This Diwali, are you really concern?

Hey Wait! You Serious?

You buying crackers for your kids & perceiving them safe? Fire can't be a source of amusement, it burns. 

I am not sure whether your child has ever given a thought to the history behind it, the significance of brightening, which source should brighten. Crackers? I am not sure too, if God likes it. Well, if it could have up to me, I would have run away. Onus is ours to handover the eternal grace & value of culture to upcoming. And a defile environment would never let you do this.

Come on, pay this perishable amount to someone like Twisha, here is the link:

http://www.souravraina.blogspot.in/2014/10/save-twisha.html 

Do it for her life & God would do it for you, and this cycle would make the world a better place. Isn't it?

I don't believe in lecturing you the hazardousness of every cracker you put on air, nor I feel doing so. But I wanna remember you that the most of the crackers your child gonna bust, are manufactured by children of his age. Child labour is worst than slavery!

Ample amount of Carbon Dioxide, Sulphur Dioxide, Carbon Monoxide, Potassium Chlorate we are going to breathe in next week. Hundreds would die, thousands would get injured, lakhs of birds & animals would suffer. 

&

PM would broom for us again to let the streets clean.

Happy Diwali !

Save Twisha

Twisha Makwana is three and half year old & the only child to her single mother. She is born with very rare birth defect isolated “Long Gap Oesophageal Atresia,” which prevents her to eat/feed by mouth. She had undergone around 20 operations (major & minor) to fix her isolated defect with no success. & had many close calls. Since then Twisha is given a spit fistula on her chest to drain her secretions/fake oral feed out and in getting her nutritious via Gastrostomy feeds.

Twisha needs true primary repair. She needs to get to Boston, MA, USA for her further medical Treatment.

In Boston there is a special clinic- Esophageal Atresia Treatment Clinic run by the Specialist Doctors and the team where they offer the world best treatment for the babies like Twisha.

They have invented a special technique named “Foker Procedure” to repair LGOA babies. In this procedure they stimulate the growth of missed Oesophagus by traction sutures. Baby is kept sedated and paralysed for couple of weeks/months. When both the ends of Oesophagus are grown long and come nearby like overlapping on each other, they are sewn together.

This Diwali, let us join together and save her life. Her mother is struggling hard to make 7.5 Crores for the treatment. Your little kindness can save her life, make Twisha & her mother smile.

Click here to donate:

http://www.twishamakwana.com/Donation.aspx

FB Page: https://www.facebook.com/missiontwisha

Contact:

Email: missiontwisha@gmail.com

Mo.: +61-425-147-970 (Sweety Makwana, Twisha's Mum in Australia)

Mo.: +91-9825323252 (Rasikbhai Darji, Sweety's Father in India)

Mo.: +91-9810570830 (Vandita Agrawal, Volunteer in India)

(Disclaimer- The post is just to support the cause and help her parents to raise the funds. I shall take it down immediately after they get enough funds)