SLC6A1 CONNECT SLC6A1 CONNECT IS A PATIENT ADVOCACY GROUP DEDICATED TO IMPROVING THE LIVES OF CHILDREN AND FAMILIES AFFECTED BY THE SLC6A1 MUTATION. OUR FOCUS IS TO RAISE AWARENESS AND FUNDRAISING TO ADVANCE SCIENTIFIC RESEARCH THAT WILL ULTIMATELY RESULT IN A CURE.
SLC6A1 CONNECT has received 21 grants from 16 known foundation funders. Revenue increased from $676,629 in 2023 to $716,694 in 2024. Most recent reported revenue: $716,694.
Annual Revenue
$716,694
Known Funders
16
Grants Received
21
Financial History
| Year | Revenue | Expenses | Assets |
|---|---|---|---|
| 2024 | $716,694 | $679,506 | $2,404,524 |
| 2023 | $676,629 | $1,264,542 | $2,299,269 |
| 2022 | $944,773 | $957,076 | $2,802,564 |
| 2021 | $984,255 | $482,756 | $2,783,114 |
| 2020 | $800,954 | $714,151 | $2,212,220 |
| 2019 | $2,176,855 | $71,569 | $2,224,812 |
Top Funders
DENVER, CO
Washington, DC
Washington, DC
Washington, DC
Mountain View, CA
JENKINTOWN, PA
ARVADA, CO
Denver, CO
Wilmington, DE
NEW YORK, NY
Showing top 10 of 16 funders.
Key Personnel
From 2024 IRS 990 filing
ANGELA MELKA
ADVISOR
GRETCHEN MCALISTER
FUNDRAISING CO-CHAIR
DR ANGELA MAZUR
ADVISOR
MICHAELLA GALLINA
ADVISOR
AMBER FREED
FOUNDER/CEO
KIMBERLY FRY
VICE PRESIDENT
CHANTAL PITTMAN
PATIENT ADVOCATE
KELSEY PIRO
SECRETARY/TREASURER
Frequently Asked Questions
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