Vishvaraj Dighe needs your help to undergo treatment | Milaap
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Vishvaraj Dighe needs your help to undergo treatment

My name is Vinayak Dighe and I am here to fundraise for my son Vishvaraj Dighe.

Vishvaraj Dighe has been diagnosed with Wolman's Disease. But he needs to undergo Stem Cell Transplantation to fully recover. The cost of the treatment will be 2250000.

Please come forward to help me save my son. Any contribution will immensely help my family. I need your support to bring them home. Do contribute and share this campaign link with your friends and family.
Estimation letter
Estimation letter
Ask for an update
12th September 2019
Dear Supporters,

Thanks for all the love and support shown towards Vishvaraj.

We have an update to share with you today. Vishvaraj Dighe had phenotype and enzyme diagnosis of Wolman's Syndrome from Laboratory tests in India. The diagnosis of Wolman's Syndrome was not confirmed on Genetic Test. Further, enzyme tests performed in Manchester ruled out the diagnosis of Wolman's Syndrome. Hence he will not be requiring a transplant.

At Milaap, we release funds raised only against utilization for the intended purpose, supported by a treatment update from the doctor as well as bills and invoices given to us. Hence no funds have been transferred utilised for Vishvaraj.

We do understand that some of you may like a refund since the original purpose was not met. - 100% of your contribution will be refunded - please reply to this email by Thursday 19th September.

Alternatively, 

We are also sharing links to the fundraisers of two more children who are also in need of urgent support. You can also choose to direct your donations to one of these children:

https://milaap.org/fundraisers/help-geet-patil

Geet Patil is 9 years old and is suffering from Aplastic Anemia. She is in urgent need of a Bone Marrow Transplant to survive.

https://milaap.org/fundraisers/help-aarohi-mandal-1

Aarohi is the 5-year-old daughter of a farmer couple from a small village in Bengal and she is suffering from Blood Cancer. She too needs to undergo a Bone Marrow Transplant soon to survive.

Note: For donors seeking refunds to donations made via bank transfer or UPI to the account number and UPI ID mentioned on the campaign page, we would request you to share the account details with us by replying to this email or reaching out to us on feedback@milaap.org.

Thank you all once again for the support.

Regards,
Team Milaap
Dear Supporters,

Thanks for all the love and support shown towards Vishvaraj.

We have an update to share with you today. Vishvaraj Dighe had phenotype and enzyme diagnosis of Wolman's Syndrome from Laboratory tests in India. The diagnosis of Wolman's Syndrome was not confirmed on Genetic Test. Further, enzyme tests performed in Manchester ruled out the diagnosis of Wolman's Syndrome. Hence he will not be requiring a transplant.

At Milaap, we release funds raised only against utilization for the intended purpose, supported by a treatment update from the doctor as well as bills and invoices given to us. Hence no funds have been transferred utilised for Vishvaraj.

We do understand that some of you may like a refund since the original purpose was not met. - 100% of your contribution will be refunded - please reply to this email by Thursday 19th September.

Alternatively, 

We are also sharing links to the fundraisers of two more children who are also in need of urgent support. You can also choose to direct your donations to one of these children:

https://milaap.org/fundraisers/help-geet-patil

Geet Patil is 9 years old and is suffering from Aplastic Anemia. She is in urgent need of a Bone Marrow Transplant to survive.

https://milaap.org/fundraisers/help-aarohi-mandal-1

Aarohi is the 5-year-old daughter of a farmer couple from a small village in Bengal and she is suffering from Blood Cancer. She too needs to undergo a Bone Marrow Transplant soon to survive.

Note: For donors seeking refunds to donations made via bank transfer or UPI to the account number and UPI ID mentioned on the campaign page, we would request you to share the account details with us by replying to this email or reaching out to us on feedback@milaap.org.

Thank you all once again for the support.

Regards,
Team Milaap
24th April 2019
Dear Supporters,

Thank you for your support.

Vishvawaraj has a phenotype of Wolman’s disease. He was diagnosed as Wolman’s disease based on low acid lipase levels and hence was referred for transplant. However, genetic tests did not confirm the diagnosis of Wolman’s disease. I have therefore referred him to the gastroenterology referral team to reinvestiage him as the diagnosis is not clear.

Please keep supporting him.

Regards,
Dr. Prashant Hiwarkar
Dear Supporters,

Thank you for your support.

Vishvawaraj has a phenotype of Wolman’s disease. He was diagnosed as Wolman’s disease based on low acid lipase levels and hence was referred for transplant. However, genetic tests did not confirm the diagnosis of Wolman’s disease. I have therefore referred him to the gastroenterology referral team to reinvestiage him as the diagnosis is not clear.

Please keep supporting him.

Regards,
Dr. Prashant Hiwarkar
Content Disclaimer: The facts and opinions, expressed in this fundraiser page are those of the campaign organiser or users, and not Milaap.
Rs.0 raised

Goal: Rs.2,250,000

Beneficiary: Vishvaraj Dighe info_outline