Image by Dmitry Schemelev

“I had no roadmap, it was just love, and a lot of trial and error.”

That is what Cynthia said when she talked about her 24-year-old son, Devon, who is autistic and learning to live more independently.

When Devon turned 18, it didn’t magically get easier. In fact, Cynthia says the hardest part came after high school. When the structure dropped away, she realized there were fewer services… and more questions than answers.

She was not sure how to help him find work, socialize, or even keep up with daily tasks. She figured it out, but not all at once, and not perfectly.

She listened, learned, and stayed close, without hovering. Today, Devon is working part-time at a local animal rescue, where he found purpose and community.

Cynthia? She says, “I still walk beside him. I also let him walk ahead sometimes.”

[Source: Autism Parenting Magazine]

https://www.autismparentingmagazine.com/adult-autism-transition-strategies/

If you are parenting an adult child with neurodivergent, ADHD, dyslexia, or other neurodivergent needs, you probably feel like you are building the plane while flying it.

There is no manual to help you along the journey, but just love, worry, hope, and a lot of questions that keep you up at night.

Will my children ever be independent? Will they be safe? What happens when I am no longer here?

Maybe you find the hardest question to be

Am I doing enough?

This blog will not fix everything. However, it will give you five doable ways to support your adult neurodivergent child while honoring your limits, too.

You are not only parenting. You are also guiding, and you do not have to do everything by yourself.

You are not fixing your child.

You are helping them live a life that feels right for them.

If your children find something that lights them up, such as a rhythm that works or people who get them included, you will feel less like a lifeguard and more like a lighthouse.

Five Ways to Support Your Adult Neurodivergent Child

Image by Matthias Oberholzer

• Let Them Have a Voice in Their Life. Start with listening, then ask, “What do you want?” Even if they struggle to answer, keep asking gently. Please support them in making decisions, even small ones. Autonomy builds confidence. Guide, don’t control. Your child needs space to grow.
• Prioritize Practical Life Skills Over Fixing. Instead of focusing on what they can not do, build on what they can. Budgeting, hygiene, cooking, managing schedules… These are crucial. Devon could not manage a planner, but he could use Alexa to remind him about daily meds. That is a win.
• Connect, Do not Correct
  Many neurodivergent adults feel like they are always being managed. Flip the script, share interests, and watch your child’s favorite shows. You can even cook together, find joy in the connection, and not the correction. “I like being around you” means more than “You did that right.”
• Build a Circle (Not a Safety Net). You do not have to do it all by yourself. Find a therapist who gets it. Join a support group (online counts). Connect with other parents to help your child build safe adult friendships and mentors. You were not meant to carry this all yourself
• Do not Lose Yourself. This one is hard, but you matter too. You need joy and rest to refresh. You do not have to be on 24/7 to be a hero parent. Cynthia started painting again. She says, “It gave me something more than being a mom. Strangely, that made me a better one.”

Your Next Step as a Hero Parent

To support your adult child it does not mean solving everything.

It means you need to show up with love, curiosity, and some tools that work.

Here’s the plan:

• Pick one of the five areas.
• Make one small change this week.
• Celebrate the progress, no matter how tiny it feels.

You should know this is not a race. Your children need you as you are.

That makes you a hero.

You may not see it at the moment. One day, your child will look back and say, “I am where I am today because my parents never gave up on me.” With that? That is more than old

Do you know of any other ways to support a neurodivergent adult child? Please share them to support a parent.

Photo by CDC

“It felt like the floor dropped out from under me.“

That’s how Meghan Herbert described the moment she got the autism diagnosis for her son, Owen when he was two. She knew something was different about him. Hearing it from the doctor hit her like a wave.

“I wanted to run out of that room and pretend it didn’t happen,” she said in an interview with Today Parents.

She didn’t run, but got up, walked out and started learning.

Source: “Autism diagnosis: Mom opens up about the moment she learned her son was on the spectrum” — Today.com

https://www.today.com/parents/mom-autism-diagnosis-son-t251695

If you’re reading this, you may be standing where Meghan once stood. You’re stunned, overwhelmed, and a little scared.

Find your calm, everything will be okay. You don’t have to figure it all out in one day.

You are your children’s greatest hero. You need to save and care for them in the journey ahead.

7 Things Every Parent Needs to Hear When a Diagnosis Changes Everything

Image from Peter Burdon

1. This Is Not Your Fault

Kindly permit me to say that again ‘this is not your fault’. It is not because of something you did or didn’t do. Neurodivergence is not a punishment. It is a different wiring. Your child is still whole, worthy, and deeply loved.

2. Grief Is Normal, So Is Joy

It is okay to cry, to feel sad, and even feel lost. You had dreams and expectations, but this diagnosis has changed the path you imagined.

Guess what?

There will also be laughter and surprises ahead, wins that will make you dance in your kitchen. Give yourself space for both.

3. You Are the Hero of Your Child’s Journey

Doctors, psychologists, educators, and therapists are your partners, yet you are the constant. You have the right to ask questions, say no, and to choose what is best for your child. Don’t be afraid to trust your gut. It is powerful.

4. Labels Don’t Limit Potential

A diagnosis is a tool, not a box.It opens the door to support, but it does not define the future. Your child can grow, thrive, and soar in ways you can not yet imagine.

5. Build a Village (Even If It’s Small at First)

No one should walk this journey alone. Find a support group. Talk to another parent. Start with just one connection because one can lead to many. Even online spaces like ‘The Mighty’, ‘Autism Speaks’, or Facebook groups can become lifelines. Sometimes, your greatest strength comes from knowing you are not alone.

6. Progress Is Not Always Linear

There will be great days. There will be days when nothing seems to work. That’s not failure; it is part of the rhythm. Celebrate the small steps. They matter more than you know. Over time, they become the milestones that shape the journey.

7. Your Love is the Best Therapy

You do not need a PhD or all the answers. You just need to show up. Read the story, ‘sing that song, and hold that little hand’. That is the power of healing, and it is more than enough.

This is What an Expert Has to Say

Dr. Rick Solomon is a developmental and behavioral pediatrician and founder of ‘The PLAY Project’, he explains:

“The most powerful therapy is a loving parent. What neurodivergent children really need is engagement, joy, and connection and that can start at home.”

Dr. Rick Solomon, in an interview with Autism Parenting Magazine, Issue 125 (2022).

As a parent, is there something you wish you had known when your child was first diagnosed? Share your thoughts in the comments.

Citations:

1. Herbert, Meghan. “Mom opens up about the moment she learned her son was on the spectrum.” Today.com.

https://www.today.com/parents/mom-autism-diagnosis-son-t251695

Solomon Rick. “The PLAY Project: Why Parent-Led Therapy Works.” Autism Parenting Magazine, Issue 125, 2022.

https://www.autismparentingmagazine.com/the-play-project-therapy-autism/

Photo by Rajiv Perera

Martin Clavet didn’t plan for this kind of life. When his son Léonard was born with a rare genetic disorder, everything changed for Martin.

Léonard couldn’t walk nor talk. He needed a walker just to move around. He also has severe food allergies, and he couldn’t eat like other kids because he can’t chew.

Martin, like many parents of children with special needs, was thrust into a world he didn’t choose. One he had to learn to survive in, fast.

He remembers the early days. It makes him feel completely overwhelmed. He doesn’t know who to ask for help. Martin was afraid to show how much he was struggling.

“I wanted to be strong for my son,” he says, “but I was drowning.”

Luckily for him, he found a support group. It wasn’t a magical fix. For the first time, he felt belonged and seen. Other parents welcomed him in, not with judgment, but with empathy.

They swapped stories, shared resources, laughed and even cried together sometimes. The group made him realize that while his journey might be different, he no longer had to walk the journey by himself.

Martin Clavet words still echo loudly.

“You can be a normal parent, even when your child has special needs, especially when you have the right support network.“

(Source: [Naître et Grandir] http://naitreetgrandir.com/en/feature/kids-with-special-needs/

Are you rowing your boat alone?

Like Martin Clavet, before he found his support group, are you carrying more than anyone knows?

Doctor’s appointments, therapy sessions, school meetings, and etc. You might be trying to keep it together sometimes with a smile that hides the cry.

Somehow, you still do it every single day. Honestly, every hero needs support. It also takes a community to raise a child. You aren’t meant to do this alone.

Why Support Networks Matter

Photo by: Ochimax studio

The truth is no one understands your life like another special needs parent. Not your best friend, your sister. Not even your neighbor. Only that mom who gets it when you say, “He didn’t sleep last night.”

The dad who truly knows what it’s like to sit through another IEP meeting feeling invisible. These are the kind of people who understand you better.

When you find those people, everything will shift in a positive way.

They will remind you, you’re not on this journey alone. Isolation will fade when you have someone who listens without fixing.

They will hand you real-life tips. What school advocate to talk to. How to apply for benefits. They can recommend a therapist who can help.

They will celebrate the wins no one else will see. Like a full night’s sleep, your child is trying a new food or making it through a meltdown in public.

They will help you breathe again. This is because having someone say, “You’re doing an amazing job” at just the right moment can be everything.

You’re the Hero Parent.

You didn’t choose this path, however you’re walking it with courage. You advocate, nurture, and love beyond limits. Even the strongest heroes need allies.

Building a support network doesn’t mean you’re weak. It means you’re smart and wise. It means you want to show up fully for your child and for yourself.

Read What This Study Published in a Journal Says

A study published in the “Journal of Autism and Developmental Disorders“ found that support groups are instrumental in providing emotional relief and practical assistance.

“Support groups enable parents to share information with one another, such as information about therapies or new programs, stories and experiences of living with autism, and advice on how to deal with different professionals. They also allow parents to vent their frustrations and have their feelings validated and understood.”

Find Your Network

If you don’t know where to start, you can try here.

• Dubai Autism & Special Needs Parent Group (Facebook)
• CANDID (Children with Additional Needs and Disabilities In Dubai)
• Local parenting groups at children’s hospitals or community centers.
• Online groups like (Parent to Parent USA)
• Facebook communities with parents in similar situations.
• Talk to your child’s school or therapist they often know of groups nearby.

You can see how Martin’s journey proves that a support network can change a whole lot of things in a positive way.

Do you have a support network? Can you please share your experience with us in the comment section?

You deserve more than just survival mode

Photo by Sora Shimazaki

Wendy is a devoted mother, she faced the daunting journey of raising her son, who was diagnosed with autism. Managing the complexities of therapies, educational systems, and societal misunderstandings, she often found herself questioning every decision.

One pivotal moment was when Wendy had to advocate for a change in her son’s therapist. She realized that consistency and understanding were crucial for his development. This decision, though was challenging, but it underscored the importance of trusting her instincts and prioritizing her child’s needs.

Throughout her journey, Wendy emphasized the significance of self-care. She understands that to support her son effectively, she needs to ensure her well-being. Her story is a piece of evidence of the resilience and the challenges that parents of autistic children face daily.

Source: Norooz Clinic – Raising a Child Who is Living With Autism: Wendy’s Story

It struck a nerve because when you’re raising a child with special needs, exhaustion isn’t just physical. It’s emotional, mental, quiet, and constant.

Let’s pause for a second and ask about something important.

How have you been coping?

If your cup is always empty, how can you pour it into your child?

This is for you. Not as a reminder of your strength. But as an invitation to care for yourself as well.

Why Your Self-Care Isn’t Selfish

You’ve probably heard the phrase,“You can’t pour from an empty cup.”

But when your life revolves around therapies, appointments, IEP meetings, meltdowns, and long nights, self-care can feel like a luxury.

It’s not. It’s survival, restoration, and it’s how you keep going.

You are the hero parent, and the anchor in your child’s storm. Even anchors need maintenance.

These are Some Simple Self-Care Strategies That Work

• . Schedule 10-minute breathers.

Even just 10 minutes of stepping outside, deep breathing, or listening to your favorite song can reset your mind.

• Join a support circle

You don’t have to walk through this all by yourself. Virtual parent groups, Facebook communities, or local meetups can offer more than advice, they can offer you understanding and support.

• Ask for help without guilt

Tag in a friend, ask a neighbor. Or let your partner handle dinner. You’re not failing, you’re human.

• Sleep is sacred

You know sleep can be erratic. Even a few hours of rest can make a world of difference. Set boundaries, and let your body recover.

• Celebrate your wins, too

Your child’s progress matters, and so does yours. Did you stay calm during a meltdown? Did you advocate during an IEP? You’re growing, too.

You Are the Hero of This Story.

You’re a parent. You’re an educator, a therapist, a warrior, and a guide.

I don’t want you to forget, you’re a human being.

You deserve joy, rest, and to feel great again.

I want you to remember what Wendy discovered, sometimes the most powerful thing you can do is say, “I need care, too”.

Hear What a Clinical Psychologist and Researcher Has to Say.

Dr. Elisabeth Dykens, a Professor of Psychology and Human Development at Vanderbilt University, has extensively researched the stress experienced by parents of children with special needs.

In a 2019 conference presentation, she highlighted the critical role of self-care in mitigating this stress. Dr. Dykens emphasized that neglecting self-care can lead to increased anxiety and depression among parents, underscoring the necessity of prioritizing personal well-being to effectively support their children.

Today, I encourage you to pause for a moment and take a deep breath. When you care for yourself, you show your children how to care for themselves someday, too.

Do you have any strategy different from the ones mentioned? Kindly share with us in the comment section, let’s learn together.

Photo by RDNE Stock project:

A few years ago, Maya, a single mom of a boy with autism, found herself crying in the grocery store aisle. Her son had just had a meltdown over a broken snack package, and strangers stared. Some judged, while a few walked away. But one elderly woman didn’t. She looked Maya in the eye and said, “You’re doing great, mama. He’s learning.”

That simple moment changed Maya’s mindset. She wasn’t failing. Her son was learning. And learning is a journey, not a race.

That’s exactly what life skills are, learning moments we plant daily. When you have a child with special needs, these life lessons become even more precious. They build confidence, independence, and pride.

They create possibility.

Life Skills Will Help Your Child Build Confidence

Mind you, life skills will help prepare your child to face life challenges. The life skills will help boost your child’s confidence. Some of them could be as simple as buttoning a shirt, setting the table, recognizing emotions, or making simple choices.

These daily wins will empower your child with confidence.

The little wins will give them the ability to tackle a bigger challenge.

As a parent, you’re not only teaching your child skills. You’re nurturing self-worth.

The Unseen Side of the Journey

I would like to be honest with you, teaching life skills is not an easy task. It takes time, patience, repetition, and more patience.

At a point you may wonder, is this even working?

I encourage you not to give up on trying.

Do you know, it takes the Chinese bamboo tree five years to break through the ground?

For five long years, it will show no sign of growth above the soil. But beneath the surface, it’s building a deep and strong root system. It’s quietly preparing for a remarkable breakthrough.

Then, in just six weeks, it shoots up over 80 feet tall.

The question is, did the bamboo grow in six weeks or five years?

Teaching your child a life skill might be like germinating bamboo; your effort, consistency, and patience may not show results right away.

But that doesn’t mean growth is not happening. It’s building beneath the surface, strong, steady, unshakable.

Keep teaching, and believing. The breakthrough is coming.

The truth is, small steps lead to big wins.When your child learns to zip a jacket or wash a cup, it’s more than a task. It’s a confidence builder. Every time you pause to teach instead of rush to fix, you’re planting seeds of independence.

That’s heroic, you’re a hero parent.

You’re not failing, many parents feel overwhelmed. You’re carving a new path.

Are you worried about how to start?

You can always start small. Think simple, one task, one goal, and one success.

Here you have 3 practical ways to begin.

• Try to break tasks into tiny steps Instead of “clean your room,” start with “let’s put your toys in the bin.” Celebrate the effort, not perfection.
• Use visuals and routines. Children thrive on structure. Visual schedules and checklists are powerful tools that reduce stress and support learning.
• Model, practice, and praise Try to show it, do it together, and then let your child try. Make sure you praise progress always to encourage the child.

Always have this at the back of your mind, “It’s okay if it takes time, it’s okay if it’s messy“, that’s life and that’s learning. This will help you build your mental muscle for the stress.

What makes it all worth it?

The day your child will make a sandwich on his own, or will say “I can do it myself”. That’s where the magic lies.

You’re not only raising children, you’re raising future adults who believe in their own abilities.

Isn’t that a dream worth the try?

Here what an inclusive educator has to say

“Every student can learn, just not on the same day or in the same way.” — George Evans

Teaching life skills is more than perfection. It’s the connection. It’s showing up again and again, even when it’s hard.

You are your child’s first teacher and hero.

For every tiny win, that’s because you didn’t give up.

I encourage you today to give yourself credit. Take a deep breath, hug your child. Then teach one small skill with great love.

If you like this content, or you have a suggestion kindly share your thoughts with us in the comment section.

Last year, on April 30th, Mariah sat in her car outside the therapy center. She was watching her son through the glass window. He was flapping his hands with excitement while sorting puzzle pieces.

Tears filled her eyes, not because she was sad, but because the world had finally paused long enough to notice kids like hers. Autism Acceptance Month gave her hope. It gave her son visibility. It gave her community.

But when the banners came down, the hashtags stopped trending. The colors faded, she felt something many special needs parents do.

Does that feeling sound familiar?

If you’re raising a child with autism, April can feel like a warm hug from the world. But what about May? June? The rest of the year?

You should always remember you’re not just a parent. You’re a hero.

Even a teacher, especially if you’re homeschooling or walking through IEPs and therapies.

So how do you keep going strong even when the spotlight dims?

I would love to talk about how you, the hero in your child’s story can keep showing up with strength, strategy, and heart all year long.

5 Ways to Support Your Child Even After Acceptance Month Ends

• Make Sure Everyday Visibility Count

Autism Acceptance shouldn’t be seasonal. You can build awareness and education right from your home.

You can share your child’s strengths with family and friends.

Celebrate the small wins. That new word, that brave step, they matter.

Let your child be seen, heard, and valued daily. It starts with you modeling it.

When others see how much you value your child, it shifts how they respond.

• Make Sure You Create a Sensory-Safe Routine

Autistic children thrive in routines that make them feel safe. Keep those calming strategies you learned in April going strong.

Use visual schedules.

Make time for sensory breaks.

Choose learning tools that align with your child’s sensory preferences.

Don’t underestimate how structure reduces anxiety. This is not just for your child, but for you too.

• Stay Connected with Your Tribe

Your support system shouldn’t vanish after April.

Join online communities or local meetups for parents of children with autism.

Keep learning through books, blogs, and professional advice.

Most importantly, connect with other parents who get it.

The journey feels lighter when you don’t walk it alone.

• Try to Empower, Don’t Overpower

As your child grows, so should their sense of autonomy. This may look different for each child, but you should have a goal.

Help your children discover who they are, not just what they need.

Give them choices. Let them express opinions, even with visuals or assistive devices. That’s how confidence grows.

• Make Sure to Refill Your Cup

You cannot pour from an empty cup. Self-care isn’t selfish, it’s necessary.

Take mental breaks.

Don’t be shy to say yes to help.

Allow yourself to grieve, to laugh, and most importantly, to breathe.

You’re not failing when you rest. You’re preserving your power.

Hear What One Hero Parent Has to Say

Ehimwenma Bello-Osagie, an autism parent advocate and educational consultant in Nigeria, emphasizes the importance of year-round awareness and support. She believes that. Vanguard News

“Every special child has a special parent who must adapt to their unique world,” and stresses the need for early detection and consistent support to use the talents of children with autism effectively.

The Reason This Matters

The truth is, your child is autistic every month of the year. And your love, your patience, your advocacy, that’s the real acceptance they need most.

I, Prof. Sherley Louis, I see you. I stand with you. And I believe in your child’s full potential, not just in April, but always.

I encourage you to continue to build a world where inclusion isn’t just celebrated once a year.

But in every day, in every classroom, at every table, and in every heart.

Are you coming across our blog post for the first time?

Kindly share your comment on this post and follow us on our social media pages for more updates.

©Prof. Sherley Louis

Dear, Hero Parent

A father once talked about the first time he sat in an IEP meeting.

He walked into the room thinking it was just a check-in. But within minutes, papers were passed around, acronyms were flying, and a dozen professionals were speaking. None of whom had spent more than 10 minutes with his daughter.

This was a brand new language, he felt overwhelmed.

He left that meeting confused and frustrated. He mentioned it later, “I didn’t know, I am making the right decision.“

But something later changed everything.He had the choice to bring someone else, an advocate.

Not to speak for him.

But to help him speak up.

That’s what advocacy looks like.And it comes in different forms, each one is powerful.

If you’ve ever left an IEP meeting feeling lost or second guessing yourself, you’re not the only one. But you’re also not powerless.

Let me introduce you to three types of IEP advocates every parent with a child with special needs should know about.

• The Parent Advocate (That’s you, the hero).

You are your child’s first and most consistent voice.

The parent advocate prepares. Learn the law. Shows up with notes, questions, and clarity. You may not have a background in education, but you have something stronger. Lived experience.

When you understand your rights under IDEA, know your child’s strengths and needs, and lead with compassion, you can dictate the tone of the room.

Always remember, you belong at that table.

• The Professional Advocate.

Sometimes, we all need a guide.A trained IEP advocate can help you.

i. Review IEP documents

ii. Attend meetings with you

iii. Offer strategies when you’re hitting a wall

They won’t take over, they will empower you.

They remind you, you’re not crazy for pushing back.That your gut matters, and your voice counts.

You can find them through local nonprofits, school districts, or online advocacy networks.

• The Peer Advocate.

These are fellow parents who’ve walked the road you’re on.

They may not have certifications, but they have wisdom, heart, and stories. A peer advocate might text you encouragement before a big meeting. They’ll share what worked for their child, and what didn’t.

They will remind you that you’re not on this journey alone. And that’s sometimes the most powerful advocacy of all.

Hear What an Educational Consultant Has to say

Dr. Danielle Cohen, is an IEP advocate and educational consultant. She emphasizes the significance of collaboration between parents, educators, and school districts.

She advocates for individual educational plans, student’s specific requirements, to ensure they receive the necessary accommodations and services to thrive academically, socially, mentally, and behaviorally.

Advocacy is confrontation. It’s a connection.You’re not “that parent” for asking questions. You’re the right parent for your child.

No one knows your child like you do.But that doesn’t mean you have to do it all alone.

In every IEP room, you deserve support.You deserve to feel seen.And your children deserve a team that truly gets them.

So before your next meeting, take a breath.Reach out, and prepare for it.Always remember the hero in this story is you.

Here’s a bonus for you, download the PDF checklist version of the 3 IEP Advocates in the link below.

If you like this post, follow us on our social media handles to learn more.

Prof. Sherley Louis

They said your child couldn’t learn like others. They told you to look for alternative centers. But deep down, you know your child is special. Not just because of autism, but because of who they are.

And now, it’s Autism Acceptance Month. Everyone is posting gold ribbons. Sharing facts. Lighting up buildings.

But you want to do something real. Something that honors your child.

But the truth is, you don’t need the world’s permission to celebrate your child. You don’t need a big campaign. You only need a shift in how you see progress.

As a parent you feel left out during Autism Awareness Month. You see the stories online. Children speaking, performing, succeeding. You may wonder, “Why isn’t that my child?”

Yes, it’s natural to think that way but comparison can steal your joy. But your child’s journey is not late. It’s just different.

You might have cried, doubts, but you can also witness a breakthrough.

Like Leila and her son Omar, from The MENA region. At age four, Omar couldn’t sit for more than a few minutes. Meltdowns were part of every day. At the majlis, at family gatherings, even at home, Leila felt the stares and the silent judgment.

Someone told her, “Maybe just keep him at home.” But Leila refused.Leila created simple routines after Fajr. She used his favorite nasheeds to calm him.

She celebrated every peaceful moment, even two quiet minutes during Qur’an time. Then, one quiet afternoon, Omar came and sat beside her. He didn’t speak.

But he gently placed her hand on the book she was reading. That was his way of saying, “Mama, I’m ready.”

Today, Omar is learning to read Arabic slowly. He still flaps his hands when excited.But now, the family calls it his happy dance.

And Leila? She says that moment on the floor, his hand on hers was the beginning of everything. When you see your children differently, you will celebrate them differently.

These are ways you can truly celebrate your child this month.

• Start a “Wins” Journal – Write one thing your child did today that made you proud. Big or small. It could be a smile, eye contact, or a full meal.
• Learn Together – Read and learn one new thing with your children. Let them ask questions, be curious together.
• Speak about Life – Tell your child what you love about them. Be specific, be sincere, every day this month.
• Create a Celebration Ritual – It can be as simple as baking together. Lighting a candle. Saying a prayer of gratitude.

If it feels right, you can share your child’s progress in your community not for praise but to motivate other parents who might be struggling.

Don’t wait for the world to celebrate your child. Do it now. Do it daily. You are their loudest cheerleader and their super hero

This Autism Acceptance Month is special. It’s about love. And your child deserves to be loved.

I encourage you to make this month a reminder that your child is not only accepted, but loved by you. Moreso by the world he’s slowly beginning to shine in.

If you like this post, kindly drop us a comment and subscribe to our monthly Newsletter for updates and Insights.

©Prof. Sherley Louis