As the Hemophilia Foundation of Michigan celebrates 70 years, we are also celebrating the people who have helped shape our story, including Lynn Ray Allen, whose lifelong connection to HFM reflects community, compassion, and continuity.

“Perhaps it’s no coincidence that HFM and I entered the world the same year,” Lynn shared. “We are both now marking 70 years of service to the bleeding disorders community.” While his own father, John, served on the HFM Board, Lynn’s personal journey began as a camper during HFM’s second summer, followed by years as a counselor, board member, and Board President during a time of immense challenge, when many in the bleeding disorders community were lost to HIV/AIDS and Hepatitis. Lynn’s leadership helped HFM grow through challenge and change.

Now, four generations of Allens continue that legacy. Lynn’s daughter Torey, a former HFM staff member and associate camp director, attends Eagles Nest Family Camp with her husband and two daughters. Her sister Megan, once a camp manager, joins with her husband and two sons, including Calyx, who also lives with hemophilia.

“HFM has been a bedrock for my family for decades, particularly because of relationships and opportunities cultivated at camp,” Torey reflected. “We look forward to participating with HFM for decades more to come.”

As Lynn turns 70, his story reminds us that HFM’s strength comes from its people, those who grow, give back, and keep the spirit of community alive for generations to come.