Charlie Gard – Not An Isolated Case

The reason we can’t and shouldn’t put aside the Charlie Gard case is that it isn’t an isolated event. If we put it aside and ‘go on with our lives’, it will only empower the hospitals and courts to make more and more decisions for our lives and not usually for the betterment of our lives.

http://www.crisismagazine.com/2017/charlie-gard-case-portends-frightening-future

Hard to Comment . . . Without Grinning!

The doctor came in looking tired and somber. “I’m afraid I’m the bearer of bad news,” he said as he surveyed the worried faces: “The only hope left for your loved one at this time is a brain transplant. It’s an experimental procedure, very risky, but it is the only hope. Insurance will cover the procedure, but you will have to pay for the actual brain.”

The family members sat silent as they absorbed the news. After a time, someone asked, “How much will it cost?” The doctor quickly responded, “$5,000 for a liberal’s brain; $200 for a conservative’s brain.”

The moment turned awkward. Several leftist family members tried to suppress a smile, avoiding eye contact with their conservative cousins. A smug liberal uncle, unable to control his curiosity, finally asked the question on everyone’s mind: “Why do liberal brains cost so much more than a conservative’s?”

The doctor smiled at his childish innocence. “It’s just standard pricing procedure. Unlike a liberal’s brain, we price conservative brains much lower because they’re used.”

The Untimely Death of Charlie Gard

A baby died in England this week. This baby’s death shouldn’t go unsung because a tiny infant showed the world what becomes of the humans of the world when the ways of the world have come to a pass that full-term, living babies can be deprived of necessary treatment and not allowed a chance at life.

Although little Charlie Gard seemed in perfect health his first couple of months of life, he suddenly started failing and ended up in a hospital with a diagnosis that could be considered a definite death sentence if left untreated. Although it was a chance, at best, Charlie’s parents researched options, begged for financial help, and got in touch with an American doctor who said he would examine the baby. Seems like a ray of home in what was being touted as a no-win situation.

Even with money in hand and a place to take their baby, the United Kingdom’s courts and doctors refused to allow the parents this option. There would have not been a single charge to the hospital for taking the baby to that one chance of help but the doctors said an adamant, unexplained ‘NO!’ and the courts backed them up on their say so. The time line for saving Charlie began in January when first diagnosed. At that point in time, the treatment just might have been beneficial giving the parents a feeling of hope in doing all they could for their first child. The doctors dragged on the process and the court trials didn’t get the immediate hearings you would think the situation merited so we end up seven months later with a baby slowly deteriorating in health.

Even in the condition he was in this month, the American doctor made the trip over to examine the baby and met with the UK doctors. A doctor in Rome offered his help on this as the Pope was also anxiously watching this turn of events. Everything was rejected and the courts sided with the doctors.

It got worse even after the parents realized that time had run out on treating their baby due to the doctors’ lack of action. They allowed that their son’s little life was fast running it’s course and only asked that they could take him home to die. This was refused. From what I read, they took the baby to an undisclosed place where the doctors removed him from his life support and Charlie died.

I only wonder how much celebration was enjoyed by those grown men who fought so hard for the death of this baby. I wonder if the judges breathed a sign of relief to have this pesky situation finally put to rest being glad little Charlie was finally being put to rest.

To basically recap: The parents of a sick baby had the wherewithal to transport him to the United States for experimental treatment. There would be no further cost to the UK hospital. The doctors refused to give the baby this once chance and regulated the time the parents could spend with the baby. When the parents persisted, the courts stepped in and took away their parental rights to do the best they could for their son.

You have to ponder what was going through these people’s minds to constantly refuse to move an inch on possibly saving this innocent child. Do these doctors have children? Would they appreciate a stranger telling them they couldn’t decide what was good for their own children? Yet, the doctors involved and the courts thought nothing of depriving this little family of their God-given free will and rather than have their word contradicted and take an ego bruising, felt it was better to get rid of the evidence . . . little Charlie Gard.

I’m thinking there are a great many people in the world today shedding tears for this family and not thinking well of how the helpless are treated under the medical guidelines of the medical health care system of the United Kingdom. A doctor vows to do no harm. I didn’t see any evidence of compassion in the events of the last few months.

Over the years, so many atrocities have been committed under the guise of medical treatment, especially in what unborn get to live and who are thrown away. It seems to follow, in a way, that if you get used to dumping aborted babies into the trash that helping a live baby to their demise would just be another day’s work. AND, if you have the backing of the court, it looks like one takes a huge chance in trusting their health and eventual outcome to the powers that be who want to run our lives.

Unfortunately, this is not isolated to the UK. People might remember Terri Schiavo who was deliberately starved to death because that was her husband’s wish with the backing of doctors in spite of her having a family who wanted to save her. Another case was the teenager, Justina Pelletier, who held by the Boston Children’s Hospital based on a doctor’s view that she wasn’t being properly treated medically. She went in a healthy young lady and finally left in need of much health care and rehabilitation from her time in that hospital.

Many prayers needed, today, for Charlie Gard’s family as well as other people/children who might be in similar situations and not allowed their freedom of choice.

Roots in the Family Tree – Memories and Surprises

I recently had my DNA analyzed by Ancestry.com and didn’t figure I would find too many surprises. I always grew up saying I was half German and half American since my mother had come from Germany and my Dad from America. Makes sense, right? I didn’t figure I would find a lot of surprises in my DNA. Wrong!

Great Britain 27%
Scandinavia 25%
Western Europe 22%
Ireland 11%
Eastern Europe 9%
Italy Greece 2%
Iberian Peninsula 2%
West Asia 1%
Middle East 1%
The last two percentages were possible but the rest is the ‘real me’ for sure. I was surprised to not have much German showing up but I do look like my Dad’s side of the family. The Irish was a surprise but a suspicion as the gene for red hair usually indicates Scotland or Ireland. I don’t have the red hair in the family but showed Scotland and Ireland in the analysis. Seemingly, my antecedents really got around.
So far, I’ve only traced my Father’s side of the family and have gotten back to the 1300’s where we have a couple of Knights and Ladies. My husband said to follow exactly from which son of a son of a son I could trace back to but it turns out that until the 1800’s, they each had one son! My great grandfather broke the tradition and had ten children and my grandfather had four children.
Seeing the names of the Aunts and Uncles (my Father’s sibling) brought back a few memories. I don’t remember my Uncle Emerson but met my Aunt Helen one time. The one, however, I remember the most without having seen her was my Aunt Viola who was married to my Uncle Emerson. It seems she was almost my second mother!
When my mother was pregnant with me, she was horribly sick the entire time. She became pregnant being underweight and weighed even less at nine months pregnant. Things, however, went well and she went home with her baby girl. Much to her surprise, Uncle Emerson and Aunt Viola showed up to visit a couple of weeks after my birth. You have to remember that back in those days, telephones were for local calls and letters took a week or more to arrive. My aunt and uncle lived in Missouri and we were in Colorado at the time. Seems that my Father panicked at my mother’s ill health and told his brother, Emerson, that if something happened to his wife, he couldn’t copy with a baby and he would like them to adopt me! My mother and Aunt Viola were friends and this was never mentioned but I can imagine she shed a few tears at not returning home with a baby. She couldn’t have children.
Well, I had a difficult time finding information about Aunt Viola for the family tree this week. When Uncle Emerson died, she kind of faded out of the family picture. My grandmother wasn’t a gem to any degree so I think Aunt Viola struck out on her own and cut her connections with the family. After a lot of digging (I’m getting good at researching family roots!), I found her and was saddened to discover she passed away in 2011! I would have like to have seen her and talked to her. So even not knowing/remembering what she looked like, it was a little sad to have missed a tiny reunion with someone that had been nice to my German mother fresh from the war and thank her for having cared about my welfare.

Charlie Gard – Medical Treatment Gone Array?

When a government is in charge of healthcare, they can also be in charge of whether you live or die. Case in the point, the medical conflict over the 11-month old, Charlie Gard in Britain. Initially, the powers that be felt that keeping him on life support was futile and the baby should be allowed to die with dignity. His parents feel he should have more of a chance and garnered every cent they could to pay for travel and treatment to America. The British medical services ‘would not allow’ that and put a date of death tag on the little boy. Thankfully, this has been extended and some good has come about on behalf of the little child.

A doctor going for cutting-edge medical treatment on the ailment of the boy and an expert in that particular field came to the UK on his own dime and spent five hours evaluating the little boy. He determined that with the help he could provide in the States, Charlie Gard could have an 11% to 56% chance of improvement. He didn’t feel he was mentally impaired. To sweeten the deal, the US Congress voted to give the parents and Charlie immediate citizenship and residence in the United States. The parents had the financial means to bring the baby over without a single penny required of the British health system. They were refused this by the British doctors and the courts. They are adamant that Charlie stays in Britain and that Charlie should die.

Recently, the doctors showed up at a hearing with brain scans purported to be from Charlie and showing low brain function. Before even talking to the parents about this, they sprung it on everyone to validate their vote for allowing Charlie to die.

You have to wonder about the mind set and callousness of a system that basically kidnaps someone’s child and takes away the parents’ right to make decisions for the child. What is wrong with doctors who refuse to consider an alternative that won’t cost them any money. Why is it so important for them to watch a baby boy die? It does make one think that pride is playing a major part in this because these British doctors have failed to help the baby and are afraid that he just might have more of a life with medical treatment in the United States. Don’t doctors take a pledge about ‘do no harm’? It is tragic, sickening, and evil to follow the news on this where doctors fight for the right to end this little boy’s life.