Precious d-sickle cell warrior TV

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philanthropist and content creator
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Let's teach, inspire and entertain you with interesting content
Sicklecell cell advocates awareness , health
Sicklecell warrior

TESTIMONY - HIV/AIDS*😭😭😭Tears of Joy streaming down my face as I share this testimony about this wonderful health breakt...
05/28/2026

TESTIMONY - HIV/AIDS*
😭😭😭Tears of Joy streaming down my face as I share this testimony about this wonderful health breakthrough, the latest technology in the field of health called

Riboceine
I am a Max Associate
I have been challenged with HIV/AIDS for over 22 years now and have been on drugs during all those years. My medical case has been managed at our local Teaching Hospital.

I was introduced to Max International by my Doctor and started using CELLGEVITY.

I started taking CELLGEVITY 2 capsules in the morning and 2 in the evening, at a point, I broke down and I thought my end has come,

I called my Doctor and after due consultations with the medical team, I was advised to increase the dosage from 2/2 daily to 4/4 daily because of the seriousness of my case,

in fact, it was a bad medical case, people thought I will not see the end of the year. Thank God, I'm alive to testify today.

After being on Cellgevity for 5 months, I got the beautiful call from my Doctor telling me that my HIV viral load that was 17,954 before I started using Cellgevity

has dropped to total Zero viral load....Pls help me give glory to God Almighty for using Cellgevity to wipe away my tears
Thank you my Doctor who introduced
CELLGEVITY to me. Thank you too, our Max family, Love you all. ✅👌

What are you waiting for place order now and thank me later WhatsApp or call ☎️ 08103531584/ 0810 353 1584




















✨ To every child fighting sickle cell with a smile despite the pain… you are the true definition of strength. 💛This Chil...
05/27/2026

✨ To every child fighting sickle cell with a smile despite the pain… you are the true definition of strength. 💛

This Children’s Day and Eid, we celebrate our little warriors who keep shining no matter the battles they face. 🌙🎉
May Allah bring healing, happiness, protection, and endless joy to every sickle cell warrior around the world. ❤️

Keep fighting. Keep dreaming. Keep believing. Your story is inspiring more people than you know. 🩸💪

Happy Children’s Day & Eid Mubarak to all Sickle Cell Warriors! 🌟❤️















4 Years Later, The Pain Still Feels Like Yesterday The Day Sickle Cell Took Both My Legs💔😭😭It has been 4 years since sic...
05/26/2026

4 Years Later, The Pain Still Feels Like Yesterday The Day Sickle Cell Took Both My Legs💔😭😭

It has been 4 years since sickle cell leg ulcer made me lose both of my legs, yet it still feels like yesterday.

The pain
The fear
The endless hospital visits
The trauma of going through surgery three different times…
The shock of waking up and realizing my life would never be the same again…

Some days, I still replay that very moment in my head.
Some days, I still cry silently.
Some days, I smile outside while fighting battles nobody can see inside.

People think healing only means the body recovering, but they don’t understand the emotional wounds that remain long after the scars close.

I may have lost my legs, but I have not lost my will to live.
I am still here.
Still breathing.
Still fighting.
Still hoping.

And even though the trauma still feels fresh, I believe one day I will heal completely — physically, emotionally, and mentally.

Maybe not today…
Maybe not tomorrow…
But with time, I will find peace again. ❤️

To everyone fighting invisible battles: please don’t give up on yourself.
Your pain is valid.
Your story matters.
And your survival is already a miracle.💔🥲

゚viralシ

05/25/2026

Strong blood, stronger heart.

75 Years of Pain, Needles, Wheelchairs… Yet I Am Still Here😭😭😭💔💔💔💔At 75 years old, I never imagined my life would become...
05/24/2026

75 Years of Pain, Needles, Wheelchairs… Yet I Am Still Here😭😭😭💔💔💔💔

At 75 years old, I never imagined my life would become a daily battle between pain and survival.

I was born with sickle cell thalassemia, and for decades my body has carried wounds nobody can truly see. The disease has stolen so much from me — my strength, my eyesight, my bones, my freedom to walk, and sometimes even my hope.

The retinopathy affected my eyes.
The AVN damaged my bones.
Multiple bone infarcts left unbearable pain deep inside my body.
And the pain crises… those never seem to end.

There are days I cry quietly because even getting out of bed feels like climbing a mountain. I cannot walk without a wheelchair anymore. Watching others move freely while I struggle with every little movement breaks my heart in ways words cannot explain.

People see an old person in a wheelchair, but they do not see the lifetime of hospital visits, blood transfusions, sleepless nights, injections, medications, and silent tears.

For 75 years, I have fought a disease that never sleeps.

Sometimes I ask myself:
“How much more can one body endure?”

But despite everything, I am still here.
Still breathing.
Still surviving.
Still holding onto faith.

If you are reading this, please be kind to people fighting invisible battles. Some smiles are hiding unbearable pain.

And to every sickle cell warrior out there — young or old — your story matters, your pain is real, and your survival is a testimony.

゚viralシ

We Went for a Routine Blood Exchange… But My 11-Year-Old Son Came Back paralyzed by stroke 💔My son is just 11 years old....
05/22/2026

We Went for a Routine Blood Exchange… But My 11-Year-Old Son Came Back paralyzed by stroke 💔

My son is just 11 years old.
An innocent child who has suffered more pain than most adults can ever imagine because of sickle cell.

Every 6 weeks, we go to the hospital for his blood exchange treatment. We follow every instruction from the doctors because we only want one thing — for our son to live a normal life.

That day felt like every other hospital visit.
We prayed, packed his clothes, and encouraged him like always.

“Mommy, will I be fine?” he asked softly.

I smiled even though my heart was heavy.
“Yes my baby, you’ll be okay.”

But few hours after the blood exchange, everything changed.

My son suddenly couldn’t move properly. His speech became weak. His little body started acting strangely. The doctors rushed around him while I stood there shaking and confused.

Then I heard the word no parent ever wants to hear…

“Your son is having a stroke.”

Stroke?
My 11-year-old child?

At that moment, my world collapsed.

I watched my son lying helpless on the hospital bed, struggling to talk, struggling to move, while machines surrounded him. The same child who was smiling before the procedure was now fighting for his life.

People don’t understand the silent battles sickle cell patients go through.
The endless hospital visits.
The sleepless nights.
The fear parents carry every single day.

Sometimes we smile outside, but inside we are breaking.

Seeing your child in pain and not being able to take that pain away is a different kind of heartbreak.

Please, if you are reading this, say a prayer for my son.
Pray for every sickle cell warrior battling silently.
And pray for parents like us who are trying to stay strong even when our hearts are shattered.

Sickle cell is not just a condition.
It is a lifetime battle. 💔

゚viralシ

05/21/2026

Stigma that comes with being a sickle cell patient 💔 #

Both My Son and His Fiancée Are AS… I Begged Them Not to Marry, But The Wedding Invitation Is Already Out 💔😭😭😭😭😔😔I am a ...
05/21/2026

Both My Son and His Fiancée Are AS… I Begged Them Not to Marry, But The Wedding Invitation Is Already Out 💔😭😭😭😭😔😔

I am a 58-year-old widow from Nigeria. My only son is preparing to get married to the woman he loves. But there is one painful issue disturbing my heart day and night…

Both my son and his fiancée are AS.

As a mother, I have begged them countless times not to go ahead with the marriage because I know the pain sickle cell disease brings to families and innocent children. I have cried, prayed, and pleaded with them to reconsider. But my son said they truly love each other and cannot separate because of genotype.

Now their wedding invitation cards are already out, and the wedding is fast approaching.

Honestly, my heart is heavy. I don’t want future children to suffer. I don’t want them to face pain, hospital visits, blood transfusions, and emotional trauma later in life.

But at the same time, I don’t want to lose my son because he feels I am against his happiness.

Nigerians, please advise me like a mother.
Should I continue to oppose the marriage?
Or should I allow them make their own decision and pray for the best?

Please, I will be reading the comments. 💔😭




















05/21/2026

Living with sickle cell, fighting with courage every day.✌️

05/20/2026

Awareness saves lives. Know your genotype👍
To avoid 👇👇

05/20/2026

God is so faithful in my life over 7 years without no blood 🩸 transfusion as a sicklecell patient 🎉🎉💃💃💃💃

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6030 Bathurst Street
Toronto, ON
M2R1Z9

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