Living in today’s world, it can be simple to forget about an important occasion like a loved one’s birthday. The fast-paced nature of life, unforeseen circumstances, or even just not remembering can cause us to miss out on commemorating an important day.
Although the birthday may have already passed, it’s never too late to make amends and show your sincerest belated wishes. In this article, we’ll explore how to express your feelings with truthfulness, personalization, and affection.
To begin, you must acknowledge that you missed their special day, but emphasize that it doesn’t diminish its importance in your heart. A heartfelt belated wish can mean just as much as an on-time one, so don’t let lateness prevent you from reaching out.
Think about what makes your relationship with the person unique and use those details to craft a thoughtful message that reflects your shared experiences, inside jokes, or precious memories. Adding a personal touch to your belated birthday wishes shows that you’ve taken the time to reflect on your bond and make your message special.
Choosing the right medium to convey your message is also essential. A handwritten letter or a carefully selected card can serve as tangible keepsakes, while a heartfelt video message adds a personal touch. The medium you select should align with your style and the recipient’s preferences.
Make sure your belated birthday wishes are genuine and express real regret for the delay. Let the person know that they matter to you and that you hold them dear, even if you didn’t acknowledge their special day on time. Your sincerity and the warmth of your words can help make up for the late wishes.
Turn your belated birthday wishes into an opportunity to highlight the positives. Celebrate their achievements, their impact on your life, or the joy they bring to those around them. Remind them of their significance and why they are so special to you. This positive reinforcement can turn a belated wish into a heartfelt celebration.
If possible, plan a special get-together or activity to compensate for the delay. This demonstrates your commitment to creating lasting memories, even if it’s slightly delayed. It shows that you’re willing to make amends and celebrate their special day in a memorable way.
A little bit of humor can also go a long way. Consider adding a well-placed joke or witty comment to your belated birthday wishes to make the person smile and lessen any disappointment from the late wishes. It shows that you can laugh at yourself, and the relationship is strong enough to handle a little lateness.
If you choose to send a gift along with your belated birthday wishes, think about the person’s interests and preferences. A thoughtful gift can show that you’ve put thought and effort into selecting something meaningful. Let this be an opportunity to make up for the late wishes and show that you care.
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.
Leave a Reply