They
tell her that heaven is where she'll be able to run and play and eat,
none of which she can do now.
Heaven is where she'll meet her great-grandmother, who shared Julianna's love of shiny, sparkly, mismatched clothes.
Heaven is where she'll meet her great-grandmother, who shared Julianna's love of shiny, sparkly, mismatched clothes.
God will be in heaven, too, they tell her, and he will love her even more than they do.
But Michelle Moon and Steve Snow explain
that they won't be in heaven when Julianna arrives there, and neither
will her big brother, Alex. She'll go to heaven before them because she
has a severe case of an incurable neurodegenerative illness called
Charcot-Marie-Tooth disease.
Her
coughing and breathing muscles are so weak that the next time she
catches even a cold, the infection could settle in her lungs, where it
could cause a deadly pneumonia. Her doctors believe that if they can
save her under those circumstances -- and that's a big if -- she will
likely end up sedated on a respirator with very little quality of life.
There's
no debate about the medical facts of Julianna's condition. But there is
debate about something her parents have chosen to do: They asked their
daughter, at the age of 4, if she would want to go to the hospital the
next time she becomes dangerously ill, or would she want to stay home,
where she would die.
Julianna has said she doesn't want to go to the hospital. She wants to go to "heaven."
Before
having these discussions with her daughter, Michelle looked online for
guidance about end-of-life talks with a 4-year-old. Finding nearly
nothing, she started a blog of her own in hopes of helping other families in the same situation. Later, she contributed to The Mighty, a website where people write about grappling with disabilities and devastating diseases.
Michelle: Julianna, if you get sick again, do you want to go to the hospital again or stay home?
Julianna: Not the hospital
Michelle: Even if that means that you will go to heaven if you stay home?
Julianna: Yes... I hate NT (naso-tracheal suction, where a tube was placed down her nose into her lungs without sedation). I hate the hospital.
Michelle: Right. So if you get sick again, you want to stay home. But you know that probably means you will go to heaven, right?
Julianna: (nods)
Michelle: And it probably means that you will go to heaven by yourself, and Mommy will join you later.
Julianna: But I won't be alone.
Michelle: That's right. You will not be alone.
Julianna: Do some people go to heaven soon?
Michelle: Yes. We just don't know when we go to heaven. Sometimes babies go to heaven. Sometimes really old people go to heaven.
Julianna: Will Alex (her 6-year-old brother) go to heaven with me?
Michelle:
Probably not. Sometimes people go to heaven together at the same time,
but most of the time, they go alone. Does that scare you?
Julianna: No, heaven is good. But I don't like dying.
Michelle:
I know. That's the hard part. We don't have to be afraid of dying
because we believe we go to heaven. But it's sad because I will miss you
so much.
Julianna: Don't worry, I won't be alone.
Michelle: I know. I love you.
Julianna: Madly.
Michelle: Yes, I love you madly. I'm so lucky.
Julianna: And I'm so lucky.
Michelle: Why?
Julianna: Because you love me madly.
Before
these conversations, Michelle says she and Steve had planned to take
Julianna to the hospital if she were to get another infection. But after
hearing Julianna's wishes, they changed their minds.
"She
made it clear that she doesn't want to go through the hospital again,"
Michelle wrote CNN in an email. "So we had to let go of that plan
because it was selfish."
While most readers left supportive comments on her blog post, some thought Michelle and Steve had made the wrong choice.
"Unbelievable
that any parent would think a 4-year-old is able to understand or make a
decision on life," commented one mother of a child with a chronic
illness. "Clearly that mother asks her leading questions. This article
sickens me."
The next week Michelle posted another blog post, further explaining their decision.
"She's
scared of dying, but has, to me, demonstrated adequate knowledge of
what death is. (J: 'When you die, you don't do anything. You don't
think.')," Michelle wrote. "She hasn't changed her mind about going back
to the hospital, and she knows that this means she'll go to heaven by
herself. If she gets sick, we'll ask her again, and we'll honor her
wishes."
She continued: "Very clearly,
my 4-year-old daughter was telling me that getting more time at home
with her family was not worth the pain of going to the hospital again. I
made sure she understood that going to heaven meant dying and leaving
this Earth. And I told her that it also meant leaving her family for a
while, but we would join her later. Did she still want to skip the
hospital and go to heaven? She did."
Should a child decide her own end-of-life care?
For
adults, end-of-life decision-making is relatively straightforward:
Basically, we get to decide how much medical treatment we want and don't
want.
But how much say should a child get? And at what age?
Without realizing it, Michelle and Steve had stepped into a heated debate.
Bioethicist Art Caplan has read Michelle's blogs, and he thinks she's made the wrong decision.
"This
doesn't sit well with me. It makes me nervous," he says. "I think a
4-year-old might be capable of deciding what music to hear or what
picture book they might want to read. But I think there's zero chance a
4-year-old can understand the concept of death. That kind of thinking
doesn't really develop until around age 9 or 10."
He
says Julianna's parents shouldn't put any stock in what she has to say
about end-of-life decisions. Maybe she chose heaven over the hospital
because she feels how much her parents hate to see her suffer; young
children often pick up cues from their parents and want to please them,
he says.
Caplan, before he started the
bioethics program at New York University a few years ago, worked at the
University of Pennsylvania and consulted on end-of-life cases at
Children's Hospital of Philadelphia with Dr. Chris Feudtner, a
pediatrician and ethicist there. Caplan respects him a great deal.
Feudtner, it turns out, disagrees with Caplan about Julianna.
"To
say her experience is irrelevant doesn't make any sense," he says. "She
knows more than anyone what it's like to be not a theoretical girl with
a progressive neuromuscular disorder, but to be Julianna."
At
his hospital, he has asked dying children her age what they want to do,
and in the appropriate circumstances, he has taken it into
consideration.
For example, he doesn't
take their opinion into account when it's a black and white decision --
children with treatable leukemia must get chemotherapy, for example, no
matter how hard they protest. But when the choice is gray, when there's
more than one reasonable option, as there is with Julianna, he has put
stock in their wishes.
As for a
4-year-old not having the mental capacity to think through death, he's
found that even adults often don't think through such issues as
carefully as one might like.
"My
86-year-old father died in April, and I'm not sure he truly got it," he
says. "He was bed-bound from cancer, and he said, 'If this is the best I
get, get me a Smith & Wesson.' Did he mean that? I don't know."
Feudtner,
the chairman of the American Academy of Pediatrics section on hospice
and palliative medicine, says as best he can tell from Michelle's blogs,
Julianna's choice for heaven over the hospital is reasonable and her
parents are right to listen to her.
"Palliative
care isn't about giving up. It's about choosing how you want to live
before you die," he says. "This little girl has chosen how she wants to
live."
Julianna is no ordinary 5 year old
Art
Caplan's words sting Michelle when she hears them. How could he deign
to understand her child? But then a few days later, she wrote to CNN to say that she understands how someone could have a difficult time understanding what she and Steve have decided.
If
you haven't met Julianna, she says, it's hard to explain how even at
such a young age, she understands the choice that's in front of her, how
she's the one who experiences the suffering and should get a say in
what will happen to her.
Source: CNN
Source: CNN
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