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DU Centre Moves to Support Faculty Member’s Child’s SMA Treatment

DU Centre Moves to Support Faculty Member’s Child’s SMA Treatment
DU’s SOL steps in to support treatment of faculty member’s child with rare genetic disorder · theprint.in

A child of a University of Delhi faculty member has a rare illness called SMA Type 2.

The child needs treatment that includes gene therapy.

The university’s Centre for Distance and Online Education has started steps to help arrange financial support.

A committee with senior doctors from AIIMS is reviewing the case and how funds could be provided.

The statement says this illness is not covered by the Central Government Health Scheme panel.

People including colleagues and family members have raised about Rs 1 crore through crowdfunding.

That is only about 6.25 per cent of the expected treatment cost.

The association says money collected for the child will be used only for her treatment and welfare.

Key facts

Condition
Spinal Muscular Atrophy (SMA) Type 2
University centre
University of Delhi’s Centre for Distance and Online Education
Committee
Includes experts and senior doctors from AIIMS
Crowdfunding raised
Around Rs 1 crore over the past few months
Share of expected cost raised
Around 6.25 per cent
Coverage noted
The statement said such diseases are not covered under the Central Government Health Scheme panel
Use of collected funds
Exclusively for the child’s treatment and welfare, according to the statement

Quotes

Kancharkuntla Praveen Reddy

President of the Centre for Distance and Online Teachers’ Association

“This situation has brought the teachers who think alike together.”
theprint.in

Sources

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