stent would stop baby Joseph from having the profound desats and still baby Joseph will have random desats (oxygen levels dropping) to 19 and sometimes lower. We can't just leave baby Joseph like this so I've made this post in hope that a go fund me or shares or something the surgeon in America that is known as the king of this condition pulmonary atresia vsd and mapcas, can help us.

So far the doctors are saying my little boys prognosis is poor, he'll never go school etc but please if you've read our story and followed our journey you'll know how wrong baby Joseph has proved them every single time, they said we'd never take baby Joseph outside and we did we took him even to my mothers house for the day and it meant to much to do this , they said he'd be born blue wouldn't cry but when my child was born on Christmas Eve he was pink and cried, they said he's brain weren't developed on scans but after a last growth scan he's brain was perfect and is perfect. they mention palliative care a lot and I know this surgeon in America can turn a bad prognosis into a good one and if that's the last resort the only resort then atleast we can say we tried everything. So please everyone I'm getting the second opinion from America in hope they can help, because that's all we have left to do. But I know it will be around 1.9million dollars, if that's £1 from everyone or 1.9 million people we'd get there, I won't bring baby Joseph home with nothing he fighted in my womb and he still fights today.

God bless you all