The Holloway Fund for Help and Hope was created to help individuals and families who have been impacted by FTD.
Our goal is to fund research and provide resources to lighten the burden of living with FTD and bring us closer to a future without this disease. My husband Lee was a gifted, brilliant pioneer in the technology industry and one of the founders of the security, performance, and reliability company Cloudflare. He was diagnosed with behavior variant FTD in April 2017.
Recently, the Holloway family’s story of Lee’s diagnosis was told in an article, “What Happened to Lee?” in the May 2020 issue of WIRED. AFTD also announced in a press release that Kristin joined the organization's Board of Directors effective April 2020.
Kristin and the Holloway family established this fund in 2019 to honor Lee's legacy.
Donations to this page will be designated 50 percent to AFTD’s support programs and 50 percent to research.
Click here to read more about the named fund.
About FTD
Frontotemporal degeneration (FTD) is the most common form of dementia for people under the age of 60. It strikes in the prime of life, gradually eroding an individual’s personality: their ability to speak, make sound decisions, control their movements, behave within social norms and relate to those they love. FTD devastates familial relationships, finances and even the health of family caregivers themselves. Currently there are no approved treatments, and most providers lack knowledge of appropriate care. Average life expectancy is 7-13 years after the start of symptoms.
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Thank you for visiting The Holloway Fund for Help and Hope in Honor of Lee Holloway.
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Donna Kobayssi donated A$505.00
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Judith Ranelli donated $50.50