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.

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۔ 💙

Some memories are beautiful… but they hurt a little too much.Sometimes I go back and watch his old videos…Sometimes I cl...
04/02/2026

Some memories are beautiful… but they hurt a little too much.

Sometimes I go back and watch his old videos…
Sometimes I close my eyes and try to remember how he looked when he used to walk.

But some days, that thought hurts a little too much.

So I remind myself — I have to be strong for him.
And truth is… he’s the strong one.

Once, we were passing by and I asked,
“Ibrahim, do you see the football statue?”
He immediately pointed towards it. That’s when I said,
“Oh wow, Ibrahim… you may be a great footballer someday.”

He smiled and said,
“No mommy… I can’t be a footballer because I can’t walk.”

For a second, my heart broke.
But then I said, “That’s okay… you’ll be an artist, because you’re already so amazing at drawing… and the way you build your little Lego worlds, maybe one day you’ll be an architect.”

And I know he will be. 🤍

There’s a quiet confidence in him when he learns like this—familiar space, gentle pace, and a whole lot of curiosity…onl...
03/26/2026

There’s a quiet confidence in him when he learns like this—
familiar space, gentle pace, and a whole lot of curiosity…
online classes might feel like a hassle for some,
but for Ibrahim, they bring comfort, accessibility,
and the freedom to learn in a way that feels right for him.
With DMD, that makes all the difference ✨

A little boy, a heart so strong,carrying more than most ever will…and still, a smile that feels like Eid 🤍Eid Mubarak fr...
03/22/2026

A little boy, a heart so strong,
carrying more than most ever will…
and still, a smile that feels like Eid 🤍
Eid Mubarak from Ibrahim ✨🌙

03/16/2026

Therapy disguised as play… and sometimes stretches too.

Behind the games and the stretches are quiet moments of courage.

For children living with Duchenne muscular dystrophy, these small routines help maintain strength, coordination, and mobility one step at a time.

And as parents, we learn that progress isn’t always loud or dramatic.Sometimes it’s simply a child realizing he’s a little braver than he was yesterday. 💛

We’ve all been down this past month—me, my daughter, and Ibrahim struggling to bounce back from a virus. And then he jus...
02/21/2026

We’ve all been down this past month—me, my daughter, and Ibrahim struggling to bounce back from a virus. And then he just laughs like this… and suddenly, everything feels lighter. That laugh is everything 🥹❤️

Every day with him is full of wonder and lessons. He teaches us to be brave, to celebrate the little things, and to love...
01/24/2026

Every day with him is full of wonder and lessons. He teaches us to be brave, to celebrate the little things, and to love without limits ✨❤️

01/13/2026

Today my heart broke and healed at the same time.
His first wheelchair… and look at him, laughing, screaming, flying.
I saw wheels. He saw freedom.
If happiness had a sound, it would be his laugh today. 💙🦽✨

Address

5900, BALCONES Drive STE 100
Austin, TX
78731

Alerts

Be the first to know and let us send you an email when Fight Against DMD posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Fight Against DMD:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram