Fight Against DMD

Fight Against DMD Dedicated to our brave son, Ibrahim, who is battling Duchenne Muscular Dystrophy — a rare and progressive genetic disorder.

Our mission is to raise awareness, share Ibrahim’s journey, and gather support for his ongoing medical treatment.

Proof that Ibbu has been given far too much access to my camera roll. 😂📸[cue suspicious background music] 🎶
08/31/2026

Proof that Ibbu has been given far too much access to my camera roll. 😂📸
[cue suspicious background music] 🎶

His version of childhood = kinda chic 😎💙
08/23/2026

His version of childhood = kinda chic 😎💙

08/19/2026

This is Ibrahim’s normal. 💙

Getting to school means a transfer from the car, settling into his wheelchair, and then heading through those gates.

It’s part of his routine, but it still takes strength — the kind you don’t always see. 💙

Ibrahim really wanted to do everything this Independence Day. 😂🇵🇰💚The snow cone, the fireworks, buying flags, getting hi...
08/13/2026

Ibrahim really wanted to do everything this Independence Day. 😂🇵🇰💚

The snow cone, the fireworks, buying flags, getting his baaja 📯, having the Pakistani flag painted on his face 🇵🇰 and, of course, a stop at the photo booth with Mama. He wore green to school and then came home and changed into another green shirt because apparently one green outfit wasn’t enough. 😂💚

He was so excited about every little part of the celebrations, and watching him enjoy it all made me so happy.

But that loud and very enthusiastic “Pakistan Zindabad!” might just have been my favourite part of the whole day. 🥹🇵🇰

Happy Independence Day, Pakistan — love, your very excited little Ibrahim. 🇵🇰💚✨

🇵🇰

Ibrahim really wanted to do everything this Independence Day. 😂🇵🇰💚The snow cone, the fireworks, buying flags, getting hi...
08/13/2026

Ibrahim really wanted to do everything this Independence Day. 😂🇵🇰💚

The snow cone, the fireworks, buying flags, getting his baaja 📯, having the Pakistani flag painted on his face 🇵🇰 and, of course, a stop at the photo booth with Mama. He wore green to school and then came home and changed into another green shirt because apparently one green outfit wasn’t enough. 😂💚

He was so excited about every little part of the celebrations, and watching him enjoy it all made me so happy.

But that loud and very enthusiastic “Pakistan Zindabad!” might just have been my favourite part of the whole day. 🥹🇵🇰

Happy Independence Day, Pakistan — love, your very excited little Ibrahim. 🇵🇰💚✨

08/01/2026

If you’ve been here for a while, you already know… Ibrahim loves a good joke. 😂💙

This time, he didn’t even let me finish guessing.

“A frostbite!” 🐊❄️

Before Ibrahim, I never understood genetics, chromosomes, or why Duchenne mostly affects boys.Now I find myself learning...
05/13/2026

Before Ibrahim, I never understood genetics, chromosomes, or why Duchenne mostly affects boys.

Now I find myself learning about things I never imagined — just to better understand my child and the condition he lives with every single day.

Awareness starts with understanding. 💙

Sometimes awareness means talking about the parts people do not see.The disease.The treatment.And the battles children q...
05/06/2026

Sometimes awareness means talking about the parts people do not see.

The disease.
The treatment.
And the battles children quietly carry through both. 💙

This morning, I was honestly very anxious.Making a passport in Pakistan used to feel like such a big hassle, and I kept ...
04/09/2026

This morning, I was honestly very anxious.

Making a passport in Pakistan used to feel like such a big hassle, and I kept wondering how we would manage everything with Ibrahim — the crowds, the waiting, the accessibility. It felt overwhelming before we even left home.

But our visit to the Executive Passport Office, Clifton, Karachi turned out to be such a positive and smooth experience. ♿✨

Ibrahim was given priority due to his disability, stayed comfortably in his wheelchair, and they even took his photo while he remained seated. The entire process was completed in hardly 20 minutes, which honestly surprised us.

There was a ramp available — though it was quite steep — but the staff immediately stepped in to help us safely take Ibrahim up and down. A special thank you to the AD, who was extremely kind and supportive throughout.

Grateful for systems that are improving, and for people who make accessibility feel real. Moments like these reduce so much anxiety for families like ours. 💙

Muscular dystrophy is a genetic condition that leads to progressive muscle weakness, affecting movement, breathing, and ...
04/06/2026

Muscular dystrophy is a genetic condition that leads to progressive muscle weakness, affecting movement, breathing, and overall strength over time.

For us, this journey has a name—Ibrahim. 💙
Through every challenge, he shows us what true resilience looks like.

Raising awareness isn’t just about information—it’s about understanding, support, and hope for better treatments in the future.

Every step he takes is a reminder: strength isn’t just physical, it’s in courage, patience, and love.

مسکیولر ڈسٹروفی ایک جینیاتی بیماری ہے جو وقت کے ساتھ پٹھوں کو کمزور کرتی جاتی ہے۔
ابراہیم کی ہمت ہمیں ہر روز سکھاتی ہے کہ اصل طاقت حوصلے اور صبر میں ہوتی ہے۔ 💙

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5900, BALCONES Drive STE 100
Austin, TX
78731

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+12062037424

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