When the new moon begins its orbit, life as we know it is going to alter, if not permanently.
At the end of this month, another moon will momentarily arrive on Earth.
Indeed, it may seem completely absurd to write or even mention that our planet will momentarily have a new moon, but it is true.
By the end of this month, a mini-moon—a tiny asteroid—will begin its orbit around the Earth and continue until November 25.
For the next week, the asteroid known as “2024 PT5” will join our moon, which has been orbiting Earth for the past four billion years, on its trip.
“The object that is going to pay us a visit belongs to the Arjuna asteroid belt, a secondary asteroid belt made of space rocks that follow orbits very similar to that of Earth at an average distance to the sun of about 93 million miles [150 million kilometers],” Professor Carlos de la Fuente Marcos said in a statement to Space about it.The population of near-Earth objects that includes comets and asteroids includes those found in the Arjuna asteroid belt.”
Leading the study team is Marcos, who is supported by a group of scientists.
The Arjuna asteroid belt is a varied tangle of space rocks, and because of its near-Earth orbit, it is predicted to round the planet once more in January.
The tiny asteroid will move at 2,200 mph and be only 2.8 million miles from Earth, which may sound like a very long way, but in space it is actually much closer than you might imagine.
The International Space Station orbits the earth at 17,500 miles per hour to put it into perspective.
“Under these circumstances, the object’s geocentric energy may grow negative, and the object may become a temporary moon of Earth,” he said. This particular object will be subjected to this process for around two months, beginning next Monday.
Saying: “It will not follow a full orbit around Earth.”You could argue that items like 2024 PT5 are window shoppers if a genuine satellite is comparable to a consumer making a purchase inside a store.”
So how do we identify it?
Sadly, you can’t, at least not with common household objects like binoculars or a telescope your mother got you.
No, because of its size, 2024 PT5 is far more difficult to see.
Marcos went on, “Most amateur telescopes and binoculars cannot resolve the object because it is too small and dim.” But the object is well inside the brightness range of the average telescope that is used by astronomers in their profession.”A 30-inch telescope with a human eye behind it will not be sufficient to examine this object; a telescope with a minimum diameter of 30 inches and a CCD or CMOS detector are required.”
Mom of Boy with Rare Condition Shares Their Life, People React Differently
Logan Pacl stands out among teenagers. At 17, he faces a rare illness known as Sanfilippo syndrome. Often called “childhood Alzheimer’s,” this cruel disorder gradually takes away a child’s cognitive skills, mirroring the effects of Alzheimer’s in older people. But he keeps fighting and uses social media to spread awareness about his condition.
At first, everything seemed normal.
Logan Pacl’s life is a battle against time. Diagnosed with Sanfilippo syndrome, often known as “childhood Alzheimer’s,” the 17-year-old from Silverdale faces a relentless genetic disorder that viciously strips away the very essence of childhood. Caused by a single defective gene, this neurodegenerative disease attacks the brain and spinal cord, leaving behind a cruel wake of lost abilities, seizures, and constant pain. It’s a ticking time bomb, as most children with this terminal illness don’t survive beyond their mid-teens.
For Logan’s family, the heartbreak began early. Born in 2007 with his twin brother Austin, Logan seemed like any other healthy baby. Both boys hit their developmental milestones—until Logan began to fall behind. A year in, the red flags emerged: while Austin was speaking, Logan remained silent. The difference between the brothers grew, signaling the start of a devastating journey.
Sanfilippo syndrome doesn’t just rob children of their future—it erases their past.
Then the news of the diagnosis hit the parents, something no one could have anticipated.
As Logan’s condition worsened, with chronic infections and a noticeably swollen belly, Noelle and William were left searching for answers. In January 2010, they learned that Logan had Sanfilippo syndrome, a terminal illness with no cure or treatment, and a life expectancy that typically extends only into the late teens. “I’ll never forget the day we got the phone call. The genetic counselor on the other end went on and on, and all I thought was, well get to the part on how we fix this. Then she said it, ’This disease is terminal, and there is no cure or treatment,’” his parents recall.
Noelle recalled her initial reaction, grappling with the news that the disease was terminal. The weight of the diagnosis was overwhelming, leaving her with a heart that felt as though it had dropped into her stomach. The severity of the situation rendered her unable to process much beyond the devastating reality.
Noelle described the experience of mourning not just the child she had but the life she had envisioned for him, a life that was abruptly stolen away. The medical advice they received was minimal and unhelpful, simply advising them to take Logan home and cherish their time with him. This lack of concrete guidance only deepened their sense of helplessness.
In their search for hope, Noelle and William discovered an experimental stem cell transplant through online research. Inspired by the success of another mother’s child, they decided to pursue the same treatment for Logan. So, Pacl went through a tough three-month treatment that was basically a bone marrow transplant. He had to endure chemotherapy to wipe out his immune system so it could accept the new stem cells. It was a risky procedure, but it seems to have helped with some of Logan’s physical symptoms.
His mother uses social media to spread awareness about his condition.
At 17, Logan’s life is very different from that of most teenagers. Losing his ability to speak at a young age was tough for him and his family, but over time, he’s become more easygoing. “Life with Logan is anything but typical. Each day is a battle to maintain the skills he still has,” his mother Noelle said.
Since 2020, Noelle has been a vocal advocate for Sanfilippo syndrome, using TikTok to share her family’s story. Her videos have reached a global audience, raising awareness about the disorder and encouraging other parents to seek early diagnosis for their children.
Although Logan’s future is uncertain, the Pacl family is committed to making the most of their time together. Noelle and William used to avoid thinking about what lies ahead, but now they focus on cherishing every moment with Logan and ensuring he enjoys his time to the fullest. Noelle notes that among Sanfilippo parents, there’s a bit of a joke that all their children seem like siblings, sharing similar features like bushy eyebrows, a low nasal bridge, and large, round stomachs.
Even with the demands of caring for Logan, Noelle keeps life as normal as possible for Logan’s siblings, Austin and Aidyn. She acknowledges that having a brother with special needs can bring its own set of benefits.
As for sharing Logan’s journey online, Noelle remains thoughtful about what she posts. While she plans to continue sharing, she’s careful to respect her family’s privacy. “We just live in the moment,” his mother said. “And if something comes up, and we’re like, we can make that, we’ll do it.”
People in comments react differently.
Mostly people express support and empathy.
- You take the most wonderful care of him. You are the greatest mom. © lauralang1108 / Instagram
But some show a bit of skepticism.
- Genuine question, what is your plan when you are gone? © devin_abq.505 / Instagram
- I just wanna know why it’s necessary. People have to publicize their children’s conditions. Why do people think that we all wanna know what’s wrong with your child? I feel sorry for the parents, but I don’t know why you want to put this all out there. I’m sure you have support group publicizing putting your child out there like this. © marlawomble / Instagram
Today, conversations about living with disabilities are becoming more open, especially on social media. Celebrities are sharing their experiences as parents of children with special needs, helping to normalize these discussions and inspire others. This shift fosters understanding and empathy, creating a more inclusive environment for everyone.
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