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Twisha Needs True Primary Repair

Twisha Needs True Primary Repair

Twisha is little amazing girl and only child to her single Mother. She is born with very rare birth defect –LGOA means she is born with an incomplete Esophagus (a tube connecting mouth and stomach), hence unable to eat/feed by mouth since birth. Australian surgeons had put their great efforts in Twisha’s treatment to fix her problem; unfortunately she is not repaired yet. Twisha has undergone around 20 Major & Minor surgical procedures with no improvement in her birth condition. To live a normal quality of life she needs to go to Boston, USA for her further Medical Treatment, as there is no effective treatment available in Australia. For more information please visit www.twishamakwana.com & follow her Facebook page- “Twisha Needs True Primary Repair”Let’s Help Twisha. Mother is raising fund to pay for her medical treatment & relevant expenses in USA. If you would like to donate for her, Please go to this link:http://twishamakwana.com/donation.htmlPlease Donate!Thank you

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