In 2006, between tours of Iraq for NBC, Sabine tested positive for the expanded Huntington's gene. His father, uncle, half-brother and brother John, would all die of
Huntington's disease (HD). John, five years older than Charles, was, before he became symptomatic, an Oxford graduate and barrister in London. In interviews, Sabine has described why he then chose to use what remaining time he had, to switch battlefields from Baghdad to the one facing HD families due to unparalleled misrepresentation, discrimination and prejudice: “My neurologist said: ‘there is nothing you can do about this disease, just live your life as well as you can.’” Sabine relates. In the coming months, however, he realised that: “The neurologist was completely wrong. There is everything I can do about this disease. The problem, is finding the time to do it all.” Among keynote lectures across four continents, Sabine has spoken at the Royal Society, the European Parliament, the World Congress for Freedom of Scientific research, the Italian Senate, the Harvard Club, and the International School for Advanced Studies in Trieste (SISSA). Sabine has become one of the foremost lay opinions on the ethics of future scientific research.
Jennifer Doudna, Nobel Laureate and inventor of
CRSPR gene editing, closed her 2017 ‘TED’ treatise on the ethics of gene editing with a quote from Sabine: “Above all else, we must respect people’s freedom to choose their own genetic destiny and strive for healthier, happier lives ... As Charles Sabine … put it, “Anyone who has to actually face the reality of one of these diseases is not going to have a remote compunction about thinking that there is any moral issue at all.” Who are we to tell him otherwise?”.Sabine contributed to the drafting of the late Senator
Edward Kennedy's last act of legislation—the
Genetic Information Nondiscrimination Act ("GINA"), designed to protect the rights of individuals with genetic predispositions in the American workplace and in insurance. Sabine was an active lobbyist in the successful implementation of the UK's
Human Fertilisation and Embryology Act 2008. The 50th Anniversary of Canada's
Gairdner Foundation in 2009, attended by 22
Nobel Laureates, was marked by a debate between Sabine and Nobel Laureate
Sydney Brenner about the future of personalised
genomics. In 2009 he was the star guest at the Italian National
Telethon, for which a film about him was produced by
Rai Cinema. Sabine is a spokesperson for Huntington's disease lay associations around the world, among them: • USA:
Huntington's Disease Society of America • UK:
Huntington's Disease Association Sabine is a member of the Global Advisory Council of the International Society for
Stem Cell Research. Sabine is Consulting Publisher to the Huntington's disease research news web platform HDBuzz, founded by
Dr Jeff Carroll and
Dr Ed Wild. Featured in the 2013 documentary
Alive & Well, Sabine discusses his advocacy work to raise awareness of
Huntington's disease. Excerpts from Sabine speeches were used by James K Wright in his song "Spring in your Step". In her
2022 New Year Honours list, the Queen awarded the Most Excellent
Order of the British Empire (OBE) to Sabine, "Philanthropist and Global Campaigner, Huntington’s Disease for Charitable and Voluntary Services". The first time in history of such awards that the words 'Huntington's disease' have been used in a citation for an OBE. == Hidden No More ==