THIS BLOD IS ALSO AVAILABLE AS AN AUDIOCAST ON SPOTIFY The second Wednesday in October is celebrated as Stem Cell Awareness Day. It's an event that CIRM has been part of since then Governor Arnold Schwarzenegger launched it back in 2008 saying: ”The discoveries being made today in our Golden State will have a great … Continue reading Celebrating Stem Cell Awareness Day
National Institutes of Health
Month of CIRM: Reviewing Review
Dr. Gil Sambrano, Vice President Portfolio & Review All this month we are using our blog and social media to highlight a new chapter in CIRM’s life, thanks to the voters approving Proposition 14. We are looking back at what we have done since we were created in 2004, and also looking forward to the … Continue reading Month of CIRM: Reviewing Review
Scientists Engineer Stem Cells to Fight HIV
Image of the virus that causes AIDS - courtesy NIH If that headline seems familiar it should. It came from an article in MIT Technology Review back in 2009. There have been many other headlines since then, all on the same subject, and yet here we are, in 2020, and still no cure for HIV/AIDS. … Continue reading Scientists Engineer Stem Cells to Fight HIV
Big time validation for early support
It’s not every day that a company and a concept that you helped support from the very beginning gets snapped up for $4.9 billion. But that’s what is happening with Forty Seven Inc. and their anti-cancer therapies. Gilead, another California company by the way, has announced it is buying Forty Seven Inc. for almost $5 … Continue reading Big time validation for early support
One family’s fight to save their son’s life, and how stem cells made it possible
CIRM's mission is very simple: to accelerate stem cell treatments to patients with unmet medical needs. Anne Klein's son, Everett, was a poster boy for that statement. Born with a fatal immune disorder Everett faced a bleak future. But Anne and husband Brian were not about to give up. The following story is one Anne … Continue reading One family’s fight to save their son’s life, and how stem cells made it possible
CIRM & NHLBI Create Landmark Agreement on Curing Sickle Cell Disease
CIRM Board approves first program eligible for co-funding under the agreement Adrienne Shapiro, co-founder of Axis Advocacy, with her daughter Marissa Cors, who has Sickle Cell Disease. Sickle Cell disease (SCD) is a painful, life-threatening blood disorder that affects around 100,000 people, mostly African Americans, in the US. Even with optimal medical care, SCD shortens … Continue reading CIRM & NHLBI Create Landmark Agreement on Curing Sickle Cell Disease
CIRM-funded medical research and development company does $150M deal to improve care for dialysis patients
Nearly half a million Americans with kidney disease are on dialysis, so it’s not surprising the CIRM Board had no hesitation, back in July 2016, in funding a program to make it easier and safer to get that life-saving therapy. That's why it’s gratifying to now hear that Humacyte, the company behind this new dialysis … Continue reading CIRM-funded medical research and development company does $150M deal to improve care for dialysis patients
Patient Advocate helps her son while helping others
A mother’s experience with severe combined immunodeficiency (SCID) is driving her work as a patient advocate on a CIRM-funded clinical trial—helping shape research that could transform treatment for children born with this rare, life-threatening immune disorder. A Personal Journey with SCID Anne Klein’s son, Everett, was diagnosed with SCID—often called “bubble baby disease”—shortly after birth through newborn … Continue reading Patient Advocate helps her son while helping others
A call to put the ‘public’ back in publication, and make stem cell research findings available to everyone
Thomas Gray probably wasn’t thinking about stem cell research when, in 1750 in his poem “Elegy in a Country Churchyard”, he wrote: “Full many a flower is born to blush unseen”. But a new study says that’s precisely what seems to happen to the findings of many stem cell clinical trials. They take place, but … Continue reading A call to put the ‘public’ back in publication, and make stem cell research findings available to everyone
Rare diseases are not so rare
It seems like a contradiction in terms to say that there are nearly 7,000 diseases, affecting 30 million people, that are considered rare in the US. But the definition of a rare disease is one that affects fewer than 200,000 people and the National Institutes of Health’s (NIH) Genetic and Rare Diseases Information Center (GARD) … Continue reading Rare diseases are not so rare