@helpkhyati
Fighting with SMA Type 1, FUNDRAISER LINKS Google Pay / Phone Pe: 9686451363
Donate through Milaap (80G Indian Tax Benefits + Overseas Donations accepted)
Donate through Milaap (80G Indian Tax Benefits + Overseas Donations accepted)
Donate through Go Fund Me
Donate through Go Fund Me
Donate through Give India (Indian, US, UK tax/Gift aid benefits)
Donate through Give India (Indian, US, UK tax/Gift aid benefits)
Donate through Impact Guru (80G Indian Tax Benefits)
Donate through Impact Guru (80G Indian Tax Benefits)
Overall Fundraising Status
Overall Fundraising Status
The New York Time Article about Khyati & SMA In India
The New York Time Article about Khyati & SMA In India
India makes many of the world’s drugs, but treatments for rare diseases like spinal muscular atrophy are imported and prohibitively costly. In desperation, parents are raising funds on social media.
NDTV News About Khyati
NDTV News About Khyati
A 10-month-old in Bengaluru, Karnataka, is fighting for her life as she waits for a medicine that costs a whopping Rs 16 crore. Diagnosed with Spinal Muscular Atrophy, type 1, the child, Khyati, needs the medicine for gene therapy before she turns 2.
The News Minute Article on SMA and Zolgensma
The News Minute Article on SMA and Zolgensma
Khyati was four months old when her parents suspected something was wrong. She was not able to lift her head up, a typical milestone for infants her age. A mont
Learn more about Khyati's story through a webpage
Learn more about Khyati's story through a webpage
BBC News
BBC News
"మాది మిడిల్ క్లాస్ ఫ్యామిలీ. నేను జీవితాంతం పని చేసినా కోటి రూపాయలు చూడలేను. అలాంటిది 23 కోట్ల రూపాయలు అంటే ఏం చేయాలో కూడా తెలియడం లేదు. ఇప్పటీ వరకూ 3 వేల మందికి పైగా దాతల సాయంతో కోటి ఇరవై లక్షల రూపాయలు సమకూరాయి. కానీ అది సరిపోదు. పాప ప్రాణాలు నిలబడాలంటే మా స్తోమత సరిపోదు"
@possiabilities Story (English)
@possiabilities Story (English)
@helpkhyati Facebook
@helpkhyati Facebook
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@helpkhyati Instagram
@helpkhyati YouTube
@helpkhyati YouTube
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