6 Years Parineeth Needs Your Help To Fight Brainstem Glioma | Milaap
6 Years Parineeth Needs Your Help To Fight Brainstem Glioma
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Rs.39,73,833
of Rs.5,00,00,000
286 supporters
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    Created by

    Manja
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    This fundraiser will benefit

    Parineeth

    from Bengaluru, Karnataka

Thank you for taking the time to visit our page.

Parineeth is 6 years young and in Dec 2019, our world was shattered after learning that our beautiful boy has a rare and aggressive brain tumor (Pons Glioma).


My Family and Friends use to call Parineeth as born Cricketer, he not only loves playing Cricket and Kabaddi.


It is breaking our hearts to see our little boy continually deteriorate at a rapid rate and with no current available treatments here in India we are forced to look for help overseas. My wife and I are determined to do everything in our power to get our son the help and treatment he needs, unfortunately the cost of the clinical trials for CAR-T Cell alone commence at $330,000 USD (Rs. 2.5 crore INR) and that’s just the deposit, on top of this is our living expenses including air fares & accommodation in the USA along with further medical treatments in the USA if any complications arise during the trail.

Any funding received will enable the chance to get Parineeth onto this clinical trial, which at this point is his only hope of survival as it is specifically designed to target the type of brain tumor that Parineeth has been diagnosed with.


Parineeth’s story


One day before Christmas (Dec 24, 2019)  we noticed Parineeth eyes got squint and was losing his balance, slurred speech & drooling and was not able to do activities he would normally do with ease. His symptoms began to rapidly escalate so we went straight to the doctor. After assessing Parineeth, we rushed to the hospital where they preformed a number of tests and subsequently delivered the news that no parent should ever have to hear... Parineeth had Diffuse Intrinsic Pontine Glioma (DIPG) an extremely rare and aggressive childhood Cancer. Which kills about many Indian children a year, and has an average survival of just 9 months from diagnosis.

DIPG almost exclusively attacks our youngest (children under 12) and most vulnerable, who should have their whole lives ahead of them and there is currently no cure. Shockingly, despite all the advances in Cancer treatments, DIPG treatment is the same as it was 40 years ago. Due to its location in the brain stem surgery is not an option and there is little other than radiation, which is not overly successful.

Thankfully, over the last 18 months there have been promising advances in overseas clinical trials. There are two lines of therapy for which there is reasonable data indicating potential effectiveness. One is CAR-T Cell Therapy, the other is ONC201 neither of which is at present available in India. The CAR-T Cell trials are being carried out in Stanford and Seattle, the ONC201 trials are being carried out in a number of units including Cleveland Clinic.
ONC2O1 has been shown to induce tumor cells to selectively kill themselves, leading to a reduction in tumor size and prevention of tumor growth. Unfortunately, ONC201 and other similar trials are not yet available in India and will be some time away.. but with DIPG, time is limited and we don't have a day to waste. This tumor is savage... words can not describe how heart breaking it is to watch him decline in just a few weeks... From cricket and kabaddi with his me to stumbling, slurring his speech and needing regular sleep. We are determined to fight and give Parineeth every possible chance.

We have created this page with two things in mind- firstly, to give Parineeth his best chance of survival and quality of life by accessing these new drugs through overseas clinical trials or on a compassionate basis. This will be costly, but it is our hope. Secondly, we would like to donate any funds not required to improve Parineeth's prognosis and quality of life, to The Cure Starts Now, who carry out much needed research, that will help other children and their families combat this horrible disease.

We are forever grateful for any contribution you can make.

Thank you for your support.

Sincerely grateful

Praveen, Devishree & Parineeth



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