Respected sir Dr Mansukh Mandaviya, Regarding Rare Diseases Policy, It's been a year. Still, Implementation is not at a good pace. CDFD's Lacks guidelines. Kindly please put special interest in this.They are so many people waiting for this policy. Thank you. Ministry of Health

Respected sir, Dr Mansukh Mandaviya As a parent of "Rare disease effected kid" requesting Office of Dr Mansukh Mandaviya Ministry of Health to please speed up the implementation process of rare disease policy . Thank you

I wish there were more services to support adults with Cystic Fibrosis. There are loads for Children With Cystic Fibrosis. Cystic fibrosis does not go away once adulthood has begun. #cysticfibrosis #disabledpersons please retweet this like crazy 🤣

If there's one thing you watch today, make it this. #LaverCup | Roger Federer

Hop cafes to discover new music.

Before giving your 100%, make sure you are giving it in a correct place.

⚠️THERMONUCLEAR BAD—Hospitals completely overwhelmed in China ever since restrictions dropped. Epidemiologist estimate >60% of 🇨🇳 & 10% of Earth’s population likely infected over next 90 days. Deaths likely in the millions—plural. This is just the start—🧵

CF patients in India has all rights to have access to the modulator.Vertex Pharmaceuticals and Ministry of Health Should look into it.Dailyhunt m.dailyhunt.in/news/india/eng…

Mallika Gollapudi Cipla Sun Pharma Lupin Ministry of Health Office of Dr Mansukh Mandaviya Cystic fibrosis patient in India are feeling very helpless as the new treatments are out of reach of the Indian patients. Please 🙏 help us.

Dr Mansukh Mandaviya Sir Please look for access of life saving drug Trikafta by Vertex Pharmaceuticals to Indian Patients of. Cystic Fibrosis. They have taken marketing permission and haven't launched the medicine in India. Also, Vertex set price so high that Indian patients can't afford Ministry of Health

No #cysticfibrosis patients should feel helpless when lifesaving drugs exist - but when Vertex Pharmaceuticals put profits before lives, this is the heartbreaking reality 😢 . #RightToBreathe #Trikafta4All #NoOneLeftBehind

Good news that these 35 children in #Ireland can now access #Kaftrio but CF Ireland also urge Vertex Pharmaceuticals to make their lifesaving drugs available to every patient in every country now, because we all know that #CFWontWait. #RightToBreathe #GlobalCFFamily #Kaftrio4All

MAY IS CYSTIC FIBROSIS AWARENESS MONTH! Please share & sign the petition! bit.ly/vsupetition #RightToBreathe #Trikafta4All #NoOneLeftBehind

We've just surpassed an incredible milestone of 100K signatures in our fight for accessible #CysticFibrosis drugs! 🎉 In the last 2 weeks alone, 40K voices joined us. Let's keep up the momentum! Sign & share to demand global access ✍️⬇️ actionnetwork.org/forms/cf-drugs… Vertex Save Us

⭐️ ⭐️ 100,000 signatures! ⭐️⭐️ Please continue to sign & share if you believe that every CF patient should have access to lifesaving drugs! #RightToBreathe #NoOneLeftBehind

‘Vertex is neither selling a new cystic fibrosis treatment in the developing world, nor allowing others to produce it; not only refusing to bring a life-raft to people drowning, but blocking others from deploying their own life-raft’ 😠💊👊 Sen. Bernie Sanders bit.ly/3Ge642g