Parents Against Injustice

BREAKING: UK hospital agrees to give Alfie Evans another chance

https://www.lifesitenews.com/news/breaking-uk-hospital-agrees-to-gi....

It seems very weird that ACH, are all of a sudden giving Alfie some leeway and that they have decided to keep Alfie on his Ventilator for a longer length of time.

Something is very wrong here?, Alfies Parents have posted YouTube videos on ALFIE ARMY FACEBOOK PAGE, showing videos of the Baby yawning, sucking on a soother, stretching, sneezing, coughing, spitting his soother out when being asked by his Parents.these videos have been seen by many persons, as well as myself.

There was also evidence that the Hospital had given Alfie the wrong dosage of medication on more than 2 different occasions, this documentation was also highlighted on the Facebook page.

So now there are serious issues of the drug errors, as well now, i have already posted the link to the drug error on a past blog.

I went to a local campaign protest the other day, and there was other certain issues that had happened, of which nobody would disclose.

The Family Division of the High Court at the RCJ, had denied the rights of the Parents, and their Application for permission to appeal was denied, as well as their Application to the Supreme Court and the ECHR..

I have also highlighted another case where the child had a very aggressive form of a brain tumour, , the Hospital stated that there was nothing more they could do,

The Parents in this case skipped the UK to Spain, in their attempt to get proton therapy in Prague.

The Parents were arrested in Spain, and put into prison, but later released and was given the go ahead to take the child for proton therapy in Prague.

The Boy is now back in the UK, and is free of the cancer ,which would of killed him, if the Parents had not taken things into there own hands, after being told that there was no more that could be done in the UK Hospital.

The Boy is now able to ride his bike and play football..

QUESTIONS ABOUT ALFIE DRUGS AS WELL

https://www.facebook.com/photo.php?fbid=1651941941592603&set=pc...

ALFIE DEFINITELY RESPONDING HERE

https://www.facebook.com/thomas.leenew.7/videos/o.425764684475548/8...

We are being blackmailed into our son's death": Alfie Evans' dad claims hospital won't let him hold toddler

https://www.mirror.co.uk/news/uk-news/we-being-blackmailed-sons-dea...

They have challenged the authority of the Hospital and now they are punished for being assertive .

The worst possible nightmare scenario.

If Alfie had of been 18 years or over, he would of definitely been placed on a DOLS, .

And the powers to be have the right to deny a Patients relative from seeing them if they feel it is not in the best interest.

Because Melody Driscol, Parents challenged the Hospital regarding her medication, the Hospital referred the issue with Social Services and the Parents had a letter from the LA, stating that she could be placed into care of the Local Authority.

Croydon mum facing court battle to keep seriously ill child

http://www.bbc.co.uk/news/uk-england-london-42583780

MUM WINS BATTLE TO KEEP TERMINALLY ILL DAUGHTER OUT OF FOSTER CARE

http://metro.co.uk/2018/01/26/mum-wins-battle-to-keep-terminally-il...

When to end a terminally ill child's life? It's an agonising decision

https://www.theguardian.com/healthcare-network/2018/mar/22/when-end...

The DRs and Paediatricians at Alderhey Children's In Liverpool have stated that Baby Alfie Evans has no quality of life,

And has stated that it is in Alfie best interest to terminate his life support.and have taken the case to the Family Division of the High Court RCJ.

Judges have ruled in the favour of the Hospital so Alfie is doomed to die.

The Baby's Parents have tried to get permission to appeal, but their wishes were denied.

There only hope now is the ECHR, and the matter is now in the hands of the European Court.

The Parents have stated that Alfie responds to them, and YouTube videos have confirmed this,Alfie is seen opening his eyes, via stimuli , he manages to suck his soother, Alfie Father asks his Son to remove the soother from his mouth, which he then spits it out.

The baby has no diagnosis yet for this brain wasting disease..

There has been an outcry by the General Public, who have emailed the ECHR, asking that Alfie should be given the chance of life, being that the condition has not even been diagnosed and that there is evidence via YouTube video that Akfie is responding to his Parents, via stimuli , opens his eyes, when being stroked on the cheek,and is seen sucking on his soother.and spitting out his soother when being asked.

Many Children are being nursed and care for at home via a tracheostomy,and connected to a ventilator , with a package of care, i for one has worked as a carer looking after a young adult with muscular dystrophy .

A recent case highlighted how Drs and Paediatricians can be very wrong. Ashya King a small Boy with a very aggressive form of a brain tumour could be very well dead by now, if it had not been for his loving Parents who had heard of a treatment abroad where he could have proton therapy.

The Hospitals stance is that there could be nothing done for the boy, only end of life care.

The Parents SKIPPED TH COUNTRY TO SPAIN, AGAINST HOSPITAL DOCTORS WISHES, HE WAS TAKEN TO A HOSPITAL IN SPAIN, A WARRANT WAS PUT OF FOR THE PARENTS ARREST, they were placed in a prison in Spain.

They were eventually let free , and took their Son to Prague for the treatment, Ashya- is now living back in the UK, with his parents and siblings, there is no sign of the cancer, he is a healthy little boy that can now play football and ride his bicycle

.https://www.telegraph.co.uk/news/health/children/11489212/Brain-tum...

Another recent case highlights the dilemma of Parents Baby Isaiah Haastrup was also diagnosed with a brain wasting disease, he was in Kings College Hospital in London,

The Hospital Trust decided it was in Isaiah best interest for his life support to be terminated, 3 Judges gave permission in the Family Division of the High Court for the life support to be terminated.

The parents took their case to the Supreme Court, their decision was that they would not overturn the decisions made by the High Court.there only hope was the ECHR, who also denied the Parents attempt for the other Courts decisions to be overruled.

Baby Isaiah died a few days later, after his ventilator was turned off.the child managed to breath unaided for 7 long hours after life support was terminated.

Could Isaiah survive if he had weaned off the ventilator very slowly,? the poor Parents will never know.

All these case including the Charlie Gard case involved Parents after to sort their legal teams, Probono, as in charlies case.

Parents involved in these tragic cases are denied legal aid, because they are Private Law civil cases.

But yet if the children had been taken into care by a Local Authority, full Public funded legal aid would of been granted.

http://home.bt.com/news/uk-news/isaiah-lived-for-seven-hours-after-...

THE JUDGE IN THE CHARLIE GARD CASE BEWILDERED BY THE LEGAL AID ISSUES REGARDING THESE KINDS OF TRAGIC CASES.

Secondly, I wish to thank all of the lawyers in this case who have assisted the court
but, in particular, the team who have worked for the parents because they have done it
not for financial reward but have given their services free. It is not for judges to make
political points and I do not now seek to do so. However, it does seem to me that
when Parliament changed the law in relation to legal aid and significantly restricted
the availability of legal aid, yet continued to make legal aid available in care cases
where the state is seeking orders against parents, it cannot have intended that parents
in the position that these parents have been in should have no access to legal advice or
representation.

https://www.judiciary.gov.uk/wp-content/uploads/2017/07/gosh-v-gard...

http://www.familylawweek.co.uk/site.aspx?i=ed187940

Mum wins battle to keep terminally ill daughter out of foster care

http://metro.co.uk/2018/01/26/mum-wins-battle-to-keep-terminally-il...