Help Khayti, a beautiful little girl was born scorching through the covid-19 pandemic. Her parents were extremely delighted to hold their newborn in their arms. But, Khayti’s ill fate doesn’t allow her to even move an inch without someone’s help.
Khayti is suffering from Spinal Muscular Atrophy- Type 1. Doctor’s said diagnosis on 17th february, earlier this year, shattered the hearts of Khayti’s Parents into million pieces.
Spinal muscular atrophy (SMA) is an inherited disease that affects nerves and muscles, causing muscles to become increasingly weak. It usually affects the infants. It can lead to death. SMA-1 is a fatal disease.Due to SMA-1, Khyati cannot breathe, the most important function of any human to survive! This adorable girl needs to be on oxygen support (bi-pap) for a minimum of 18 hours each day. She cannot lift her neck to swallow her own spit. She cannot have food or move her arms to reach out to her favorite toys.
The Doctors from Bangalore Baptist hospital informed Khyati’s Parents, “SMA-1 treatment should be done before she turns 2.” This infant has faced multiple problems uptil now. But, there’s a silver lining. There’s a cure for Khyati’s grave illness. Through Gene therapy, Khyati can lead a normal life; Zolgensma, the world’s most expensive medicine exported from the US, can save Khyati’s life. One shot of this drug can keep khyati a new life.
But, the last hurdle that Khyati needs to jump across is the cost of Zolgensma. This Medicine costs a whopping $2,168,188 USD For the middle class family of Nagumantri, it’s difficult to collect such huge amount of money. But, With your Generous Donations, Khyati has been able to raise $2,138,188 USD. Surely, another $30000 USD can help her afford treatment.
Will you join hands and help her reach Zolgensma?
Direct Bank Transfer:
K Dinesh Kumar
Adyar branch, Chennai, Tamilnadu, India
Account No: 918010017092327
IFSC CODE : UTIB0000082
MICR code : 600211006
BIC Code (Swift) : AXISINBB