Iama2cmdindia

15/05/2026

Are you a paediatric physiotherapist, contact us please

22/04/2026

Rare diseases are usually discussed in terms of diagnosis.

On April 24, please join us in the International Forum “Rare Women” – a global conversation hosted in Russia and streamed in English.

For the first time, the focus shifts from the child’s condition to the person who holds everything together: the . Because behind every treatment pathway, every decision, every outcome – there is her.

This year’s theme is vitality – the inner strength that allows women to keep going, support their children, and stay present in their own lives.

Together with speakers from different countries, we’ll explore:
– how women sustain themselves under constant pressure
– how they become true partners in treatment
– what changes internally when life is reshaped by a rare diagnosis
– and where the strength to continue actually comes from

This is not a medical discussion, it’s a shift in perspective.
Join us to listen, reflect, and be part of a growing international dialogue.
📍 April 24 | 10:00–18:00 (GMT +3)
📍 Online | registration required
📍 English broadcast available
https://lnkd.in/gqSZT-rh

20/02/2026

31/01/2026

👉 Raise awareness | Start conversations | Support research 🤝

Because awareness is the first step toward a cure.😇

21/01/2026

A family | A big belief | A future we are fighting for 💫
When family comes together, your power multiplies 🫶🏻

It was Ishika’s 2nd birthday and happiness was truly all around✨

I don’t know what the future holds, but aaj bahut acha hai and kal aur bhi acha hoga. Hope is stronger when it’s shared.

On this special day, my family came together to record this video in support of LAMA2 Muscular Dystrophy.

This is not just a video—it’s love, belief, and a promise to keep going 🙏🏻😇