Lama2 India

Ultra rare disease | No Cure | LAMA2 Congenital Muscular Dystrophy | Merosin Deficient CMD |
| muscle wasting disease | instead of muscle building, everyday child is loosing the muscle

🇮🇳 India has 1.4 billion people but we are connected with 60+ LAMA2 CMD families who once felt completely alone.

This video is not just content. It is a call for connection.

📢 If you are:
	•	A parent
	•	A doctor, geneticist, physiotherapist, or researcher
	•	A policymaker, advocate, or supporter of rare diseases
	•	Or someone who believes every child deserves a chance

👉 You are part of this journey.

🤝 How YOU can help:
	•	Share the videos
	•	Talk about LAMA2 CMD
	•	Connect families to us
	•	Help us find undiagnosed children
	•	Stand with rare disease parents who fight every single day

Because when awareness grows, hope follows.

📩 Connect with us:
👉 🌐 www.lama2india.com

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