Nominate for Gentle Giant Award!
Do you have a pituitary HCP who has made a profound difference in your care or your life? A real “Gentle Giant”. We want to hear about them! Help us recognize the amazing professionals who go above and beyond by nominating your favorite doctor. Your story can help shine a light on the heroes in our community and inspire others on their journey. Submit your nomination today—we can’t wait to celebrate them with you!
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Patient’s Corner
Introducing Patient’s Corner, a place for you, the patient, to share your stories. If you have a story you would like to share please contact us below.
Patient story:
Panhypopit patient in a bind as Humatrope is discontinued
Tara Cummins, a pituitary patient in Klamath Falls, Oregon, says she’s at her wits’ end because the medication she depends on, Humatrope, is being discontinued by pharmaceutical giant Eli Lilly. Humatrope is Lilly’s version of somatropin, used to keep people like Cummins alive. Cummins suffers from panhypopituitarism, which developed after pituitary failure soon after a hysterectomy done in 1992 to counter painful recurring ovarian cysts. She also experienced pituitary failure.
Cummins has no health insurance because she makes too much to qualify for Medicaid and cannot afford to buy insurance on the individual market. In addition, when she had insurance, it didn’t cover the medication she needed. She sued the insurance company, saying, “Policies are allowed to be changed and modified to under-cover conditions or medications or exclude treatment for certain conditions. Early on after my settlement with the insurance company (where I still maintained my policy) they changed the terms of the policy, leaving me with a choice of having insurance but not coverage (or adequate coverage) for the somatropin which left me with out-of-pocket expenses that almost no one would be able to afford. With no insurance, I could qualify for patient assistance directly through the manufacturer. The term used was being under insured; as if I had any option to be more insured.”
So, Cummins has been paying for doctor visits on her own and she relies on Eli Lilly’s patient assistance program for free access to her medication: 1 mg each night. At age 63, it’ll be a little more than a year before the retiree qualifies for Medicare. In the past, she took Pfizer’s version of the medication, Genatropin, but Pfizer discontinued its patient assistance program two years ago, and the medication costs between $5,800 and $16,000 a month if you don’t have insurance.
Cummins says she hopes to get one more shipment from Eli Lilly, which would last her about four months. She says she’s been told that her life expectancy without the medication is about two years.
Complicating matters, Novo Nordisk’s Norditropin Flexpro subcutaneous solution for injection, is on shortage as of September. On ashp.com, the shortage is attributed “to increased demand and manufacturing delays.” The site notes that Ferring has Zomacton available; that Genentech discontinued Nutropin AQ Nuspin presentations in December 2024; that Pfizer has Genotropin available (but discontinued the patient assistance program); and that Sandoz has Omnitrope available.
In addition, Cummins had her thyroid removed and relies on natural thyroid medication. However, the FDA announced in August that it wants animal-derived thyroid medications off the market because they are not FDA approved and “contain many compounds that are uncharacterized for safety and effectiveness.” The FDA estimates that “1.5 million patients received prescriptions for these medications from U.S. outpatient retail pharmacies in 2024.”
PNA Spotlight: Dr. John Boockvar
This month the PNA Spotlight focuses on Dr. John Boockvar, vice chair in the Department of Neurosurgery and director of the Brain Tumor and Pituitary/Neuroendocrine Center at Lenox Hill Hospital in New York. He also serves as a professor of neurosurgery and otolaryngology/head and neck surgery at the Donald and Barbara Zucker School of Medicine at Hofstra/Northwell in New York. In addition, he directs the Laboratory for Brain Tumor Biology and Therapy at the Feinstein Institutes for Medical Research.
Dr. Boockvar did his undergraduate work at the University of Pennsylvania and followed in his father, grandfather, and great-grandfather’s footsteps to earn his medical degree from SUNY Brooklyn-Downstate Medical Center. He completed a surgical internship and neurosurgical residency at the Hospital of the University of Pennsylvania. He then did postdoctoral research training in neuro-oncology at the University of Pennsylvania Cancer Center, supported by the National Institutes of Health. He later served as professor of neurological surgery at Weill Cornell Medical College/New York-Presbyterian Hospital where he was co-director of neurosurgical oncology, head of the Laboratory for Translational Stem Cell Research and director of the Brain Tumor Research Group.
Dr. Boockvar was kind enough to answer a series of questions from the PNA. His answers follow.
Tell us about your educational journey. What stood out to you about each of the places where you spent time studying?
I did my undergraduate training at the University of Pennsylvania, and I think that’s where I was really taught neuro-psychopharmacology. There I met pharmacology professor Steve Fluharty, who really got me thinking about chemistry of the brain, pharma-therapeutics of the brain, and the blood-brain barrier. That was really impactful for me, as an undergraduate studying biology. Then I went to medical school at SUNY Downstate in Brooklyn. This was during the HIV AIDS epidemic in the early 90s, and so our hospitals were overrun with HIV/AIDS patients. It was really an incredible time to be a student, and to be hands on, battling one of the most dangerous, challenging diseases ever known. It instilled in us a strong work ethic that served us well decades later during the pandemic. We were well trained for that. I went back to Penn as a neurosurgery resident, where I fine-tuned my surgical acumen.
“When it comes to neurosurgery, the surgeons who train you become your mentors. You’re always a mosaic of the of the people that you trained under. “
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Pituitary Patient Toolkit
Seventh Edition - Now Available!
The Pituitary Patient Resource Guide Seventh Edition is now available! Be one of the first to have the most up-to-date information.
The Pituitary Patient Resource Guide a one of a kind publication intended as an invaluable source of information not only for patients but also their families, physicians, and all health care providers.
It contains information on symptoms, proper testing, how to get a diagnosis, and the treatment options that are available. It also includes Pituitary Network Association’s patient resource listings for expert medical care.
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