Announcement from the Child Neurology Foundation

On behalf of the CNF:
Applications for the 2017 Harnett Mini-Grant: Now Being Accepted

In January 2014, the Harnett Mini-Grant was founded by Mr. Michael Harnett, as an enduring memorial to his nephew, Brendan Michael Harnett.

Brendan was was diagnosed with infantile spasms and passed away before his first birthday.

Each year, CNF is proud to partner with the Harnett family in honoring Brendan through the offering of one $1000 grant to assist a family with a child diagnosed with infantile spasms. This grant can be used to pay for eligible expenses not covered by insurance.

Applications for the 2017 Harnett Mini-Grant are now being accepted through October 15, 2017.

The recipient family will be announced during Infantile Spasms Awareness Week (ISAW), December 1-7, 2017.
To learn more about this grant, click here.

Jessica Gladwell

Jessica Gladwell

Jessica Gladwell is one of PW's consultants and patient editors. She has lived with late-stage, chronic Lyme and POTS since circa 2002. She has also served as a caregiver to close family members with late-stage, chronic Lyme. Before diagnosis, she served as a business consultant for a large corporation and PM for a small digital branding agency. Now, she is proactive in the rare and neurological disease community, spreading awareness and advising on matters of health and lifestyle when living with a chronic illness.

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