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Twisha is little unfortunate angel, 3 years 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. Twisha is fed via a Gastrostomy button on her
belly, which delivers her milk direct into her stomach. And to manage
her secretions, she has an Esophagostoma (an artificial opening of her
upper esophagus on right side of chest). To live a normal quality of
life she needs to go to Boston, USA for her further Medical Treatment.
Unfortunately In USA her treatment will occur in substantial amount of
money, which we are not able to cope with. We need financial help to
get Twisha to Boston, USA. For more information please visit
www.twishamakwana.com & follow her Facebook page- www.facebook.com/missiontwisha
Let’s Help Twisha. We are raising funds to pay for her medical
treatment & relevant expenses in USA. Twisha's treatment cost is
estimated to be 1.2M USD. 720K USD has been raised so far! If you
would like to donate for her, Please go to this web link to proceed
your contribution : http://www.twishamakwana.com/Donate.aspx
Please Donate!
"Ocean is created with every single
drop of water." Any size donation is highly appreciated.
Please keep Twisha in your prayers and share her cause in your
circle to expand needed help and support for her.
Thank you very much
Sweetie Makwana & Twisha's Mum
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