- Jaxon Buell was diagnosed with microhydranencephaly, a severe brain malformation for which there is no known cure
- Jaxon Strong Facebook page garnered more than 200,000 "likes" and global attention
(CNN)Jaxon
Buell was born without a large part of his skull and brain. Doctors
told Brandon and Brittany Buell their son wouldn't live past a few
weeks. In August, the family celebrated his first birthday.
After
many months of tests and misdiagnoses, doctors finally diagnosed Jaxon
with microhydranencephaly, a severe brain malformation for which there
is no known cure.
Jaxon's short life
has not been without struggle, and his parents' candid accounts on
social media have garnered global attention.
In a September Facebook post,
Brandon Buell explained the couple's decision to continue the pregnancy
after learning at a 17-week untrasound their son had something wrong.
"When
we first learned there were concerns for Jax during the pregnancy, we
were given the options of carrying him to term or having an abortion
because there was the unknown issue. No doctor could tell us exactly
what was wrong or what to expect, but we did make sure to ask if Jaxon
was in pain or was suffering, and we asked if there were any added risks
for Brittany during the pregnancy or potentially at time of delivery.
Since the answer to both questions was "no," we never came close to
considering abortion. Yes, we are Christians, and our faith has
certainly been vital during this entire journey for our family, but
we're still realists. Had there been any suffering in the womb or a
danger involved other than Jaxon possibly not being able to live outside
the womb because of the concern for his head and brain, then we
certainly would have had a different discussion. However, that wasn't
the case, and it was our choice, and only our choice."
A Facebook page, Jaxon Strong, has over 200,000 "likes," and a GoFundMe page has received nearly $100,000 in donations, which go toward the family's monthly expenses, including Jaxon's medical bills.
Jaxon
cannot eat on his own and relies on a feeding tube for nutrition but
his dad tells CNN it's one of the only differences between him and most
other children.
"He's going to always
to be very small. At this point he's 13 months old and he weighs just
over 12 pounds. He's certainly not suffering whatsoever, he's actually
still thriving. He really is a normal baby in so many ways: He cries, he
goes to the bathroom, he wants his dirty diaper off... Jaxon is
virtually perfect."
The
parents know that Jaxon will need a miracle in the long term, but are
taking each day as it comes and relying on faith to help them through.
"We
had a faith that we will continue the pregnancy and hopefully we
wouldn't lose him. And now we are today where he's not showing signs of
going anywhere. He is -- you can tell -- so loved, he has the brightest
eyes, he recognizes so many things, he's so alert. We are just aware of
the miracle of what he's doing and also the reality of what may happen
tomorrow," Brandon Buell told CNN.
Via (CNN)
No comments:
Post a Comment