As Li-Fraumeni Syndrome Awareness Month approaches in March, we are gearing up for our fifth year of awarding LFS Hardship Grants on March 20th: LFS Awareness Day and Living LFS founder Jen Mallory's birthday!
We'll begin accepting applications for LFS Hardship Grants from eligible families and individuals on February 6th.
We are absolutely thrilled to announce a special matching gift opportunity:
An anonymous donor has generously agreed to match donations for LFS Hardship Grants, up to $40,000!
With your help, on March 20th we can award up to $80,000 in LFS Hardship Grants!
This money will provide much-needed relief and hope for people who are struggling with the myriad costs of life with LFS, which can be financially devastating:
- Extensive annual surveillance
- Costly out-of-pocket medical expenses
- Long distance travel to cancer centers for specialized treatment
- Living expenses during and after treatment
- Loss of income while caring for loved ones in treatment
This is an incredible opportunity to double your impact, and to make a significant difference in the lives of those with LFS who urgently need our help.
To ensure your donation is matched, please make your gift by March 6th, 2025.
Here's how you can contribute:
- Give at livinglfs.org/donate
- Donate to our Facebook fundraiser
- Mail a check to Living LFS, 4020 Greenmount Crossing Dr. #353, Shiloh, IL 62269 and write LFS Hardship Grants in the memo line
Living LFS, Inc. is a qualified 501(c)(3) tax-exempt organization, so your donations are tax-deductible to the full extent of the law. Living LFS' Federal Employer Identification Number (EIN) is 47-1326501.
On LFS Awareness Day, March 20, let's show the Li-Fraumeni syndrome community what we can do!
Please, donate today, and share this great news to anyone who can help us reach our goal.
Thank you for your compassion and your support!