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Tag: Chance

  • Mum Told To Abort Baby By Dr, But Mum Would Not Give up

    I received the awful news that there’s no fluid left around my baby the deepest pool was 1.8cm because of this my babies lungs can’t develop so if it survives full term we won’t get more than an hour with him before he passes away, this is what we were told 4 months ago.

    Doctor after Doctor told me there was NO HOPE, NO CHANCE of survival, one Doctor even told me I was wasting NHS money and time continuing with this pointless pregnancy and just to abort it and move on.

    This was not a thing to discard this is my child, a much wanted and tried for baby boy, even if I only get to hold him for a minute it would be worth it.

    Did my baby not deserve a chance to fight for the right to live, I messaged into Mums advice and asked if there was anything I could do to give my baby more hope.

    One woman (I wish I could remember her name) told me to drink water as if it were going out of fashion, just drink, drink, drink, I followed her advice and my baby thrived, he grew, he made it to 32 weeks before deciding it was time to meet his mama.

    Samuel Chance was born on July the 26th, he took a breath, he screamed a tiny sound, an hour passed and he was still with me.

    Samuel is still in the special care unit and fighting every day, he is gaining in weight and in strength this boy won’t give up and neither will I.

    Thanks Mums advice for believing in Hope and helping me to stay strong for my baby boy!!!

    I want to urge mums out there not to give up if you have a glimmer of hope you have to hold on to it.

  • One Boys Fight For The Right To LIVE

    One Boys Fight For The Right To LIVE

     

     

    Alfie Evans is at Alder Hey Hospital in the PICU. He has been hospitalised continuously since December 2016, dealing with chronic seizures of an undiagnosed disorder. The hospital has given up on him and applied to the High Court to remove parental rights and withdraw ventilation to end Alfie’s life. Yet Alfie and his parents are FIGHTING!

    Alfie has been been at Alder Hey in Liverpool PICU since December 2016. After a year of being there, this hospital has still not done procedures which should have been done a long time ago, like a tracheostomy and a PEG tube. This would be done immediately as soon as Alfie gets to the European hospital who is ready and willing to take him. The only thing stopping him from going to this hospital – is Alder Hey and their turning to the court. They have given up on him!

    One Boys Fight For The Right To LIVE

    Alfie’s parents are in court tomorrow , as the hospital wishes to appoint a guardian.

    Alfie has been given a chance at this European hospital who is waiting for Alfie to try and treat and diagnose his illness.

    Alfie has not been diagnosed with a terminal illness, HE IS STILL UNDIAGNOSED. Yet, ALDER HEY have put in an application to REMOVE HIS LIFE SUPPORT!

    Please do not let them do this to him. Lots of disabled children live happy lives. Alder Hey say that “Treatment is futile” and He has “no quality of life.” Being disabled, doesn’t mean his life should be written off.

    One Boys Fight For The Right To LIVE

    Alder Hey say that Alfie is “insensate” and that He “feel nothing”. Alfie does react, He stretches, He sneezes, He opens his eyes, He sucks a dummy, HE IS AWARE! and HE IS LOVED

    Please sign my petition so that Alder Hey will #RELEASEALFIEEVANS. https://www.change.org/p/we-demand-alder-hey-to-release-alfie-evans-to-a-hospital-of-his-parents-choice

  • My Baby Has An Inoperable Brain Tumour

    This is Edie Molyneux, she is three years old and was recently diagnosed with an inoperable brain tumour, her only chance for survival is a hospital in Mexico who have a number of success stories through this condition.

    She has a condition known as DIPG, Diffuse Intrinsic Pontine Glioma, commonly referred to as pontine glioma, infiltrative brainstem glioma, or DIPG, is a rare tumor of the brainstem that occurs almost exclusively in children. A pontine glioma occurs in a most delicate area of the brainstem (the “pons”), which controls many critical functions, including breathing and blood pressure. Its location, as well as the way it infiltrates normal brain tissue, makes it especially difficult to treat.a rare cancer affecting children.

    Which in Edie’s case is a tumour in the centre of her brain, making it unreachable by uk standard methods without poisoning her whole body, this is where Mexico come in, they have the advancements to treat and shrink the tumour and have 2 cases of No Evidence Detected in other children.

    However we need to raise £300,000 to make this possible, every share, awareness raised and £1 means the world to us.

    Here is a photograph of Edie and a scan photograph of her tumour, also a link to her fundraising page, thank you ever so much, your support will be eternally appreciated.

    Come on Mums advice ladies lets help this little girl, how much do you pay for a bottle of wine or a chocolate bar? Every pound could make a huge differnce and save this precious angel https://chuffed.org/project/the-spider-ede-appeal

    A Chrismas Miracle is what we need

    All my love,

    Emma Fessey

     

    My Baby Has An Inoperable Brain Tumour