Twisha Makwana a 3-year-old girl is suffering from a rare birth defect i.e. she is born without food pipe and hence can’t eat anything by mouth to stomach. Her mother, Sweety Makwana, injects formula milk directly into Twisha’s stomach to keep her alive. There is another tiny hole on Twisha’s chest from where she spits her saliva.
The mother’s heart dies every minute she sees those holes on Twisha’s tiny tender body, she sees her crying when Twisha gets feed via tube, when Twisha undergoes the painful dilation every second day, when she sees other children going to schools and learning the lessons of childhood which Twisha is devoid of, when Twisha is denied small happiness like playing in a park, when she sees that Twisha wants to eat her favourite chips but the fear of choking haunts and holds her back… Life is too harsh on her. She deserves to live a normal life…
Twisha has already undergone around 20 operations on her little fragile body in Sydney, Australia, which have been failed to cure her. There is a possibility to grow her own food pipe via Foker Treatment at Boston Children’s Hospital, USA. The cost of this treatment is estimated to be $1.2M USD, which is beyond her poor mother’s reach. Her courageous mother has managed to raise $750K USD so far. A determined mother is nearer to her mission to save her only daughter but still way short of the actual amount of funds needed for her daughter’s medical treatment.
If only 4000 People will donate 100$ each, Twisha will survive. Please donate generously to save Twisha. She is a brave little soul and with your support will survive to grow even stronger. Please DONATE via http://twishamakwana.com/help-her/donate-money/ For any query, you can contact her mother on +61425147970 or email [email protected] Please keep Twisha in your PRAYER to heal and cure her. You can also help her by SHARING this post as much as you can to expand needed help and support to Save Our Twisha.
Twisha is being raised like a normal child, but she doesn’t yet know of her deformity. She is in pain. She is in distress. Life throws daily challenges on her. She gets choked every now and then. But the brave girl keeps smiling. Please help her live, help her take on the world, help humanity…
Billionaires, celebs, CEOs from across the world took up the Ice Bucket Challenge to raise funds for ALS in 2014. Will they or will YOU come together to raise funds for Long Gap Oesophageal Atresia (LGOA)? Twisha’s mother has set up Mission Twisha to make people aware about LGOA, and help children born with this rare disease to get the best possible treatment available regardless of their race, creed and gender. While the NGO has been established to support a bigger cause, she wants to start with Twisha because if she fails today to save Twisha, she will never be able to save another.
Every Prayer Counts…
Every Cent Counts…
Sources:
http://www.ndtv.com/article/blog/my-3-year-old-daughter-needs-your-help-617843
http://www.indianlink.com.au/super-mum-sweety/
government and billionaire don’t really care, if they did they would have helped. A life is a life….they should do the operation for the pipe first and then the parents can pay the money in installments….but i guess people don’t really give a shit …all we want is money.
Anonymous. Are you in the hacking business.. or the money business?
option three.