Reviewing politics
and culture since 1913

  1. Politics
  2. Health
9 February 2016

#Match4Lara: Lara has found her match, but the search for mixed-race donors isn’t over

A UK blood cancer charity has seen an “unprecedented spike” in donors from mixed race and ethnic minority backgrounds since the campaign started. 

By Barbara Speed

Lara Casalotti, the 24-year-old known round the world for her family’s race to find her a stem cell donor, has found her match. As long as all goes ahead as planned, she will undergo a transplant in March.

Casalotti was diagnosed with acute myeloid leukaemia in December, and doctors predicted that she would need a stem cell transplant by April. As I wrote a few weeks ago, her Thai-Italian heritage was a stumbling block, both thanks to biology (successful donors tend to fit your racial profile), and the fact that mixed-race people only make up around 3 per cent of international stem cell registries. The number of non-mixed minorities is also relatively low. 

That’s why Casalotti’s family launched a high profile campaign in the US, Thailand, Italy and the US to encourage more people – especially those from mixed or minority backgrounds – to register. It worked: the family estimates that upwards of 20,000 people have signed up through the campaign in less than a month.

Anthony Nolan, the blood cancer charity, also reported an “unprecedented spike” of donors from black, Asian, ethcnic minority or mixed race backgrounds. At certain points in the campaign over half of those signing up were from these groups, the highest proportion ever seen by the charity. 

Subscribe to the New Statesman today for only £1 a week.

Interestingly, it’s not particularly likely that the campaign found Casalotti her match. Patient confidentiality regulations protect the nationality and identity of the donor, but Emily Rosselli from Anthony Nolan tells me that most patients don’t find their donors through individual campaigns: 

 It’s usually unlikely that an individual finds their own match through their own campaign purely because there are tens of thousands of tissue types out there and hundreds of people around the world joining donor registers every day (which currently stand at 26 million).

Though we can’t know for sure, it’s more likely that Casalotti’s campaign will help scores of people from these backgrounds in future, as it has (and may continue to) increased donations from much-needed groups. To that end, the Match4Lara campaign is continuing: the family has said that drives and events over the next few weeks will go ahead. 

Select and enter your email address Your weekly guide to the best writing on ideas, politics, books and culture every Saturday. The best way to sign up for The Saturday Read is via saturdayread.substack.com The New Statesman's quick and essential guide to the news and politics of the day. The best way to sign up for Morning Call is via morningcall.substack.com
Visit our privacy Policy for more information about our services, how Progressive Media Investments may use, process and share your personal data, including information on your rights in respect of your personal data and how you can unsubscribe from future marketing communications.
THANK YOU

You can sign up to the registry in your country via the Match4Lara website here.

Content from our partners
Lives stuck in limbo
Rare Diseases: Closing the translation gap
Clinical leadership can drive better rare disease care

Subscribe
Notify of
0 Comments
Most Voted
Newest Oldest
Inline Feedbacks
View all comments