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17th May 2020
Dear Donors,

As you are aware of my Baby's condition. We are taking her to Rainbow children hospital for check ups every alternate days which is costing us nearly 10k for medications. Right now, I'm withdrawing 75,000 from the campaign to use it for the same.

Thank you. 
Dear Donors,

As you are aware of my Baby's condition. We are taking her to Rainbow children hospital for check ups every alternate days which is costing us nearly 10k for medications. Right now, I'm withdrawing 75,000 from the campaign to use it for the same.

Thank you. 
5th May 2020
Dear Supporters,

My baby is again admitted in the hospital for the same cause. Its been more than 2 years we have been taking care of her by providing treatment at home with very fewer days of hospitalization; however, now again he condition gone worse, intestinal absorption and dis-motility factors come up again.

With my earnings and I was able to manage so far; however, with this episode of hospitalization facing very difficulty to continue with the treatment. Our parental-hood is stopping us say no to break the treatment and her innocence signs making us cry every minute.

She is been fighting since 4 years with the multiple surgeries and her body is full of needle pricks for the diagnosis and cannulas. We really don't know whats making her to fight with the rare disease and where is her life hanging.  

Regards,
Ravi
Dear Supporters,

My baby is again admitted in the hospital for the same cause. Its been more than 2 years we have been taking care of her by providing treatment at home with very fewer days of hospitalization; however, now again he condition gone worse, intestinal absorption and dis-motility factors come up again.

With my earnings and I was able to manage so far; however, with this episode of hospitalization facing very difficulty to continue with the treatment. Our parental-hood is stopping us say no to break the treatment and her innocence signs making us cry every minute.

She is been fighting since 4 years with the multiple surgeries and her body is full of needle pricks for the diagnosis and cannulas. We really don't know whats making her to fight with the rare disease and where is her life hanging.  

Regards,
Ravi
27th August 2019
Dear Supporters,

Once again I thank each and everyone for extending your support for my child's Mid-Gut disorder problem. As you all know she under went for 5 surgeries and its been more than 2 years for now after 5th surgery of Bishop-Loop ileostomy/Stoma (means one edge of the Large Intestine kept out with a bag to collect stools on regular basis and protect it from outer infections), we have been maintaining it and taking care of the clinical process at home with regular followup visits to Gastroenterologist and Surgeon.

Next step is to do another surgery to close the stoma; however, we are not able to take a decision now as she is slowly started recovering now. Though she is 3 years 7 months old now but still she looks like below 1 year kid. Per Neurologist there is a huge delay in the development due to lack of nutrition and hospitalization for long period (more than a year).

Now i am trying to manage all medical expenses with my earnings; still holding the further surgery part as doctors not able to give any guarantee and may or may not see the re-occurrence of the problem due to previous diagnosis. So, we are not able to take risk at this time. We are at-least quite happy that she is now able to recognize us and hopefully she will be bit more fit though it may take longer time than usual.

We would like to wait for few more months on her growth and other behavior and then think about next surgery part. Once again thank you all and will share you all with the further updates with development process.

Regards,
Ravi. V
Dear Supporters,

Once again I thank each and everyone for extending your support for my child's Mid-Gut disorder problem. As you all know she under went for 5 surgeries and its been more than 2 years for now after 5th surgery of Bishop-Loop ileostomy/Stoma (means one edge of the Large Intestine kept out with a bag to collect stools on regular basis and protect it from outer infections), we have been maintaining it and taking care of the clinical process at home with regular followup visits to Gastroenterologist and Surgeon.

Next step is to do another surgery to close the stoma; however, we are not able to take a decision now as she is slowly started recovering now. Though she is 3 years 7 months old now but still she looks like below 1 year kid. Per Neurologist there is a huge delay in the development due to lack of nutrition and hospitalization for long period (more than a year).

Now i am trying to manage all medical expenses with my earnings; still holding the further surgery part as doctors not able to give any guarantee and may or may not see the re-occurrence of the problem due to previous diagnosis. So, we are not able to take risk at this time. We are at-least quite happy that she is now able to recognize us and hopefully she will be bit more fit though it may take longer time than usual.

We would like to wait for few more months on her growth and other behavior and then think about next surgery part. Once again thank you all and will share you all with the further updates with development process.

Regards,
Ravi. V