Save Our Twisha
Update: https://www.gofundme.com/surgery-for-twisha
I am Twisha, 3 years old girl, born in Sydney, Australia. I was born with very rare birth defect called Long Gap Esophageal Atresia, which means I was born with an incomplete Esophagus, hence I am unable to eat by my mouth. I have already undergone around 20 various (Major & Minor) surgeries in Sydney, Australia, with no success to cure my condition.
Where there is no Cure,
There is Hope.
Where there is Hope,
There are Miracles!
I can be cured, if I am taken to Children's Hospital Boston, MA, USA. But my treatment cost is around $1.2M USD! My mum, Sweety Makwana is trying to raise the funds needed for my treatment so that I can eat by mouth one day. My dad left me and my mum, when I was only 5 months of age. And he never come back to see me. Now, my Mum is my Dad; like 2 in1!
My Mum is working so hard to ensure my addmission into Boston Children's Hospital, MA, USA. She knocking every possible door to ask for help. So far, she has managed to raise around $720,000 USD!! Please Help my mum to raise remaining portion of my treatment cost.
PLEASE DONATE BY YOUR HEART via this campaign or Twisha's website http://twishamakwana.com/Donation.aspx
"Ocean is created with every single drop of water!" Any size donation is highly apprecaited.
To know more about me, Please google my name: "Twisha Makwana" Or visit my website: www.twishamakwana.com
Contact of my Mummy:
Ph: +61425147970 (Australia)
E: [email redacted]
FB: www.facebook.com/missiontwisha
Twitter: www.twitter.com/missiontwisha
Thank you,
Your little Twisha
