Kathy Giusti
![Kathy Giusti](/assets/img/authors/unknown.jpg)
Kathy Giusti
Kathy Giustiis the Founder and Executive Chairman of the Multiple Myeloma Research Foundationand the Multiple Myeloma Research Consortium. In 1995, following her diagnosis with multiple myelomaat the age of 37, Giusti discovered that there was no research at all going on to create drugs for MM. Together with her twin sister, she founded the MMRF to fund innovative myeloma research and drug discovery...
NationalityAmerican
ProfessionActivist
CountryUnited States of America
cancers hope
I hope I can become a voice for all cancers and all patients.
approved both fda helped life multiple opened six span taken
In 15 years, we've raised $225 million, sequenced the myeloma genome, and opened 45 trials of 23 drugs - six approved by the FDA - which have doubled the life span of multiple myeloma patients. I've taken both Velcade and Revlimid, which we helped develop.
I always say, the greatest cost of leading is the cost of paving the way.
complex environment incredibly
Our healthcare environment is incredibly complex and is changing rapidly.
cancer family institute mom proud sister test time wait wonder
Every time I go back to the Dana-Farber Cancer Institute to wait for my test results, and I wonder if I've relapsed or if I'm doing okay, I don't think about my company. I'm proud of everything we've done, but at the end of the day, it comes back to family. I'm still a wife, a mom, a sister - all of those things.
accelerate mission
The most important thing a leader can do is set the vision and don't stray. We said, 'We are a research foundation. Our mission is to accelerate cures.'
cell fortunate needed stem
When I got really sick and needed a stem cell transplant, I was fortunate to have a twin sister as the donor.
although centers genetic including information massive mutations provide sequence technology valuable whether
Although not yet routine, many cancer centers have the technology to sequence some or all of a patient's cancer genome. This can provide massive amounts of valuable information about your cancer, including whether you have genetic mutations and other abnormalities for which new drugs are available.
academic access miss offered options rare treated treatment treatments
Being treated by a doctor who specializes in your kind of cancer is so important, especially for those of us who have rare or very rare cancers. They will have access to newer treatment options that may be offered only at big academic cancer centers, so you don't miss out on treatments that could help you.
despite diagnosed expects fact happen healthy men multiple otherwise rare surely three tom women
Despite the fact that one in every two men and one in every three women will be diagnosed with cancer in their lifetime, no one ever expects it to happen to them. I surely didn't. I was an otherwise healthy 37-year-old when I was diagnosed in 1996 with multiple myeloma, the same rare cancer Tom Brokaw has.
attract discovered funding knew money provide quickly raise scientists
I quickly discovered that scientists go where the funding is, so I knew I had to start a research foundation. If you don't raise money and provide research grants, you'll never attract scientists, and if scientists aren't working on a cure, there isn't going to be a cure.
cancer critically disease fact happy lose sight word
I'm happy to say that I am in remission. That R word is something critically important to cancer patients, especially in a disease like myeloma. But I never lose sight of the fact that there is another R word called relapse.
assume cherish gift gives learned seize
If I've learned anything, it's to live in the moment, and the gift that cancer gives you is, you just assume I'm only here today, and I am going to seize that moment and cherish it.