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The Milla Goni Family Foundation is a private corporation based in CARLSBAD, CA. The foundation received its IRS ruling in 2020. It holds total assets of $2.6M. Annual income is reported at $534K. IN 2022, THE FOUNDATION CONTINUED ITS COLLABORATION WITH FIQUI PERU, UNDER THE "SUMANDO MANANAS" (ADDING TOMORROWS) PROJECT. DURING THIS THIRD YEAR, THE PROJECT OFFERED WORKSHOPS FOR PARENTS LED BY SPECIALISTS COVERING VERY IMPORTANT ASPECTS OF CYSTIC FIBROSIS (CF). IN ADDITION, THE PROJECT CONTINUED TO IDENTIFY NEWLY DIAGNOSED CF PATIENTS AND HELD INTERVIEWS WITH THEIR PARENTS TO HELP THEM UNDERSTAND WHAT CF IS, ITS IMPLICATIONS IN THE LIFE OF THEIR SON/DAUGHTER, AND THE FUTURE HANDLING AND TREATMENT REQUIRED, TO IMPROVE THE QUALITY AND LIFE EXPECTANCY OF THEIR CHILD. THESE PATIENTS WERE OFFERED ACCESS TO THE GENETIC STUDY NEEDED TO IDENTIFY THEIR SPECIFIC MUTATION(S), WHICH IS CRITICAL INFORMATION TO PLAN MEDICATION AND TREATMENT NEEDED BY EACH PATIENT. TOWARDS THE END OF 2021, THE PROJECT FUNDED THE VIRTUAL ATTENDANCE OF A TOTAL OF 20 PHYSICIANS WORKING WITH CF PATIENTS TO INTERNATIONAL CF CONFERENCES (NORTH AMERICAN CYSTIC FIBROSIS CONFERENCE IN NOVEMBER, (CONTINUED BELOW). Contributions to this foundation are tax-deductible.
THE FOUNDATION COLLABORATED WITH FIQUI, A NON-PROFIT ORGANIZATION IN PERU ON A PROGRAM TO IMPROVE THE DIAGNOSIS, TREATMENT, QUALITY OF LIFE AND LIFE EXPECTANCY OF PATIENTS WITH CYSTIC FIBROSIS IN PERU THROUGH TRAINING, EDUCATION AND AWARENESS. THE TRAINING COMPONENT WORKS WITH CAREGIVERS AND PATIENTS, GENERAL PRACTITIONERS/PEDIATRICIANS, SPECIALISTS IN CHARGE OF CYSTIC FIBROSIS PATIENTS AND PHYSICAL MEDICINE/REHABILITATION TECHNOLOGISTS TO ENSURE TIMELY DIAGNOSIS AND TREATMENT OF PATIENTS. A SOCIAL STUDY WILL ASSESS NEEDS OF CYSTIC FIBROSIS PATIENTS IN PERU IN ORDER TO IDENTIFY AREAS FOR FUTURE PROGRAMS.
Expenses: $60K
IN 2022, THE FOUNDATION CONTINUED ITS COLLABORATION WITH FIQUI PERU, UNDER THE "SUMANDO MANANAS" (ADDING TOMORROWS) PROJECT. DURING THIS THIRD YEAR, THE PROJECT OFFERED WORKSHOPS FOR PARENTS LED BY SPECIALISTS COVERING VERY IMPORTANT ASPECTS OF CYSTIC FIBROSIS (CF). IN ADDITION, THE PROJECT CONTINUED TO IDENTIFY NEWLY DIAGNOSED CF PATIENTS AND HELD INTERVIEWS WITH THEIR PARENTS TO HELP THEM UNDERSTAND WHAT CF IS, ITS IMPLICATIONS IN THE LIFE OF THEIR SON/DAUGHTER, AND THE FUTURE HANDLING AND TREATMENT REQUIRED, TO IMPROVE THE QUALITY AND LIFE EXPECTANCY OF THEIR CHILD. THESE PATIENTS WERE OFFERED ACCESS TO THE GENETIC STUDY NEEDED TO IDENTIFY THEIR SPECIFIC MUTATION(S), WHICH IS CRITICAL INFORMATION TO PLAN MEDICATION AND TREATMENT NEEDED BY EACH PATIENT. TOWARDS THE END OF 2021, THE PROJECT FUNDED THE VIRTUAL ATTENDANCE OF A TOTAL OF 20 PHYSICIANS WORKING WITH CF PATIENTS TO INTERNATIONAL CF CONFERENCES (NORTH AMERICAN CYSTIC FIBROSIS CONFERENCE IN NOVEMBER, (CONTINUED BELOW).
The Milla Goni Family Foundation typically selects its grantees rather than accepting unsolicited proposals.
The Milla Goni Family Foundation is headquartered in CARLSBAD, CA.
| Name | Title | Compensation | Benefits | Total |
|---|---|---|---|---|
| Alexandra Milla | DIRECTOR | $0 | $0 | $0 |
| Sebastian Milla | DIRECTOR | $0 | $0 | $0 |
| Maria Milla | SECRETARY & TREASURER | $0 | $0 | $0 |
| Marcos Milla | PRESIDENT | $0 | $0 | $0 |
Total Giving
$207K
Total Assets
$2.6M
Fair Market Value
$2.7M
Net Worth
$2.6M
Grants Paid
$0
Contributions
$0
Net Investment Income
$93K
Distribution Amount
$0
Total: $2.1M
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