Fight Against DMD

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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.

10/21/2026

Behind every smile are fears I rarely speak about, tears I hold back, and a heart that’s still learning to carry it all.

I can’t change his diagnosis, no matter how much I wish I could. But if I could take away every struggle, every pain, every fear and carry it all for him, I would. A thousand times over.

Because more than anything, I just want him to have the happy, beautiful childhood he deserves. ❤️

Don’t say we didn’t warn you. ⚠️🤭�
10/17/2026

Don’t say we didn’t warn you. ⚠️🤭�

10/03/2026

Apparently, dreams come with sprinkles. 🍦✨ Thank you Footsteps School for capturing this little glimpse into Ibrahim’s imagination. 🤍

🍦✨

10/01/2026

What may look like a lot to the world is simply part of his everyday.

And through it all, he laughs. ❤️

Just Ibrahim, living his Thursday.

Fantastic Mr. Fox, ready for movie night. 🦊🎬Complete with his very own stolen chicken. 😂🐔          HopeForIbrahim
09/19/2026

Fantastic Mr. Fox, ready for movie night. 🦊🎬
Complete with his very own stolen chicken. 😂🐔

HopeForIbrahim

09/07/2026

“I’m Ibrahim. I have DMD, but I’m still strong.” ❤️🎈

This World Duchenne Awareness Day, we stand with the message: Access changes lives.

Access to care, treatment, support, education and opportunities can change the course of life for children living with Duchenne.

Today, we raise awareness for Ibrahim and for every child living with DMD. ❤️

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 😎💙

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. 💙

Address

5900, BALCONES Drive STE 100
Austin, TX
78731

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