The Wishing Factory

The Wishing Factory Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from The Wishing Factory, Charitable organisation, 5 GF, Hind Industrial Estate B/H Hotel Parkway, Dadar West, Shivaji Park, Mumbai.

The Wishing Factory is an ISO certified (ISO 9001:2015) not-for-profit organisation dedicated to improving and enriching the lives of underprivileged Thalassemia ‘Warriors’ in India.

Yeh toh bas woh hai jo nazar aata hai…Asli kahaani toh aur gehri hai...The visible deformities are only one part of thal...
04/08/2026

Yeh toh bas woh hai jo nazar aata hai…
Asli kahaani toh aur gehri hai...

The visible deformities are only one part of thalassemia.
Behind them lies a lifetime of transfusions, challenges, and silent battles.

Every beat comes at a cost.

Swipe through to understand the cause behind each change.


Not all heroes wear capes. Some wear quiet smiles, steady hands, and show up every single day without asking for recogni...
01/08/2026

Not all heroes wear capes. Some wear quiet smiles, steady hands, and show up every single day without asking for recognition.

Surta Ram Ji wasn’t just part of the journey, he was the comfort, the trust, and the constant behind it.

Years of care, countless lives touched, and a presence that can’t really be replaced… only deeply missed.

Retirement isn’t an end here, it’s just a pause on a legacy that will keep living in every warrior he’s cared for.

Meet Yuvraj.A 13-year-old who loves flying kites, exploring new things, and spending every chance he gets outdoors.Stand...
31/07/2026

Meet Yuvraj.

A 13-year-old who loves flying kites, exploring new things, and spending every chance he gets outdoors.
Standing beside him through it all is his elder sister, Manasi.

Most siblings fight over the TV remote. Yuvraj and Manasi share something far bigger. Hospital corridors. Blood transfusion days. And a courage no child should ever have to learn so young.

From Poincha, a temple town about 50 km from Vadodara, the siblings travel with their parents every few weeks to receive their blood transfusions, often on the same day.

Their journey also highlights why early diagnosis matters.
Manasi was diagnosed with thalassemia intermedia only at the age of five. By then, Yuvraj had already been born. Without timely awareness or genetic counselling, the family never had the opportunity to understand the condition early enough.

Both siblings were initially diagnosed with thalassemia intermedia, requiring only intermittent transfusions. As their blood requirements increased, they were later diagnosed with beta thalassemia major. Today, they receive regular blood transfusions and lifelong chelation therapy together.

Their story reflects the reality of many families in rural India, where delayed diagnosis and limited awareness continue to change lives. Sometimes, delayed diagnosis doesn't change just one life. It changes an entire family's story.


A simple question. A common myth.Can thalassemia carriers donate blood?The answer isn't a straight yes or no—it depends ...
30/07/2026

A simple question. A common myth.

Can thalassemia carriers donate blood?

The answer isn't a straight yes or no—it depends on your health and the blood bank's screening.

Swipe through to understand the facts, bust the myth, and share this with someone who might have the same question.

Because awareness saves lives just as much as blood does. 🩸

The poster is from 2022. But the message is still relevant.If you're planning a family, ask about HPLC screening.If you'...
27/07/2026

The poster is from 2022.
But the message is still relevant.

If you're planning a family, ask about HPLC screening.
If you're a healthcare professional, help make that conversation routine.

Because prevention begins with one question!

Meet Romik Patel.Before Romik was born, his parents had already lost their eldest daughter to thalassemia at just two ye...
24/07/2026

Meet Romik Patel.

Before Romik was born, his parents had already lost their eldest daughter to thalassemia at just two years of age. Like any family, they hoped their next child would be different.

But when Romik was born in 1994, he too was diagnosed with thalassemia major.

Many people believe that if one child is born with thalassemia, the next won't be. In reality, genetics doesn't work that way. When both parents are thalassemia carriers, every pregnancy carries a fresh 25% chance of a child being born with thalassemia major. The probability resets each time, regardless of previous pregnancies.

Romik's story is a reminder that these aren't "one in four children" across a family. They're one in four chances with every pregnancy.

Growing up in Awakhal, Romik never let his diagnosis define his future. Starting with a small mobile repair shop, he adapted with time and now runs a stationery, photocopy, and electrical supplies business, serving his community with quiet determination and resilience.

Today, Romik's journey reminds us that while we can't change genetics, we can change outcomes through awareness, carrier screening, and timely diagnosis.

Because every informed decision has the power to change a family's story.


If you’re looking for beautifully handcrafted Rakhis that carry meaning beyond just a thread, this is your stop. 💛Made b...
21/07/2026

If you’re looking for beautifully handcrafted Rakhis that carry meaning beyond just a thread, this is your stop. 💛

Made by Hiral Shah - a Thalassemia warrior herself, each Rakhi reflects strength, resilience, and heart. Despite her own journey, she continues to support fellow warriors by contributing a part of the proceeds towards their care and wellness. ✨

This Raksha Bandhan, celebrate your bond while becoming a reason for someone else’s smile.

To order, reach out to Hiral on her Instagram ID.

An empty desk.An empty spot on the field.For a Thalassemia Warrior, life pauses every 15 days for a blood transfusion.So...
20/07/2026

An empty desk.
An empty spot on the field.

For a Thalassemia Warrior, life pauses every 15 days for a blood transfusion.

Some make it back. Some leave behind spaces that can never be filled.

Your blood donation can help change that story.

Donate blood. Save lives.

Meet Kana. Her birth name is Lish*ta, but everyone lovingly calls her Kana.She is five years old, loves playing with her...
17/07/2026

Meet Kana.

Her birth name is Lish*ta, but everyone lovingly calls her Kana.

She is five years old, loves playing with her kitchen set, and her favourite meal is bhindi ki sabzi with mag bhat.

Kana is the youngest of five daughters. The eldest is healthy, one sister was born prematurely and sadly passed away, another lost her battle with thalassemia at just two years old, and during another pregnancy, prenatal testing revealed thalassemia major, leading the family to make the difficult decision to undergo a medical termination of pregnancy.

When Kana's mother became pregnant again, her family was reassured that everything was normal. However, Kana's condition was not identified during pregnancy, and after she was born, she was diagnosed with thalassemia major.

Today, her father, a rickshaw driver, works tirelessly to support her treatment. Yet, Kana continues to smile, play, and dream like every five-year-old should.

Her story reminds us that timely screening, accurate diagnosis, and greater awareness can change lives.
Because every child deserves the chance to grow, dream, and simply be a child.💙


How often do we stop at the first diagnosis?When a child is diagnosed with severe anemia, the immediate focus is natural...
15/07/2026

How often do we stop at the first diagnosis?

When a child is diagnosed with severe anemia, the immediate focus is naturally on treatment. But what if treatment is only one part of the conversation? What if the more important question is the one we haven't asked yet?

Not every case of severe anemia has the same underlying cause. While iron deficiency is one of the most common reasons, some children may be living with inherited blood disorders like thalassemia that require further investigation. Without timely testing and the right diagnosis, that possibility can remain hidden.

This isn't about questioning doctors or replacing one diagnosis with another.
It's about asking whether we're looking closely enough.

When severe anemia appears on a report, should we also ask what lies beneath it? Could earlier investigations lead to earlier diagnosis, stronger screening, and better preventive care?

Maybe the answer isn't always more treatment.
Maybe it's one more question.
Could it be more than anemia?

What do you think? Is this a conversation we should be having more often? We'd love to hear your thoughts.

Address

5 GF, Hind Industrial Estate B/H Hotel Parkway, Dadar West, Shivaji Park
Mumbai
400028

Opening Hours

Monday 10am - 6pm
Tuesday 10am - 6pm
Wednesday 10am - 6pm
Thursday 10am - 6pm
Friday 10am - 6pm
Saturday 10am - 6pm

Telephone

8448449544

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