Don’t miss our first LIVE expert roundtable discussion

Pour yourself a cup of coffee and join us LIVE on Friday, July 9th from 9:00 to 10:30 am, PST, (12:00 to 1:30 pm,...

Ionis Rare Disease Webinar series on Acromegaly

If you missed this fantastic event, here is an on-demand video you can watch at your leisure. In this second installment of the Ionis'...

How Cushing’s Disease Helped Shape Sharmyn’s Wonderful Life

On Cushing's Day, we share Sharmyn McGraw's blog on her journey with the disease. From her Blog - "Now twenty-one years in remission from a...

Celebrating 20 years of patient support at the Pacific Neuroscience Institute

The Pacific Neuroscience Institute is celebrating 20 years of their pituitary patient support group! Ever since April 2001, when the first meeting was held,...

A view of pituitary disease across the globe

From the desk of J D Faccinetti, co-founder - The World Alliance of Pituitary Organizations, WAPO is attempting to provide a world view of...

A muse for Rare Disease Day

From Jorge D Faccinetti, co-founder - Today is Rare Disease day. It is encouraging and gratifying to see the many organizations that participate by...

News from the California Center for Pituitary Disorders at UCSF

From our friends at UCSF: Read this great update with links to articles on telemedicine for patients with pituitary disorders, making surgery safer during the...

The unrecognized caveats of pituitary conditions

From Lewis S Blevins, Jr., M.D. - Today on Dr. Blevins' Corner: An elderly man underwent removal of the thyroid gland many years ago due...

Should we answer surveys, share our experiences, participate in drug trials, engage with others?

From J D Faccinetti co-founder - Unwanted surveys, polls, unsolicited robocalls, panels, emails, and text messages seem to be the order of the day,...

Looking Forward: A Time of Hope for Pituitary Patients

From the desk of Linda M. Rio, MA, MFT - Marriage and Family Therapists and PWN contributor - Hope, in such a year as unique as...

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