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The Jayden DeLuca Foundation is proud 

to announce our

Patient Assistance Fund Program!

 

Click HERE to Download the Application

 

The Patient Assistance Fund is designed to assist families with children that have been diagnosed with Congenital Heart Defects (CHD). Individuals should document they are a member of a community area served by the Foundation.

**All applications require appropriate requested documentation.

Please submit PAID receipts with your application**

 

Financial assistance may include, but is not limited to:

  • Travel assistance related to CHD medical care
  • Medical bills related to CHD and not covered by insurance
  • CHD specialized equipment not covered by insurance

Applications are reviewed and awarded on a quarterly basis by a Third-Party Committee.

There is a reimbursement limit of  $1,000 per family, per awarding session. 

The third-party committee reserves the right to approve or deny applications as they deem appropriate.

Reimbursement applications are for travel and medical needs.

The terms of approval for applications are subject to change at any time.

Applications deadlines are as follows:

  • March 31st
  • June 30th
  • September 30th
  • December 31st

Submit all applications to: info@jaydendeluca.com

Or mail them to:

Jayden DeLuca Foundation

12639 W. Explorer Drive #140

Boise, Idaho 83713

 

Please review all Terms and Conditions from the application before submitting.

All applications require proper documentation as requested. 

The terms of the application are subject to change at any time. 

Click HERE to Download the Application

 

“Fifty years ago we would have known her heart was the problem but have not been able to repair it. Fifteen years ago the heart/lung bypass machine was not advanced enough and would have destroyed her kidneys during her surgery. It is only today, with all our medical advancements, that my baby could be ok. The words thankful do not even begin to describe how we feel.”

- Gracen’s Mom

“I wanted to thank you again for your gift. The money has already gone to good use. There was a patient from Idaho with PH that needed oxygen on the airplane and we could not get it funded, so we used Jayden’s fund to pay for it so the family could go home sooner. We have recently sent in 4 different pulmonary hypertension papers to medical journals on different aspects of PH in children.”

- Dr Dunbar Ivy,  The Children's Hospital - Denver, Colorado