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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. João Paulo Almeida, MD PhD
This month the PNA Spotlight focuses on Dr. João Paulo Almeida, the Robert L. Campbell Scholar in Neurological Surgery, Associate Professor of Clinical Neurological Surgery and Director of Skull Base and Pituitary Surgery at Indiana University/IU Health in Indianapolis. He earned his medical degree at the School of Medicine of the Universidade Federal do Ceará and completed his neurosurgery residency at State University of Campinas. He also trained at Toronto Western Hospital / University of Toronto as a clinical fellow in neuro-oncology and skull base surgery and cerebrovascular surgery. He then served as an advanced endoscopic and open skull base surgery fellow at Cleveland Clinic, in Cleveland, Ohio. He joined Mayo Clinic in Jacksonville, Florida in 2021, and came to Indiana University last year. Dr. Almeida answered a few questions from PNA. His answers are below.
Please tell us about your educational journey.
I was born and raised in Brazil. I did my original residency training in São Paulo, where I worked with a very well recognized team in microsurgery. In 2016, I came to the University of Toronto in Canada for a fellowship in skull base surgery. I spent two years with that group, and then I went to the Cleveland Clinic in Ohio for one additional year of fellowship. Then I returned to Toronto, and I spent one more year as a cerebral vascular fellow there. In 2021, I joined the Mayo Clinic in Jacksonville, Florida, where I stayed for three years as an assistant professor and associate surgeon. In November 2024, I came to Indiana to become the Robert Campbell associate professor of neurosurgery in the Department of Neurosurgery at Indiana University in Indianapolis. I am the director of skull base surgery for the Indiana University Skull Base program, and I am director of skull base programs for the Department of Neurosurgery, and the director of the micro neurosurgery at the Skull Base Laboratory here at Indiana University.
What led you to be interested in pituitary medicine, and who are your mentors?
I have been lucky to have multiple mentors. It all started when I was in medical school. Initially I was trying to find mentors to help me with research, and I was lucky enough to be in a hospital where Dr. Jackson Gondim practiced.
“I have been lucky to have multiple mentors. It all started when I was in medical school.”
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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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