David Mitchell has an incurable blood cancer called multiple myeloma. The price of his current drugs is more than $875,000 per year. Like millions of Americans, David needs innovation and new drugs to survive, but he believes drugs don’t work if people can’t afford them. After more than 30 years at a D.C. policy and communications firm, he retired in December 2016 to devote his full energy to helping change policy to lower prescription drug prices. Patients For Affordable Drugs mobilizes patients and allies at the federal and state levels and does not accept funding from any organizations that profit from the development or distribution of prescription drugs. It is one of our favorite organizations, and the only one of its kind on the Hill doing this work without the funding of big pharma. Leveraging the power of patient stories, P4AD works on a bipartisan level to create policy change in favor of reduced drug pricing and eased accessibility to necessary medications and treatments. Their work is remarkable, and we are proud to have their founder on the show!
Tune in as David shares:
how he was first diagnosed with multiple myeloma after experiencing severe back pain
that he’s been on maintenance drugs continuously for the past 10 years — and these drugs are what have kept him alive
that at the time of his diagnosis, the median age of survival for his form of cancer was 3-5 years; that has now increased to 8-10 years
that myeloma mutates and finds its way around drugs — so when treatments stop working, patients typically pass
that he plans to live to 95 and die of something else entirely
that the disadvantageous side-effects of his drugs are manageable in comparison to the cancer itself
how his wife stepped up as a fearless advocate for him until she herself endured breast cancer and its accompanying treatments (she’s a survivor!), and he stepped up for her
his belief that no cancer patient should endure the “acute” stages of diagnosis and treatment alone
the importance of looking after his physical and emotional health, and why it’s vital his work be meaningful
what P4AD does: how they help patients share their stories and are creating communities among these patients
that P4AD not only engages patients, but patients are also among their staff
that there is no free market for drugs, and that drug companies have created monopolies to set drug prices and protect those monopolies in whatever way they wish
that pharma invents groups akin to P4AD, including Patients Rising and the Alliance for Pharmaceutical Access
how insurance and drug companies monopolize pricing and gouge patients
where he sees the breakdown of the medical system in the US: that it’s systematically designed without the patient’s access to affordable, comprehensive care in mind
an acknowledgement of systemic racism in medicine
that he is also a recovering alcoholic — and has been for 30 years
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