Jin Popyliole, 63, was diagnosed with sarcoma, rare and aggressive cancer, and fears that she would die in pain.
Jeddah tells a final patient today, deputies: “I have gone through a good life, I would like to choose a good death.”
Jin Popyliole, 63, was diagnosed with sarcoma, a rare and aggressive form of cancer, and fears that can die in pain.
“I feel passionate about it. It is about choosing in a liberal society. I understand about 80 % of the voters in favor.
“It is not about to force anyone. He is about not to die in an uncomfortable or painful way. Who wants it?
“When you have a final disease, the fact that it may happen to you, it is difficult to imagine what it looks until it happens.
“Who knows how my end will be. I have lived a good life and I would like to choose good death. I feel everyone should have the right to this option.”
Jane said that she removes a borrowed blond hair, to show the reality of living with peripheral cancer, that she got full support for Tony's husband, 62, and her two children. She also told how they made the difficult decision to explain her three grandchildren, between the ages of 15, 13 and 11.
She said: “We were honest with them, it is clear that we distinguished between their ages. I have made it clear to them that this is very important for me and my beliefs. It is about choosing.
“We will all die, and this is certainty.
She said that her youngest granddaughter was upset, but she was invited to the oncology unit to see the work they are doing
“Sometimes the unknown is more frightening than well -known. We talked about it and it was really useful. I didn't get complaints about NHS, my treatment and care, I couldn't asked for more,” said Jin, who supports dignity in the death group.
Jin was first diagnosed in August 2023 after falling. X -rays revealed that there is something wrong and in November the word “cancer” was first used.
“It took a long time to treat. They were trying to find whether in my blood or bone,” she said.
No more test was diagnosed in Birmingham only after rare soft tissue cancer was diagnosed.
Jane said her life has completely changed over the past 18 months: “I moved from the work point for three days a week, as she worked as a quality manager in care homes, driving everywhere, and being an active member of society, and I have a social life with my grandchildren, to how I am now.
“It is an aggressive and rare cancer. It is strange, because the word“ station ”was used from Go Go. When we went to the date, Tony took a pen and paper to write everything. When I looked at it it was on the ground and was crying.
“I just said” Why do you do that? “It took a long time for me to reconcile with it.
Since the diagnosis, it has undergone radiotherapy and is now in its third path of chemotherapy. But she received the devastating news that cancer had extended to its lungs and liver.
She said, “I have my moments down, but I try to stay positive. I do not think about the schedule, and I take it moment by moment.
“I feel that I still have a purpose in life, I can still make a change. By supporting this bill, I can still make a change to other people.
“I have never smoked and I have been vegetables since I was twenty years old. I lived a healthy life. But I never asked,” Why am I? “If I get what I call” thinking stink “, then I take myself to bed.”
“Even if this law is passed, it may not help me. It is the first step in a long process. But I hope my story, my image, my legacy helps to change the opinion of someone.”
Jin's message to the deputies
Dear members of Parliament,
I and the writing below write to you and you are preparing to vote on the bill of death with the help of its third reading. We are a group of people with end diseases from all aspects of life and regions of the country, but we stand united with one message: Please vote for change, our death depends on that.
I live with terminal sarcoma, rare soft tissue cancer. I receive excellent care from my medical team, but every day I am afraid that I will die with pain. It will allow me to choose death with the help of living better now, with comfort in knowing that I will have an opinion on how I die if my pain becomes unbearable.
I know that people with cancer may die badly, and I managed to manage a care house and saw the residents die without taking advantage of this choice. I don't want to travel to Switzerland to die. My cancer has spread and I find it difficult to move, so travel hundreds of miles is hard for me. In addition, it costs 15,000 pounds, and who has this type of money lies?
People who signed this message all have different experiences with their diseases. Some live with permanent pain, and some live in fear of how they died, although they receive excellent care like me. Some suffer from motor neurons and may soon lose their ability to speak. They want to use their voices to fight for change while they are still able to do so.
Without the law of death with help, our options are very limited. Unfortunately, some people suffer at the end of their lives, although excellent careful care. Hundreds every year take their private lives, and they often die alone and unit, while keeping their plans secretly from their families. Some, if they have money, travel abroad to die, and they often die sooner than they want, so that they can do the trip.
If we live in Australia, New Zealand or some American states, we will have this option at the end of our lives. There is no reason that prevents us from not joining hundreds of millions of people all over the world who already have a death option with help.
We have given us the Kim Lidepter bill. The draft law includes the most important guarantees of the world, such as the need to evaluate it by two independent doctors and a committee, including a judge or a senior lawyer, a social worker and a psychiatrist to ensure that the person who dies is chosen free from coercion.
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Kim, the draft law committee and all deputies during the report phase worked hard to ensure that this bill is applicable, safe and practical, while giving people who die like us the sympathy and choice we request.
We write to you not only for our death, but for the sake of our families that do not want to see us, we are suffering, for all those who went before us and died before the law changes, and for all everyone in this country who may want this choice in the future, and who deserve better than the dangerous and spontaneous blanket to help.
Please vote for selection and mercy. Please vote to support the death bill with help. Vote for us. When we cannot stay, let's choose how to go.
You sincerely,
Jane Boubleliole, lives with the station Sarkoma
